Save Nil’s Life !
I am starting a campaign for Nil Güleç who is the daughter of my close friends Ali and Nihan Güleç. Nil was diagnosed with spinal muscular atrophy (SMA) type 2. In order to have a better future, Nil has to receive a genetic therapy called Zolgensma. Zolgensma costs $ 5k, with additional expenses the total amount reaches $ 5k. Zolgensma approval only covers children under 2 years. Nil is 18 months old. We have a fight against the clock. She must receive her treatment in the United States. Below, you can find the story of Nil and her family. Your donations will be greatly appreciated. This campaign is dedicated exclusively to Nil.