FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
|
Thread Tools | Display Modes |
![]() |
#1 | ||
|
|||
Member
|
As some of you will know I have written to Angela Vincent and the national hospital of neurology.
Today I recieved a reply from the national hospital of neurology. In the letter it says they can only see me via a referral from my gp or consultant. It states "From your letter it does sound as though investigation and management has been entirely appropriate and would have followed the same lines that we would have undertaken in London. I am very sorry not to be able to help further in this matter, but I do wish you all the best" Well you can't say I didn't try! I just don't know what to do next. Love Rach ![]() |
||
![]() |
![]() |
Thread Tools | |
Display Modes | |
|
|
![]() |
||||
Thread | Forum | |||
ALS Update | ALS | |||
My Update | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Update | Occipital Neuralgia and other Cranial Neuralgias | |||
Update on my son | Thoracic Outlet Syndrome | |||
Update | Peripheral Neuropathy |