Shielding rights of persons with disabilities Author Mugambi Paul

The views expressed here are for the author and do not represent any agency or organization.

 Mugambi Paul is a public policy,  diversity,  inclusion and sustainability expert.

Australian Chief Minister Award winner

“excellence of making inclusion happen”

 

 

The COVID-19 pandemic has turned our everyday lives upside down. Recently, its impact on persons with disabilities has been felt in almost all spheres of life.

More barriers on inclusion have been identified by different studies by by individuals with disabilities, organizations of persons with disabilities, governments and also other stakeholders.

For many reasons, people with disabilities are among the groups most at risk in this pandemic. Their often compromised health status means they have a high risk of adverse outcomes if they get the virus; their need for personal care and support with everyday living makes it more difficult to take effective precautions such as social distancing; and, the well-documented inability of health systems to respond adequately to people with disabilities means health services will struggle to provide them with quality care during the pandemic.

People with intellectual disabilities in particular will find it difficult to understand what is happening during this time and are very susceptible to isolation and loneliness. For some, the restrictions on visitors to family or group homes, and limited access or support to use online technology, have meant little or no contact with friends and family for months.

The same story is affecting blind and vision impaired persons. Not even many are aware the proper wearing of masks. Most adverts are too visual thus rendering communication barrier.

 

Needless to say, the role of health services in Kenya is by the county governments.

This has seen had failed to quickly recognize and respond to the greater risks of COVID-19 on people with disabilities, leaving this community disproportionately affected by the pandemic. Early emergency plans focused on older people. In Kenya we are yet to see disability specific pans or even outlined measures by both national and county governments on disability corona response.

Additionally, in other jurisdiction we have seen development of disability advisory committees which is quite important in ensuring article 4 of the UNCRPd is implemented.

We hope soon we can have a disability telephone help line dedicated towards addressing the challenges.

Some silver lining has been seen in some nations on the reopening up of economies by provision of disability inclusive plans and actions.

Will African countries follow same way or we shall ensure protection of rights of persons with disabilities ins not achieved?

 

 

 

Why we must dismantle social ableism Author Mugambi paul.

The views expressed here are for the author and do not represent any agency or organization.

 Mugambi Paul is a public policy,  diversity,  inclusion and sustainability expert.

Australian Chief Minister Award winner

“excellence of making inclusion happen”

 

 

As COVID-19 has drastically changed the way we live and relate to one another, Kenyans with disabilities like me have been living in fear, not just of the virus, but of community attitudes to our lives and existence. The pandemic has brought to the forefront deeply ableist ideas held by our society that see disabled lives as disposable. Our lives are not worth living, and are not worthy of the same care and protection. Our deaths do not carry with them the same grief and sorrow that abled deaths do. We are casualties that must be accepted for the greater good of our economy.

This discourse has dangerously manifested in our hospitals, shaping COVID-19 triaging policies and the way medical professionals treat persons with disabilities– with or without the virus.

Globally, its evidently clear some nations they have   disregard for lives of persons with disabilities.

People with disability have been identified as particularly “vulnerable” to this potentially deadly illness. If only we all had the freedom to decide who, and how many people, we have contact with in our own homes.

.

For instance, president of South African President Cyril Ramaphosa has expressed sadness over the death of Nathaniel Julius, a teenager with Down syndrome, during a police operation.

 

I have been continually shocked and angered by triaging guidelines that override shared decision-making processes, fail to acknowledge disproportionate rates of disability amongst already oppressed communities – such as rural and slum dwellers.

I affirm due to the changing times I have had from senior leaders, journalists, business persons who believe we should position life to normalcy.

It’s okay – COVID only really kills old and disabled people. If you’re young, you’re strong and healthy and won’t be at risk. The people who die from COVID don’t really have a quality of life anyway. We really do need to open up the economy for the rest of us. With resources so scarce and hospitals overwhelmed we need to priorities those of us who would actually survive.

 

 

For many persons with disabilities, hospitals are already traumatic places where we are spoken over, invalidated and dehumanized. Frequently they are places that deprive us of care, brutalize our bodies and result in our death. How do we begin to confront the even more explicit violence in our healthcare system COVID has triggered? When I think about the not-so-distant future, and try to imagine how our disability community is coping, I am filled with anguish thinking of the scars these triaging narratives will leave. I think of the trauma being resurfaced for hundreds of thousands of disabled people who have already suffered mistreatment at the hands of healthcare systems, and I think of those persons with disabilities who would’ve survived COVID, had things been different. I vow to remember them and keep working towards a world grounded in disability justice, where no one is disposable and we can receive the care that we need. As Mpofunamba1 articulates in one of the music track attitudinal barriers do exist where women with disabilties are even questioned which animal impregnated you. As f women with disabilities are not supposed to enjoy sex and give birth. Several studies have shown increase of gender-based violence against persons with disabilities.

Based on a biased understanding of appearance, functioning and behavior, many consider disability a misfortune that make life not worth living. To promote the rights and dignity of persons with disabilities, we must dismantle social ableism and embrace disability as a positive aspect of the human experience.

The world’s population is ageing. By 2050, people over the age of 60 are expected to account for 21 per cent of the global population. About half of them will live with a disability, making this the largest community of persons with disabilities—and one of the most stigmatized and neglected.

The deprivation of liberty on the basis of disability is a human rights violation on a massive global scale. As Mpofunamba1 I say it is not a “necessary evil” but a consequence of the failure of States to ensure their obligations towards persons with disabilities.

 

 

 

Parents, You Matter!” Guest author Alison

The views expressed here are for the author and do not represent any agency or organization.

 

I have been thinking hard about how important a parent is in the life of a special needs child…

It’s been a while since I wrote anything about autism. It’s been a crazy season – being home, working from home, and helping the kids with their schoolwork, etc. There is something I have learnt during this season, though. Parents are very important. Parents matter. Parents are special people.

Parents, let me encourage you today.

You know your child better than anyone else

Picture this. You take your child for a therapy session, and they are crying all through. The therapist tells you that things will get better with time, but at the next session, things are the same. You try a few more sessions, and nothing changes. Then you start to notice that your child cries every time you are leaving for the therapist’s clinic, or every time the therapist is just about to get to your house for a session. At this point, you, as the parent, make an executive decision and stop the sessions. Why? Because you know your child best.

I have been there. I have had to make this decision several times. Initially, I felt that I should have tried just one more time, then I realized that it was up to me to make sure that my child was happy and at peace. Nobody else could have done it for me.

You communicate best with your child

Maybe your child is not yet speaking. Maybe you are longing to hear that first word. Can you tell, however, when your child is sad? Can you tell when he or she wants to have a meal or go to the bathroom? Most likely you can, especially when nobody else can tell what your child is trying to communicate.

How does this help? Imagine you go for a therapy session, and the therapist asks your child to do something. Your little one does not respond, and the therapist is stuck. You then offer to try and talk to your child, explaining the instructions. He or she quickly responds by doing what the therapist has asked. Do you see what I mean? Parents always know how to communicate with their kids.

Parents, don’t beat yourself up just because your child is not speaking. There are other ways that kids can communicate like sign language, using technology, writing, using pictures, etc. Find the best way to communicate with your child.

You want to help your child out of love

Nobody wants your child to acquire skills as much as you do. Nobody understands how important it is for your child to be independent like you do. Your love for your child is what drives you to hire therapists, follow the home program, buy equipment, etc.

You may, however, find that the people you hire to help your child are doing it for the money. Others may be doing their job just because it is a job, not because they love working with your child. The bottom line is, your love for your child is what will drive you to keep going, to keep learning, to keep training, and to keep waiting patiently for a skill to be mastered.

I just want to encourage a parent here. The world will not always accept our children for who they are. It is up to us to show them how to love children who are abled differently, and to show them that being different is not a bad thing. Also, surround yourself with like-minded people, people who will support you on your parenting journey, people who will love and accept your child just as they are, and people who may even offer to watch your child while you catch a breather!

You are your child’s greatest resource

Parents, you are your child’s greatest resource. You provide them with love and care. You make sure their environment is conducive to learning. You purchase all that they need for therapy, school, etc. You feed them and clothe them. You teach them the things that only a parent can. You pay for therapy sessions and school. Parents, you rock!

In this season when accessing services is hard, I believe that parents can still do something with their children. What have seen your therapist do that you can do at home? Find out what activities your child can do to improve in areas in which he or she has challenges. For example, if your therapist has mentioned fine motor skills in the past, look for videos with fine motor activities you can do at home. Also, for those who are doing teletherapy, it’s important to remember that a good session works best when you are there to help with setup, resources, etc. You can also opt to get a therapist to come up with a good home program for your child which you will implement.

See how important you are, dear parents?

One last thing, though. You need to recharge from time to time otherwise you will burn out. Find a way to catch a break whenever possible. You need it.

 

How Do Disabled People Feel About Discussing Their Disabilities? Guest author A Pulrang

The views expressed here are for the author and do not represent any agency or organization.

 

 

 

For people with disabilities, talking about our disabilities is complicated.

Sometimes, when people ask their perennial questions, or just look at us in a certain way, we can almost hear them say it:

“Go on! Do that thing you do, where you remind me how my own little problems aren’t so bad. Do that ‘inspiration’ thing that makes me feel better about myself for admiring you.”

What does it mean when a wheelchair user speaks at a political convention? What does it mean when a blind person gives a motivational speech, when an amputee engages students or employees on “disability awareness?” What does it mean when any disabled person, in the ordinary course of their day, is asked to explain their disability, or tell their disability “story?” And what does it mean when the disabled person tells their story? And what does it mean when they say, “No, not today. Not here. Not for you. I’m not here to be your inspiration.”

From a non-disabled point of view, it must sometimes seem like we disabled people can’t make up our minds. That’s because the whole subject is fraught with conflicting choices, each with pluses, minuses, and even moral implications.

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Do we raise awareness, or mind our own business? Do we welcome questions from the curious, or draw clear boundaries to guard our privacy. If we want a better world for disabled people, what is our own obligation to further that goal? Will we share our most profound experiences and thoughts about disability, and for what purpose — or whose?

Some of us are quite anxious to tell our stories to anyone who will listen. It can make us feel less alone with our burdens and traumas. Some of us draw strength and purpose from telling our stories of triumph over adversity, dispelling myths about disability, or advocating for better disability policies and political power for disabled people. Despite popular rhetoric about “not letting disability define us,” a great many of disabled people do organize much of our lives around our disability experiences and identity, and we do it intentionally, joyfully.

