copaxone.livejournal.com
Copaxone Chat
http://copaxone.livejournal.com/tag/personal%20stories
MS Watch by Shared Solutions. The National MS Society. 03 April 2007 @ 01:50 pm. And my MS/Copaxone experience.). Whoa, new members! Hi everyone. Feel free to say hi and start chatting. Also, if you know of anybody who might be interested in this community, please pass the URL along. Here's a little bit more about me - well, not such a little bit, but less than I. Some symptomy stuff, some diagnosis stuff, then some Copaxone stuff. Viewing most recent entries.
copaxone.livejournal.com
Welcome! - Copaxone Chat
http://copaxone.livejournal.com/259.html
MS Watch by Shared Solutions. The National MS Society. 29 March 2007 @ 12:04 am. The community's still really new, so feel free to introduce yourself and start things up while I put on the finishing touches. Check out the community's info page if you have any questions, or drop me a line at electrablue@livejournal.com. 3 comments Leave a comment. Anonymous) on June 14th, 2007 04:31 pm (UTC). Is there any help for the cost of this drug? On September 7th, 2008 11:45 pm (UTC). 3 comments Leave a comment.
copaxone.livejournal.com
Welcome again! (And my MS/Copaxone experience.) - Copaxone Chat
http://copaxone.livejournal.com/754.html
And my MS/Copaxone experience.) - Copaxone Chat. MS Watch by Shared Solutions. The National MS Society. 03 April 2007 @ 01:50 pm. And my MS/Copaxone experience.). Whoa, new members! Hi everyone. Feel free to say hi and start chatting. Also, if you know of anybody who might be interested in this community, please pass the URL along. Here's a little bit more about me - well, not such a little bit, but less than I. Going to get sicker, all the while telling me how. I started Copaxone in the beginning of Dec...
copaxone.livejournal.com
copaxone - Profile
http://copaxone.livejournal.com/profile
Created on 29 March 2007 (#12602726). Last updated on 27 August 2010. All Members , Moderated. This is a new community for Multiple Sclerosis patients, caregivers, professionals, and any others who have experience with or questions about the MS therapy Copaxone (glatiramer acetate). It can also serve as a general discussion forum for the disease itself, if such conversations and questions arise - which they probably will! The rules are pretty much the same as any other community:. Sorry for the rant....
copaxone.livejournal.com
Copaxone Chat
http://copaxone.livejournal.com/tag/admin%20stuff
MS Watch by Shared Solutions. The National MS Society. 29 March 2007 @ 12:04 am. The community's still really new, so feel free to introduce yourself and start things up while I put on the finishing touches. Check out the community's info page if you have any questions, or drop me a line at electrablue@livejournal.com. Viewing most recent entries.
smile-interuptd.livejournal.com
smile_interuptd - Profile
http://smile-interuptd.livejournal.com/profile
For Long-Term Bells Palsy Sufferers and Friends. Created on 19 March 2003 (#956373). Last updated on 18 May 2015. Long-Term Bells Palsy Sufferers and Friends. Bells Palsy Info @ Neurology Channel. All Members , Moderated. Welcome to Smile Interrupted. A community for, but not exclusive to, long-term sufferers of Bell's Palsy. The duration of Bell's can cause numerous short- and long-term physical problems, including constant facial and nerve pain, damage of the eye, and hearing loss. Let us not forge...
smile-interuptd.livejournal.com
Hi there.: smile_interuptd
http://smile-interuptd.livejournal.com/15470.html
So I'm going to be a hypocrite and talk now and hope someone listens. My neurological troubles have increased tenfold in the past year - I got diagnosed with Multiple Sclerosis. I've been occasionally checking out MS communities, which generally produce the same result. Last year I had to move back in with my mother, who I have a tenuous relationship with. She keeps insisting that my cases of Bell's palsy (the first in 1999, the second in 2003) are absolutely. Post a new comment. Post a new comment.
smile-interuptd.livejournal.com
Hello, I'm new here :): smile_interuptd
http://smile-interuptd.livejournal.com/16077.html
Hello, I'm new here :). Auckland, New Zealand. Do you currently have Bell's Palsy? Did you experience any common "warning signs" before it set on? I had a headache and I was incredibly tired the night before I woke up to an even worse headache and swollen face, etc. How long have you had Bell's and what percent recovered are you? I first got it almost 3 years ago, I would say I'm about 75% recovered. What treatment, if any, did you undergo/are undergoing? How did treatment affect your condition? We will ...
smile-interuptd.livejournal.com
First post to smile_interrupted - hiya!: smile_interuptd
http://smile-interuptd.livejournal.com/15031.html
First post to smile interrupted - hiya! Do you currently have Bell's Palsy? Did you experience any common "warning signs" before it set on? I had a headache and earache on that side for three days before it started in. How long have you had Bell's and what percent recovered are you? It started seven days ago, and so far, it hasn't recovered a lot, but it feels like it's getting better. What treatment, if any, did you undergo/are undergoing? How did treatment affect your condition? Question for you all:.
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