Although the workplace was toxic, it was a steady income. Including when my spaciticy in my right leg makes it so hard for mobility 😕I just don’t know how to remain positive with this condition.
Well, after 38 year, four consultant neurologists and three GPs, I'm cured!
Yes, I don't have PPMS (or any other kind of MS for that matter).
My latest consultant says that my brain is in excellent shape . . . .nothing to see.
(But then there never was)
My spine is clear of the lesions first seen...
Long shot! I’m based in York (UK) and would love a pal similar age to me (31) that I can meet up with, go for coffees and things with ☺️I work at my local hospital and have met a couple of patients in passing with MS but never had a proper face to face chat with someone with this condition, I really...
I was diagnosed with RRMS in 2022. It’s been a journey in trying to educate myself and people close to me about MS. I wrote a blog post last week that friends tell me gave them a better insight into and understanding of MS.
This isn’t a sales pitch, I understand hypnotherapy isn’t for everyone. Bu...
Hi all who read and respond.
I’m a 44 year old female.
I have endo - pocs and need my lumbar puncture to confirm MS, I have lesions on spine and Genu of brain.
I would be educated in certain things like sensory issues/ cognitive issues as I am a mother to a child with special needs and have ...
I have secondary MS for the Last. I think 10 years it has progressed worse and I’m seeing my neurologist. I have been on nine different DMD over the 27 years of having MS and I did not stay on them for long because I found that they were giving me side-effects. Because I hear there is a lot of new ...
I was wondering if anyone here has started on HRT in their mid 40s and found it helped with MS symptoms at all, along with other things (please feel free to share 'other things' if you are comfortable as I have read HRT can help with issues such as loss of libido and with pain and dryness you-know-w...
Need advice or anyone had or having a problem getting their private pension from work. After being officially diagnosed in early 2022, I was still working but had quite a bit of time off due to MS problems. Our HR officer had asked me if I had considered retiring early due to ill health. This would ...
Hello everyone, ive been having suffering from mild cognitive fog for a couple of years now not knowing what was causing it and blaming it on university ect. Ive been diagnosed with MS this year which is making me think it was probably due to this. Recently it has gotten much worse. All of my senten...
How'd you say is the best way to differentiate a new symptom (you think) from being a relapse or maybe PIRA without involving MRIs and such? Also I'm talking more about cognitive symptoms, not something physical and more "evident".