Like to find out more on MS, all i can"t find any thing about pain on it and if it is part of the illmess.

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Pain and MS
* Pain is a common occurrence in MS, with 30-50% of patients experiencing pain at some time in the course of their illness. Pain typically is not associated with a less favorable prognosis, nor does it necessarily impair function; however, since it can have significant impact on quality of life (QOL), it needs to be treated appropriately. Pain in MS can be classified as primary or secondary.

* Primary pain is related to the demyelinating process itself. This neuropathic pain is characterized often as having a burning, gnawing, or shooting quality. Nonpharmacologic techniques, such as use of imagery or distraction, can be helpful. Transcutaneous electrical nerve stimulation (TENS) is useful in some patients. Pharmacologic approaches include prescription of tricyclic antidepressants as first-line drugs. Anticonvulsants, such as carbamazepine, phenytoin, or gabapentin, can be added as second-line agents.

* Secondary pain in MS is primarily musculoskeletal in nature, possibly due to poor posture, poor balance, or abnormal use of muscles or joints as a result of spasticity. Nonpharmacologic treatment for secondary pain includes moist moderate heat, massage, physical therapy, and exercise (eg, stretching). Pharmacologic agents include nonsteroidal anti-inflammatory drugs (NSAIDs) or other analgesics. Use of narcotics seldom is indicated.

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www.webmd.com

Great site for so much info! :)

i would suggest www.nationalmssociety.org they have a lot of info and there is a forum at www.msworld.org or.com i cant remember. but my girlfriend has ms and it can be very painful for her to walk at times, and a lot of the times when it is sunny out.

yes pain unfortunately is part of MS. It comes from the nerve damage that is done because of the disease. Getting hot emphasizes side effects of the disease (that part will improve once the person has cooled down) I have alot of pain in my feet (I have MS) because the nerve signals just don't throught to them anymore, some days it really hurts other not to bad. I am on my feet all day at work which I am sure doesn't help either. When the person gets fatigued the symptoms can be stronger too: time to rest when that happens. The National MS Society is a great website and has lots of links to other websites. Also Montel Williams has a website very informative on both.

unfortunately, there is some nerve pain associated with this disease. Sometimes, my legs hurt very badly after standing for a long period and sometimes, i get pains in my arms. hard to describe them, though. a good neurologist should be able to prescribe a medication for you if you are having nerve pain. its never been too bad for me. =]

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Like to find out more on MS, all i can"t find any thing about pain on it and if it is part of the illmess.

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