…all such a pain!
… Is everyone else also in constant pain?! In 4 years (since diagnosis), throbbing / burning pain in my feet / lower legs has been constant. There’s never a second of the day or night when I don’t feel it. They give me Amitriptyline for it and that doesn’t even touch it so I dont bother with that anymore, but I’m curious to know if this constant, unrelenting pain is something everyone experiences and if so, how do you deal with it?
I work full time and just live my life, ignoring MS as much as humanly possible but this constant pain is just boring and I’d love to know if there are any recommendations to help it! Thanks! 💛
remove all fruit that has citrus , or everything that has citrus and the burning will stop. Also find yourself splina and that will help you also to most of Ms symptoms. take care.
No, MS is so different for everyone that not everyone is going to experience pain. my feet feel either randomly warm or cold some of the time but I wouldn’t describe it as pain. But lots of people will share your experience too. Its really important this doesn’t affect your sleep. Have you tried asking your doctor for a different medication? There are other medications which might work better than amitryptyline for you. I’ve heard of people using heat pads or magnesium supplements as well.