I am desperately looking for a pair of shoes for my 22 year old son with DMD. His foot drop is really bad with his little toe curling underneath his foot. Any advice?
My name is Margarita, I live in Ukraine, Kirovograd. I have a son, who is ill with Duchenne. My name is Margarita, I live in Ukraine, Kirovograd. I have a son, who is ill with Duchenne. He is now 10 years old. Doctors diagnosed the illness at the age of 6.5. In Ukraine, no onetreats such children. Therefore, we are forced to travel to Israel each year toseea neurologist. There we learned howto swim in the pool, ride a horse,dospecial exercises (such asstretching)every day. For 2 years we have been able to stop the disease. But last 2 years my son fells woster than it was early. Iwould liketo communicate withtheAmerican parents and doctors whoprobablyknow more about new medicinesor methods for treating this condition. My email my-science@ukr.net. If you have a free time write me on my email I wiil wait.
hi carol - just ran across ur page & wanted to say HI - I was brought to tears when I read that you never thought you'd see the day your son turned 22. Our Levi just turned 3 and was recently dx w/ DMD - all we want is for him to turn 22, 32, 42, 52 etc. we have great family helping us and PPMD has been amazing. Your son looks so happy. and thaty's all we want for Levi and his 2 older bros who do NOT have DMD. well just want to say HI perlita
Carol, thanks for the link to the article about the brain and Duchenne. Did you ever take Daniel to a neuropsych when he was younger? I am thinking about doing so for Cory after reading the article.
Hi Carol. Thanks for the link to the article, I look forward to reading it. I am sorry to hear of all your recent troubles. When it rains it pours! Lets talk soon.
Carol, I would love to meet you--Wednesday would work. This sense of insanity is overwhelming, every step of the way has been frustrating. When Cory started kindergarten there were some problems at school which after trial and error turned out to be Aspergers. Good news, he was set up with an IEP and his school has been really great. He was also toe-walking at 6 so we went to his ped. who sent us to a ped. orth. surgeon. Dx was idiopathic and they casted him. That didn't do much so he suggested surgery, I said no (surgery when dx is idiopathic?). November '08, a teacher's off-the-cuff comment "he walks like one of my MD students" sent me through this latest labyrinth trying to get a dx. One dr. told me to go to a child psych. Finally found MDA through the internet and got a dx in Jan and genetics lab in March. But that is about all they can offer. Many hours of research and I have found very interesting work on the connection btwn autism spectrum and DMD. I just really need to find the best place to take Cory for real help.
Hi Carol. I just joined PPMD and was looking for parents of children with DMD in Montana. I live in Missoula and my son Cory is 8 yrs. I thought I should introduce myself here because Paula H. mentioned your name to me. Just wanted to say hello.
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"Hello, Dear Carol! I wrote to you the letter to your email again"
Hello, Carol! I wrote to you the letter to your email.
My name is Margarita, I live in Ukraine, Kirovograd. I have a son, who is ill with Duchenne. My name is Margarita, I live in Ukraine, Kirovograd. I have a son, who is ill with Duchenne. He is now 10 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 asstretching) every day. For 2 years we have been able to stop the disease. But last 2 years my son fells woster than it was early. I would like to communicate with the American parents and doctors who probably know more about new medicines or methods for treating this condition. My email my-science@ukr.net. If you have a free time write me on my email I wiil wait.
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