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What Next For PWDs As Government Excludes Them From COVID-19 Intervention Programme

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As the effect of the virus bites hard, the government stepped in to cushion the effect by providing palliatives to citizens.

BY OYETUNDE TOBI

he outbreak of COVID-19 in Nigeria like in other countries, brought the nation to its knees as all sectors of the country were halted. From agriculture to economy down to sports, the outbreak of the pandemic continues to affect every single person but in different ways.

As the effect of the virus bites hard, the government stepped in to cushion the effect by providing palliatives to citizens.

The Nigerian Government claimed to have spent billions of naira in palliatives distribution across the country. Despite this spending by the government, People with Disabilities have continued to lament their non-inclusion in the programmes as well as not carrying them along in the post-COVID-19 plans and information.

Assessing the palliatives programme, a joint report by civil societies revealed that the aid was hijacked and diverted by politicians.

A survey was carried out across Lagos State and one of the respondents of the survey claimed that a lot of the palliatives came from the NGOs, private organisations and individuals and they are more than what the government shared.

Recounting how they were affected by the virus, PWDs said despite being the most vulnerable to the outbreak, they did not receive any help from the government.

Ada, a special needs lady, said she had to rely on help from family members during the lockdown to survive.

She said, “Several measures have been taken since the outbreak of the virus but less consideration was given to us as people with disabilities and we are the most vulnerable in the society.

“While I could not go to my work and had no money coming in, I had to rely on assistance from family and friends.

“The government said they shared food materials but we only heard about them in the media.”

Lanre, a resident of Ketu, a Lagos suburb, who works as a cobbler despite his disability, said patronage dropped significantly, forcing him to to close his shop till the government fully opened the economy.

He said, “When I did not get palliative from the government, I was relying on the money I had saved.

“When it finished, I went to open my shop but nobody patronised me for about a month and had to close it until now that everybody is coming out.

“During that period of lockdown, feeding and paying bills was hell for me because I do not have anybody to meet for assistance and my family had to eat.”

Condemning the palliatives distribution process, CSOs in the country noted that the major problem was the inequality in the distribution of the relief materials.

CSOs noted that some clusters got more than others while the government ignored the PWD clusters.

“There were problems of distribution as some clusters got more packs than others, and the whole process became chaotic.

“There was the issue of coordinating with the PWDs. A better result would have been obtained, if there had been a relationship with the Joint National Association of Persons with disabilities, and Lagos State Office for Disability Affairs.

“Identifying who to give the palliative would have been easier if the synergy was there, synergy was clearly absent,” the CSOs said.

Suggesting the way forward on inclusivity and engagement with PWDs, President, Association for Intellectual and Developmental Disabilities of Nigeria, Mrs Joko Dawodu Omotola, said while the neglect by the government could not be described as deliberate, it should immediately move to ensure PWDs were well catered for even beyond COVID-19.

She stated that 50 PWDs from clusters were able to get support from private individuals and non-governmental organisations.

She said, “The Lagos state government was looking for ways to alleviate the sufferings of the people so what they did was to quickly give palliative but was not properly planned because I don’t expect the state to want people with disabilities to struggle with the other set of people in getting palliative.

“For stabilization, financial support is needed. Aside from finances, needs of the clusters are being considered, we have advocate groups with intellectual disabilities and there are so many in our clusters that have severe conditions that parents need to stay and sit with them before they can eat and do anything.

“It is sad to say that we are the most neglected but we have been trying to create awareness and as soon as COVID-19 is over, we can then swing into action.”

She also urged the government to push for a balance in matters concerning PWDs, adding that the government should include PWDs in its social intervention programme.

Omotola advised all state and local governments to replicate the establishment of PWD commission by creating functional offices that should be manned by the different PWD clusters at their levels to deal with the challenges facing the PWDs effectively.

Similarly, Dr Adebukola Adebayo, Chairman, JONAPWD Lagos State Chapter and Disability and Inclusive Development consultant, stressed the need for the government to give economic packages for minor and major businesses, individuals and organizations.

