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World Autism Day: How 15-Year-Old Kanyeyachukwu is Painting His Way into History

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As Nigeria joins the rest of the world to mark World Autism Day, a 15-year-old Nigerian autistic artist, Kanyeyachukwu Tagbo-Okeke, has shattered expectations with his extraordinary artistic feat.
World Autism Awareness Day is an international observance dedicated to raising awareness about autism spectrum disorder (ASD) and promoting acceptance, inclusion, and support for individuals with autism.

Observed every 2nd April, the date was designated by the United Nations General Assembly in 2007 to highlight autism as a growing global health issue and encourage worldwide support for individuals with autism and their families.

After spending three months working tirelessly on a canvas spanning an astonishing 12,303 square metres, Kanye has achieved what many deemed impossible.

His artwork, entitled “Impossibility is a Myth,” surpassed the previous record of 9,652 square metres. The project, which began in November 2024, was completed with the support of JC Best Schools and aimed at raising autism awareness.

In an exclusive interview yesterday with Kanye’s mother, Dr. Silvia Tagbo-Okeke, she said Kanye’s passion for painting is more than a hobby; it is his life.

She explained that the journey had been both a financial and emotional investment for Kanye’s family, who have poured countless resources into making his dream a reality. Kanye’s mother reflected on the challenging yet rewarding journey of her son’s record-breaking artistic achievement.

She noted that, over three months, Kanye, a 15-year-old with autism, completed a remarkable 12,303 square-metre painting, a feat many believed impossible for someone with limited verbal abilities.

Despite the numerous challenges, including financial strain and the daily commute to his school, Kanye’s passion for painting drove him to overcome every obstacle.

His mother emphasised the importance of love, support, and acceptance in fostering his potential.

According to her, Kanye’s work not only serves as a personal achievement but also aims to raise awareness for autism, acceptance, and inclusion.

She said her ultimate goal for Kanye is his independence, expressing hope that one day he will thrive on his own.

“I would say relief. It has been a long journey, three months actually. There is a sense of relief and accomplishment, not for me, but for Kanye. As you can see, the canvas is huge. It’s 12,303 square metres. If somebody had said, ‘Okay, a 15-year-old autistic boy with limited verbal speech can do this,’ a lot of people would say impossible. That’s what it is, the Impossibility Myth. However, nothing is impossible; once you set your mind to it, definitely you can do it.

“A whole lot of things went into Kanye creating this amazing work We had to go every morning to his school. We would drive to his school and then get the space for the first stroke of the brush. But the Chief of Defence Staff was really amazing. He gave us the first break we had by providing us with a 760th goggle ladder for the first stroke of the brush as part of their army-civil relationship. After that, we moved the canvas to his school, JC Best, and then we started painting. It was a bit hard, but looking at it today, it was worth it.

Dr. Tagbo-Okeke has good advice for parents with special needs children.

“The impact we want it to have on other children on the spectrum is for people to accept them for who they are, for inclusion, for awareness for those people that are not aware that there is even anything like autism. So basically, the things that Kanye is trying to achieve with this monumental work are autism awareness, autism acceptance, inclusion, and neurodiversity,” she said.

When asked what she hoped for his future concerning this huge project, she said she wanted her son to be self-sufficient.

“For me, I just want Kanye to be independent. That’s all. Independent. As parents, we don’t want our children to suffer, especially when we are no longer there. So that’s my goal for Kanye, that if I’m no longer there, he will not suffer. That’s just it.

“We have to tell them about Kanye. We have to create an environment of love and acceptance for him. Everybody, my kids, the first thing we talk about is Kanye. We tell people about him so that they understand that being different is not bad. He’s just different. He just thinks differently,” she said.

She said his cousins, his grandma, granddad, extended family, and friends all supported him.

Kanye’s mother noted that for anybody, not even someone on the autism spectrum, to be able to achieve this feat, they must enjoy painting.

“Painting is his life. Painting gives him joy. Painting is just part of him. That’s why it wasn’t that hard for him to do this. As I’m talking to you, every day he would dress up in his main clothes. He wants to paint. It’s not work for him. It’s just like breathing for him. That’s why he’s able to do it. And if you lay another canvas like this for him, he will still do it without breaking a sweat.”

