A question is coming I promise: I can relate to all of these different sensations. I live in texas and am terrified about the cold weather which won't be coming for quite sometime, but it scares me. Maybe that's because it was so cold when in was diagnosed and my hands would feel completely curled up in a ball and while I could pick things up I was unable to set them down.
I take Baclofen for the spastiscity and muscle spasms and I am so thankful that it takes care of that type of pain. After being paralyzed and having to learn to walk again the feeling that was coming back was pain I had never felt before and was so hard to describe. As far as nerve pain goes I take Neurontin. Has anyone been on Neurontin and Lyrica at different times and can try to give a description as to how one works better than the other. My problem is that the Neurontin takes care of most of nerve pain but my hands continue to twitch and when I wake up in the morning my feet and ankles have such a horrible sensation that I feel like I need to go to the hospital - it's that bad (i would not go to the hospital again unless I ABSOLUTELY had to after the time I spent there - a month was long enough for me) Has this happened to anyone. Another question: Has anyone had any convulsions or seizures when they wake up? Not sure what to call them but whenever I wake up, no matter what time, My head thrashes forward than back a few times and it almost seems I have no control over my body. I have to hold onto the ceramic part of the sink so I won't hit it. I have already hit the bridge of my nose and chipped a tooth in doing so. I don't know what to call this but I have made an appt with my neurologist but can't get in until August 1 and am really scared. Also, I have a problem urinating. I have to push really hard no matter how bad I have to go. In conclusion, I would really like to know what works best for nerve pain, whether Neurontin or or Lyrica. Neurontin works other than the bottom bart of my legs. I should be grateful that it works that well, it is much better than what I went through before the scripts were ordered. But am curious about Lyrica. My neurologist mentioned it as an alternative but as I said the neurontin was working so well(other than the lower half that I didn't want to change anything.) Thank you for listening - I know we all have different experiences with our own Transverse Myelitis and I appreciate your time. Wish I could find a support group nearby. While I can't donate just yet I will be able to do so in September and it will be very worth it. On Mon, Jun 25, 2012 at 6:50 PM, Janice Nichols <jan...@centurytel.net>wrote: > I would start with Baclofen first - I think it works great. You > need to take all through the day, morning, noon and night. It really > does help a lot. > Janice > > *From:* Elizabeth Clark <xbeecla...@gmail.com> > *Sent:* Monday, June 25, 2012 2:36 PM > *To:* 'Janet Dunn' <j.d...@shaw.ca> ; tmic-list@eskimo.com > *Subject:* RE: [TMIC] Looking for input. > > > Coincidentally, someone from a different TM support group recently > expressed similar difficulty and here’s a response that may be of help…*** > * > > **** > > > > > “Hi all, > > I am new to this group and was hoping you folks could give me some > advice. I am recovering from transverse myelitis. I was unable to walk for > six months and had complete paralysis from the waist down for three months. > I am now able to walk again, but have severe hypersensitivity to hot and > cold and get stabbing pain in my legs particularly at night. What do some > of you do for the pain? I am looking to avoid narcotics and habit forming > medications. Any advice you have would be greatly appreciated.”**** > > -----------**** > > “My relief came from flexeral (sp) which helped the spasms and cymbalta, > which helped with the neuropathic pain. When I get localized brutal nerve > pain in my spine (rare), only tramadol helps.”**** > > **** > > **** > > *From:* Janet Dunn <j.d...@shaw.ca> **** > > *Sent:* Monday, June 25, 2012 12:29 AM**** > > *To:* tmic-list@eskimo.com **** > > *Subject:* [TMIC] Looking for input.**** > > **** > > Hello Everyone - not sure who is on here anymore. > > I have written in before, several times in fact, bemoaning the issues that > I have with the cold cold winters that we get up here in northeastern BC. > > Now, it is the heat. My question is this: does excessive heat cause > issues like the cold does? I have never noticed it before, but this year I > quit taking Lyrica, and I cannot get the spasming in my leg to stop, no > matter what I try. I am wondering if stopping the lyrica has contributed > to the increase in pain, or if it is heat related? > > Thanks for your input. > > Janet**** >
