Help For Little Kris
Spende geschützt
19-month-old Kris was born with spinal muscular atrophy. Spinal Muscular Atrophy (SMA) is a genetic neuromuscular disease characterised by muscle atrophy and weakness. The disease generally manifests early in life and is the leading genetic cause of death in infants and toddlers.
Because Kris doesn't have enough strength, he can't sit or walk on his own and his parents are taking care of him 24/7. At the end of May this year, the U.S. Medicines Agency approved a ground-breaking drug called zolgensma, which cures the disease in ONE SINGLE DOSE. However, this medicine is only suitable for children under the age of two and costs an astronomical £2M. Help us raise £100.000 before Kris reaches 2 years old.
We can do this together!
Because Kris doesn't have enough strength, he can't sit or walk on his own and his parents are taking care of him 24/7. At the end of May this year, the U.S. Medicines Agency approved a ground-breaking drug called zolgensma, which cures the disease in ONE SINGLE DOSE. However, this medicine is only suitable for children under the age of two and costs an astronomical £2M. Help us raise £100.000 before Kris reaches 2 years old.
We can do this together!
Organisator
Child Safe Foundation
Organisator
England