She admitted that a lot of money went into the venture.

“The paint alone cost hundreds of millions. My husband and I, we had a donor, but the money didn’t go far at all. We had to put everything we had. We made unimaginable sacrifices, but we are glad those sacrifices were made. As we celebrate World Autism Day, mine is autism awareness. Tell people about your child.”

She further urged parents with autistic children to accept their children for who they are and show them love, saying that it is difficult because, at times, such challenges can be difficult to deal with.

“But always show them love because they don’t just come and say, ‘I’m just going to misbehave today.’ Something triggers it. Show them love. Show them attention. And just have it at the back of your mind that every child, if the right resources, the right time, the right attention, the right love is given to a child, they normally excel.

“And to everybody out there, no child should be left behind, no matter what. Every child matters, irrespective of the diagnosis.”

Kanye’s brother, Ozichukwu Tagbo-Okeke, said he’s very proud that someone he is related to and so close to, whom he loves, is accomplishing such a great feat.

“I’m lost for words. It’s really amazing seeing him soar to the heights that he’s getting to. When he was small, he used to like drawing and colouring, and they saw that he had an interest in that. So, from that interest, they pushed him, and they pushed his dream for him to accomplish what he has accomplished today.”

He said his brother’s achievement showed parents that their special needs children can accomplish their dreams if supported by their parents and society.

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GTCO conference highlights urgent need for early Autism support, societal inclusion

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The Guaranty Trust Holding Company’s (GTCO) 15th Annual Autism Conference has underscored the urgent need for early autism support and greater societal inclusion in Nigeria.

Oyinade Adegite, Head of Corporate Communication at GTBank, reaffirmed the bank’s unwavering commitment to raising awareness about autism and promoting a more inclusive society for individuals on the spectrum.

The conference, which opens today, July 15th to 17th at the MUSON Centre, Onikan, Lagos, aims to spotlight the critical importance of early intervention and the need to cultivate an inclusive environment where individuals with autism can thrive.

Speaking during a press briefing ahead of the conference, themed “From Awareness to Action: 15 Years of Advancing Autism Inclusion.

Adegite expressed the need to engage directly with communities to raise awareness and promote understanding that individuals with autism are simply different, not deficient. 

She stressed the importance of fostering a welcoming environment for those on the spectrum. “We often wonder what truly matters, and one answer is amplifying the voices of those who are usually unheard. Sometimes we speak up, and sometimes we feel ignored.

 This frustration is even more profound for children and adults who struggle to express themselves. It’s crucial for society and communities to recognize and respect these differences.”

Dr. Grace Bamgboye, an expert in speech and language therapy, highlighted how crucial early detection and support are in enabling children with autism to thrive. 

“The sooner we can identify autism and provide intervention, the better the chances for these children to succeed,” she explained.

Autism advocate Solape Azazi shared her own journey navigating the challenges faced by families. She pointed out the pressing need for increased support and resources, noting, “Too many families are left to manage on their own without access to the tools and assistance necessary to help their children flourish.”

“For the past 15 years, GTCO has remained deeply committed to advancing autism awareness and fostering inclusion across Nigeria. Through its ongoing initiatives, the organization has created a supportive space where individuals with autism and their families can share their stories, find community, and gain strength from shared experiences.

This year’s conference will offer a variety of engaging sessions—including hands-on workshops, specialized clinics, and advocacy-focused discussions—all aimed at deepening public understanding and encouraging greater societal acceptance.

With appropriate support systems and access to necessary resources, people on the autism spectrum have the potential to live rich, purposeful lives and make meaningful contributions to their communities.

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Group demands 5% legislative seats for women with disabilities

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A disability rights group, under the auspices of Network of Women with Disabilities (NWD), has called for 5% of legislative seats to be specifically reserved for women with disabilities in the Reserved Seats for Women Bill currently under review by the National Assembly.

Lois Auta, President of the Network, has urged the National Assembly to ensure inclusive representation in the ongoing constitutional review.

 In a memorandum presented during the Zonal Public Hearings, she called for five percent of the 181 proposed additional legislative seats for women to be specifically set aside for women living with disabilities.

