I’ve had CFS/ME ~30 years, which is progressive neurological illness and can cause one to be slowed or bedridden. It’s relatively obscure, about 10 million cases worldwide. Last month I got 2 new diagnoses which may or not be related but are also neurological. One is peripheral neuropathy in the feet. Symmetrical Burning is all consuming. Currently taking Percocet but doctor not inclined to continue it. This is causing anxiety and panic to the max as no other relief in sight.
The other is hand tremors, shakiness. Doc says may be Parkinson’s! I can’t see a neurologist until the end of Feb, 2019. This is scary, thinking of all the possibilities and images. I’m 65+, a little young for this elder disease.
Is there anyone here in similar state - dealing with consuming pain and not having a certain path out; anxiety; fear... ? How do you cope? Thanks.
The other is hand tremors, shakiness. Doc says may be Parkinson’s! I can’t see a neurologist until the end of Feb, 2019. This is scary, thinking of all the possibilities and images. I’m 65+, a little young for this elder disease.
Is there anyone here in similar state - dealing with consuming pain and not having a certain path out; anxiety; fear... ? How do you cope? Thanks.