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Treatment criteria?

Hello,

I'm a pretty infrequent poster, but avid reader on this forum. This revimmune treatment seems to be very promising to say the least. I was diagnosed in 2005 but had symptoms going back to 2000. Currently asymptomatic with the exception of some tingling in my legs after exercise. Would someone with no disability be allowed into this trial? It would be great to stop progression before any real damage has been done.

ps. Best ...
Read more : Treatment criteria? | Views : 2319 | Replies : 4 | Forum : Revimmune (cyclophosphamide or cytoxan)


MS-Exercise

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Read more : MS-Exercise | Views : 4079 | 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 : 5067 | 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 : 4240 | 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 : 1526 | 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 : 1687 | 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 : 2517 | 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 : 1967 | 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 : 1860 | 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 : 2811 | Replies : 0 | Forum : Low Dose Naltrexone


 

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