There\'s hope - maybe I do have PD after all.
I now have a new glimmer of hope that it is not ALS after all (movement specialist MD wanted me to see an ALS doctor …
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Parkinson's Pain - Does it exist? YES YES YES - Why do we not talk about our chronic pain? I'm in pain every day now and my so called MOVEMENT DISORDERS SPECIALIST refuses to even accept the idea that it's painful so therefore I'm going to look for another doctor. What to do and where to go? I'm so frustrated and hurting this morning and oh so tired from lack of sleep because it's too painful to stay in bed. Why isn't Parkinson's listed as a chronic pain disorder like all the others that get so much attention? I'm going to sound like a whiney baby in all this but I'm beginning to wonder "why not?" since nothing else works anyway! Thanks for listening to an old tired out person here! ParkieJan
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I am taking aleve every day . It almost feels like arthritis pain or burning.
ShellJ
Is it cold and rainy the Jan? That always makes it worse. I would put on my sassafras face if I were near you and you could come watch the old men squeeze my balloon boobs. There did that make you smile. Hope so. Hang in there warm weather is coming and we always feel better then. Sass.
Sassafras
Sass, It's been rainy and stormy here the last two days but not cold. It's been in the 70's. Thanks for the smile for the day. Hugs, Jan
parkiejan