Donación protegida
Dear Friends,
Can you please support me in helping a little girl Angelina Kovalchuk, born February 21,2018. She was diagnosed with Spinal Muscular Atrophy, stage “I”. It is a rare neuromuscular disorder. She cannot move, she cannot swallow food, she is bedridden and the disease progresses very quickly. At the moment she requires the special feeding through the tube with amino acids mixtures, vitamins and very expensive medications.
In Europe, there is a medication SPINRAZA which cured and brought many patients to a full recovery. Even in USA, in December 2016, it became the first approved drug used in treating this disorder.
Please join me in collecting funds and make sure Angelina LIVEs and ENJOYs this beautiful world!
I deeply appreciate all your help
Can you please support me in helping a little girl Angelina Kovalchuk, born February 21,2018. She was diagnosed with Spinal Muscular Atrophy, stage “I”. It is a rare neuromuscular disorder. She cannot move, she cannot swallow food, she is bedridden and the disease progresses very quickly. At the moment she requires the special feeding through the tube with amino acids mixtures, vitamins and very expensive medications.
In Europe, there is a medication SPINRAZA which cured and brought many patients to a full recovery. Even in USA, in December 2016, it became the first approved drug used in treating this disorder.
Please join me in collecting funds and make sure Angelina LIVEs and ENJOYs this beautiful world!
I deeply appreciate all your help
Organizador y beneficiario
Oksana Heba
Organizador
Walled Lake, MI
VASYL HEBA
Beneficiario