Hi all,
I know you already know how good the MNDA is, but today I got my first experience of what the association can do for me.
In my welcome post a couple of weeks ago I outlined my plight with trying to get a diagnosis and the seeming lack of support from the NHS.
I sent an e-mail to MNDA yesterday asking for help and within 1 hour of receiving a reply I have already had a very lengthy conversation with Caroline Davis at Queen Elizabeth Hospital MND team which is part of the NHS and I will be getting an appointment with a specialist hopefully as soon as next week.
regards
Les Cotterill
I know you already know how good the MNDA is, but today I got my first experience of what the association can do for me.
In my welcome post a couple of weeks ago I outlined my plight with trying to get a diagnosis and the seeming lack of support from the NHS.
I sent an e-mail to MNDA yesterday asking for help and within 1 hour of receiving a reply I have already had a very lengthy conversation with Caroline Davis at Queen Elizabeth Hospital MND team which is part of the NHS and I will be getting an appointment with a specialist hopefully as soon as next week.
regards
Les Cotterill
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