[En Français] We are reaching out to you with hope and urgency. Amina is a bright and courageous child battling an incredibly rare condition known as bilateral congenital femoral deficiency (CFD Type 2) and bilateral humero-radial synostosis with ulnar aplasia. This condition affects only 1 in 100,000 individuals, and without treatment, it severely impacts their quality of life.

There is hope, however. The eminent Dr. Ratnav at Manipal Hospital in India specializes in treating this condition, and we are fortunate that Amina has been accepted for treatment. This treatment offers a real chance for Amina to lead a normal, healthy life.

But we need your help. The cost of the treatment is €30,000, and we cannot do this alone. We are reaching out to our community, friends, and compassionate strangers to help us raise the necessary funds.

Every donation, no matter how small, brings us one step closer to giving Amina the life she deserves. We also ask you to share this message with your networks to help us reach as many people as possible.

Thank you from the bottom of our hearts for your generosity, support, and love.

You can donate thru:

 Cotizup:  https://www.cotizup.com/-cotizup-com-foramina

GoFundMe:  https://www.gofundme.com/f/help-amina-to-reborn-again-with-a-normal-life

Or thru our website:  https://www.mahealthfoundation.org/donate or By Check payable to MAHF