Looking for
something specific?

Hi there, I've had RRMS for almost 20 years, am seriously thinking about stem cells, mesemchemal ones, prices seem to vary and experience feedback too... Anyone here had done it already or thinking about it? I've checked out a few options in Antigua, Costa Rica and Romania/Russia, my neuro says ther...

Hi everyone, I received a call from my nuro this morning to say they have accepted me for stem cell therapy. I'm both excited and slightly terrified. Has anyone else had stem cell therapy? Looking for advice on success and experience really. Thanks x

Afternoon, So I’m literally one step away from Being offered stem cell treatment (HSCT) for my MS at Sheffield. Question: “If official offered the treatment, should I…?” The more people speak with the more I want to hear. I’m aware it’s scary and let’s be honest brutal, but potentially longer...

Hi all, Out of interest, if you had an option which of the above would you opt for, the stem cells being from one's own bone marrow? If the lemtrada had not performed as well as expected on all 4 counts, namely symptoms, MRI results depicting prominent inflammation in key areas, 3 relapses in 7 mo...

Hi all, I have been diagnosed since 2008 but never had any DMDs offered to me until earlier this year. I turned them down to join the STREAMS trial which involves taking intravenous stem cells harvested from my own bone marrow. Is anybody else on the trial? There are only 13 patients on it in the U...

http://www.dailymail.co.uk/health/article-4369310/Musician-RELIEVED-diagnosed-MS.html Is their stem cells in this country now ? This guy says its £80,000 privately . Rachael X

Hi all, I shared a couple days ago my youtube channel about sharing my Stem Cells Transplant process and what I am going through. Today the doctor came in and told me that my isolation was lift (after 1week2days of transplant) because my white blood cells were high enough. He says he's surprised of...

Has anyone heard of research of stem cells directly into the spine? My neurologist mentioned it last September and said I would be a good candidate for trials. I spoke to my ms nurse this week and she had heard about it but it wasn't being trialled in this country and she is now on long term leave....

I am anxious to chat with any one with MS who is interested in having Stem Cell Therapy possibly in Mexico.