Yukhym Vykhopen
Yukhym Vykhopen with tuberous sclerosis received the so much needed rehabilitation at the Olinek Center in Poland.
Yukhym Vykhopen with tuberous sclerosis received the so much needed rehabilitation at the Olinek Center in Poland.
One more victory for our USA Resettlement Program: on June 28, Maksym Kadubets received his Zolgensma.
During the star-studded annual event in Franklin, a popular American country singer purchased an auction package donated by one of our loyal supporters.
Yeva Sharko has received Zolgensma at the Children’s Hospital of Los Angeles as a U4U parolee and our USA Resettlement Program.
Ksieniia Karimova’s fundraiser is closed! BfS has collected and transferred $13,920 to cover Ksieniia’s treatment for phosphate diabetes in Israel
The second child in a healthy family, Tymofii was developing normally in the first days, however, he sadly faced the early onset of SMA already in the third week after birth. The genetic testing soon confirmed the Type 1 diagnosis and tore the parents’ hearts forever apart.
In these 2 years, the family had to learn to build their life into Tymofii’s routines and devices. Tim is taking Risdiplam as a part of Genetec’s Early Access International Program.
The members of the BFS Board of Directors Nataliya Miller and Matt Lambert have been interviewed by KUTV CBS 2 channel
BFS congratulates Dima, his family and the team of volunteers! We are endlessly happy you’ve been given this amazing chance before the age of 2! Hope, the rehabilitation is easy, and the effects of the therapy are going to be stunning. Wishing Dima all the health on the planet!
Sofiia Mykytiuk is 9 months old, she has SMA Type 1. The family decided to immigrate to the US 5 months ago as “Uniting for Ukraine” program participants. After long examinations and tests, Sofiia qualified for Zolgensma therapy and received treatment at Los Angeles Children’s Hospital right after Christmas 2022.
BFS expresses enormous gratitude to all medical professionals and volunteers who made this life-saving journey for Sofiia a reality!
BFS has raised $9,950 for Oleksand’s annual hormonal therapy with Genotropin.
Sasha needs to take the synthetic form of the hormone of growth on a daily basis. This way his body and internal organs will form properly.
Thank you for supplying Sasha with this treatment for one year!