He added that the system has to be put in place for disability inclusion which should be by defaults from the government.

Adebayo said, “In the case of children with disabilities, does the government have the knowledge or understanding of how to cope with these children or are they building capacity for staff but as the case may be?

“I have not seen any interventions to strengthen the capacity of government officials on how to include the disabled in their interventions.

“Secondly, CBN came with an intervention to support small and medium scale enterprises in order to get their business back on tracks. There have to be lots of supportive systems from the government to buy into the products produced by the PWD’s and also to access the market easily.”

Adebayo also urged CSOs to find a way to get people’s support whether the government was inclusive or not.

He added that when the government fails to carry out its responsibilities, CSOs and private organisations should fill in the gap by calling the government to its responsibilities or approaching private individuals who will be willing to assist PWDs clusters in the country.

This report was done with the support of the Internews

I lost my sight due to my husband’s neglect…Patience Francis, a blind woman from Bokkos regrets

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Patience Francis is a blind woman from Bokkos local government of Plateau State, she was not born blind, it came to her later in life.

She dropped out of school at primary class four, when her father forced her into early marriage with a man old enough to be her father.

The marriage ended her formal education.  She gave birth to two children before her husband died.

After his death, she got married to a man who had two wives, she had four daughters, two out of the four died.

At a time, in her second marriage, she developed eye problem, which gradually led to total blindness due to lack of care from her husband.  Then later, they divorced.

As a woman with blindness, she met another man and got married again. That’s her third husband and she is still living with him. He later became partially blind, as a result of this, he lost his work as a security man in a private organization.

In this interview with Bulus Baba Izang, she shared how she coping daily and what she wants government to do to alleviate her suffering.

TQM. Did you not go to the Hospital for help when you had eye problem?

I did, but, because, l doesn’t have money and support, I went there late. It was the Church l worship and our Traditional ruler that gave me money and took me to Hospital, where l was operated on, upon all the pains that I took from the operation, l did not gain my sight back.

I am grateful to the Church Community and Our Traditional ruler for the support they gave me.

TQM.  Are you doing something for a living?

One of my daughters is selling firewood, l am helping her to sell it, while she is selling sweet potato at the local market.

TQM. Is the house you are staying owned by your husband?

No.  The owner gave us two rooms, and say we should give anything we can afford. We have been giving him #500.00 per month.

TQM. How do you get money to pay for the rent?

I go to some of my relations, who help me with food and money, after I help them in processing their harvested crops.

TQM.  What about your Children? Are they grown up?

My oldest son is missing I don’t know where he is, he has taken to drugs. And my daughters are married, but they are having financial and marital difficulties. So there is little assistance coming from them.

TQM. Do you have any appeal to make?

I am appealing to the government to help with money to start a small business.

TQM.  What kind of business do you have in mind?

I want to be selling grains, I mean food items.

TQM. We wish you the best in life.

Thank you.

Chidi Olujie, NNAD President elected as the Vice President of African Deaf Initiative

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Chidi Olujie in his Facebook account in a write up titled “Another Feather to the Cap” announced that he has been elected as Vice President , African Deaf Initiative (West African Regional Representative).

He conclude by saying let’s get African Deaf Community working through improved access.

Teach me how to do something, I don’t want to be a burden to others…Asade Amalam, a woman who become blind three years ago seeks help

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Asabe Amalam is a woman with visual impairment who became blind three years ago, she is married and she gave birth to ten children but unfortunately two of them dead. Although, she is from Bokkos Local government of Plateau state. She stays in Danbish in Barkin-ladi local government of Plateau state.  with her husband and children.

Losing her sight made her to be staying with one of her daughter who is married to a man from in Bokkos for proper care.

In this chat with our correspondent Bulus Baba Izang, she spoke on her inability to work after losing her sight.

TQM: What is the cause of your blindness?