PROMOTED

At the same time, disabled people have mixed feelings about sharing our experiences with others. We all have different ideas about the pros and cons of sharing our stories, raising awareness, and “educating” non-disabled people about disability. And what we think about it can change from day to day, from person to person, and situation to situation.

To understand how disabled people struggle with these questions of sharing, educating, advocating, you need to explore some of the positives and negatives we juggle every day.

Positives

First, some disabled people find sharing their disability stories therapeutic. Many who were disabled later in life need to tell how they became disabled. And talking about our disabilities and everyday struggles with ableism can help all of us clarify how we feel about our disabilities.

While few of us like to admit it, many of us do in fact crave sympathy or at least empathy. Getting a positive, supportive response to our disability stories can be validating. It can, at least in the short term, compensate for some of the negativity and unvarnished prejudice we encounter regularly. And genuine empathy can actually make our lives easier by reducing misunderstandings and judgment.

There is also the practical benefit, or necessity, of sharing something about our disabilities in order to get help and accommodations that we need to survive, and that can help level the playing field for our ambitions. Having to reveal private information in order to obtain equal opportunity is a constant burr in our sides. But it is the most consistently beneficial payoff for this awkward exchange.

Finally, some of us choose to embrace being spokespeople of sorts for the disability community, and the cause of disability rights and justice. Some disabled people commit themselves to advocacy, motivational speaking, writing, and educating the public … all of which call for some degree or another of personal sharing. These commitments can give purpose to a disabled person’s life, if purpose is missing or uncertain. It can give meaning to a person’s disability, if meaning is important to them. For some of us, it’s also a living, and a potentially useful one.

The benefits available to disabled people for sharing our stories, experiences, and feelings are fairly familiar. It’s the negatives people tend to forget, but that are constantly on disabled people’s minds, precisely because they are so common and cut so deep so often.

Negatives

For a start, constantly retelling our disability stories can be a seductive trap. We tell it again and again, sometimes on request, or else in search of some resolution that never comes. We stagnate or worse, spiral further into depression and trauma. Also, other people’s curiosity about disability and disabled people’s stories tends to have a very short shelf-life. While they start out craving answers and compelling narratives, most people quickly get sick of them, especially if they fail to fascinate or uplift. Regardless, fixation on our own personal stories also makes it less likely that we will discover the broader disability community and disability issues, and that is a real loss.

Another problem is that many of us quickly come to realize how easily the visibility we craved for so long, and we finally seem to be getting, can be misused, no matter how carefully we craft our messages. As any disabled person who has addressed a political audience can attest, you never know just how much of your specific message gets through, and how much is drowned in a sea of sentimental responses to our very presence. Do audiences come away with a new understanding of health care, or home care, or accessibility? Or do they leave uplifted or amazed at how articulate the disabled speaker was, and how brave?

The most important thing to remember, but so many people miss, is that sharing our stories and educating people about disability always costs us something. The novelty of attention and praise eventually wears off, and you find yourself giving and giving, with little in return. Even if you are being paid … and far too many disabled public figures aren’t paid for what they give … sharing yourself, your passion, and your hopes with strangers takes a toll. And even the best audiences have little ability to give back.

Yet, disabled people are often expected to share our stories and enlighten others on disability matters … as if it’s our unique duty and special mission in life as people with disabilities. A calling is a personal choice. A duty is more of an imposition. A lot of people don’t understand the difference. On the personal level, friendly curiosity about our disabilities can quickly turn to sour resentment when we don’t immediately satisfy it. And demanding to be “educated” is often used as a “put up or shut up” answer to being called out for accessibility failures or other kinds of ableism. If we don’t agree to open ourselves up at all times and give free education, then ongoing ableism is implied to be our fault.

So, when is it okay, and when is it inappropriate to ask disabled people for their stories, or for help on disability issues?

Situations

Obviously, it depends partly on what kind of relationship you have with the disabled person. It’s rarely if ever appropriate to ask a disabled person you don’t know to tell their story, or explain intricacies of the disability experience to you. Asking a coworker or casual acquaintance may be alright, if you do it with care and listen for signs of receptiveness or reticence. You can deepen your relationship with family or close friends with disabilities, by inviting them to share deeper experiences and feelings. But this kind of closeness should never be mistaken for open-ended permission. Having a family or professional connection to disability isn’t a special permit to pry. Neither is having a disability yourself. A disabled person may trust you more if you’re disabled too,, but your disability status doesn’t guarantee access.

It also depends on the time and setting. Certain subjects and avenues of conversation are appropriate in some places and occasions, out of place in others, and totally bizarre or even creepy in still others. Think of how doctors and lawyers feel when people at cocktail parties ask them for medical or legal advice. It’s often like that for disabled people. We feel like everyone’s public encyclopedia of all things disability. No place is taboo, no subject off limits. At any moment, we can be prayed over in the frozen foods aisle, asked in a coffee shop how we have sex, or grilled in the lunchroom on which disability terminology we use.

If you want to engage with disabled people, and learn about disability issues and culture, that’s great! Please do both. But remember that each disabled person is an individual, and we each make our own decisions, using our own criteria, for when and how we want to share, explain, and educate others, from perfect strangers to those closest to us.

In the end, sorting the good from the bad, the appropriate from the burdensome, isn’t that complicated after all. It’s a bit like intimacy and consent. Talking about disability with disabled people can be enormously rewarding for both parties, but only when the disabled person is a willing participant. While some of us consciously choose to be as open and forthcoming as possible, none of us feels that way all of the time.

Above all, no disabled person should ever feel obligated to share, or shamed for not sharing. this is also my school of philosophy . as a Public policy diversity and inclusion expert I celebrate diversity in full.

Dream of Corona from a Disability lense Author Mugambi Paul

With the recent occurrence and high prevalence rate of Covid 2019 in Kenya having recorded over 32 thousand cases in August 22nd.

I wish to retaliate what front line soldiers and policy makers need to put in place to ensure those individuals with disabilities and those who are acquiring a disability in this period are well taken care of and granted the best of serf=vices.

 

The Kenyan health workers should

  • Know about people’s rights
  • Protect people’s rights

People should get the health care they need during coronavirus.

Convention on the Rights of Persons with Disabilities is a law that protects the rights of people with disability around the world.

The Convention is called the CRPD for short.

The CRPD says discrimination is never ok. CRPD says people with disability

  • Have the same rights as other people
  • Must be respected

The CRPD says people with disability have the right to

  • Be included in their community
  • Make their own decisions and

During a pandemic some rights are very important.

  • The right to life
  • Good health and health care
  • Information like Easy Read.
  • People with disabilities deserve to get treatment and medication just like other persons.

People with disability have the right to make choices about their health.

This includes having support to make choices. Supports include

  • Aids like a cane or wheelchair
  • Support workers or family

Communication:

People disability have the right to communicate how they choose.

  • Kenyan sign language
  • Braille
  • Easy Read

Plain language.

Last to be served last one to eat: Author Mugambi paul

The views expressed here are for the author and do not represent any agency or organization.

 Mugambi Paul is a public policy,  diversity,  inclusion and sustainability expert.

Australian Chief Minister Award winner

“excellence of making inclusion happen”

Globally, Evidence is emerging that persons with disabilities are being disproportionately affected by the Coronavirus pandemic and emergency policy measures being undertaken are not enough.

This is to say the marginalization that existed before covid is still being multiplied and increased due to lack of inclusive disability response starting from the world health organization and the governments.

 

The COVID-19 crisis is taking a grim toll on human lives across the globe. Although the complete impact is yet to be fully comprehended. The coronavirus pandemic has changed almost every aspect of normal life, from grocery shopping to work, from exercising to socialising. While the changes, brought on by fear of infection and the state-mandated quarantine –– which has been in place in Kenya since March 20 –– are difficult and inconvenient for everyone, for those living with disabilities across Kenya, the virus crisis has posed a unique threat to their ability to access basic healthcare, education and to their own individual autonomy. 

 the risk the pandemic

is exposing for gains made towards the Sustainable Development Goals (SDGs) is becoming evident. What this global emergency is also revealing, is that

these 17 goals are, in fact, our best option to recover better and to overcome similar crises in the future.  

Policy statements need to manifest in concrete action.

In other words, inclusion and empowerment of persons with disabilities is essential to ensuring that persons with disabilities are not left behind.

 

 

 As governments rush to respond to the virus, it is more critical than ever to guarantee that measures taken are fully inclusive.

 

 

of persons with disabilities and prevent human rights violations from taking place. More importantly several studies from the UN body, research institutions, disability sector, individual testimonies and government have shown no disability desegregated data has been recorded up to date. Disability is prevalent throughout Kenyan society, though that prevalence isn’t always represented in policy-making. No less than 15. 10 percent of the population of Kenya lives with a permanent difficulty or limitation, according to organization of persons with disabilities data.

 Additionally, disability is present in 2.2 percent of Kenyan households, according to official data of KBs 2019 census. 

 

 

As a public policy scholar am yet to understand why governments are able to give geographical location, gender age and not disability desegregated data !

Is this not a form of exclusion?

At least 70,000 Americans with disabilities have died in the last 120 days without being on the radar. Those in nursing homes are referred to as ‘elderly,’

with ‘underlying conditions,’ or ‘vulnerable.’ These are euphemisms that avoid using the word “disability”. This diminishes and ignores civil rights protections

for millions.

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Policy makers need to realize that when persons with disabilities are not being counted, they are being locked out of interventions.

The distribution of the cake needs to be served in an inclusive manner.

 

For many countries in Africa they have formed emergency response committees with uyt representation of persons with disabilities.

Should disability persons organization publish experts with disabilties since governments have failed to ensure representation?

Persons with disabilities in low income countries face substantial challenges in terms of achieving self-representation,[1] inclusive employment[2] and integrated education.[3] The Convention on the Rights of Persons with Disabilities (CRPD)[4] outlines a framework for the inclusion and self-advocacy of persons with disabilities, while the Sustainable Development Goals (SDGs) commit to ensure that global development processes are disability inclusive.

 

 

 

Moreover, several general protocols have been made but without any reference on how interventions will be carried out for persons with disabilities.

Additionally, after 4 months of COVID  2019 several countries have started to some sort of disability protocols, of which they contain minor concerns of persons with impairments.

