It is currently Fri Jan 20, 2017 12:03 am

News News of ThisIsMS

Site map of ThisIsMS » Forum : ThisIsMS

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.

Chronic Cerebrospinal Venous Insufficiency (CCSVI)-

« Moderator's Note: This is the original thread that began the discussion of CCSVI here at ThisIsMS. Its status was changed to "sticky" to make it easy to find for people to get a historical perspective on the development of the discussion here. There are also several good references cited which may or may not be available in the other threads. NHE »
    ------------------------------------------------------------------------------
Dignan recently posted the link to Dr. Paolo Zamboni's abstract on ...




Weird

I stopped taking Mirapex about three days ago to see what it would be like not to take it. Well the last two nights I have had night sweats so bad that I had to get up during the night and change. I usually take three 5 mg Mirapex a day to control my RLS. For the life of me I can't figure out why this is happening. Has anyone else had these night sweats ...
Read more : Weird | Views : 1448 | Replies : 1 | Forum : General Discussion


Possible MS dx

Awaiting appt. with Neurologist and gathering all the information I can. It feels soooo overwhelming!

so glad there are places like this to help!
Read more : Possible MS dx | Views : 1179 | Replies : 0 | Forum : Introductions


Pain after shot

I'm wondering if anyone experiences pain after a Copaxone shot. Not the normal bee-sting type feeling. Occasionally, after I give myself a shot, I get a sharp pain, which will become a dull ache, and it usually lasts at least a day. I got it again last night after injecting into my abdomen. It was pretty painful, and is still tender this morning. I don't think it was because I hit a nerve or muscle, ...
Read more : Pain after shot | Views : 2192 | Replies : 3 | Forum : Copaxone


Copaxone \ HiCy Reasearch

This video explains evrything about why Copaxone is being used after HiCy treatment. The Speakers are the resaerch team at Johns Hopkins.

This video is VERY VERY informative

http://video.google.com/videoplay?docid ... 0908357407


Enjoy,
Chris S.
Read more : Copaxone \ HiCy Reasearch | Views : 2624 | Replies : 7 | Forum : Revimmune (cyclophosphamide or cytoxan)


Original HiCyers

Sorry to hear the bad news Keri and Chris. Glad to hear that Mel's MRI turned out ok.

Could anyone who is in touch with Dr Kerr or Dr Gladstone please find out how the partcipents of the original Johns Hopkins and Stony Brooks trials are faring now? It would shed a lot of light on the speculations surrounding reactivation.

Thanks!
Read more : Original HiCyers | Views : 2507 | Replies : 6 | Forum : Revimmune (cyclophosphamide or cytoxan)


FOR WOMEN

I feel very very sad :cry: Yesterday night me and my boyfriend wanted to go out and have fun,as every Saturday happens here in Greece.So,i wore nice clothes to be prety and also wore 'high 'shoes(i do not know the english word...).That was mistake,bad choice because i could not walk on them!i felt AWFUL!... :cry: ...
Read more : FOR WOMEN | Views : 1860 | Replies : 8 | Forum : General Discussion


Bowel Health - Cause and Effect

For me, from when I was diagnosed six years ago I was convinced of the link to my bowel.
This has been confirmed without any doubt when after a particularly stressful time at work I came out in nasty itchy rashes.
I went to a Kinesiologist who looked at what was causing me such allergic reactions. This guy has identified and confirmed the whole problem. He maintains that, every person he has ever met or ...
Read more : Bowel Health - Cause and Effect | Views : 9005 | Replies : 28 | Forum : Regimens


Controlled My MS for 6 Years

Hi all,
It is good to be part of this forum.
I was diagnosed six years ago. No doubt my story is the same as most when dealt such a bombshell. I am sure there are those worse off than myself and we all know what a horrible disease MS is. I guess I was and still am lucky. I have never been able to accept how I should have this disease and set about ...
Read more : Controlled My MS for 6 Years | Views : 1422 | Replies : 0 | Forum : Introductions


 

Login  •  Register


Statistics

Total posts 235728 • Total topics 25500 • Total members 16781


Contact us | Terms of Service