I don’t know, but gradually overtime, I started losing my sight, l became completely blind about three years ago.

TQM: Have you been to Hospital for medical care?

Yes, I have been to Sabon Laying, a medical center in Mangu local government of Plateau state, I even tried traditional medicine without success.

TQM: Where you privileged to have any formal education?

No, l did not go to School.


Asabe Amalam

TQM: What was your work before your present condition?

I was selling meat. I buy cow meat, goat meat and even bush meat, and resell them.

TQM:  Now that you have lost your sight, are you doing something?

I am not doing anything, what can a blind woman do?  I am not doing anything.

TQM: But people who are visually impaired are doing so many things.  May be, you don’t know that you can do something even with your disability, especially if someone teach you how. 

I, doing something at my age and condition?

TQM: Yes, but will you like to learn?

Yes, I will like to learn, if actually, l can do something.

TQM: Have you received any support from the government or other persons in your condition?

Yes, in the village, people assisted me.

TQM: What will be your call to the government in terms of coming to your aid with assistance?

The government should help me with food and money. And If someone can teach me something to do, please I need that help also to be earning a living without being a burden to others.

TQM: Thank you Mama, we wish you good health.

Thank You, May God Bless you


This story is part of The Qualitative Magazine Project “CONNECTING OUR VOICES TO THE WORLD”-propagating the potentials and challenges of Persons with Disabilities in Plateau State supported by VOICE NIGERIA

The Carted away CACOVID palliatives by Lagos residents is meant for PWDs and other indigents…Lagos govt

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Lagos State Government has condemned the vandalization of the warehouse at Mazamaza.

In a statement by Abisola Olusanya,  Acting Commissioner for Agriculture In the state, the government said the warehouse houses the food palliative packages donated to the State government by the Private Sector Coalition against COVID-19 (CACOVID) group.

“The State Governor, Mr. Babajide Sanwo-Olu had on September 22nd 2020 formally taken receipt of the food palliatives from the CACOVID team meant for distribution to the indigent,” the statement said.

“The Government notes that the warehouse in question is not State owned and its usage was made available to the CaCOVID group. The State Government had been allowed to commence rebagging of food items allotted to it from the quantities meant for South West States.

“The rebagging was being done to account for each beneficiary receipt, as was required and monitored by the CACOVID team.”

The government said the distribution was on-going but had to be halted due to protests, before the invasion of the warehouse Thursday.

“For effective distribution of the food palliatives, groups such as Transport Unions, Ethnic Groups, Religious Associations, Artisans and Tradesmen Association, Marketmen and Women Association, People Living with Disabilities, Orphanages and Old Peoples’ Homes among others were being used as distribution channels to their members.

“The State Government however regrets the invasion of the warehouse and appreciate the support offered by the CACOVID group to the citizenry of Lagos.”

You will recall that Lagos residents on Thursday attacked a warehouse where COVID-19 palliatives were stored at Mazamaza community of Lagos.

The community is located in Oriade Local Council Development Area of the state.

Video clips circulating across social media showed that the residents, led by some hoodlums, gained entrance into the warehouse and looted COVID-19 food aid.

A resident told this newspaper that a bonfire was set at a junction not far from the warehouse, after which palliatives were carted away.

The looted items were branded as COVID-19 palliatives.

The development comes against the breakdown of law and order following Tuesday night shootings of #EndSARS protesters at Lekki.

Numerous organisations and public institutions were set ablaze across the state on Wednesday.

Premium Times

Nigerian digital ID initiative for people with disabilities wins Mission Billion Challenge

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Trust Stamp and Yoti CEO recognized on leadership lists

Finalists of Mission Billion Challenge 2020, a World Bank-sponsored initiative that seeks to ensure inclusivity of digital identity systems for vulnerable groups of persons, have been unveiled with the work of a Nigerian participant winning the top most prize. A biometrics provider and CEO have also won awards for work on technology benefitting social inclusion and development, with announcements from Trust Stamp and Yoti.

