Dear, Abby Bronson! I prepared a project to help children in Ukraine, I sent it to our Ministry. I constantly learn something about muscular dystrophy from your sites. Finally, the Ukrainian neuroscientists have interested in my materials. I have seen that I should help not only my family but also to other families in Ukraine. We must see how parents live in USA.I invite you and somefamily to us in Ukraine. Our family is ready to welcome you and we want very strong to stay to summer camp in USA with my son. He is 9,5. Help us. How I can do it? In Ukraine isn`t camp for Muscular Dystrophy. I'm afraid to lose time.
Hello! My name is Margarita, I live in Ukraine, Kirovograd About my family: . I have a son, who is ill with Duchenne. He is now 9 years old. Doctors diagnosed the illness at the age of 6.5 . In Ukraine, no one treats such children. Therefore, we are forced to travel to Israel each year to see a neurologist. There we learned how to swim in the pool, ride a horse, do special exercises (such as stretching) every day. For 2 years we have been able to stop the disease. But I would like to communicate with the American parents and doctors who probably know more about new medicines or methods for treating this condition.
I want to participate in different Parents’ Projects for Muscular Dystrophy online. There may already be drugs that can cure my son. Please help us, because we are lonely here with our problem.