***12/3: THANK YOU, THANK YOU, THANK YOU!! We are at 100%! Little Anika will be on her way to get needed therapy in January 2021. Thank you for every single share, every single donation, thank you for your faith and kind words.*** Update 10/24: Dear Friends! Anika is gaining weight and for any healthy baby this is great news, but not for Anika. She is now 3lbs away from being rejected by the hospital to get Zolgensma. Please share and donate as there is not much time left for this little angel.***
To find out more about Anika visit: https://helpanika.com/
From Anika’s dad: God bless you, kind people. My only child, Anika, has a very rare illness. She has a Spinal Muscular Atrophy (SMA type 1). Her breathing and swallowing are deteriorating and the rest of her muscle functions will deteriorate in time. However - there is a hope. There is a gene therapy option called Zolgensma and to get this one time therapy the cost is 2.1 million euros.
It is very time sensitive. Time is not a friend for only child right now. Especially with the cost of the therapy.
I would like to ask anyone who can contribute and save the life of my daughter, to click on the below link and donate. I still strongly believe that there are good hearted people out there.
Every donation counts! Help us to save this young life today!
Thank you again, and God bless you.
- Timothy Arndt
- Jasna Markovic
- ED 70247
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