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Caregiving for MS/TNA
Im a new member to this group but I see many of us share the same concerns about what to do and how to cope. We all have to take it one day (hour) at a time and do the best we can. Sharing information on succeses (and failures) can be a big comfort to others who are taking the same path. MD's dont have all the answers... so the best informed deceison comes from getting good information. We were at 2400mg of Carbamazepine per day and still getting pain when in bed. Just had MVD and so far so good (3 weeks)... now at 1200mg /day
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Hi Rich and welcome to Neuro Talk. Here is the link to our MS forum..http://neurotalk.psychcentral.com/forum17.html
It's a very active forum and you'll find information and much support there. I'm glad you've joined us. :) |
Hi Rich http://www.freesmileys.org/smileys/greet013.gif and http://bestsmileys.com/welcome/18.gif
Please feel free to roam around and join in anywhere.... Hope to see you around the boards!!! http://www.freesmileys.org/smileys/ad/hiya.gif Abbie |
Hello Rich and Welcome to NeuroTalk. Hope you take a look around and I see Alffe had given you directions to our MS forum. NT is full of so much info and the members are very friendly and helpful.
Please make yourself at home and join in anywhere.. http://dl7.glitter-graphics.net/pub/...gdba0e340m.gif |
Hello and welcome to Neurotalk - you will find many great people here!!
If you need anything just ask - I will try and help you if I can Thanks and i'm looking forward to seeing you around the forum soon. Alison |
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