Anyone else get a dreaded brown envelope arrive on the doormat and think 'great another fight to face!' I think the endless reviews of Personal Independence Payment for those of us with MS is absolutely disgusting! I mean did I miss something? Or is there suddenly a cure for Multiple Sclerosis that ...
Does anyone follow/recommend any sort of special anti-inflammatory diet for those with MS? I'm pretty healthy don't drink, don't smoke and practice very low impact yoga. I just wondered if anyone on here swears by a specific diet.
Thank you x
#diet#workandplay#nystagmus#tremor#yoga
Hello fellow MSers
Nice to meet you all. Newbie MSer here.
I am usually nervous when joining group but I came across Shift MS by chance and appreciate I found a place where others have questions and worries that I also share. It's refreshing since those around me sympathise but don't understand.
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My MS journey started in 1989 with what transpired to be optic neuritis.
Living in London in a bachelor pad that resembled a scene from the movie Animal House after a major relapse and a dose of steroids life went on. Yes rugby was a non starter but the chaos of a 20 year old continued at a ridiculo...
To anyone this applies to, what were your feelings when you started using walking aids? I am pretty much at that point and just the thought of it scares me probably irrationally so
Does anyone take any kind of vitamins? I currently take vitamin D3, tumeric, magnesium and omega 3 all high strength. Just wondering if anyone had any suggestions of any more I can add into the mix 😂
We’ve just launched Shift.ms polls! Take part in the first poll below👇
*Bonus points if you can leave a comment and let me know: are you happy with how long it took?
How long did it take you to get diagnosed with MS?
When do you tell someone your dating that you have ms? I told the last person on the 5th date and they got upset with me for not telling them sooner. I didn’t feel comfortable with them sooner and it didn’t seem like he was that into me.
Hellur to my Ms peeps,
Just wanted to ask about any recommendations on any Ms related things I should look into in Calgary, Alberta to deal with my MS (support groups, activities, specialists to help build my MS team there). If you also have any fun suggestions for activities I would love to know...