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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.

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...

Well… I guess I’m a part of the MS gang now! 🧡 Im a fresh newbie, I got my diagnosis yesterday after struggling since last year and to say I feel overwhelmed is an understatement but… we’re here now! My MS nurse was incredible with me yesterday, so knowledgeable, reassuring and just so supportiv...

Hey! I’m a complete newbie to your community - it’s lovely to meet you all. I wonder if anybody can help - I was diagnosed (pretty out of the blue, but I know how lucky I am to get a quick diagnosis) on Monday 6th March after experiencing tingling, numbness and a lack of mobility in my right leg. T...

I was diagnosed in September 22, I’m awaiting the results of my 2nd mri which will determine which type of ms it is, I was just wondering what questions I should be asking my neurologist so I can be fully prepared when I see him

Who else is on zeposia? What have the relapses been like..? I’m newly diagnosed -1yr- RRMS. Began treatment shortly after.

hi everyone! I have recently been diagnosed with RR MS. I have new lesions in my brain, and they have offered either Kemsimpta or Ocrevus. I am leaning towards Ocrevus because the thought of injecting myself scares me but i wanted thoughts or advice on anyone who is on both and what are your side ef...

Hi! I was just diagnosed with MS in December so it’s new to me. I’m in Sweden. I have four young kids and live a pretty busy life. Looking forward to hearing your stories.

I went in for headaches and it turned into something more. I’ve been diagnosed with MS, showing lesions in my brain and a new one a little over a month later as well as some evidence in my thoracic spine, specifically at T9 along with Oligoclonal bands in my CSF. They believe they’ve caught it early...

I went in for headaches and it turned into something more. I’ve been diagnosed with MS, showing lesions in my brain and a new one a little over a month later as well as some evidence in my thoracic spine, specifically at T9 along with Oligoclonal bands in my CSF. They believe they’ve caught it early...

Hi, looking for some specific ms buddies here. I was diagnosed at the end of September. I haven’t yet been given a date to see an MS nurse or clinic. What length of time did people wait recently to be seen initially ? #newlydiagnosed #treatment #glasgow

Hi all, I've recently been diagnosed with MS. I was diagnosed with a different condition but now they have confirmed it's MS. I know very little about the condition and how it's is going to affect my life. I'm 26 with a new born baby and I work full time on nights. Any advice would be great Thank yo...

Hi I’m Tye! I’m new here . Recently diagnosed at 37 and awaiting my first dr visit with the nuero after receiving the call that i have MS. What should I expect? I’m just soo lost and frustraited rn and monday can’t come soon enough so I can receive treatment. I’m having trouble dealing with the pain...

Hi I’m Tye! I’m new here . Recently diagnosed at 37 and awaiting my first dr visit with the nuero after receiving the call that i have MS. What should I expect? I’m just soo lost and frustraited rn and monday can’t come soon enough so I can receive treatment. I’m having trouble dealing with the pain...

I just kind of wanted a bit of a moan & vent to a supportive ear. I volunteer with St John ambulance and have been for years, however, yesterday, MS took over everything! the pain I was in was excruciating the amount of walking I had to do I couldn’t lift someone in a carry chair and had to get hel...

Hi everyone! My name is Lauren, I was diagnosed with RRMS 3 months ago. My first symptom was numbness in my feet; and within a few weeks I was paralyzed from the neck down. The nerve pain was so extreme I couldn’t be touched. My body wasn’t responding to prednisone or plasmaforesis—-so I’m currently...

https://youtu.be/wvQXygHtYzc

Hi guys! I am new to the MS community. It all started last year 3 months after having my second baby. It started with legs going numb, then pins and needles, fatigue , slurred speech, tightness around stomach and like a vibration throughout body when I bend my head down. I had a emergency section o...

Hi everyone. I got diagnosed with ms two weeks ago. Neurologist told me I had lesions on my brain and spine. I have no idea what type of ms I have or what will happen now! I keep reading about different treatments etc and I feel like I'm in limbo! Been told I will be referred to a ms nurse and that'...

Hi everyone! I do need a bit of help and I'm trying to keep as short as possible. I could call myself a newly diagnosed, though it has been almost a year since my first MRI and the discovery of lesions. Briefly, in December 2021 started to hear some sounds (like music), for about 5 minutes in th...