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Looking for MS support groups and warriors in the area. I started on Aubagio in October and the last month have been experiencing numbness and electric shock in my feet and ankles. Has anyone else had similar?

Hi, I got diagnosed 3 days ago with RRMS. I'm 45 and my symptoms started 6 weeks ago. MRI of brain and spine showed numerous lesions in my brain and 2 on my spine. It's all come as quite a shock. When I met the neurologist last week I was told I would have to have 7 different vaccines before medi...

Hi, I'm from Glasgow Scotland. I was diagnosed in 2019. Looking for people to chat to xx

My neck feels like it needs a good massage and now and agin it crunches is this MS related thanks

I was diagnosed last September,it started with numb toes and travelled up to my waste in a few days,it was my first attack so don't know how it goes,was on a iv steriod for five days,and started gylenna in November,all symptoms have subsided but my feet are still numb,will it eventually go away??

I was doing really good for a while but now I'm feeling low again. Can't take this anymore not fair 😞

I am having double vision . Booked in to an experienced optician next week. I have read in various formats that certain specific lenses can help with double vision. I mainly get this at night and when I am tired. Does anyone have any suggestions , I would be very grateful.

M. S. and the heat in las vegas 😪

Just started on Zeposia this week and am blown away by the food restrictions. Anyone here using the med and can share their experience? I started experimenting by eating some of the "maybe" foods and will keep doing so as I go along.

Hello, I was hoping to find out more about others experience with optic neuritis and how long it has tended to last? Is there anything that helps? I've had the condition for a good few months now and I'm worried that it will have lasting damage to my vision? I'm currently in the process of official...

Hi all I had a Mri in Feb it showed several small bilateral periventricular and T2 deep white matter and FLAIR signal abnormalities and dymelation is within the differential I have problems with spinal cord as well. Symptoms started last year Numbness in leg Then I have tingling very often in diffe...

Has anyone had botox in the bladder to stop incontinence and if so has it worked 🤞🙏

Read a lot of posts about struggle on here so Here’s something that might help you keep doing ‘YOU’ when your struggling takes practice but 🤞might help - https://www.youtube.com/watch?v=3NHZkQ57wzE https://www.getselfhelp.co.uk/docs/STOPP5.pdf

I have been taking fingolimod for three years and it is fine and I am satisfied. I got a letter through the post from the NHS which read that they were changing Fingolimod to a new manufacturer and it is cheaper. Cuts in the NHS I guess. Also, I checked my supply and discovered that I had two too ma...

New video online! Today I talk about my story... about the things MS has taken away from me and how I adapted to being chronically ill and STILL doing what I love. Yes, its motivation wednesday 😄 Check it out 🧡 https://youtu.be/clIF5jOVu0c

Hey guys my name is Gary and I just joined what looks to be a really cool MS site!!! So I am from Memphis, TN but live in Denver, CO. I have been living here with my husband for about 15 years. I was diagnosed with MS in 2012. Would love to make some new friends with MS on here so hit me up any...

Good morning! Yesterday I had my MRI results that showed no lesions, this of course is amazing news and I am very thankful. My neurologist said for now we are ruling out m.s. While I am massively relieved about this it leaves me more worried about the symptoms am I feeling and wondering if I am act...

I am currently taking steroid tablets over 5 days at home. Those were prescribed by GP (it wasn't easy to get prescription) for very serious relapse - I wasn't able to walk. What is concerning, that my MS nurse advised me not to take them, only wait and see, maybe it will improve by itself! And that...

Hi, I was diagnosed rrms after 4yrs of symptoms last July. Im unsure of if and when to contact my ms nurse. Im currently experiencing intermittent sharp stabbing pains on left side of head ( had before, neurologist aware) its driving me mad and my doctor couldn't find anything. Its really ramped up ...

Saying hello, first time on Shift. Took me 6 months to be diagnosed after years of symptoms and a bit of medical gaslighting thrown in. I've been on Copaxone, Gilenya and currently on Tysabri. Having a difficult time the last couple of months in work with my boss, which is not helping my fatigue or ...