Has anyone heard of ‘MS burn out’, ?
My neurologist thought that this was where I was at, about 2 years ago. Whereby the patient doesn’t get worse NOR become any better, just remaining as you are.
Here I’ve found although having to go private (cos going public is an absolute disaster) I read with most of you, you have an MS team, & an MS nurse who will call to your homes re- assessing how the mser patient is doing.
This amazes me to be frank, as it’s not happening with those in Ireland (Rep of) π€
Thank you in advance.
Jane
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