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I was born into a loving family, but life wasn’t always easy. Both of my parents passed away when I was young, leaving me and my brother under the care of my uncle, my father’s brother. In their home, I grew up alongside my cousins, who were my age, and together, we faced the trials of life...

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...

Hi all, I’m newly diagnosed of RRMS. Despite I have multiple denyelinating lesions in my brain and spinal cord, my simptoms so far have been relatively mild and disappeared in a few weeks. Doctor said he thinks I should go on a highly active treatment as soon as possible to slow down the progression...

What’s everyone’s thoughts on this medication ? Is it real ? It is in trials to see if it can regrow mylien

Just wondering if anyone has tried the Tao Patch that I keep seeing? Suppose to use your body’s own energy to help restore balance, ease pain and reduce MS symptoms? They are expensive but last for 2.5 years so it really breaks down to $26/month. It’s a 90 day trial so it seems legit. I’d rather...

I had my annual check up with my consultant 2 hours ago at RUH Bath. Here is a brain dump of our discussion, while it's fresh in my mind, in case it helps anyone else with RRMS/SPMS who takes a T Cell based DMD: - Lymp count was 1.3 and right where they want it. - The very slow annual increase in...

I am helping to shape a guide called "Alternative Treatments and Complementary Medicine – Looking for evidence and knowing the risks" for this excellent organisation https://senseaboutscience.org. I was contacted by them via the work I do for the MS Society. Does anyone have personal experience of ...