This Is MS Multiple Sclerosis Knowledge & Support Community

Leetz I am so sorry about your test results. I can imagine how frustrated you may feel. Just remember to not lose hope. MS is an uphill battle. This is one of my favorite quotes and it definitely applies to this. "If you are going to win any battle, you have to do one thing. You have to make th...

I really like this topic. I know all drugs have risks but I have been counting the days until I am able to get it. Im willing to take the chance because I want to walk better. If I got scanned and had CCSVI I would more than likely have the procedure. That's why I love this website-so much info and ...

I am so sorry. I hope I didn't offend anyone, I think you guys are great and I learn something everyday on here. I used the wrong wording. I did have success for a while but I had a huge attitude of faith, positive thinking etc. That makes everything better no matter what the treatment is. So I woul...

Mine are adipose cells from myself. I had this last year and it worked so well. I walked normal and had no symptoms for several months. But, I quit taking my medicine. So this time I am doing a trial on myself. Im going to continue my medicine, get the treatment and see if it last longer. I am very ...

I am in Costa Rica right now about to get stem cell treatments.

I mean really, whoever they are, they will realize that people only resent you when you care that much about them. They look at you like you are weak. And it is nice to see there are people who actually still love so deeply. I mean, would any of you do the same thing? Would I? Its thoughtful beyond ...

Obviously someone that cares alot.

No offense taken at all. I just do better when I am on my meds. Ive tried it both way and have MRIs for my own curosity. I used to say I hate drug companies etc. I am against the monopoly of the drug lobbyists but it is the difference between day and night when I stay on my meds.

Daisy 3, Not to put a damper on it but stem cells are more of a placebo mind over matter thing. If you can afford it every 4 months or so, it is great. Dont get discouraged. They do tend to give you alot of false pretense, and oddly enough don't even wear gloves during the procedure. Im a nurse and ...

Hey Daisy, I want to put scans up to but of my MRI's that show how my disease modifying medication is helping extremely. How have your MRI's of the brain turned out? As far as this other stuff people are scanning, hopefully there really isn't a problem with your veins. From my experience, going the ...