This is our resource for parents and teachers of children with CMT. We've included several Muscular Dystrophy Campaign leaflets here, since much of the problems that are faced by our children are applicable to children with any neuromuscular condition. See the Resources for Parents and Teachers page here: cmt.org.uk/Resources_for_Pa...
Resources for Parents and Teachers of... - Charcot-Marie-Too...
Resources for Parents and Teachers of Children with CMT
Written by
Joel
To view profiles and participate in discussions please or .
Not what you're looking for?
You may also like...
Diagnosing CMT in children?
Hiya, I'm new here just looking for some advice and help with a few things :)
Bit of background, I...
Blurred periphial vision with CMT....?
Hiya, I have CMT, Type 1a as well as my 3 children, my sister and my dad. Question: have any of you...
Cmt and progesterone
Hi, does anyone have any knowledge of the effect of progesterone on cmt? I have cmt1a. Seems to be...
Medication for children?
My almost 4 year old daughter has cmt type 1a. Every night she wakes with cramps, this happens...
Hnpp and cmt
Hi I hope that this is the right place that I have came to. I got my diagnosis yesterday it was...