The winners of the Challenge were announced by the World Bank on October 21.

Identification for Inclusion (ID4I), a Project by Ibiyemi Ayeni under the banner of Special Olympics Nigeria, highlights the problems hindering persons with intellectual disabilities from getting a digital identity in the country. It also proposes what can be done to remedy the situation, especially as the country plans to establish digital identification for at least 150 million of its citizens in the next three years.

Kiva Protocol’s Sierra Leonean solution emerged second in the Challenge. This is an open source technology used for the issuance of digital identity credentials. The system can host citizen identity wallets and support affordable and compliant customer identity verification for financial institutions.

The third on the winning list is the Mobile Vaani, a project by Gram Vaani in India that aims at reducing exclusion by leveraging Interactive Voice Response (IVR) technology to help citizens register grievances through voice mail. The solution also proposes strategies to reduce exclusion from the public service because of digital ID system limitations.

Other pitches that featured among the top six of the Challenge entries include those of Mastercard and Trust Stamp, an online and offline privacy-enhancing authentication system; FlexID, a digital identity wallet that makes it possible to receive, store and share identity credentials; and the digital KYC for farmers by Uganda’s Laboremus Group, a fast and simple verification system that uses the Ugandan national ID cards to empower the underserved rural folks.

The Mission Billion Challenge is an annual prize of the World Bank which rewards projects that seek to explore how better vulnerable persons can have access to digital ID systems while ensuring their safety and integrity. The project is in line with the United Nations vision of digital identity for all by the year 2030. The Mission Billion Challenge has three categories namely, the Global prize, the Wuri West Africa Prize and the Information Prize.

Trust Stamp’s innovations reap multiple awards

Trust Stamp, while it did not finish on the Mission Billion podium, has also been recognized for its authentication technology and efforts to support inclusion this month, the company said in a news release.

The company did make the short list of the World Bank ID4D Billion Mission Global Prize for its Inclusive Identity entry made in collaboration with Mastercard.

Other recognitions received by Trust Stamp include placement on The 2020 Inclusive Fintech 50 and Tracxn’s Top Emerging RegTech Startups of 2020 list.

The company said it is being rewarded for its technological innovations in the domain of identity authentication especially in fostering financial inclusion and resilience, protecting data privacy while minimizing risk, and rapid growth in the regulatory compliance space.

Yoti’s CEO among Meaningful Business top 100 leaders

Robin Tombs, Chief Executive Officer of digital identity solutions provider, Yoti, has been included in the Meaningful Business Leader 100 for 2020, a distinction that honours outstanding business leaders across the world who are combining profit and purpose for the realisation of the United Nations Sustainable Development Goals (SDGs).

Tombs has been recognised for his company’s efforts, since 2014, to contribute towards one of those goals which pushes for the establishment of a legal identity for all.

“We are delighted to recognise Robin Tombs as part of the Meaningful Business 100 for 2020. In what has been a challenging year for everyone, the MB100 provides an inspiring reminder of the brilliant work being done around the world to solve the biggest issues we are facing today,” said Tom Lytton-Dickie, Founder and CEO of Meaningful Business.

Yoti said in a statement that though the year has been a difficult one, it was a pleasure to find their CEO among some of the best business leaders from across 34 countries of the world.

Capacity of Organization of People with disabilities were built to carry out the advocacy on Global Disability Summit commitments

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By Chris Agbo

Disability Rights Advocacy Center (DRAC) once again from 14th -16th October 2020 in Abuja hosted the second edition of the Disability Rights Fund (DRF)’s Strategic Advocacy training for her grantees and other Organizations of Persons with Disabilities (OPDs) in Nigeria.

The Strategic Advocacy 2.0 training was organized to further strengthen the strategic advocacy capacity of the Nigerian grantees through training and sharing experiences; to orient the grantees on the practical utilization of the Advocacy Strategy Paper 2020-2024 and its policy brief developed at the first training held in October 2019. The training also facilitated the positioning of interested grantees to the three advocacy clusters established by the advocacy strategy and to develop the terms of reference for each of the formed clusters to guide operations of the clusters.

