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Hi been seeing neurologist for 5 weeks, been suffering with double vision, pins/ needles,falls,headaches, no sleep, tired for last 22 months, had head scan which is clear, had spine scan but results shows bulging disks in neck and wear and tear on lumbar spine, I had lumbar puncture yesterday and lo...

Does anyone else get this.... I am seeing double but only in my right eye pain under and to the back of my eye. Been of phone with the ms nurse she said it doesn’t sound optic neuritis or classic symptoms of. Please I Just want to know if I’m going mad or not

Wtf just had to cancel a booking for a long weekend with guests at a big cottage as part of my now postponed civil partnership celebrations, casually mentioned got MS so additional factor in not having large gathering due to COVID risks. Having mentioned cancelling party, not able to book the bloom...

Hi everyone, I have just read something about brainstem lesion. In 2018 before I started any treatment, I had a brainstem relapse that caused numbness on face and tongue, and reduced hearing. I am quite worried about this, as I believe if you have a relapse in that area, it is a part of the brain...

Can someone help me? I’ve searched the web and all the MS sites and can’t find the answer. I would like to hear from someone who has symptoms daily that come and go. Like everyday. For instance I permanently have numb feet but sometimes in the day it travels up to my knees then goes away back to jus...

I have been on Tec just over three weeks and third week on two tablets of 240. Last four days extreme diarrhea also nausea and stomach cramping. Spoke with MS nurse who said was probably at stomach bug. Everything I have read in the booklet and on here suggests could be a side effect which I told h...

He says, "I am interested to know if any of you who have COVID-19 are suffering from a persistent loss of smell and taste and how has it affected your life? Please let us know if smell training makes a difference." - Here is the full post: https://multiple-sclerosis-research.org/2020/06/mscovid19-lo...

Hi my name is Erika Iam 32 years old, I was diagnosed in 2012, am taking tysabri. I got married two years ago( I have a 14 year old son now, doctor said am stable and am good to start planning on having a baby but for that I would have to change my treatment to Ritaxon, I’ve read it’s good to start ...

Hello all, Well I don't know where to begin!? Guess I should start here. Joined this site nearly 4 years ago just after I was diagnosed. I have had this thing approximately 20 years. Not on any medication, not that there seems to be much, the same as help with this - not much. I suppose when I w...

Hi, hoping for some advice - I have emailed my neurologist but waiting a while to hear back so thought I'd see what people on here think. I work as a secondary school teacher. Have been teaching remotely but deciding about returning. This week there is a training day (staggered in small groups) the...