 

Its only south Africa who have made major attempt of having disability inclusive response protocols and interventions.

Obviously, this is a step in the right direction but more needs to be done to ensure no one is left behind.

Likewise, in other countries like in Kenya having sign language interpretor on the TV screen during the Corona state address seem to be an already concluded assumption that they have addressed the communication and inaccessible information gaps.

Does this mean that all persons with disabilities have accessed the information?

the Kenyan social protection policies seem to be driven ‘smoothing

out’ variations in incomes over the lifecycle, I argue  that ‘the dominant effect

of social spending in the Kenya is to redistribute income across people’s own life. For example the recently launched “Kazi kwa mtaa programme”

aids citizens to pay taxes of what they have.

 

The policy brief offers 4 recommendations on how governments can best mitigate the economic fallout of the COVID-19 crisis and protect informal workers:

list of 4 items

  • Continuing emergency income support for workers and businesses operating in the informal economy 
  • Reforming social-assistance schemes to extend beyond the poor—both horizontally and vertically—to ensure that the “missing middle” will have access to

them

  • Ensuring that social-assistance measures are a part of a larger relief package and include loan repayments, rent and utilities payments, and tax breaks

on essential goods

  • Safeguarding women’s access to these benefits

list end

On the other hand, In the book Good Times, Bad Times challenges popular misconceptions about the welfare state

. The book deconstructs the view that ‘welfare’ is exclusively

about out-of-work benefits and that those who are in receipt of such benefits are

somehow ‘other’ to the rest of ‘working Britain’ (a term favored by our current

political leaders). Hills challenges these misconceptions with detailed evidence

demonstrating that in fact we all benefit from the welfare state over the life-course,

getting back what we put into the system. The welfare system in Kenya and most African countries

covers universal entitlements such as education, health care, pension provision, and

youth protection except for the very wealthy), and as such it is something that all of us

make use of at varying points in our lives: when we have children; when we become

unwell; when we need healthcare; and when we grow old.

Hills explains that whilst the welfare system is redistributive (poorer households

do get more out of the system and richer households put more in), the system is

also redistributive for individuals over the span of their own lives – so effectively

he argues that we are all paying for own services and benefits in a kind of ‘savings

bank’ (67). This is the case for all families, with even the poorest 10th of the population

paying in half of what they take out. The rich contribute more because of

the principles that the system was founded on: that benefits and services should go

to people according to their need (as opposed to whether they can pay for it); and

that the taxes we pay should be in proportion to our incomes.

 

In the COVID-19 pandemic, persons with disabilities may face heightened risks, such as increased exposure rates, due to numerous barriers in the humanitarian response. For example, barriers in accessing life-saving information, protective measures and other essential humanitarian services on an equal basis with others. Gaps in the preparedness and response plans increase these risks even further. 

As we hurtle towards the 2030 Sustainable Development Goals deadline, governments are accelerating investments in both social protection and disability and gender equality. This presents

an opportunity to gain a deeper understanding of how social protection can not only reduce poverty, but also contribute to disability mainstreaming. Disability mainstreaming is

vital to achieve sustainable poverty reduction through social protection. In turn, poverty reduction, for instance, through greater income equality and

security provided through well-designed social protection promotes disability inclusion.  

Social protection, particularly in the form of cash benefits, has already proven its ability to 

address multi-dimensional and intergenerational poverty for persons with disabilities of particular are men, boys, women and girls with disabilities

 in different contexts, including increasing women’s savings and investments in productive assets or improving girls’ school enrolment and attendance. Yet, this

potential can also be belied if programmes are poorly designed or executed, resulting in further entrenching prevailing gender inequalities. More needs

to be done to understand how and why programme design and implementation can either strengthen or worsen impacts for women and girls.  

  1. All means all! we cannot have proper digital inclusion if we leave people behind;
  2. We need stronger connections between schools, families and students because connections lead to commitment

list end

 

       

What lessons can African nations learn?

We need to activate disability emergency mode when the glbe is doingit not just to react after the race has already kicked off.

We may have lost many persons with disabilties either through hunger, loneliness, lack of health services, covid itself and other preexisting conditions.

Organizations of persons with disabilities need to ensure duty bearers accountable to them and if need be seeking legal address. For instance. 

Over 1,000 web accessibility lawsuits have been filed in 2018.

Companies like Nike and Amazon are being sued for failing to make their content accessible to deaf, hard of hearing, blind, and low vision users.

       

Conclusion:               

Covid19 has created new societal challenges and exacerbated existing ones however plethis is also an opportunity to rebuild our society in a more equitable

Corona 2019 why did you’ve it imprison the blind? Author Mugambi paul

The views expressed here are for the author and do not represent any agency or organization.

 Mugambi Paul is a public policy,  diversity,  inclusion and sustainability expert.

Australian Chief Minister Award winner

“excellence of making inclusion happen”

 

 

 

As a blind person for the past 23 years, I thought I had seen it all! Oh boy, was I ever wrong! After many years of practice at being blind, I have found something that is sending me for a loop.

COVID-19 has done it to me!

My world now is cold, untouchable, lonely at times–which is something hard to handle. I am not so sure I could survive the new world we are all experiencing if I did not believe that my “Heavenly Father” would not be here to catch me when I fall.

Going for a walk, if anyone is passing me by, I’m always wondering if they will possibly get me sick. Going to a market or moll and trying to get assistance, while everyone wants to run away from you. No getting together with friends because no one wants to come and visit, scared we pass the virus to one another. Walking onto a bus and being scared that the person who previously occupied the seat you are now at had the virus.

Or, a simple walk in a park and getting lost because all the roads have no traffic to give me a sense of direction. Yes, to me, this was probably one of the hardest things to handle. My world is open when I have sounds of traffic or sound barriers to help me to be able to be independent daily.

My rural places like playing fields and parks is a place I have known for the past 23 years and I am very used to going there. Now this park and field of play is very different for someone who has no sight. No children in the playground, nobody bringing the dogs to the park, no one bringing me coffee and conversation, and no cars to give me direction as to where the roads are.

The world I knew had familiar sounds to help give me direction, and this I knew was a world that was easier to deal with in my daily life. I also use a white cane and now people are scared. Put jump very first since thy know viruses can spend time on metallic objects. How does a blind person keep social distance from a sighted guide?

 

 

I also have had others say that many in the markets get upset when I use the white cane.

Now I can honestly say that the world as a blind person is hard to cope with! If I did not live in a house with a yard and with a great garden to take care of and give me joy, my world would have been lonely and hard to handle for the foreseeable future.

Meetings online may give me many hours of involvement with my community, but the time spent on electronics is starting to drive me crazy.

I love to attend meetings in person and the opportunity they provide to get to know others and how they are engaged in our community. Now this opportunity is also lost, and I find that the computer does not bring the same spirit into my daily routines.

So, for all of these reasons, “blindness” has imprisoned me again. But this time it feels like I have moved from a minimum-security prison to a maximum-security one.

Disabilities that Complicate Substance Abuse Treatment and How to Overcome Them Guest author Patrick Bailey

The views expressed here are for the author and do not represent any agency or organization.

 

The last thing a person recovering from alcohol addiction needs is yet another obstacle to getting back to the life they know and love. Well-managed inpatient drug and alcohol treatment centers should ensure a physical disability does not impede full recovery.

Disabilities and Substance Abuse

People who suffer from physical disabilities have a higher risk of alcohol and drug abuse. The National Rehabilitation Information Center (NARIC) shows that about half of Americans who suffer from a disability are also likely to suffer from substance abuse (co-occurring disorders or dual diagnosis). That’s compared to 10% of the general public.

Disabled World reports that those with mobility issues—disabilities like amputated limbs, spinal cord injuries, orthopedic disability, arthritis, deafness, vision impairment, or multiple sclerosis—are two to four times more likely to abuse drugs or alcohol.

Yet an anonymous survey reveals that of those suffering from a spinal cord injury or traumatic brain injury (TBI) and also seeking addiction treatment, about half are refused admission to inpatient drug and alcohol treatment centers.

A report from the American Association on Health and Disability (AAHD) shows that physical accessibility negatively impacts the success of treatment for those with disabilities every day.

According to the Centers for Disease Control and Prevention (CDC), one in five American adults has a disability. Most worrisome for those in an inpatient facility are mobility and visual or auditory challenges that prevent them from taking full advantage of the treatment offered them.

Alcohol and drug abuse can complicate treatment for the physically disabled by interfering with therapy, rehabilitation, counseling sessions, and medications.

Overcoming Barriers to Treatment

For this reason, a physically accessible treatment center is essential to those who have both physical limitations and addiction challenges.

Group therapy and support groups can dispel social isolation and offer a healing environment for both those who suffer from addiction and their families. However, an additional layer of support is required for those with an additional disability.

Inpatient drug and alcohol treatment centers can offset this by removing or altering potential barriers to their disabled clients.

The Americans with Disabilities Act (ADA) requires that all private accommodations and commercial facilities that are not residential facilities remove barriers to communication and access that would negatively affect individuals who are disabled.

For this reason and others, a viable treatment facility must accommodate those who are disabled, ensuring they have complete access to the facility.

Making Rehab Accessible

Three factors that can affect a person’s ability to function:

  • A person’s mental, emotional, and/or physical state doesn’t function properly. This can include hearing or memory loss.
  • Activity limitations. Inability to carry out normal tasks.
  • Participation restrictions. A person who cannot participate fully, or not at all, in daily life activities because of their limits. This impacts the way the individual engages in work, social, recreational, or health-related activities that are critical for their health and well-being.

Some of the modifications needed for the disabled include:

  • Ramps and elevators that offer mobility-specific features.
  • Wider doors and hallways for those in wheelchairs or other mobility devices.
  • Power-assisted doors.
  • Even, slip-proof floors.
  • Prominently displayed braille and other sensory navigational features.
  • TTY options on phones for the hearing impaired.

Other Physical Disabilities

Physical disabilities are not confined to one’s ability to walk without aid. They may result from a birth defect, an accident, a disease, or age. Anything that prevents or diminishes a person’s ability to engage in social activities is a disability

Physical disability includes chronic health conditions that prevent a person from participating fully in their day-to-day life. This includes a variety of autoimmune diseases. Some diseases can become a secondary disability that must be considered in one’s drug or alcohol rehab.