Auta emphasized that the proposal is not a matter of benevolence, but one of fairness, justice, and equal rights.

“True representation is about justice, not sympathy. Women with disabilities deserve a constitutionally guaranteed presence in Nigeria’s political system,” she said. 

“At least five percent of the proposed special seats for women should be allocated to this group, and all legal and constitutional language must reflect inclusivity and a rights-based approach.”

She also advocated for comprehensive reforms within political parties to create pathways for women with disabilities to contest and assume leadership roles.

She emphasized the need for political spaces to be accessible, highlighting the importance of inclusive campaign venues and polling stations.

 She also proposed the creation of an Electoral Support Fund specifically designed to support candidates with disabilities.

The President of the NWD urged legislators to take bold and timely action to guarantee that women with disabilities are given reserved seats, stressing that this is essential for achieving truly inclusive governance.

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Children with special needs in England are 20 months behind their peers by age five, report reveals

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A new report has revealed that five-year-old children with special educational needs in England are now 20 months behind their peers, raising concern over a widening gap in the country’s education system.

 The Education Policy Institute’s (EPI) annual report, published on Tuesday, warns that, five years after the pandemic, the attainment gap for these children continues to widen, with little sign of recovery.

 The disruption caused by Covid, including school closures and reduced attendance, has left disadvantaged pupils and those with special educational needs struggling to catch up.

Though the disadvantage gap at primary and secondary schools narrowed marginally between 2023 and 2024, it says disadvantaged pupils remain significantly behind their peers, with the gap up to a month wider than before the pandemic.

The gap has grown yet wider among children in reception class right at the start of their education, with pupils with special educational needs and disabilities (Send) the most severely affected, the EPI analysis shows.

In 2024, five-year-olds with education, health and care plans (EHCPs) – legally binding documents that outline the additional support required – were 20.1 months behind their peers, the widest gap on record since EPI analysis began more than a decade earlier.

Five-year-olds from lower-income families than their peers are also falling further behind, prompting warnings that the impact of the pandemic has had “long-lasting effects on infants’ development”.

Natalie Perera, EPI’s chief executive, said the report showed that five years on from the pandemic the education system had yet to recover.

“Our youngest and most vulnerable learners are still paying the price. This should be a significant concern for policymakers,” she said. “Without swift action, we are baking lifelong disadvantage into the system. Higher levels of funding for disadvantage, addressing student absence, and fixing the Send system, which is at crisis point, are urgent priorities.”

The EPI report compares pupil attainment in 2024 with the previous year and with 2019, the year immediately before the Covid-19 pandemic, based on economic disadvantage, Send, gender, ethnicity, English as an additional language (EAL) and geography.

It finds that fewer disadvantaged young people are participating in education post-16 than at any point since 2019, resulting in more than one in five disadvantaged 16-year-olds out of education or training.

At key stage 4, which culminates in GCSEs and in education for 16-19-year-olds, the attainment of white British pupils has declined since 2019 relative to all other ethnic groups and girls have “made consistently less progress than boys across secondary school once their attainment at age 11 is taken into account”.

John Barneby, the chief executive of Oasis Community Learning multi-academy trust, said: “The growing inequalities facing our youngest and most vulnerable children –particularly those with Send – are deeply concerning and risk entrenching disadvantage for a lifetime.

“Addressing these challenges requires bold investment and a shared commitment across society to give every child the opportunity to flourish and find their place in the world.”

Pepe Di’Iasio, the general secretary of the Association of School and College Leaders, said: “From a government whose mission is that background should not be a determining factor in success, we need to see more purpose and positive action.

“The gap identified between five-year-olds with special educational needs and disabilities and their peers is particularly alarming, and emphasises how important it is for the government to get right its planned reform of a system that is under unsustainable pressure and is not working well for anyone.”

A Department for Education spokesperson said: “This report lays bare the widening disadvantage gap this government inherited, and which we are working flat out to solve through the plan for change.

“From next year we will be investing £9bn per year in a revitalised early-education system that helps get children ready for school, with working parents receiving 30 funded childcare hours a week, an almost 50% increase in early years disadvantage funding, and a strong new focus on improving the quality of reception-year education.”

The Guardian 

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