Does anyone else get really bad pain at night? The restlessness is pretty well controlled, especially since I have managed to get back on the pramipexole, my chemist called to let me know he had managed to get it again m which was good of him.
I truly feel I can't take the pain much more, it is not just in my legs but all over, even my hair follicles hurt if you can imagine. I am not sure if it is the RLS, as I have been told that I have an autoimmune disease in the crest spectrum. The thing that makes me connect it to RLS is that as soon as it gets dark, it starts, and calms down somewhat at dawn.
My Doctor just says oh dear, but will not offer me anything but tramadol, and Diazepam for muscle spasms.
I hope you are all doing as well as possible,
Hugs Cazx