Examples include:

  • Asthma
  • Allergies (environmental and food)
  • Crohn’s disease
  • Irritable bowel syndrome (IBS)
  • Ulcerative colitis
  • Diabetes
  • Migraine headaches
  • Cerebral palsy (CP)
  • Cystic fibrosis
  • Epilepsy
  • Fibromyalgia
  • Multiple sclerosis
  • Rheumatoid arthritis
  • Spina bifida
  • Spinal cord injuries
  • Loss of a limb
  • Traumatic brain injury
  • Cancer
  • Lupus
  • Sickle cell anemia

Learning Disabilities

The best inpatient drug and alcohol treatment centers also make accommodations for clients with learning, sensory, and mental disorders.

A learning disability alters the way a person can listen, speak, read, spell, and/or think. Such a disability impedes a person’s ability to process, recall, and/or express information.

Clients with memory problems often have trouble communicating and have a hard time performing school or job-related tasks.

Chronic health conditions such as physical disabilities are risk factors on their own. Add to that a substance abuse problem and removing as many barriers as possible is essential.

Will the “Disabled” Kenyans cry foul after being left in Coronavirus conversations? Author Mugambi Paul

In order not to live the disabled Kenyans who are the largest minority, who make up 15 % of the population.
I opine, disabled Kenyans they deserve not to be left behind.
There is an urgent need for Ministry of health in Kenya to address the rights and needs of disabled person throughout all COVID-19 planning and response.
In other words, for maximum community results in the recent updates from the national and county governments there is the need to close the glaring gap of inclusivity.

Available facts:
Children and adults with disabilities and older adults are 2-4 times more likely to be injured or die in a disaster due to a lack of planning, accessibility, and accommodation. Most people with disabilities are not inherently at a greater risk for contracting COVID-19, despite misconception that all people with disabilities have acute medical problems.
Kenyan government Actions taken now can make a big difference in COVID-19 outcomes
Additionally, the disability sector from both the state and non state actors need to raise the voice not just to remain mum.
Are disabled persons represented at the national emergency committee established by the president?
Are the needs of the disabled catered for in the contingency plans?

Lessons learnt:
One of the greatest lessons in the fight of HIV aids in Kenya is that the disabled persons were not involved nor consulted in the plans strategies for combating the menace.
It took few disability stakeholders to get the national aids control council to ensure inclusivity is realized.
When shall the disabled stakeholders learn not to be left behind?
Should the disability society be involved after the rest of the population? we
Moreover, USAID was very critical in supporting disabled stakeholders in achieving active disability engagements.
Worst still, many disabled persons weren’t aware of how to prevent themselves from the HIV AIDS infection. Many disabled Kenyans died, and many being taken advantage of by the society perceptions and behaviours [HI 2007]
This is because of the late response to the needs of disabled persons.
Several studies showed the greater involved of disabled Kenyans in awareness, contributed to reduction of stigma and discrimination associated with disability and HIV aids.
It also ensured representation in National aids committees, and prevention promoted reduction of spread of the disease. [NACC 2008, Liverpool 2007 HI 2007[.

Role of the disability sector:
Needless to say, disability stakeholders can play a crucial role by facilitating support to the ministry of health on inclusive strategies which will address the needs of the disabled Kenyans.

Legal Obligations and Training
On the other hand, Public and private agencies that provide services to persons with disabilities must be aware of their legal obligations and must train their employees appropriately. When public and private agencies and businesses are unclear about their legal responsibilities, there are no limitations in providing greater than minimum levels of support and services to persons with disabilities. Lack of understanding is NEVER an acceptable reason for failing to meet legal obligations, including throughout emergency circumstances.
Furthermore, the ministry of health has a has a legal obligation to provide equal access to public health emergency services to disabled Kenyans, including throughout a pandemic since our president issued an executive order
Coupled with the support one of the pillars of the big 4 agenda, of Kenyan 2010 constitution on right to access to health services and international conventions.

Needs of disabled Kenyans:

I observe disabled Kenyans require the same resources and assistance that all citizens deserve.
in other words, adequate information and instructions, social and medical services, and protection from infection by those who might contracted the virus. However, some disabled Kenyans may have needs that warrant specific reasonable accommodation by the public and private sectors that may not be necessary for Kenyans without disabilities. This is not much to ask since the current strategies by both national and county governments have not addressed the reasonable accommodations.

For instance, Communications Authority has approved sending of bulk information messages on coronavirus by the Ministry of Health to all subscribers of local mobile phone operators.
I beg to ask:
Are persons with intellectual impairment, Deaf, Blind, psychosocial disabilities able to consume this information?
1. Can the government provide alternative formats of communication in awareness raising? Disabled Kenyans need to be informed of why Ministry of health believe that certain actions are warranted, to be given an opportunity to ask questions and receive answers in an accessible format, and to be afforded the opportunity to object and propose alternative solutions.
2. Another example, the Bagathi hospital has been designated to be the official self-quarantine place.
Has it met accessibility standards?
Are the beds easily accessible and user friendly to Kenyans with mobility impairments?
Moreover, in some places, the distribution of protective equipment, food, and medical supplies might be warranted. If Point of Distribution locations are established, government and private stakeholders must address how these supplies and equipment will be distributed and accessed by disabled Kenyans, elderly and others who have difficulties in movement and lack means of travel. Disabled Kenyans have the right to receive services in the most integrated setting appropriate to their needs.
All in all, the existing legal protections of disabled Kenyans remain in effect under all circumstances. These protections are not subject to waivers or exceptions, even during public health emergencies or declared pandemics.
I Hope there will be no contrition on this journey of ensuring disabled become part of the solutions.

The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy, diversity, inclusion and sustainability expert.

Celebrating our super parents: Guest Author Odumbe Kute

It occurred to me yesterday after something I posted that prejudice and discrimination, whether conscious or sub-conscious is a very big deal in our lives.
I’ve been a disability and human rights activist for over 24 years and the one thing that rings true through all the work I’ve done around the world is
this. No amount of legislation, education and advocacy will ever cover for ignorance and prejudice about disability that is experienced every single day
by those affected.

It’s not just the general public. The worst offenders are family, close relatives and people who masquerade as friends. The thing is this. Most people
act the way they do, discriminate like they do, judge like they do, say really stupid and very hurtful things like they do, gossip like they do, show their
prejudice like they do because they’re afraid. You’d like to think that they’re just ignorant, but the truth is that they’re afraid. Afraid of what is
different, afraid of their own insecurities, afraid of how they would cope if they were ever in a situation where they would acquire a disability, give
birth to a child with a disability, have a spouse who acquires a disability or have to care for someone with a disability.

They go around calling themselves “normal”, whatever the hell that is. Here’s a wake up call. At least 1 of every 5 people in the world has a disability
of some sort, most of them hidden and not visible to people. It could be mental health, it could be chronic back pain, it could be sickle cell, it could
be a neurological condition ranging from autism to ADHD, it could be any number of debilitating conditions that people are shit scared to talk about for
fear that they might get labelled or judged. They refuse to look at it as a disability. They only choose to consider disability as a physical and medical
thing.

I haven’t even begun to talk about the hundreds of thousands of parents who have a differently abled child. Our society is brutal. Take the mothers of
kids with a disability from autism to CP, from physical to sensory disabilities. Those who stay in relationships and marriages after giving birth to a
differently abled child are considered the lucky ones. But are they really? Most mothers of children with a disability are single because they’ve been
abandoned at the traffic lights. They’ve been ostracized and become outcasts in their own families, in their marital families, amongst their friends and
relatives. They are seen as vessels of witchcraft, accused of bringing forth defective offspring that sully the gene pool of the family. They not only
have to deal with the challenges their child or children face, they are also as individuals, totally discriminated against and judged for every move they
make.

Let me tell you something about these women. They are amazing. They are Ninjas. They are super women, most of whom have to give up their entire lives,
their hopes and dreams and they sacrifice everything to give their differently abled children the best chance they have in life. They live isolated lives
because of the open and mostly hidden discrimination they face by people closest to them. But the one thing that will never be taken away from them is
their resolve, unconditional love, determination and sheer stubbornness in not giving up their default role as primary care givers to their children.

Most if not all these women go through hell every single day to make sure that their children have the best they can have in life, despite their individual
means. Some can hustle and get a shilling here and there, some don’t have that opportunity. Even for families who would ordinarily be financially stable,
the cost of therapy, medication, education, nutrition – you name it, is capable of bringing them to their knees. Some of these women cry themselves to
sleep every single night praying to their God and asking why he or she has forsaken them. And yet, the next morning, they wake up and do it all over again.

I submit to you that you “normal” people as you call yourselves; you people who have perfect lives that allow you to pass judgement over those who have
a different life; you people who stare and shake your head in disgust at a mother whose autistic child is having a melt-down in a supermarket and saying
that “what is wrong with that mother, her child is spoilt”; you people who have the luxury of not knowing the pain of a mother with a non-verbal autistic
child who is in unbearable pain and distress and unable to express themselves; you people who judge and come out with ignorant and stupid comments like
“that one was bewitched”, “that one’s dowry wasn’t paid and that’s why they have a disabled child”, “that one must have done something in a previous life”
– I submit to you that whichever God you pray to is kind enough to have spared you and gave you the right to be ignorant and stupid. Because if you were
ever in the situation that others are in, society has to be lucky that your not one of the ones who will be able to cope with the burden and responsibility
of caring for and loving someone who is different. Pray to that God of yours to never put you in a situation that you become disabled, a spouse or child
of yours becomes disabled, or you give birth to a child with a disability.

Why have I written this post you may ask. It’s because of the sheer amount of in-box messages I’ve got from parents of children with a disability, mostly
those on the autism spectrum, who were absolutely furious that I had to explain that my son is autistic to parents that commented on my post and took the
“your child is bloody spoilt” view. There is a parallel here to real life where the constant need to explain to those who are discriminatory and prejudicial
has become tedious for them and enough is enough.

Let me conclude with a simple example. A couple of weeks ago, a distressed mother on one of the support groups posted a question asking what they can give
their autistic child to calm them down when she has guests. Let me first say, many kids on the autism spectrum will be on medication, and this should only
be for their benefit and if it improves their development. But the thought of having to medicate your autistic child to make it easier for guests? I was
like – Fuck that. The only intervention needed is to bitch slap those guests out of your house. If your own guests cannot come to terms with the fact that
your child is autistic, they have absolutely no right to be guests in your home, let alone friends.

