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...
Cmt and progesterone
Hi, does anyone have any knowledge of the effect of progesterone on cmt? I have cmt1a. Seems to be...
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...
Medication for children?
My almost 4 year old daughter has cmt type 1a. Every night she wakes with cramps, this happens...
JOINT PROBLEMS and CMT
I have had CMT for most of my adult life but was only diagnosed when I was in my late 40's. I am...