The Program Officer of DRF in Nigeria, Theophilus Odaudu in his opening remark said that DRF began grantmaking in Nigeria in 2018 with six grantees namely: Disability Rights Advocacy Centre (DRAC); Centre for Citizens with Disabilities (CCD); Independent Living Programme for People with Disabilities (ILP); Family Centred Initiative for Challenged Persons (FACICP); The Albino Foundation (TAF); and Joint National Association for Persons with Disabilities (JONAPWD) but currently, DRF have 13 grantees namely: Association of Lawyers with Disabilities in Nigeria (ALDIN); Centre for Citizens with. Disabilities (CCD); Disability Rights Advocacy Centre (DRAC); Deaf Women Aloud Initiative (DWAI); Inclusive Friends Association (IFA); Lionheart Ability Leaders International Foundation (LALIF); Nigerian Association of the Blind, FCT chapter (NAB-FCT); Nigeria Association of the Blind, National (NAB); She Writes Woman Mental Health Initiative (SWW); The Albino Foundation (TAF); TheseAbilities Women and Youth Empowerment (TAWYE); The Irede Foundation (TIF); and Voice of Disabilities Initiative (VDI).

He stated that three of the DRF/DRAF grantees are leading separate coalitions, that is: DRAC is having a National Coalition grant to lead a coalition working on disability disaggregated data comprising DRAC, JONAPWD Anambra State, Disability not a Barrier Initiative (DINABI), and Mimijiean Foundation; IFA is also leading a National Coalition comprising IFA, Haly Hope Foundation (HHF), FAECare Foundation, and Advocacy for Women with Disabilities Initiative (AWWDI); and The Irede Foundation leads a Mid-Level Coalition comprising The Irede Foundation (TIF), Festus Fajemilo Foundation (FFF), and Children Developmental Centre (CDC).

He informed that they have spent over six hundred thousand US dollars in Nigeria through these grantees carrying out different projects that geared towards promoting the rights of persons with disabilities.

Speaking further, he expressed satisfaction that more groups representing excluded disability clusters are also joining the DRF grantees family such as She Writes Woman (Mental Health), Irede Foundation – Parents of children with disabilities and LionHeart Ability Leaders International Foundation – DeafBlind.

He welcomed the new grantees such as Deaf Women Aloud, She Writes Woman, Irede Foundation, Nigeria Association of the Blind, Voice of Disability Initiative, LionHeart Ability Leaders International Foundation and TheseAbilities Women and Youth Empowerment (TAWYE) etc.

He also said that DRF cannot support all organizations of persons with disabilities because advocacy is capital intensive but DRF can give recommendations for OPDs to approach other donors.

He expressed sadness over the death of Executive Director of one of the grantees Mrs. Foluke Idowu of Independent Living Programme for People with disabilities and a one minute silent was observed in her honour.

The Executive Director of DRAC, Dr. Irene Ojiugo Patrick-Ogbogu in her speech welcomed OPDs present at the event. She expressed gratitude to DRF for always choosing DRAC to host DRF events in Nigeria and for the support DRF is giving Nigerian OPDs in both financial grants and technical support. She urged participants to take the training seriously and acquire important advocacy skills because it is geared towards achieving the ultimate goal of inclusion for persons with disabilities in Nigeria.

The event witnessed the presence of the Executive Secretary of National Commission for Person with Disabilities, Hon. James Lalu who expressed his gratitude in the way DRF brought together leaders of disability community and urged the participants to put in their best as they learn new ways in advocating for the rights of persons with disabilities. He demanded that the communique of the workshop be sent to him at the end so that it can also serve as guide which the commission would be using to perform their duty. He called on every member of OPDs to always approach the commission with ideas that will be beneficial to persons with disabilities.

