Help Little Behiye Get Her Life-Saving SMA Treatment Before It’s Too Late

Hello,

My name is Samet, and together with my wife Sıla, we are the proud parents of our beautiful 19-month-old daughter, Behiye.

When Behiye was 17 months old, our world changed forever — she was diagnosed with Spinal Muscular Atrophy (SMA) Type 1, a rare and life-threatening genetic disease that weakens the muscles and makes it difficult to move, swallow, and eventually breathe.

Behiye is a bright, joyful, and strong little girl. She loves to smile, listen to music, and hold our hands. But SMA doesn’t wait — and she must receive her life-saving treatment before turning two years old for it to be effective.

We are doing everything we can. I work as a security officer in the private sector, and my wife takes care of Behiye full-time. However, the cost of this treatment is far beyond what any normal family can afford.

That’s why we are reaching out to you — kind people from around the world — to help us save our daughter’s life. Every donation, big or small, brings us one step closer to giving Behiye the chance to grow up, to walk, to play, and to live the life she deserves.

Please share our story, pray for Behiye, and help us reach our goal.

From the bottom of our hearts — thank you for giving our little girl a chance at life.

With love and gratitude,

Samet & Sıla

(Parents of Behiye, SMA Type 1 Fighter )