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I have RRMS and its been slowish in development. Im now on ocrevus but things are happening with my cognitive behaviour - memory, focus, clarity of thought, problem solving. This has been getting gradually worse for a few years, but i knew my job inside out, so not too much of a problem. Of course i...

I usually kee things bottled up but here goes im struggling to let the fact I’ve been diagnosed with ms sink in I feel like guilty for putting my gf and family through it and my temper sometimes gets the better of me and I say stuff I don’t mean I’m on tysabri round 5 coming up soon and diluxatine f...

Diagnosed in December 19, after private MRI, as a result of my acupuncture Dr recommending it. Went into hospital with suspected tumour on the spine. Another MRI and CT and just before I left, the Consultant told me that I had MS. I left hospital in a daze, thinking of wheelchairs, dribbling and bl...

Hey Peeps. Spoke to the consultant yesterday, my yearly follow-up which went ok apart from mentioning about armpit, arm and neck and shoulder pain. I was referred to the breast clinic in March which they checked me over and just said lumps were normal and having no history in the family was a good...

Hey all 🙂 im hoping this is common with others suffering MS.... people just dont seem to understand anything about it or what you might be going through! Friends... family and work colleagues see you looking normal and presume everything is fine.... I never want to come across dramatic but sometime...

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I've secondary progressive ms , I went from rrms about a year ago as me and my family were suffering really bad with the neighbours anti social behaviour I mean bad , no help from police or any other authority, I went to my doctor and cried, I felt so low I couldn't see away out plus ide just had ...

I am due to go on holiday on a canal boat with 8 extended family in mid September. It was booked a year ago but since then my SPMS has got much worse. I know I won't be expected to do much at all but I have started using a wheelchair inside the house after having many falls and I know there isn't ro...

I am due to go on holiday on a canal boat with 8 extended family in mid September. It was booked a year ago but since then my SPMS has got much worse. I know I won't be expected to do much at all but I have started using a wheelchair inside the house after having many falls and I know there isn't ro...

Hi all New to the site. Been given 3 options for treatment and I am siding with Rebif as we are thinking of starting a family soon. What’s people’s thoughts on it? So much information to take it. I’m feeling very confused and overwhelmed. Got diagnosed about 3 weeks ago. Thanks in advance Lucy