Are there any services out there that specifically provide mental health support for children/ young adults with Duchenne?
The parent has tried to access support through their health services but hasn't been able to get any.
Are there any services out there that specifically provide mental health support for children/ young adults with Duchenne?
The parent has tried to access support through their health services but hasn't been able to get any.
We are lucky enough to have a Neuromuscular Adviser in Devon and Cornwall, I would usually be asking them for advice.
Where are you based? I would be very sad if the peron's diagnosis has anything to do with them gaining access to support. Are they verbal? I would assume so.
Hi, this might be helpful
Someone to talk to is a peer to peer support where a volunteer is assigned to you to talk about what it’s like to have a deteriorating condition https://www.musculardystrophyuk.org/news/news/peer-support-someone-to-talk-to/