The Muscular Dystrophy Campaign Nigeria (TMDCN) is a registered charity dedicated to improving the lives of people living with muscular dystrophy and other neuromuscular conditions through awareness, education, advocacy, support, and research.

Our services include:

• Information and education
• Peer support through the TMDCN Connect Network
• Patient registry enrolment
• Advocacy and awareness campaigns
• Research collaboration
• Signposting to specialist healthcare services
• Small Business Start-up Support subject to funding availability 

Our services are available to individuals living with muscular dystrophy and other neuromuscular conditions, their families, carers, healthcare professionals, researchers, and organisations interested in collaborating with us.

No. TMDCN is not a healthcare provider. We do not diagnose conditions or prescribe treatment. We provide reliable information and, where possible, connect individuals with appropriate healthcare professionals and specialist services.

Yes. We can provide information on the diagnostic process and signpost you to hospitals or specialists that offer relevant diagnostic services where available.

The TMDCN Connect Network is our peer support community for individuals living with muscular dystrophy, their families, and carers. Members can connect with others, share experiences, receive support, and access reliable information.

The TMDCN Patient Registry securely collects information from people living with muscular dystrophy and other neuromuscular conditions. The registry supports research, improves understanding of these conditions in Nigeria, and helps ensure Nigerians are represented in global research initiatives.

Yes. We are committed to protecting your privacy. Any personal information you provide is handled securely and used only for the purposes you have consented to, in accordance with applicable data protection requirements.

No. Joining the registry does not guarantee access to treatments or clinical trials. However, it helps advance research and enables us to share relevant research opportunities when available.

This programme provides small grants to eligible individuals living with muscular dystrophy and other neuromuscular conditions to help start or grow small businesses, promoting financial independence and sustainable livelihoods.

Applicants must meet the programme’s eligibility criteria, including demonstrating financial need and submitting a viable business plan. Funding is limited and awarded following an assessment process.

We occasionally provide limited financial or welfare support through specific programmes or grants when funding is available. Unfortunately, we cannot guarantee financial assistance to every applicant.

You can apply by completing our Volunteer Registration Form. If your application is successful, a member of our team will contact you to discuss available opportunities.

We welcome partnerships that improve awareness, diagnosis, care, advocacy, education, or research relating to muscular dystrophy and other neuromuscular conditions.

You can support our work by donating, volunteering, partnering with us, fundraising, or helping raise awareness in your community.

You can reach us through our contact form, email, telephone, or social media platforms. Our team will respond as soon as possible.