The Outrage of the missing data of women with disabilities in Kenya “where are you my sisters?” Author Mugambi Paul.

The upcoming international women day’s gives scholars, practitioners and other public policy stakeholders to ask ourselves the pertinent question.
Has Kenya done well in advancing the rights of women and girls with disabilities?
Has Kenya broken the barriers of inclusion of women with disabilities?
Has the disability space been accommodative of women with disabilities?

As a public scholar I join in the reflection of the Kenyan disability public space.
Absolutely not, this is one of the debates which the stakeholders in the disability sector need to engage.
Are women with disabilities actively engaged?
I live that to other analysts. As a matter of principle, I say representation matters.
On the other hand, I thank the president of Kenya having appointed Madam MUkhobe at the highest decision-making organ in the country since 2013.
Where is the Data and statistics of the disabled?
Numbers don’t lie.
Globally disabled persons are at 15 %.
3.8 of the are persons with moderate to severe impairment.
5.1 % of the children with disabilities are below the age of 14.
0.7 % have severe functional impairment.
19 % are women with disabilities world report 2011.
To put matters into perspective, In the latest 2020 national council of population report has no data of women or girls with disabilities.
Does this mean that women and girls with disabilities do not get pregnant?
Are women and girls with disabilities not sexually active?
Different media channels on a weekly basis in Kenya have been reporting of how women and girls with disabilities have been experiencing gender-based violence in the hands of family members or even under the institutions mint to support them.
I believe This is another big blow to disabled persons in Kenya after the release of Kenya bureau of statistics 2019 census report. Which in essence reduced the data of disabled Kenyans.

Will disability sector continue with the same old ways of addressing this challenge?
Will the disability sector move out of board rooms and actualize the dreams of girls and women with disabilities?
Does the national council of population have a disability mainstreaming committee?
The lack of disability desegregated data will obviously affect planning and service delivery for girls, boys, men and women with disabilities.
In other words, the national council of population affirms that women and girls with disabilities have never experienced gender-based violence nor gotten pregnant.
Let me remind the disability stakeholders women with disabilities are more likely to experience sexual violence than women without disabilities.
This is also coupled with disabled Kenyans who face barriers to accessing services in both public and private sectors.
Most disability policy stakeholders know the barriers that disabled Kenyans face but have refused to actualize them.
Disabled Kenyans persons have been left chanting in the social media as a tool of advocacy.
Am not surprised to note in March 4th, 2020 a person with physical impairment was begging for a wheelchair on in one of the social media platforms.
Which system works for disabled Kenyans?
Will the Big four agenda be realized for disabled persons?
When will Kenya declare begging an economic enterprise for disabled persons since the constitution provisions aren’t working for disabled Kenyans?
several studies show Women and girls living with disabilities often face additional marginalization in their experiences of abuse as well as specific barriers to accessing services, due to:
• economic and/or physical dependence on the abuser, which challenges efforts to escape (particularly within family and sometimes institutional set ups. Several research in Kenya have indicated women with disabilities have suffered from forms of abuse specific to women living with disabilities (e.g. withholding of right medications, like the case of national children council exposed by NTV Kenya in 2019.
research done by women with disabilities organizations in Kenya show denial of assistive devices is also rampant.
Additionally, there is also refusal to provide personal care), which are less documented and may not be explicit within legal definitions of abuse.
For instance, Menstrual Health in Kenya: Landscape Analysis published in May 2016 never showed the extent to which women and girls with disabilities can’t access sanitary pads.
As Well lack of or limitations in physical accessibility of venues for women with disabilities still remains one of the barriers.
Furthermore, perceptions by service providers like health continue to plague the system in place.
This is because many believe that they cannot provide services for women with disabilities given their resource or capacity limitations. Mainstream women organizations and women service providers have not entrenched any inclusive measures of engaging or consulting women with disabilities.
In other words, lack of programming informed by and implemented in consultation with Kenyan women with disabilities or misinterpretation of their needs in escaping and overcoming the abuse they have experienced. Thus, having gaps in collaboration between disability organizations and service providers supporting survivors, as well as assumptions by each group that survivors are served by the other. A study by Kenya national human rights commission in 2015 indicated low sensitivity among law enforcement personnel or other service providers, who may not inquire about abuse by caretakers, or disregard reports from women with visual, speech/communication or motor coordination disabilities (e.g. cerebral palsy), assuming they are intoxicated or are not serious in their claims. The KAIH who have been working closely in the legal apparatus affirm that biases among judicial personnel and courts is evidently seen.
For instance, cases of provision of preferential treatment to the abuser in child custody due to the victim’s disability (

What can disability sector and stakeholders do to change the narrative?
Develop Strategies and tools to prevent violence against women with disability. E.g. have inclusive training tools on gender violence.
Ensure collection of data collected is gender, age and disability desegregated in reporting and monitoring
Share best practices of gender and disability equitable practice
develop inclusive Referral system and services which can assist in responding to women with disability who experience violence
have more role models among women with disabilities.
Collaborative initiatives with the mainstream women organizations
list end support men with and without disabilities who are supporting reduction of gender-based violence initiatives.
Conduct inclusive training to service providers in both health and law enforcing agencies.
Ensure engagement and meanful consultation with women and girls with disabilities from rural and urban set up.
This will actualize the slogan not living any one behind as the sustainable development goals advocate.
global commitments 2018.

In conclusion:
The truth of the matter is Kenya is known to have progressive disability
related laws and policies but poor implementation is the order of the day.
As a result the dire state of affairs of women with disabilities is not due to lack of new ideas. The biggest problem is lack of capacity to take up and implement the new ideas in existing policy documents.

The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy, diversity, inclusion and sustainability expert.

Disabled Kenyans outcry of the elusive accessible housing plans: Author Mugambi Paul

According to the Convention on the Rights of Persons with Disabilities it recognizes the right of persons with disabilities to adequate housing and their right to social protection (article 28). The Convention was adopted in 2006 and ratified by 180 countries, where Kenya is one of the earliest countries to do so.
more importantly in 2017 Kenya adapted the big 4 agenda where affordable housing is one of the key issue.

Where are we:
Arguably, there have been back and forth debates on how the public will be entitled to the affordable housing schemes in Kenya.
There has no been any agreeable way between the 3 arms of government and the public at large.
The lack of public participation in the affordable housing seam to have reached rock bottom.
This is coupled with lack of clear policy frameworks which could ultimately have guided the process.
In Jamuhuri 2019 the president of Kenya seem to have soften the stand on involuntary housing contribution. This has led to treasury in 2020 February budget policy estimates to the Parliament to say that it will allocated 0 budget for housing plan.
Although the private sector is investing on the housing agenda.

What’s happening at the National level?

In 2015, the UN Member States adopted the Sustainable Development Goals which call for access for all to affordable housing and implementation of appropriate social protections systems for all, including persons with disabilities (Goals 11 and 1).
But Kenyans with disabilities remain largely invisible in the implementation, monitoring and evaluation of these commitments. Notably, Lack of reliable and timely data, evidence and research on persons with disabilities continue to pose challenges to the inclusion of persons with disabilities and the full implementation of Sustainable Development Goals, including Goals 1 and 11.
This is affirmed by the latest Kenya bureau of statistics 2020 where disabled numbers dwindled.
Lessons for policy makers in the disability sector:
Mobilization of expertise on disability inclusion in housing agenda needs to be considered.
Disabled persons organizations need to participate in public participation forums to ensure their issues are hard by the ministry of housing and transport.
The disability sector policy makers need to resource and facilitate disabled Kenyans to this process of ensuring inclusive measures are observed.
The disability sector should demand 15 % of the housing units being constructed to be accessible and owned by disabled Kenyans.
The UN report 2018 shows that despite the progress made in recent years, persons with disabilities continue to face numerous barriers to access affordable and adequate housing and a disproportionate number of persons with disabilities are homeless. They face many barriers that prevent them from enjoying their right to adequate housing, including higher levels poverty, lack of access to employment, discrimination and lack of support for independent living.
On the other hand, On 19th February 2020 the gavel fell on the
58th session of the UN Commission for Social Development,
which agreed the text of the historical first United Nations resolution on homelessness. A serious violation of human dignity, homelessness has become
a global problem. It is affecting people of all ages from all walks of life, in both developed and developing countries.
Relevance of data:
Globally, 1.6 billion people worldwide live in inadequate housing conditions, with about 15 million forcefully evicted every year, according to UN-Habitat,
which has noted an alarming rise in homelessness in the last 10 years. Young people are the age group with the highest risk of becoming homeless.

The UN Commission’s resolution recognizes that people are often pushed into homelessness by a range of diverse social and economic drivers.

“It could happen to anyone. It’s not always drugs, alcohol. It’s not always something external. Life happens. And life can happen to a whole lot of us.
It did during the great financial crisis, and it could very well happen again”, said Chris Gardner, who had described his experience of homelessness in
his bestselling book, “The Pursuit of Happiness”.

“We, as a great human society, we are diminished, we lose the gift of their creativity, the gift of their curiosity, the gift of their potential when it
is marooned by all downstream consequences of homelessness”, said Mary McAleese, Former President of Ireland.

“I will never forget my first experience with homelessness. I, unfortunately, was born into a family plagued by a chain of events which included domestic
violence”, added Chris Gardner. “My one regret about being here today is that the two most important people in the world to me couldn’t be here today‐‐‐I’m
referring to my granddaughter and my goddaughter. One of them says that she wants to become the President of the United States and the other one says
that she wants to become an astronaut and go to the moon. And you know what I say to both of them every day? Let’s go!!! THAT’S THE POWER of ONE!”

In its resolution of the UN Commission for Social Development calls for a response by all sectors within Governments and societies. The Commission recommended
the resolution for adoption by the UN Economic and Social Council later this year.

The Commission also celebrated the
25th anniversary of the World Summit for Social Development
and its Copenhagen Declaration. Stakeholders and experts from all over the world expressed strong support for the work of the Commission, noting that
the outcome of the Copenhagen Summit remains relevant today and continues to guide social development in their countries.
Kenya ministry of social protection was recognized on this event.
All in all with the current trends in Kenya it remains a pipe dream for having accessible housing in place.
This is because there are no adequate measure or regulation in place to ensure real inclusion is achieved in housing agenda.
What remains is the low confused undertones among the Kenyan disability community without knowing which direction to take!

