I cant take the hell of constant sweating and how bad the spasticity is in my legs and arms , 😔 is anyone else dealing with these constant issues to and if so how do you manage to cope with them ?
I saw my consultant today and finally feel like she’s listening to me. My lymphocytes are back to normal levels six months after cladribine just need more bloods in October and I’m ready for year two. As I failed in my attempt at my MRI in June not sure how effective the tablets have been for me ...
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Need some advice please guys. Has anyone else lost their ability to urinate following an excessive hospital stay due to a physical trauma. Recently I broke my femur so was hospitalised. Whilst in hospital, I was urinating via a long term catheter. My bladder had gone into retention caused by the tra...
Hi- with Covid really just passing through my area I have restarted my PT. I left off in December when they shut down. He left me with some good exercise options and I tried some of the other options so readily available on-line.
The good news is that I think I have been able to maintain strength p...
I'm now 55 i was diagnosed in 2013 and i have just carried half disbelieving that i have ms but have got to a stage that i have had to tell work and everyday is a uphill struggle and my neurologist said that it may be time to take early retirement and I havent got a clue where to start.
Hi, I’m Kim !
I’m 48, about to be 49 .
I’ve had RRMS for 11 years now . What a blow to be hit with in your 30’s . I was diagnosed the same time I had to get breast surgery . My now , EX husband wasn’t too much of a supportive man during my years of battling meds and seeing which ones helped 🙁 But...
So I was at my Neurologist and her assistant stated to me that I should be a lot worse than what I am! My neurologist agreed.. so this of course got me thinking of the future. I have decided that I do not want to get bad, I know some people r and are happy and that’s their choice and right. I have t...