Looking for
something specific?

I have come across this on the web. They have a treatment that suppose to correct the immune system so it won't attack your nerves anymore. Has anyone heard of this. Www.hsctmexico.com

I am sharing my personal MS journey this MS Awareness Week, because I want other people suffering with this disease to know that they’re not alone in their experiences. There is plenty of hope, laughter and joy to be found alongside MS, and I hope that through sharing my story, I can help others fin...

Today I celebrate for the reasons noted above. It was nine years ago that I had HSCT! I’m not suggesting a treatment of any kind. I’m just advising you of my positive news

#IHAVEMS The Chief Executive of the MS Society (Nick Moberly) was the Chief Executive officer at Kings College Hospital , when they’re ’mistake caused my disability, after the succesful HSCT Treatment that I had. He ignored my letters to him, but he had Julia Wendon respond about the issue. The deta...

You ought to. It is a brilliant patient focused resource. If you ask him nicely it is free. The big US MS meeting has just ended. It is called ACTRIMS. This is an excerpt from Prof G's report 'There were excellent talks on the biology of myelination and remyelination and their complexity. The que...

Hello everyone hope you’re doing good I diagnosed with PSMS 5years ago and walking is so hard for me .. my Dr in San Jose suggested me to do AHSCT! Has anyone did this process? And was it helpful?

Ocrelizumab (Ocrevus) 6 monthly infusion ? Or HSCT (stem cells) ? Whats your thoughts which would you be going for ? Thank you

Hi. Hope your great where ever you are in your journey with MS. I have a question for all those on Tysabri infusions or have used it. I have been on the infusions for last couple yrs and I have been having relapses that have been ignored. Now a mri has shown new changes and they have offered me HSCT...