The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy, diversity, inclusion and sustainability expert.

The Deep Crises in the Kenyan disability sector Author Mugambi Paul.

Kenya is a country faced ultimately by many challenges as a developing nation.
Issues of disabled persons seem to be hanging in the Kenyan movie of activities.
No one or any institution seems to understand how to handle the first pace changes taking place in the global disability sector.
The disability sector seems to be blaming each other for the failures and the inadequacies felt by the wanjikus with disabilities.
Issues ranging from lack of representation in the building bridge initiative, lack of adequate data from the Kenyan bureau of statistics to delayed
Service delivery.
Let me not dwell on the Corana virus.
As a public policy scholar let be engrain me to the importance of collecting desegregated
data for disabled. Persons.
According to standard media, the release of additional census data by the Kenya National Bureau of Statistics (KNBS) should be a wake-up call to policy makers in both the county and national governments. The numbers present valuable information on trends and patterns within the country’s demographic that should inform policy decisions and resource distribution
This was after the realise of the numbers byt the Kenya bureau of statistics. Unfortunately, for disabled person it was a bitter peal to take having lots of expectations.
The data presented seem to have reduced the numbers of persons with disabilities.
What happened?
The reality check indicates the lack of proper representation and lack of technical knowhow of disability data desegregation took place.
did the disability sector participate in the cycle of activities at the Kenya bureau of statistics?
The data released seems to be negative.
Reasons?
First application and training of the use of the Washington group of questioners was not properly conducted.
Secondly no pilot activity was done on how to collect disability desegregated data.
Thirdly the training of enumerators was a second thought.
Fourthly, were the organization of disabled persons involved in the process?

Facts for consideration:
It is well known. That
An estimated one billion people worldwide live with disabilities. Of the world’s poorest people, one in five live with disabilities.
Notable, in developing nations like Kenya conditions where we lack material resources as well as opportunities to exercise power, reach our full potential, and flourish in various aspects of life. (WHO and World Bank, 2011).
Globally, People with disabilities were not listed as a priority in the Millennium Development Goals. This is also true in the Kenyan context where disabled persons are not listed in the big 4 agenda. As a result, there is exclusion from many development initiatives, representing a lost opportunity to address the economic, educational, social, and health concerns of millions of the Kenyan’s most marginalized citizens (UN, 2011). In contrast, for the 2030 Agenda for Sustainable Development, United Nations member states pledged to leave no one behind, recognizing that development programming must be inclusive of people with disabilities.
Expected irreducible minimum:
To ensure disability-inclusive development, disability data must capture the degree to which society is inclusive in all aspects of life: work, school, family, transportation, and civic participation, inter alia. Disaggregating disability indicators will allow us to understand the quality of life of people with disabilities, towards developing programs and policies to address existing disparities.
Opportunity for Kenya disability movement:
Kenyan disability movement should stop board room meetings among themselves and join where the cake is being mashed and prepared.
At the Global Disability Summit in July 2018, the World Bank announced new commitments on disability desegregated data support to countries.
Specifically, the Bank pledged resources to strengthen disability data by scaling up disability data collection and use, guided by global standards and best practices.
This commitment is aligned with the World Bank’s October 2015 pledge to support the 78 poorest countries in conducting household surveys every three years. Regular household surveys are an excellent option for disability measurement, as they can be stratified to oversample people who are more likely to experience limited participation in society. In multi-topic household surveys, disability data can be collected along with other socioeconomic data, enabling a richer analysis of the experiences of people with disabilities. Finally, regular household survey programs can measure the change over time and space in key indicators such as the frequency of types of disability, severity of disability, quality of life, opportunities and participation of people with disabilities, and rehabilitation needs. For example, the recently launched 50×30 initiative may offer a good opportunity to collect disaggregated farm- and rural-related indicators by disability status
The Kenyan disability sector should stop ghetorization of disability issues and we shall realize real mainstreaming when we speak to where barriers exist.
It is encouraging that more disabled persons in the social media are demanding a specific census for persons with disabilities.
Weather this will be executed time will tell.
All in all, we need a model survey for disabled persons in order to have proper planning and ensure we get the Kenyan national cake.

The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy, diversity, inclusion and sustainability expert.

Will you Be my Valentine? “Tips for an extra special day with your blind partner” Author Mugambi Paul

Friendship, love, and romance are in the air with Valentine’s Day in Nairobi..

Whether you’re on your first date, or it’s your tenth with your true love, planning the right date night, getting the right flowers, a gift, dinner reservations,
etc can be a bit stressful.

And you may imagine that going on a first date with someone who is blind or visually impaired can even be more awkward.

But in reality, going on a date with someone who is blind or low vision is no different than dating any other person.

Here are a few tips for sighted companions or partners to help make your date memorable.

#1 Sighted Guide

Consent is key! Once you’ve selected a place, made a reservation or planned an activity, don’t forget to brush up on your sighted guide technique.

There is an etiquette to offering sighted guide assistance to a blind person. Always ask first, don’t grab or push.

Now a days I combine my White cane experience with Sunu Band
to navigate indoor spaces like restaurants and cafes. Moreover, it has aided me with the line like at theaters, so I know when it’s my turn to move up in the queue.

The Sunu Band is also great for when you are doing a sighted guide as the blind or low vision person being guided retains awareness and more control.

#2 Be descriptive

But not overly so – allow your partner the chance to soak in the ambiance.

Now that you’ve arrived at that fancy, romantic restaurant or place, offer a lite description of where you are to your partner.

Allow your blind partner the chance to ask about his/or her surroundings.

#3 Don’t just read the menu

make it conversation instead of reading a list.
You know Nairobi hotels and restaurant do not offer braille, or large print menus, you have to check with your partner their preference.

If those aren’t available, you can start by asking what are they’re in the mood for drink and food? If it’s a place you know well, make a recommendation
or mention the specialty of the house.

But whatever you do, don’t order or speak for your blind or low vision partner. Especially, don’t allow waiters or staff to ask you to speak for your blind
partner.

In the event it happens, tell your waiter to direct the question or comment to your partner.

#4 Table manners are still king

And throw away the messy stereotypes. Enjoying a meal with someone who is blind or low vision is just like eating or drinking with anyone else. Again being
a little bit more descriptive is good.

When the meal arrives, you may offer a quick description of where things are on the table. For example, your wine glass is to your left or at your 9 O’clock.
Sometimes using the clock reference is helpful.

Remember, don’t overdo it and stress about the vision impairment. Just be yourself and enjoy each other’s company through great conversation, drinks, and
food. At the end of the date, the most important thing is that you both have fun.

Additionally, everyday should be a valentine.
You should even practise self-love.
Self-love means allowing yourself to be happy. Too often, we manipulate ourselves instead of increasing the amount of joy we bring to our lives.

So, every day, do things that make you feel good. Even 10 minutes of self-care can add up and make you feel much better in the long run. But you’re worth
more than 10 minutes. You are the most crucial person in your life. Act, accordingly, show love, and be open to receive love.
All in all, do things that fulfill your soul. Get rid of people who don’t make you feel good.
What others say or think about you has nothing to do with reality. It’s just their perception.

Sure, we’d all like to be around people who are kind and loving, but the harsh reality is that rudeness exists. Yet, it doesn’t need to affect you and
especially not your wellbeing.

The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy, diversity, inclusion and sustainability expert.

“DISABILITY LENCE” The unspoken truth of the Kakamega school tragedy! Author Mugambi Paul

In the recent past more schools in Kenya are reporting deaths and newly disabled pupils in unclear circumstances. Yet we have lots of resources’ and commitments towards achieving sDG number 4 and meeting the Kenya 2030 vision.
Kakamega school is not the last in this zero-game played by lack of observation of accessibility standards.
Kenya has lots of different pieces of legislations which needs harmonization and have a clear state organ to lead in implementation.
In September 2019 a classroom crushed at Precious Talents Top School in Nairobi killing 8.
Up to now no one has been convicted nor a report produced.
How many more should die or get disabled?
I opine that Schools have become death traps for future leaders and different influencers.
The unspoken truth is that the lack of observation of built accessibility standards seems to be the major setback towards this issue.
How many more will die or get disabled so that policy makers will protect the innocent lives?
Schools are meant to be safe heaven away from the harsh times in Kenya.
I believe the different policy makers seem not to grasp what is ailing lots of buildings in the country.
Kenya seems to be mark timing on the root course of collapsing of buildings and stampede in build environment.
The voice of the disabled:
the disability sector in Kenya have maintained the traditional tune of wait and see who will blink first.
I observe that more persons have become disabled in search kind of disasters.
How are disabled persons included in disaster management?
How are the newly disabled persons included in the new club membership?
What are the support measures put in place to ensure the persons who have acquired disabilities have a smooth ride of inclusion?
According to different studies, it is moment like this when the disabled persons organizations and allies of the disability sector are needed to raise the voice of accessibility.
It would be prudent to see policy makers within and without the disability sector setting record stay straight on having national accessibility standards.
One of the commitments made by the Kenyan government is about inclusive education in July 2019.
Could the stakeholders in the disability sector stand up and make a statement?
Shall we continue to be left behind?
Disability media reporting:
This is one of the major gaps in the media industry.
The exact desegregated data of the newly disabled persons is not given nor reported.
Recommendation:
The national construction authority needs to conduct an accessibility audit of all schools.
This will aid the non-compliant schools to be shut down by the ministry of education.
The national construction authority has the capacity in resource mobilization and expertise in built environment.
Moreover, what they might need capacity on is technical support on conducting inclusive audits.
When will the ministry of education issue a decree on accessibility standards in school just like the way the Cabinet secretary ordered pregnant girls to be admitted in form one?
All in all, as a public policy scholar I believe disability mainstreaming will be achieved when all institutions take responsibility and not to wait for a policing unit to actualize inclusion.
When we make built environment accessible for all it benefits everyone not the disabled only.
The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy, diversity, inclusion and sustainability expert.

The cost of remaining mum on Kenyans living with disabilities and individuals with chronic illness Author Mugambi Paul

Research shows that most chronic illnesses can affect every single part of individuals life, but it doesn’t really look like it. Some chronic illnesses have constant pains and fatigue among individuals [WHO 2011].
On the other hand, I have engaged several individual in the social media platforms.
This has led me to learn several lessons
You might not know a person is suffering if you don’t communicate ]HI 2011].
I classify some of these individuals as having invisible disabilities.
This is to say invisible disabilities mean that often times,
people don’t believe that actually individuals can be sick. This leads to people saying common things that, despite usually having good intentions, can come off as rude,
dismissive, and ableist.

