@username
Please wait...
For a better experience get the Shift.ms app
Sort by

@pearhouse 

Last reply

pearhouse

Teacher with MS

Hi, I’m a teacher in England. Diagnosed in September, awaiting to start treatment. I had optic neuritis last year and recently I’ve noticed a small patch of my eyesight blurring. I got in touch with the MS Team at the hospital, they said this is likely a relapse triggered by stress or other things, ...

@89scott 

Last reply

89scott

Blame

Does anyone blame themselves for getting MS like for having an unhealthy lifestyle before

@Nora107 

Last reply

Nora107

@JamJam79 

Last reply

JamJam79

Sometimes I just feel overwhelmed

Vibrations, migraines, almost too much pain to bare, dizzy, fatigue all at once and for long stretches of time like this has been going on for months nearly daily. Yes I've talked to my PCP and my neurologist and both suggest physical therapy which I've done twice in the same year with no help. My p...

@Marcovio 

Last reply

Marcovio

Allergies blah ..

Good morning or good night. Was wondering what type of allergy pills do you take? I was feeling weird and off balance, as well as feeling of maybe passing out. I know that allergies in the air can cause that to the autoimmune we have, but my question is what allergy OTC do you take? I take Allegra,...

@Jodie Louise 

Last reply

Jodie Louise

Newly diagnosed

I was diagnosed last week with RRMS. I started off with double vision in April and then started to get numbness and tingling in my legs, arms, back and torso. I also have the zapping sensation down my body when I bend my neck. I have active and old lesions on my brain stem, neck, upper back and lowe...

@PenfoldNuke 

Last reply

PenfoldNuke

Feeling worthless

I’m I the only one but when I go out with my family on days out I feel like a burden as I’m so tired and always in pain

@rlmandyml 

Last reply

rlmandyml

New to shift..

But I’ve had my MS diagnosis for quite some time. Could use some support or just cool people to talk with. Right now my life is overtaken with MS this and MS that and I’m sick of it. If you don’t have it, you don’t understand it; so I’m hoping to find normal ms people surviving this encapsulating di...