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Yesterday I was sat in car when suddenly I started to choke as I had swallowed my own saliva when I took a breath. Had my head out of car door trying to clear my throat as couldn't communicate to my daughter too pat me on the back. After, I said to my daughter "if that happens again pls can you pat ...

I recently decided to start telling people I have MS. I have been very private about my diagnosis since I was diagnosed about 3 years ago. I felt like a huge weight was lifted off my chest! My friends encouraged me to go further with sharing as a healing tool. I decided to create a blog about mother...

Hi! I have just been diagnosed with MS after having a big ‘flare up’ - For months I lost all feeling down the left side of my face, then I lost my balance and was very nauseous for a couple of weeks! Saw a neurologist, had an MRI scan and on the 3rd January this year he confirmed it is MS. I don’t h...

I have had covid which has taken me of my feet .I am really scared that I won't get the use of my legs back this time. Feel that no one is listening to my concerns .

I went out today with my wife and my bestie and I fell in the toilets. My wife had to come help me up. I couldn't get up. I have never been so embarrassed and mortified in my life.

Anyone else have MS within their family

Brain fart (or was it a man moment) as meant to post this earlier. Craig Watson is inviting you to a scheduled Zoom meeting. Topic: Monthly session for PP or SP Time: Feb 16, 2022 04:00 PM London Join Zoom Meeting https://us02web.zoom.us/j/89438670495

Did you tell your employer about MS?

Hi All, just wondering if there are any other new MS moms/parents out there ? Our little one is due mid Jan and would be great to link up with some other new parents.

When you feel like you're failing your child but he gets scouted to play for a championship football team whilst you work full time and run him around where he needs to be 👌💪👊

I was diagnosed with MS after telling my doctor for two years that there was something wrong with me. My doctor never took any notice of me until the end of 2019 when I finally got to see a neurologist and got a head scan . In February 2020 this year I was told I had MS. Since then I’ve been tryin...

I’m currently relapsing whilst on Ocrelizumab. How bad do my symptoms have to be to take the risk of having steroids now, and further reduce my immunity?

Years ago I needed to change my life completely. Why? That was not my choice but my health conditions. I was diagnosed with MS and it felt heavy to carry with me. I was afraid to dream about the future or even live a day with love, care, and understanding to myself. I felt guilty when I wanted to ...

Hi all! I was diagnosed very recently with MS, on Feb. 26th 2020. Feb. 12th, 13th, 14th '20 I had a Methylprednisolone cure for 3 days, which didn't help me out of my relapse. Complaints are getting worse and my neurologist says DMT is not an option right now because of the corona virus. He says "I...

Hi :) I was diagnosed with Fibro 12 years ago. Nearly 6 months ago I woke up unable to walk, my legs and back just wouldn't hold up. My hands were numb at times with pins and needles, head felt empty or weird - this had been preceded by months of vertigo, pain, overheating bouts through summer etc. ...

My mom has primary progressive MS. She falls all the time. We went on vacation a few months ago (Disney) and she had 2 scary falls, i finally convinced her to be in a wheelchair the rest of the trip, which Disney is very good about that. I just found out she fell last week IN THE STREET and could...

Pauline

Just want to share a horrible walking moment I had yesterday. I went for a job interview in the hub of the city. I checked out where it was and parking thought I’ll be ok walking there with my sticks. Well I thought wrong, there was construction on the building next door so lucky when crossing the...