This Is MS Multiple Sclerosis Knowledge & Support Community

I don't go on thisisms and one of the elders here summed it up. Alive and well and not suffering from SPMS although I'm not 100% symptom free, I can still jump and have balance, as well my bladder is still functioning. I've also learned that I had venous reflux in my legs and recently had vein ablat...

Hi Lorreena,
That name needs to be changed! Getting angioplasty done to correct a vein problem does not cure the problems with MS!

I have a personal plea for donations towards Dr. Siskin’s clinical trial which has started and will show that people with Multiple Sclerosis are suffering from CCSVI and it's treatable. Our fundraising goal is $10,000, if each of the people on my friends list can donate $5.00 we will have almost rea...

I have a personal plea for donations towards Dr. Siskin’s clinical trial which has started and will show that people with Multiple Sclerosis are suffering from CCSVI and it's treatable. Our fundraising goal is $10,000, if each of the people on my friends list can donate $5.00 we will have almost rea...

What is wrong with all you people? And what's with all the 1-post newbies? There is a 30 page thread on this forum discussing this dr. and his treatment. HE HAS A WEBSITE ADVERTISING HIS TREATMENT! Maybe there's too much detail in the post. I'm sure flashhack will edit it as soon as he can, but gee...

Hi FlashHack, While I am extremely happy for you I am begging you to please please please edit out the hopsital specifics from your blog. I know you are coming from a good place in putting it there but every time Dr and location specifics have been posted that facility ends up getting shut down alm...

Rokkit wrote:

Lifegirl wrote:It's not okay to mess up other people's chances of getting treated. It's great you had results and we have been very clear about not using names and places.

Whoa, Lifegirl, getting treated by Dr. Siskin is not a secret. He has a website.

No kidding, but the untruths are unacceptable!

Your foolish lies and comments are more than self serving, they put this whole project at risk and you know nothing about it.

Whoa ... let's all calm down a minute. Take a deep breath ... Everyone knows about Dr. Mehta in Albany. Heck, his information is on clinicaltrials.gov ... It's the ones who are treating privately that we need to keep quiet. I'm doing the exact same thing ... withholding a bunch of doctors names I k...

Posting the names and hospitals of doctors is what is getting in the way of our patient-doctor privacy! Stop it.

The Multiple Sclerosis Society is so full of shit! They are only worried about their next dollar. If they truley represented the people then they would be supporting the decision of the MS community. So to hell with them. What have they done anyway?

Class Action World First register at this site http://classactionworld.com/forum/profile.php?mode=register&redirect=viewforum.php?f=1&start=0 Then sign in and go to http://classactionworld.com/forum/viewtopic.php?p=2949#2949 and tell your story. My string is CCSVI let's keep it all together ...

It's so good to hear such an encouraging update on Melissa! I pray she continues to do so well and regain her health!

So happy for you heather! I love to hear how well you are doing. Keep it up! Hopefully the rest of us will get there too!

I was wondering if any one knew why it is that some people are actually being treated with he liberation treatment of opening the veins but most of us are not? Maybe the answer is out there? but I'm so new to this site and confused by it still as well, there is just so much to read and I just don't ...