Jasmine was born in 2010 with hip spica and hypotonic muscles. She and her mum have been going to regular rehabilitation sessions ever since. The hip dislocation was corrected by surgery, but over time it was discovered that she has an incurable muscle disease (Urlich muscular dystrophy), which is a constant deterioration. Jasmin finds it increasingly difficult to walk and tires quickly, but they go outdoors a lot in a wheelchair because he loves being outside with his brother. Since then, his illness has also affected his digestion and breathing, which have been corrected by PEG implantation. This helps her to get the right nutrition, and at night the breathing machine helps her to get the right oxygen. Despite the difficulties, Jasmine is a smiling, happy little girl who loves to read and experience things.

Please support Jasmine and her Family so that she can have all the opportunities that will help her to live a happy life!