I am a physiotherapist and have been working for very many years with boys who have Duchenne abd their families throughout our large state I coordinate the multidisciplinaryneuromuscular clinc at my organisation Montrose Access and run a seating clinic every month.
About my family:
I have four adult children and eight grandchildren
I count my the families involved with the duchenne community as my very dear friends
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PPMD advise me to send you my question concerning to night splint. I saw your video clip about PT and use it as guide line for my boy.
My boy start walking with legs inward toe movement sometimes. I much concern if it is because of night splint. My family stay in Vietnam where we cannot find splint particularly for Duchenne boy, so we have to copy from internet and order (casted). So, I worry if it is suitable or not.
Hi Helen, we are both that is Colin and I attending the conference in Baltimore, Sol from the physio practice you visited while you here asked me to ask you to please a bring a copy of the book you were talking about if possible, thanks and look forward to seeing you in July XXX
It is good to see you on the web. are you going to present at the congerence again this year? I will see how it goes and may surprise everyone and arrive, it just depends how the next few weeks go.