Yes. SMA Hope Foundation Nigeria is a registered foundation in Nigeria and is committed to accountability and long-term stewardship.
FAQs
Answers to common questions about SMA, the foundation, and how to help
Understanding Spinal Muscular Atrophy and the work of supporting affected families can bring up many questions.
We have gathered the most common enquiries we receive about the condition, our foundation, the book When Every Breath Matters, and how you can offer meaningful support.
Spinal Muscular Atrophy is a serious genetic condition that causes progressive muscle weakness and can affect breathing, feeding, and movement.
Yes. Families can use the contact form and choose Family support, or email help@smahope.org.
Yes. Donations from Nigeria and outside Nigeria are supported through Paystack.
Yes. Use the contact form with Partnership or Book enquiry, or email help@smahope.org.
Use the contact form and select Partnership / collaboration or Media / speaking invitation, or email partnerships@smahope.org.
A Note on Medical Information
While we strive to provide clear and accurate information about Spinal Muscular Atrophy based on lived experience and established medical consensus, the content provided by SMA Hope Foundation Nigeria is for educational and awareness purposes only.
It should never replace professional medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding your child's specific health needs.
Still Have Questions?
If you couldn't find the answer you were looking for, or if you are a family needing specific guidance, please do not hesitate to reach out to us directly.