The workshop was facilitated virtually by a seasoned consultant based in Lusaka, Zambia, Wamundila Waliuya who was also the facilitator in the first edition of the workshop in 2019. The co-facilitators were Theophilus Odaudu, DRF Program officer in Nigeria and DRAC Program Officer, Noel Balogun.

The participants were taken in the following activities in the three days long workshop; progress on the implementation of the advocacy strategy, they scored themselves based on action taken in the last one year to ascertain progress made, they were guided for the expected outcome in the coming year. There were review of the Capacity assessment of the organizations, SWOT analysis review, Advocacy issues review, Advocacy Audience Allies and Partners Engagement Process, Alliance Building as Engagement Activity, Strengthening Alliance Building, Strategic Approaches of Advocacy and Strengthening Use of the Approaches, Lobbying and Influencing styles and Role play, Research and policy analysis and working with the media.
The participants went into groups to identify priorities, design advocacy programme in line with the Global Disability Summit. The groups worked on Empowerment of persons with disabilities, Sexual Reproductive Health Rights of Persons with disabilities and Inclusive Education.

A participant, Barrister Daniel Onwe, President of Association of Lawyers with Disabilities in Nigeria, also made a presentation on Strategic / Public Impact Litigation, stating how litigations can help to advance the rights of persons with disabilities in Nigeria.

Some notable advocates at the workshop were Chidi Olujie (President, Nigerian National Association of the Deaf (NNAD) Lawrence Idemudia (Centre for Deaf Inclusion), Beatrice Mube (Mimijean Foundation), Obinna Ekujereonye (NAB FCT), Barr. Ikem Uchegbulam (National Civil Service Association of Persons with disabilities), Hauwa Ojeifo (She writes Woman-Health Initiative), Comrade Musa Muazu Musa (National Commission for People with disabilities), Haruna Mohammed(Nigerian National Association of the Deaf(NNAD), Damian Okechukwu Ivom (The Albino Foundation),  Celine E. Osukwu (Divine Foundation for Disable Persons), Hauwa Ojeifo (She writes Woman-Health Initiative), Olanike Akinola (Network of women with disabilities in Nigeria) Crystal Chigbu (Irede Foundation), Bilkisu Ado Zango (NW Zononal Coordinator JONPWD) Agbo Christian (The Qualitative Magazine (TQM) and many others.

World White Cane Day: NAB FCT rallies to create awareness in Abuja, demands motorists respect for the white cane

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by Chris Agbo

The Nigeria Association of the Blind FCT Chapter on Tuesday organized a rally to mark World White Cane Day.

The members of the association and other members of disability community marched from L.E.A Primary School Jabi to Laps New World Hotel Jabi, Abuja, the venue of the celebration. In their rally, they were sensitizing the public on what the white cane means to the blind and why it is important for motorists to take cognizant of the white cane and ensures that they give any person with a white cane the right of the way on our roads.

The event which ought to have been taken place on 15th October 2020, the actual date to mark International White Cane Day was sponsored by Disability Rights Fund(DRF) and it was also supported by Sightsavers.

The Chairman, Nigeria Association of the Blind FCT Chapter, Mr. Obinna Ekujereonye in his opening speech said that the event could not take place on the 15th October because of some circumstances beyond the control of their executive but by God’s grace, the event is taking place. He said that the event is important to the blind people because it is a day whereby awareness is being created about the white cane and what it means to persons with blindness.

He said that the white cane signifies independence to the blind people and fortunately the theme of this year’s celebration is promoting independence and productivity. He said that the white cane is what a blind people use to navigate his or her way and when they can successfully navigate their way, they must have had some level of independence and with that they can be productive.

He urged government and even the public to enhance the inclusion of the blind people by ensuring the partways are properly closed, cars not allowed to be parked on the partways, ensures that there are no obstacles, white cane should always be respected on Nigerian roads.

He also called for full and immediate implementation of the Nigeria Disability Act to address the numerous challenges of not only the blind people but persons with disabilities in general.

