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Welcome Avengr, great to have you here.:)
Spasticity, the MS perk we all know and hate.:mad: There are some meds out there to help, but nothing is going to make it go away completely. Mine is medium to mild, so I use stretching exercises and that helps to relax them a bit, so I can sleep. I've used Lioricel/baclofin (SP), in the past, with little success, but it has helped others, so you may want to try it. |
Hello
Hi, I'm Raeleen - 43
dx 03/98 RRMS From the PNW :) |
Hi all the new folks.
Raeleen - when I saw PNW my first thought was peripheral neuropathy. I'm guessing you mean pacific northwest? avengr13 - seizures? Me too. 1993-1994, about 5 years into this MS adventure. I'm very thankful they went away. bettycas - where in Miami? I worked all over that town. Tom |
for me only meds and laying in bed eventually works for spasticity.
then massage, heat and muscle relaxants. welcome to NT. |
New member...
Hi, my name is Sue. I've been an MSer for a few years. Diagnosed in 92. Have been taking gabapentin for nerve pain since Sept. '12 but have gained much weight. Weaning myself off to see if I can lose the extra weight. Took Copaxone daily shots for about 5 years. Currently not taking anything for MS except Cymbalta for depression. Basically upbeat person who sees the best in folks and loves animals.
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hi sue, welcome to NT,
i love animals too but don't have any. i use my friends'. i love animal shows and nature shows on tv. |
Welcome Sue, nice to meet you. :)
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Hi Sue, welcome to NT. :)
Jappy |
Hello, I'm new?
My name is Kristin, I was just diagnosed six months ago. 12/11/2012 RRMS
This is all so new to me,overwhelming. I am thankful to all of you who are so kind and so brave to share your stories. Thank-you!:) |
Welcome home Kristin, I'm glad you are here for you, as you for us.:hug:
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