Dotun Tejuoso Muscular Dystrophy Foundation

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Dotun Tejuoso Muscular Dystrophy Foundation We support people living with Muscular Dystrophy or any form of disability and there families in Africa Especially Nigeria.

Understanding Duchenne Muscular Dystrophy starts with awareness. Today, we are pleased to join BCOS Mid-Morning Show for...
14/09/2026

Understanding Duchenne Muscular Dystrophy starts with awareness.

Today, we are pleased to join BCOS Mid-Morning Show for an important conversation on Duchenne Muscular Dystrophy (DMD) — a condition that affects children and families in profound ways.

Our Founder, Mr. Dotun Tejuoso, will be joining Dr. Joy Alejo, Consultant Paediatric Neurologist, to discuss the realities of muscular dystrophy, challenges around diagnosis and care, the experiences of patients and families, and what needs to change.

At the Dotun Tejuoso Muscular Dystrophy Foundation, we believe that no person living with muscular dystrophy should be invisible, undiagnosed or left without support.

We are working to improve awareness, early diagnosis, access to care, patient support and data for people living with muscular dystrophy and related neuromuscular conditions in Nigeria and across Africa.

📺 BCOS Mid-Morning Show
📅 Monday, 14 September 2026
⏰ 10:30 AM
📍 BCOS TV Studio, Ibadan

📡 Watch live on Facebook: BCOS TV Live
▶️ YouTube:

Join the conversation. Share this post. Help us raise awareness.

Because every person living with muscular dystrophy deserves to be seen, heard, diagnosed and supported.

RareDiseasesNigeria NeuromuscularDisorders DisabilityAdvocacy MuscularDystrophyAwareness Nigeria Ibadan PatientAdvocacy RareDiseaseAwareness CountedConnectedEmpowered

Today. I’ll be having an important conversation about Duchenne Muscular Dystrophy (DMD) and the realities of living with...
14/09/2026

Today. I’ll be having an important conversation about Duchenne Muscular Dystrophy (DMD) and the realities of living with muscular dystrophy in Nigeria.

I’m honoured to join Dr. Joy Alejo, Consultant Paediatric Neurologist, on the BCOS Mid-Morning Show tomorrow, Monday, 14 September, at 10:30 AM.

For me, this is more than a television appearance.

As someone living with Becker Muscular Dystrophy, I understand personally what it can mean to grow up with symptoms that are not properly understood, to wait years for a diagnosis, and to navigate life with a condition that many people have never heard of.

But I also know that my story is not unique.

There are many children and adults across Nigeria living with muscular dystrophy and other neuromuscular conditions who remain undiagnosed, misdiagnosed or without adequate support.

That is one of the reasons I founded the Dotun Tejuoso Muscular Dystrophy Foundation and why we are working with our clinical partners at UCH Ibadan and others to build the Muscular Dystrophy Registry Nigeria (MDRN).

We need better awareness.
We need earlier diagnosis.
We need better access to care.
And importantly, we need data — because people who are not counted can easily be overlooked.

I’m looking forward to having this conversation, sharing both the patient perspective and the advocacy work we are doing, and hopefully reaching more families who need to know that they are not alone.

📺 BCOS Mid-Morning Show
📅 Monday, 14 September 2026
⏰ 10:30 AM
📍 Ibadan
▶️ Live on BCOS TV Facebook & YouTube

If you can, please join us — and share this post.

Let’s keep putting muscular dystrophy on the map.

Counted. Connected. Empowered.

RareDiseasesNigeria PatientAdvocacy DisabilityAdvocacy NeuromuscularDisorders Nigeria MDRN DataEquity CountedConnectedEmpowered

Understanding Duchenne Muscular Dystrophy starts with awareness. Today, we are pleased to join BCOS Mid-Morning Show for...
14/09/2026

Understanding Duchenne Muscular Dystrophy starts with awareness.

Today, we are pleased to join BCOS Mid-Morning Show for an important conversation on Duchenne Muscular Dystrophy (DMD) a condition that affects children and families in profound ways.

Our Founder, Mr. Dotun Tejuoso, will be joining Dr. Joy Alejo, Consultant Paediatric Neurologist, to discuss the realities of muscular dystrophy, challenges around diagnosis and care, the experiences of patients and families, and what needs to change.

At the Dotun Tejuoso Muscular Dystrophy Foundation, we believe that no person living with muscular dystrophy should be invisible, undiagnosed or left without support.

We are working to improve awareness, early diagnosis, access to care, patient support and data for people living with muscular dystrophy and related neuromuscular conditions in Nigeria and across Africa.

📺 BCOS Mid-Morning Show
📅 Monday, 14 September 2026
⏰ 10:30 AM
📍 BCOS TV Studio, Ibadan

📡 Watch live on Facebook: BCOS TV Live
▶️ YouTube:

Join the conversation. Share this post. Help us raise awareness.

Because every person living with muscular dystrophy deserves to be seen, heard, diagnosed and supported.

RareDiseasesNigeria NeuromuscularDisorders DisabilityAdvocacy MuscularDystrophyAwareness Nigeria Ibadan PatientAdvocacy RareDiseaseAwareness CountedConnectedEmpowered

Our Founder & Executive Director, Adedotun Tejuoso, will be joining News Central TV’s Breakfast Xtra to discuss the real...
05/09/2026

Our Founder & Executive Director, Adedotun Tejuoso, will be joining News Central TV’s Breakfast Xtra to discuss the realities of living with Muscular Dystrophy in Nigeria and the urgent need for greater awareness, research and improved access to care.

The conversation will highlight the challenges faced by individuals and families living with muscular dystrophy, including delayed diagnosis, limited access to specialist care and genetic testing, and the need for stronger patient data and research.

At the Dotun Tejuoso Muscular Dystrophy Foundation (DTMDF), we remain committed to changing this narrative by advocating for better care, supporting patients and families, strengthening research, and building systems that ensure people living with muscular dystrophy are not left behind.

📺 Breakfast Xtra – News Central TV
📅 Sunday, 6 September 2026
⏰ 9:00 AM WAT
📍 DStv Ch. 422 | GOtv Ch. 23 | StarTimes Ch. 274
▶️ Live on YouTube:

Tune in, share the conversation, and help us raise awareness.

Awareness. Advocacy. Research. Action. 💙

RareDiseases PatientAdvocacy DisabilityInclusion MuscularDystrophyAwareness HealthcareNigeria MedicalResearch NewsCentralTV

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No 1, Jericho Idi Ishin Road, Jericho GRA
Ibadan
234

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