Support for our Young People with CMT - Charcot-Marie-Too...

Charcot-Marie-Tooth UK

1,688 members667 posts

Support for our Young People with CMT

Joel profile image
Joel
1 Reply

We try to provide support for the Young People who have attended our Young People's Weekends in person, or by phone, email or Facebook.

There is an active "CMT Kids" Facebook page, but this is a closed page, and your membership of it will need to be approved by Karin Rodgers - if you'd like to email her to explain your links with CMT and CMT United Kingdom, please email karin@cmtuk.org.uk

You can find the CMT Kids Facebook page here: bit.ly/aaqcHE

Written by
Joel profile image
Joel
To view profiles and participate in discussions please or .
1 Reply
CMTerSam profile image
CMTerSamVolunteer

Go CMT Kids :D

Not what you're looking for?

You may also like...

CMT in young people

Hi My Name is Sean Paul and im 29. My CMT results in having a bad tremor in my hands and i just...
SPJCurry profile image

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...
Cindyyb profile image

Stem cell treatment for CMT

There is a clinic in Cancun (world stem cells) that offers stem cell treatment for CMT sufferers....
Etxalar profile image

Speech Problems with Type 1A CMT

I was only diagnosed with Charcot Marie Tooth 1 years ago because the doctors I consulted in...

Struggling with cmt child

Hi all. My ten year old son has CMT and was diagnosed four years ago. He is now very frustrated and...
Asyeda profile image

Moderation team

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.