Theophilus Odaudu, Program Officer, DRF Nigeria in his presentation of what white cane is all about and the history said that the cane is white for easy identification, saying that if the cane is black or any other colour, it can not be seen easily by a motorist, and again, the white cane is a symbol of identity for a blind person.

Speaking further, he said that in countries like America, there is a legislation on white cane and there is a penalty for anybody who fails to take cognizant of the white cane on the road. The white cane must be white with red down and its length is from the chest of the user and the user is expected to use it to identify all obstacles ahead. He also said that technology have improved the effectiveness of the white cane before there are some white cane which can dictate an obstacles from afar with some other function that makes it more convenient and user friendly.

He expressed joy that on October 15th, during the celebration of world white cane day with the Minister of Humanitarian Affairs, Disaster Management and Social Development, Haijah Umar Farouq, she promised that she would made available white cane with recent technology for blind people in Nigeria. He charged NAB FCT to follow up on that to ensure that the Minister keep her promise.

The event also witnessed drama showcasing the discrimination the blind face in our society whereby people think that a blind person should not be independent. It should be the responsibility of the person’s family to take care of the person. Again, the person have no business coming out alone, so if there is no one to assist the person to navigate, the person should stay indoors.

The event also witnessed giving of words of advice and encouragement to other younger persons with blindness from the older and well experienced ones.

Be proud and focus, Lucy Mailafia advises persons with albinism

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Lucy Mailafia is a lady with albinism hailed Akwanga LGA, Nasarawa State but now resides in Jos, Plateau State. She is a staff of The Albino Foundation (TAF), Plateau State. Her father had minor albinism while her mother doesn’t. She is only girl in the family of six and the only one with albinism.

She had her primary and secondary education in Nasarawa State and now she is in Plateau State working with TAF, Plateau State Chapter.

She had a chat with our correspondent in Plateau State, Bulus Baba Izang and she shared her challenges, her love life and her future aspiration.


Lucy Mailafia

TQM: Can you tell us about the challenges you’ve encountered as a person with albinism?

The major challenge I am facing is poor vision and the sunburns especially when I was in school. I had to practically go very close to board to see properly but overtime I made some friends whom I could collect their notes and that made it easy for me as a child, I had no idea that exposure to the sun wasn’t good for my skin but I got to learn a lot about myself as I grew older.

TQM: Tell us when you got to join The Albino Foundation?

I got to know about the albino foundation in 2015 but joined officially in 2017.

TQM: How does it feel to be a part of The Albino Foundation?

It is a family. We are close knit and look out for people with albinism, it feels good to be a part of it.

TQM: Are you in a relationship?

I have been in a couple of relationships but I won’t give details (laughs).

TQM: What are your future goals and what is your advice to people with albinism?

I would love to further my studies to PhD level and my advice to people with albinism is that they should not lose focus or give up on what can be achieved. You can do it if you will to do it.

TQM: Thank you for your time. We wish you the best.

Thank you for having me.


This story is part of The Qualitative Magazine Project “CONNECTING OUR VOICES TO THE WORLD”-propagating the potentials and challenges of Persons with Disabilities in Plateau State supported by VOICE NIGERIA

Kano State govt captures PWDs in the 2021 Budget

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People with Disabilities have been vividly captured in the 2021 budget of Kano State.

This was reaffirmed by The Director Planning at the Ministry of Planning and Budget, Alhaji Muntari Ado Yakassai on Monday when the Leadership of the National Association of Persons with Disabilities(JONAPWD) led by the Northwest Zonal Coordinator National Association of Persons with Physical Disabilities (NAPWPD) and Chairperson NAWOJ Kano Bilkisu Ado Zango paid him a courtesy call in his office.

This is an indication that persons With disabilities have been captured in a budget sub code under the Ministry of Women Affairs and Social Development.

TQM learnt that it is a fit achieve by resilient advocacy of the persons with disabilities in Kano State and it is going to enhance the implementation of the project designed for persons with disabilities.