Looking for
something specific?

I follow this doctor on YouTube named Aaron Boster. He’s pretty knowledgeable and can help a lot of you get answers to your questions. I know a lot of you or newly diagnosed and I think you can learn a lot and benefit from this YouTube channel. He’s a really good guy from what I see and knowledgea...

If you are a mortgage holder, see if you have critical Illness coVer as you may be eligible

Nine months ago, my life changed when I was diagnosed with MS in 2023. The journey since has been nothing short of transformative—physically, mentally, and emotionally. I’ve faced challenges I never imagined: enduring relentless relapses, the disconnection of not being able to feel my hands, feet, o...

I am so disheartened by the interactions I’ve had on this app, in leas than 24 hrs. So far it has been a slew of judgment and mansplaining about MS. Like most things in life, I don’t really care how other people approach their health, as long as I’m not being pressured to go along with it. My orig...

So my mri results came back with lesions to the neck spine and brain I was referred to one of the top neurologists for ms here in Northern Ireland, but I feel like I’m in limbo,the supposed wait is 70 WEEKS! new symptoms come and go but most recently I’ve developed a limp and my foot is agonising to...

Hi I'm sorry if this is a bit personal but I'm wondering how often does everyone relapse? I'm newly diagnosed and wanting some more info and support.

I know this is embarrassing and tmi but does anyone have issues holding there pee? I’ve had too many accidents recently. I haven’t started treatment yet and am still newly diagnosed so still have to talk to my neurologist about it :(

Hi all 👋 I've recently these last two weeks been having stabbing pains in the left side of my head. They last between 30 secs and a couple of minutes but I've noticed I'm having them more frequently like 10-15 a day. Not sure if its ms related or not? My hubby thinks its because im so tired all the...

Hey there, newly diagnosed and awaiting starting treatment. I have been reading some of the posts here and it's really nice seeing others who understand how it feels to be in pain all the time and all the other feelings that come with MS. Thank you

Hey there! Newly diagnosed this summer and have been putting off starting a treatment out of anxiety and fear. I’m trying to determine which is better, Tysabri or Zeposia. Anyone have any input on either medications? Curious of side effects, efficacy, etc. Thank you!