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MS-Exercise

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Read more : MS-Exercise | Views : 3999 | Replies : 19 | Forum : General Discussion


Another story

Sorry, I'm a sucker for these stories.

http://c.moreover.com/click/here.pl?j13 ... 6&w=464753
Read more : Another story | Views : 4996 | Replies : 16 | Forum : Stem Cells


Reiki

Does anyone do it regularly?

Family and friends are raving about it and keeping suggesting it to me (on the verge of pushing it on me) and I am intrigued. But also nervous about it. I'm not sure if I want someone messing around with my energy/electricity considering I have problems with it already.

I'd appreciate hearing your thoughts on it. :)
Read more : Reiki | Views : 4210 | Replies : 26 | Forum : General Discussion


Hi All

Hi everyone....glad to have found this site!

My name is Steve, 40 years old, and diagnosed with RRMS back in December following a fairly debilitating attack. I've been lucky enough to enjoy good health for my entire life, having rarely ever seen a doctor until a few months ago. Unfortunately, all of that changed back in late November.

Right around Thanksgiving, I noticed a tingling/burning in my left leg, and I recognized the sensation as ...
Read more : Hi All | Views : 1504 | Replies : 3 | Forum : Introductions


New to the Site

Hello to all!

I just came across this site - and am eager to get into it more! I've been diagnosed for a year and a half - after a 5 year struggle! Just started Avonex, also on Lamictol. Most days are great, but some days really really suck!

Glad to be here! Any advice welcome!
Read more : New to the Site | Views : 1651 | Replies : 2 | Forum : Introductions


Would appreciate new friends/contact

My name is Cindy and was diagnosed with RRMS in early 2002.
Have been reading this wonderful forum for several months... this is my first post. Just turned 51, I am in North Carolina, originally from CA, USA.
At this stage, there is no pain but my mobility is really bad.
I'm not sure what I want to say--other than I just have to get started and actually reach out/connect this time...
The bottom line, ...
Read more : Would appreciate new friends/contact | Views : 2486 | Replies : 10 | Forum : Introductions


Research article

A research article on Campath - but not from the Cambridge team overeeing the trials.

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Read more : Research article | Views : 1954 | Replies : 0 | Forum : Campath (Lemtrada, Alemtuzumab)


Tovaxin Extension Study Blood Drawn

Ok people. Had my blood drawn today (02/25/08) for the Tovaxin extension study. Here's a link to my journal (blog) about the Tovaxin extension study http://blog.360.yahoo.com/pvns2005 I won't be on this forum allot so if you have any questions please email me or post a comment on my journal (blog). Email and all my contact information are on my profile.

This is what we been waiting for.
Read more : Tovaxin Extension Study Blood Drawn | Views : 1815 | Replies : 0 | Forum : Tcelna (Tovaxin)


New book on Lyme (MS?) including LDN

New book: The Lyme Disease Solution by Ken singleton. MD

Lyme is still a controvercial area, good to see an MD weighing in. He also has a chapter on the use of Low Dose Naltrexone LDN in treating
Lyme. Here's the intro http://www.lymebook.com/lyme-disease-low-dose-
naltrexone-ldn

Just thought I'd point this out, since I have a positive Lyme PCR from
Igenex, and that is likely the cause of my "MS". I ...
Read more : New book on Lyme (MS?) including LDN | Views : 2779 | Replies : 0 | Forum : Low Dose Naltrexone


Gadolinium/blood draws

I really don't sit around contemplating disaster, but this has been on my mind since before the Gadolinium issues came up. Since I have been in this trial, my trial days have been set up like this; I have an MRI and get injected with contrast then I go to my site for tests, injections and BLOOD DRAWS. My common sense alarms have been going off about the blood used for my vaccine being full ...
Read more : Gadolinium/blood draws | Views : 2691 | Replies : 11 | Forum : Tcelna (Tovaxin)


 

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