The one I’ve heard the most is something that has undoubtedly been said to every person with an invisible disability or illness – the dreaded ‘but you
don’t look disabled nor sick!’. This happens all too often as an offhand comment, but it’s also been followed by heartbreaking situations like eventually losing friends
who haven’t believed that chronic illness or having impairment was real because people don’t look or act sick in the way they think one should be?
So, to give you a bit of a crash course, here’s some examples of what NOT to say to people with chronic illness.

‘But you don’t look sick!’

Yep, I know – but I am. These five words reduce health down to appearance, which is not the case at all. You might be saying this with the best intentions
(hopefully shock, because someone look ~too stunning~ for someone who’s actually very ill) but what it actually does is hits on one of the biggest fears of chronically
ill people – that people don’t believe them.
Actually,
Personally, whenever someone says this, it just reminds me of the many times people haven’t believed I can’t see because I didn’t *look* Blind. You might mean it supportively,
but all I hear is doubt.
This is because am super in mobility and orientation especially in familiar territories.
Sometimes it’s an anxious moment for me when individuals with out disabilities just plainly discuss behind my back “look at him, he is just pretending, he is comfortable” not knowing I have to go an extra mile to orient myself, secondly he or she doesn’t know that I have to do it since I don’t have alternative.
Additionally, I note that Not all illnesses are visible.
I can guarantee you; every chronically ill person has tried absolutely everything they physically and financially can. I cannot think of one person who’s
simply said, ‘ah bugger, I’m chronically ill. I’m not going to bother trying things to feel better!’
Trust me, some have tried it all; all the doctors’ and specialists’ suggestions, and yes, a bunch of the tinfoil hat ones too (desperation and lack of medical
answers make for strange bedfellows).

Examples of suggestions of what my friends the blind community and other persons with disabilities have tried including: various supplements, Chinese herbs, marijuana, LSD, ketamine, essential
oils, drinking their own urine, crystals, B12 shots, spirulina, charcoal, detoxes and juice fasts, prayer and religion – the list goes on,
as a blind fellow you can guest which one of them, I have tried I’ll let you ponder on which).

And before you ask, yes
You have seen many disabled persons, the chronic ill persons going to work, or you saw a photo of one catching up with a friend on the weekend. That’s irrelevant to whether he or she look ‘okay’ to you now
He or she still remains ill, and he or she maintains his or her impairment since they do not disappear.
According to several studies they indicate the nature of chronic illness is, sadly, extremely can be unpredictable. One can have totally manageable levels of pain and fatigue one day, and barely able to
walk the next. Sometimes it’s because one accidentally overexerted himself and went over my limits, but sometimes symptoms flaring can be completely random.
If you find it annoying, just try to imagine how frustrating it is for individuals with chronic illnesses. Regardless, some have always sick and in pain – some days some are just able to manage
it (and hide it!) better than others.

‘You just need to snap out of it and push through.’

‘Pushing through’ actually makes someone, and many others with chronic pain and illness, worse.
In Kenya and other developing countries there is no particular policy framework addressing concerns of persons with chronic illnesses although a mention here and there on different framework.
Most families carry the burden of taking care of chronic ill individuals and this affects the economic and social wellbeing of the society at large. The resources used to trat could have been used for other functions [ILO 2017, undp 2016].
Its high time we have particular social protection measure to address persons who have chronic illnesses.
Moreover, one of the major experientials in the disability world and chronic illness which seems to be similar is the way the society expects us to push ourselves beyond our limits
Obviously its so great to push beyond limit but this doesn’t apply to all persons. What the society doesn’t understand persons with disabilities and individuals with chronic illnesses are not a homogenous group.
one is sick or disabled every single day, and know their body and their limits better than anyone – so telling one to ‘push through’ is actually
the worst possible advice. When you’re talking to someone with disability or a chronic illness, remember just because you’d be able to manage something, doesn’t mean
they can or should. Don’t assume someone’s health and limits for them. It totally removes their agency as a human being.
Besides having a disability some individuals might also be having chronic illnesses.
‘You’re too young to be sick!’ or sometimes for disabled persons they say woyee woyee how comes he is blind?

Yep! He or she is young! And sick or having a disability! It sucks. But sickness and chronic illness isn’t exclusively the domain of the elderly; people of all ages can get sick. The society needs to understand that Doesn’t
make their experiences less valid, or their identities abnormal. They just sick in a cool young person way, I guess. I don’t know – it’s a weird thing to
say, so just don’t.

‘If you stopped talking about it all the time and looked on the bright side, you’d feel better.’

I do! To be totally frank, as a blind fellow if I didn’t look on the optimistic side, I wouldn’t be alive right now. Being blind for 23 years now it’s not a walk in the park.
It takes strong will to be in this unjust society.
This also applies to other fellow disabled persons.
Needless to say,
Being chronically ill is also tough as hell, and many chronic
illnesses have strong ties to mental illness. One has to look on the bright side A LOT, otherwise their depression and just the daily battle of being sick
would drag one down and some can’t be able to get out of their beds.

All in all, people should be able to talk about their lived experience as much as they deem appropriate, and disability and chronic illness is not spoken about
enough. Let them vent, let us explain, let them talk about their day!

The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy, diversity, inclusion and sustainability expert.

Why the disability movement in Kenya should stop crying faw

Over the years the Kenyan disabled haven’t got enough opportunities in many spheres of life.
This is because of overreliance of the old tricks and lack of change of tact in the advocacy engagement processes.
Unfortunately, it’s true, many disability private and public initiatives have taken place either as a second thought or organized by the few politically correct individuals.

So, if we know this to be true, what are we doing about it?
Most of the time Kenyans with disabilities have not grabbed the recent social, economic or political opportunities.
For instance, after the 2007 post-election violence there was no representation nor disability mainstreaming agenda in the Kofi anaan initiatives.
This scenario has been repeated once again in the building bridge initiative.
The disability
movement is not represented and right now is when the disability keyholders are trying to unmask the already cooked food.
The disability movement in Kenya forgets so easily if you were not on the table in preparation of meal.
You don’t have manors to demand for the cake.
It’s prudent to say the Kenyan disability sector will just get the breadcrumbs.
This is seen by upcoming mobilization of groups of disabled persons to play to the gallery even when the building bridge initiative report is yet to be made public.
The reality of the day there is not a living systematic structural engagement of disabled persons.
The barriers to public participation are either because of financial reasons or even a few individuals who have held the disability sector on ransom.
Am not surprised that currently we have an amorphous body called
Caucus on Disability Rights Advocacy.
Additionally, we still have another platform still championing on the global commitments made in July 2018.
All of these platforms still have the same individuals and agencies.
Does the common Wanjiku with disability aware of these platforms?
Is the voice of rural disability hard in these forums?
What are the tangible benefits to the change of the implementation of legal or policy frameworks?
What are other alternatives to ensure real and proper public participation and engagement of many disabled persons can be achieved rather than the few elites in the disability movement?
I opine that in article 2 of the constitution of citizen participation and article 54 should be made a reality and mandatory.
Moreover, the movement needs emancipation from the tired narratives and demand what is rightful.
For example, why do the mentioned platforms do not engage in the recent happenings as reported in the media like how children with disabilities were mistreated.

Why has the disability movement kept mum on the gazettements done by government of Kenya?
The jury is out there!
This is evidenced by below article.
http://www.mugambipaul.com/2019/09/03/why-the-disabled-kenyan-man-missed-the-land-comission-job/land
The young and vibrant individuals with disabilities have a role to play.
Do not mind the lack of mentorship in the sector.
Rise up and contribute to the transformation.
Through this the youth can reduce social media lamentations.
Research shows 80% of disabled are between the ages of 18 and 64 – the workforce age.
This can have creative and innovative outcomes for the disability movement.
Additionally, the legal processes in Kenya have not favoured the disability sector.
As penned in my past articles we should await 2021 to have the repeal of the 2003 persons with disability act.
Moreover, we still have the 2006 disability policy still in draft form.
Does that sound an alarm?
Historically in Africa Kenya is admired for having best practises in disability sector but this tale is being overtaken by Rwanda and other African countries.
For instance, Kenya disability sector has been agitating for improved accessible public transport.
This hasn’t taken place and now Rwanda is boasting of implementing accessible transport by acquisition of accessible buses and subsidized fairs for disabled persons.

What more can be done?
It’s been my experience that disability sector wants to be seen as benevolent, accepting of all disabilities, and up to date in compliance. The reality is that
many don’t want to bother as long as their image is intact.
As illustrated in many forums organized by the disability sector and non-disability sector members, they don’t provide alternative formats of information or observance of reasonable accommodation.
If the disability sector made it mandatory to preach water and Drink water, I believe things will not be the same for future disability generations.
As a public scholar and a person with lived experience of being disabled.
I have a dream that one day the sector will stand tall and read declaration.
“We the disabled of Kenya from across our great Country;
Recognising the sovereignty of the Constitution of Kenya and of the great people of Kenya, 15 % of the Kenyan largest population.
Appreciating that the Constitution of Kenya is the consensus document that reflects the ‘voice of the People of Kenya’ and has ring-fenced and protected Clauses for all including disabled and other marginalized groups through various provisions.”
We express our disappointment in the lack of leadership and strong commitment by the duty bearers to ensure the implementation of the article 54 provisions.
We therefore have the following Irreducible Minimum

————

I passionately believe that If Kenyans with disabilities think everybody has value, everybody can be capable, and no one should be excluded. I make an appeal go and Tell your CEOs, board of directors in the disability sector and allies of the disability movement to join and rise to the occasion and change tact.
Why should the disability movement be singing to the second fiddle?

The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy and diversity and inclusion expert.

Why the Kenya Revenue Authority should partake responsibility of tax exemption for the disabled Kenyans!

