Diana’s Story — A Little Girl Fighting for Life ]

— I’m a dad of a beautiful two years old girl named Diana — a little angel who has filled our lives with love and laughter.
We are from Iraq and currently live in the United Arab Emirates.
I hope every parent who reads Diana’s story will feel her struggle and help her complete the next stages of her young life.
Diana is a bright and loving girl who once spent her days playing, laughing, and taking her first steps.
But one day, everything changed.
She was diagnosed with Spinal Muscular Atrophy (SMA) Type 2, a rare and life-threatening genetic disease that slowly weakens the muscles.
What began as slight difficulty standing and walking has turned into a serious medical crisis.
Without urgent treatment, SMA will continue to progress, affecting her ability to breathe and eat — and eventually putting her life at risk.
There is one hope — a life-changing treatment called Zolgensma, a groundbreaking gene therapy that replaces the missing gene responsible for SMA.
This treatment has the power to stop the disease and give Diana the chance to live a healthy, normal life.
However, this hope comes with a huge challenge: the treatment costs $2 million USD.
Without it, Diana’s condition will continue to deteriorate, leaving her future uncertain.
We can’t do this alone — we need your help to save Diana.
Every donation, no matter how small, brings us one step closer to giving her a second chance at life.
Even one dollar or one euro can make a real difference.
If you cannot donate, you can still be a hero by sharing Diana’s story with your friends, family, and social media.
Every share helps us reach more kind-hearted people who can make a difference.
Your kind words, encouragement, and prayers mean so much to Diana and to us.
Together, we can give Diana the greatest gift of all — the gift of life.
From our hearts, thank you for your kindness, generosity, and prayers.
You are not just helping Diana — you are giving her a future. ❤️