Please help me save my niece!
Hello to anyone who's reading this,
I'm a German university student who wants to save her niece from a cruel fate.
My niece Milana was diagnosed with muscle atrophy SMA2. For everyone who doesn't know what it is: Spinal muscular atrophy type 2 (SMA2) is a genetic neuromuscular disorder that affects the nerve cells that control voluntary muscles (motor neurons). Without treatment, progressive muscle weakness develops in babies with SMA2 between ages 6 and 12 months. Babies with SMA2 can sit without support, however, they cannot stand or walk independently. Feeding and breathing problems also develop.
Most infants die due to not getting the proper treatment and medicine they need since it's very expensive! I don't want my niece to share the same fate..
Her birthday was on the 29th of August, she turned one year old. She's just a little baby who is in dire need of getting the proper treatment! My relatives in Russia cannot pay for the therapy and the medicine she needs as fast as possible! I can't stand by and watch her die slowly and painfully, which is why I open up this gofundme, hoping to get enough money to save her life..
Please, if you can at least donate a small amount of money..please do so!
If you know an organization or a doctor or anyone who can help her out,please contact me as well!
Share this with your friends, family and on social media! The more people see it, the more likely are the chances to find some help or get enough money!
I'm grateful to any euro or dollar that will be donated..
All donations will be spend to get Milana her medicine and therapy!