CMT
Options
Lucysmumx
Community member Posts: 1 Listener
Hi my name is Helen my 15 year old daughter has CMT or also known as HMSN Hereditary Motor Sensory Neuropathy it is a rare muscle wasting disease which affects the hands & feet mainly but there are many other symptoms.
Comments
-
Hi @lucysmum.
It is great to have you here I do hope that we can offer you both support/advice.
Please have a good look around the site & please let me know if there is anything else that I can help you with ??? We have a very active online community where you can talk to other people in similar situations as you.
Please please let me know if I can assist you further ??? -
Hi @lucysmum,
Welcome to Scope's online community! It's great to have you here.
There's plenty of groups and discussions for you to get involved with, whether it's just for a chat, or to ask for some help and support.
If you have any questions, please do get in touch!Liam
Brightness
Categories
- All Categories
- 13K Start here and say hello!
- 6.6K Coffee lounge
- 69 Games lounge
- 385 Cost of living
- 4.3K Disability rights and campaigning
- 1.9K Research and opportunities
- 199 Community updates
- 9.2K Talk about your situation
- 2.1K Children, parents, and families
- 1.6K Work and employment
- 767 Education
- 1.7K Housing and independent living
- 1.4K Aids, adaptations, and equipment
- 586 Dating, sex, and relationships
- 363 Exercise and accessible facilities
- 737 Transport and travel
- 31.6K Talk about money
- 4.4K Benefits and financial support
- 5.2K Employment and Support Allowance (ESA)
- 17.1K PIP, DLA, and AA
- 4.9K Universal Credit (UC)
- 6.2K Talk about your impairment
- 1.8K Cerebral palsy
- 868 Chronic pain and pain management
- 180 Physical and neurological impairments
- 1.1K Autism and neurodiversity
- 1.2K Mental health and wellbeing
- 317 Sensory impairments
- 818 Rare, invisible, and undiagnosed conditions