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Hello, just got my ms diagnosis so haven't got my ms nurse in place yet, I started amitriptyline 10mg a week ago and I believe is causing me to have blurred vision and pain in my eyes, has anyone else had this please, have tried to contact the doctors with no success so far and also ms nurse but as ...

I have blurred vision to the point I can’t read I had optician today and my eyes are healthy but issues may be behind my eye obviously I googled I know bad idea i can’t see anything if u was to wave at the side of my eye could this be a flare up or something totally ms unrelated any advice will be g...

I have had blurred vision in my right eye for about 4 days now getting progressively worse. I had 4 relapses in 4 months and was dx in March ‘24. It has been about 2 months relapse free now for me but concerned this may be the start of another. Ironically I had my first loading dose of ocrevus yeste...

Hi, Newly diagnosed last month after symptoms starting last December, the MRI showing 4 spinal legions and the lumbar puncture from hell 😂 I've done a lot of research into diet, exercise and supplements. I've been gluten and dairy free since June and in the gym 3 times a week. It started with th...

I read that in most cases of OP , the eyesight is restored some if not completely after time has passed with or without steroids, however i have had optic neuritis in my right eye with no improvement for 19 years. Anybody else? I can see everything through a very dim view like when you come in a ro...

For the last six years or so I have had a multitude of issues hysterectomy do to adenomyosis parathyroid condition resulting in surgery the diagnosed with fibro one doctor said she thinks I may have ms due to my wide spread symptoms I am on a waiting list for an mri but here is some of my symptoms b...

Hi All, Diagnosed after around 2 months of private testing, all started after what was supposed labyrinthitis [I was unable to move without vertigo, double vision, fatigue and completely hearing loss in left ear] I then developed a hemifacial spasm in my left face which varies in severity, asked ...

Hi, I've just taken my last loading dose of Kesimpta yesterday and over the past few weeks I've noticed my skin is really sensitive to heat, pain and to touch. I get gel nails done every few weeks and noticed last week my skin burned and stung under the UV light which never happend before I started ...

Does anyone else have this and have any advice? Long story short, if my body temperature increases some of my symptoms worsen. Eg if I went in a sauna, my mobility would worsen for a day. If I manage to go for a run on a treadmill, my vision worsens for about 15-20 mins. Anyone suffer with it too?

Wanted to ask who was also following the Overcoming MS Diet? I have since about 3/4 months after my diagnosis, and want to encourage others - it was a big shift, but haven’t had any symptoms since the ones that first got my diagnosed (double vision). Plus 3 years of stable MRI readings. Just wan...