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:

For older children:

Muscular Dystrophy Campaign’s resources for children with neuromuscular conditions:

(Don’t forget this guide is not specifically aimed at children with CMT, and may talk about children with conditions that are much more severe than CMT.   Don’t be alarmed, and just take from them what is appropriate for your child.)

CMTA’s leaflet about having children with CMT – this is from the USA, so not all the information will be relevant to us in the UK.

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Last Updated: Monday 17th December, 2018