Lizzy,

Did this problem start once you began the novatrone? You know once you took that you had some swelling, and I know that can cause pain in the extremities.

As for myself I have that everyday, but that's part of my Fibro.

hugz Sis :)

Right now I am having the same problem...it is so painful, especially when I take the pressure off of them. Haven't heard of any help or anything....would like to know myself what is going on. LOTS OF LOVE.

I get pain in my feet and hands, but I also was wondering about the novatrone? Hubby also gets his feet pain from neuropathy, so anything is possible... hugs
Morgaine

thanks to you all so much the problem started before i started the novathrone.i forgot to mention i also get a sore tongue lol.suny a good idea the parafin.im going to try that on my hands and feet alas;not my tongue lol thanks again loads of love lizxxxx

I have pain all the time in my feet and the ankles....I heard Montel Williams explain his MS and sounds exactly like mine....my hands have the same problem....gotta love/hate MS..the only thing that helps are hot oil rubs, hot baths, surprisingly hot tea and warm blankets....go figure..good luck.

Hi sis, what you are describing is neuropathy which occurs quit often with people with MS. Usually what is given is neurontin or cymbalta which is a newer antipressant. If they give you the neurontin please be careful ... often docs will start you on a high dose versus starting low allowing your body to tolerate it slowly. It is a wonder drug for the pain, but it is horrible if given to much to fast...feel like you are in a fog etc. Best wishes... love Carol

oohhh neuropathy we are very knowledgable in this house with that...hubby has diabetes and neuropathy ...he takes neurontin and amnitryptiline(sp) for it and it works well for him. But I tried the neurontin for my neuro pain and I puked my guts out, was allergic to it :( anyways now I am on nrcotic pain med and supposed to be on wellbutrin but well I haven't refilled it yet lol...but I am getting by with out it ;) just my pain med and baclofen right now ;) but I have to say my pain got the best of me last night...not what liz has thonot the feet I had spasms and leg pain. But anyways good luck lizz
hugz and sorry for the rambling on and on lol
Morgaine

i have the sore feet and hands but only effects my left hand but both feet. the only thing I';ve found to help is hot tub water or the foot messagers you put your feet into. I know the hot water is a no no for ms but i also have fibro and if it works to relieave the pain i will do it.

I haven't been offically dx'd yet. I've had two MRI's which show brain lesions. but yes,the soles of my feet hurt so much of the time. Hands, too, but it feels like deep tissue in my hands that hurts. The area between my thumb and forefinger. It's really hard to try and explain to anybody how it feels...

thank-you all so much for your replys but not been well again and i have only been poopping on for a min or teo here and there i see the neuro next month and i am going to ask about these meds some of u mention then hopefully i be back to happy feet and hands lol thanks again love lizxxxxx