This Is MS Multiple Sclerosis Knowledge & Support Community

With all the positive noise concerning this subject I can't believe not one person has replied to my post, I was just hoping for some encouraging feed back/advice.......what ever..!!

Hi,
Has anyone experienced or know of anyone who have had HSCT, looks a hopeful treatment.. thanks.

Hi Scotland, not a user name I'd expect from someone in Canada..
Is the much noise regarding stem cells in your parts - nothing for us in the UK..

Hi Scotland,
I take two x 5mg caps each morning, very early days for me only a matter of weeks from which I'v not noticed any difference really ?

I am 48 and was Diagnosed in February 2011 with RRMS, not on any other med's.

Hi,
Any views or experience with Mito Q - Thanks.

What about stem cells ?

Hi, I'v read various comments about stem cells not being a serious break through for pwms and many other conditions, after watching a documentary with Steven Hawkins, I am so optimistic that stem cells are the way forward in the fight against many conditions up to now incureable, or am I missing som...

I was put on Avonex, injected myself at 10:30pm after going to sleep I woke at 2:30am paralised, which lasted for four hours, my MS nurse said I could not relate it to Avonex as no body had reported symptoms of this kind and to persavier, the following week the exact same thing happened again, again...

Hi,
What kind of toxins are you talking about ?

Hi,
Has anyone had any experience with parathyroid disease or have any information in potential connections with MS ? I'm from the UK and have been diagnosed with RRMS..

Has anyone had or heard of any experiences with AS in regards to MS ?

Thanks for replays, My neuro explained my CSF as clear and commented it as unusual, and me a difficult case to read ? My most recent MRI indicated all activity as calm / no hot spots although my symptoms seem to be worsening with no remission which I'v never experienced even though my neuro insists ...

I have recently received blood results as all normal, is that likely for someone with aggressive RRMS, a recent LP was also clear, confused !!!!

Comments appreciated.

I was tested for CCSVI in Scotland UK ( EHC ) and was informed everything was clear so was deemed non compatible for the procedure ?