During the past 3 decades in Kenya there have been numerous changes in our society with respect to the management and treatment of people with disabilities.
Of course, there ar numerous success stories of actual improved disability mainstreaming.
How did the changes occur?
Many legislative and societal changes have taken place for instance, the disability act of 2003, the UNCRPD 2006 and the 2010 constitution and several disability related regulations. Furthermore, these gains have been necessitated by the lobbing and advocacy by disabled persons and their organizations.
On the other hand, Disability mainstreaming and work to end discrimination against disabled persons have been on both government and non-state actors’ agendas for decades. Why is disability mainstreaming still important?
Some of us feel that “everyone” in government and non-state actors who include development and human rights organisations are well aware of the issues. But the truth is that in organisations without
any explicit focus on disability mainstreaming or disability social justice, the levels of awareness for disability-based discrimination (and the need to end it) tend to be uneven.
Am not surprised by the inaccessible built environment, inaccessible information or the negative attitudes which still exist among the Kenyan society.

Efforts to promote disability equality remain limited and often isolated. Some would prefer to drop “disability” altogether, busy as they feel with all those other
issues that must be “mainstreamed” – good governance, environmental protection, HIV/AIDS prevention, “you name it!”

most government and private entities normally pass on the back when dealing with disability matters!
I opine that ignorance in the Kenyan society is very expensive for disabled persons.
Why should and institution require permission to offer disabled person a service?

As citizens we do not require permission to get a passport, when one has Malaria a disabled person doesn’t require permission.
Why does Kenya revenue authority run away from its responsibilities?
As long as one has uploaded the right documentation there is no need of putting more barrier for the disabled persons.
Why are policy makers silent on this injustice?
Most top government policy makers and stakeholders have done benchmarking of disability services in other countries and they know how good and proper systems work for the people.
Why are they not actualizing simple and impactful solutions to the disabled persons?

. But there are at least five reasons why “disability mainstreaming” must continue:
list of 5 items
1. Organisations that are committed to universal human rights have a responsibility to ensure their work respects and promotes human rights. Disabled rights
are human rights, enshrined in widely accepted international treaties as the Convention on the rights of persons with disabilities UNCRPD 2006.

Any rights-based approach that neglects disabled persons rights is inadequate.

2. International movements and campaigns rally large numbers of disabled people. Disabled persons make the largest minority group in the world

if government institutions who are the planners, implementers and evaluators ignore disabled interests and needs, and refrain from
engaging disabled persons as interlocutors, collaborators and allies.
They will never get it right!
3. Many development and human rights agencies are into education and campaigning – i.e., they attempt to spread ideas around, and to mobilise others to
join them in their cause. The messages they convey, implicitly or explicitly,
influence people’s minds: research has shown that campaigning can reinforce or weaken people’s value systems – broadly speaking, what they consider to
be “good” or “bad”, “right” or “wrong”. (See for example the gender mainstreaming angle.
Hence, it is important to avoid reinforcing values that condone discrimination and other violations against disabled persons
which would be in stark contradiction with the development and human rights goals most of us defend.
The disability organizations need to take lead in voicing what needs to be don on tax related concerns.
Disabled persons should not just be raising concerns on the social media but take the demands to the Kenya revenue authority.
The Kenya revenue authority need to work along side disabled persons in order to ensure smooth and faster process is achieved.
4. disability -based violence is not only one of the most pervasive human rights violations, it also jeopardises development. For example, large numbers of disabled persons have experienced delayed service delivery due to the bureaucratic processes. For instance, delayed in tax exemption renewal, with
dire consequences for their physical well-being, their mental health and their social status. Getting tax exemption is right, but y risk their
lives because of high cost of transport, psychological wellbeing. The Kenya revenue authority should know that most disabled persons are unemployed and for those who do not get access to the service
are likely to feel abused, something is deeply wrong.
Additionally, the Kenya economy is highly affected by wastage of hours on the road.
The tax exemption should have been simplified through decentralization of Kenya revenue authority services at the county.
In other words, if the digitalization process ways actualized the staff at Kenya revenue authority would be able to automatically issue exemption certificates without delay.
The disability mainstreaming focal point person at Kenya revenue has to actualize the dreams of disabled persons by ensuring the system works beyond himself or herself.
Are there government institutions, private sectors who have been given tax relief by the Kenya revenue authority for promoting disability employment and improving access for disabled persons in Kenya?
5. In terms of efficiency, any organisation has a responsibility to serve the disable persons who need their service.
Disabled persons should not be treated as second class citizen in government services.
Siting an example in 2019 May the Kenyan government in collaboration with world bank launched the braille version of the 2030 vision which in essence non blind persons read a decade ago. Is this fair?
The Kenyan policy makers need to stop the mancantile policy process and adapt solution-oriented policy and procedures.

The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy and diversity and inclusion expert.

am I a indigenous disabled person Retracing my roots: Author Mugambi Paul.

As I joined the cultural exchange activity during the triple A assembly in Brisbane.
Many thoughts came to my mind.
When one of the tour guides gave me one of the traditional instruments to test.
It reminded me of my indigenous roots as a disabled person.
The tour guide and fellow Australian African award team were mesmerized how I blew the wind instrument with ease.
The thoughts which were in my mind were the lack of water access in 2019 in my rural village while have seen sufficiency of water through out in may stay in Australia.
The land where they don’t have enough water sources like Kenya.
Secondly, I thought of how my community has eroded the culture activities and materials.
I resolved to start a Canberra cultural center which will defiantly bring back my indigenous culture.
I remembered I never so my grandfather whom am named after.
He died as a hero fight for the rights of the people during the colonial era.
Stories are being told of how he never entertained colonial rule.
He was a strong defender of women rights.
Could I have inherited his traits?
I sometimes run away from my passion of advocating for the rights of disabled persons, but I find myself back.
Could this be my purpose of life?
Grandpa just whisper to me!
If he was alive, I believe the Kenya gender story would have been different.
All is not lost.
We as the exposed energetic and intellectually grown up have to rise to the occasion and bring back our culture alive.
For once I thought the aboriginals are related to my indigenous culture.
As a public policy expert am now duty bound to restore the history for the sake of future generation.
Australia celebration of the indigenous cultures and the multicultural events and activities have really restored hope and faith that we can live together and enjoy every one’s cultures.
I believe other expertise is needed to initiate restoration of indigenous culture. More so I will be digging out the indigenous disability culture.
How many fellow Africans are ready to travel the unchartered roots of our cultures?
We need to tell our story no matter the decades and the distorted narratives that have prevailed.The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy and diversity and inclusion expert.

The Blocks to Disability Leadership and the mercantile economy of Kenya Author Mugambi Paul

Should disability leaders give up their work?

What world you do when you are in an office and all documents are inaccessible?
What would you do if you turned up for work and you had to climb a 3-meter brick wall to get into the office?
Ask the Nyeri law courts.
What about if everyone conducted team meetings
using PowerPoint and print materials?
How would you feel if you complained and nobody seemed to care?
The Kenyan public space has basically normalized this habit.
Yet, Kenya is the signatory and has domesticated the UNCRPD.
Kenya is known worldwide to have progressive laws and policies.
Imagine if we would have at list 10 % implementation of accessibility!
Let me give an example of the normalcy which occurs daily.

Some contemporaries of mine went to work the other day.

No big deal, hey. Lots of people go to work every day.

The difference is these colleagues are disability leaders. They are well respected in their various fields and regularly lead the public conversation about
disability. They are somehow not tough people I know, allot much gets in their way.
They mostly forget to bring the cows home by not demanding what’s is rightfully and constitutionally there’s.
!
This is to say, most of the public and private conferences in Kenya are held inaccessible areas.
Mostly, the disability leaders aren’t able to transact their work obligations as expected because the workshops and business areas are normally inaccessible. Very inaccessible. Should I say even the Kenyan parliament is among the list?
A place where the largest minority or marginalized group are supposed to find solace.
Should we continue with boardroom discussion on how to make accessibility real?
Or just continue with our social media rhetoric discussions?
Should we wait for another Kibaki moment to actualize the dreams of our heroes and heroines in the disability world?
Where is the accessibility voice space?
Who should be bringing the sector in to order?
The government and human rights bodies in Kenya “hamwoni hi ni dhuluma?” What I am
particularly annoyed by isn’t the inaccessibility, well actually that does annoy me, rather I’m very annoyed that a bunch of disability leaders have continued this trend to
work expecting to perform at their usual high standard, and they are unable to do so.

Most of them can’t live the venues or have alternative mode of communication.
That’s why in Kenya we are still talking in boardrooms about accessibility.
If one day the disability leaders walked out in protest of inaccessible venues and products it will be the turning point.
Through a social media survey, I actually noted that some disabled leaders aren’t involved by public and private entities into workshops.
They are normally left out and remain in offices.
There bosses tend to claim they are stubborn when they demand for reasonable accommodation.

How many local and international conferences have taken place in Kenya and accessibility becomes an afterthought?

This is a total distress and lack of engagement.
This affirms why disabled persons are not represented in most of the forums and become last to be remembered.

How is that the answer? Should disability leaders be giving up their work, or should conferences and workplaces be more committed to ensuring accessibility?

Newsflash: accessibility isn’t an extra or a nice thing to have, its mandatory if you want disabled people in the room. If you think diversity is of any
value at all then accessibility is part of your regular processes, it’s just how you operate. You budget for it, make it happen, build it in from the outset.
You choose venues that work, and make sure there are rapid responses to any issues that arise. You don’t argue and able plain and put the onus back onto
the disability leader to get less disabled, you take responsibility for making accessibility happen and you fix it quickly when it doesn’t.
which government building in Kenya is accessible for the disabled persons?
Most importantly, you make sure the people designing the access are those who know about access and have professional experience in accessibility.
This means they will also be disabled people. These access experts should be paid for their work, just like your sound technicians and caterers.
Obviously, lack of recognition of disabled experts has been normalized by the system, which we need to break.
and that makes it unusual. Most incidents of inaccessibility happen to individuals, often in workplaces that aren’t supportive or have managers who think
they know better, or they are single barriers affecting individuals at offices, seminars rather than everyone, so we never hear about them.
Mostly when organizers realize their mistake.
They normally result in a formal apology during the final plenary. Unfortunately, most of the disability leaders accept and move on.
Additionally, most apologies do not include a commitment to recruit disabled people onto the organising committee in the
future, nor did they include a reference to the same situation happening at the previous conference and this incident being a repeat.

There are still significant barriers to disability leadership.

The views expressed here are for the author and do not represent any agency or organization.
Mugambi Paul is a public policy and diversity and inclusion expert.