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Funded!

6 months of Aybars SMA1 TYPE (Spinal muscular atrophy) treatment

Collected amount

$765
51%
Goal $1,500

Remaining days 0 days

This project has finished.

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the flag image of country Aybars Karadağ
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Hi,

My name is Aybars. I'm a 6 month old baby. I have spinal muscular atrophy called SMA Type 1; this is a deadly muscle disease.

Unfortunately, the gene therapy fee is $2,132,000. And it's too expensive for us to afford. I have very little time for treatment to take place. Even the smallest help in this difficult process will be a breath for me, a step for my future. I need your support. Can you help me please? I love you all.

The future of Aybars is in your hands

Dear benefactors, the future of Aybars is in your hands. Our little baby is struggling with a muscle disease called SMA Type-1. Her only hope is Zolgensma gene therapy.

Payment of the $ 2,156,765 treatment fee specified for this treatment is only possible thanks to the help of you, our valuable people. There is little time for cure to take place. Even your smallest help in this difficult process will be a breath to Hifa, a step for her future. Please give Hifa a helping hand. Her beautiful future is in your hands.

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