Our beautiful little boy, Mamoun, has been diagnosed with Spinal Muscular Atrophy (SMA) Type 2, a rare genetic disease that gradually weakens the muscles needed to crawl, stand, walk, swallow, and eventually breathe.

After months of searching for answers, our family made the heartbreaking decision to leave behind our home, our jobs, and our loved ones in hopes of giving Mamoun access to the specialized care he urgently needs.

Despite every challenge, Mamoun continues to greet each day with a smile. He is now receiving medical care and rehabilitation to help preserve his strength, improve his mobility, and give him the best possible future.

Treatments such as Zolgensma, Spinraza, and Evrysdi can slow the progression of SMA, but they are among the most expensive treatments in the world, costing from hundreds of thousands to over $2 million, in addition to the ongoing costs of therapy, rehabilitation, specialist care, and medical equipment.

Your support will help cover these essential treatments and the many expenses that come with Mamoun’s care. Every donation—no matter the amount—brings him one step closer to a brighter future.

If you can’t donate, sharing his story can make a world of difference.

Thank you for standing with our family and giving Mamoun the chance to keep smiling, growing, and reaching the milestones every child deserves.

To ensure complete transparency, donations will be received by our trusted family friend, Mr. Adam, in France, who will securely transfer the funds to our family for Mamoun’s care. We are deeply grateful for your trust, generosity, and support.