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

Follow-up: Release the Hounds

I got out of bed this morning at free-fall speed. Unfortunately, my legs hadn’t received the same instructions. I hit the floor like a bowling ball dropped into a lake, then walked to the bathroom like a newborn giraffe discovering gravity. I immediately knew I’d fucked up. Apparently, I’ve now g...

@Aleighan 

Last reply

Aleighan

Feeling so let down

I had bad reaction to broumvi and its been awful since. I had it on 3rd of sept. Ive been gp, ive been a&e, contacted ms team multiple times. And here i am crying at home cause i cant take feeling this ill. I dont know what i need to do to get some help. Its so hard to cope with. I get take paraceta...

@brittxrose7 

Last reply

brittxrose7

Recovery & Ms

Is anyone in recovery who also has ms? I really need to talk to someone who gets it. Iykyk

@bigAlreeves 

Last reply

bigAlreeves

My kids don’t deserve this.

I lived across three states Missouri Arkansas and Illinois when I was younger and I hate Having to be sick to the extent I can’t even get out of bed. They should be out there like me when I was younger not deliberately buying their properties as close as possible to mine is simply because they are w...

@elev 

Last reply

elev

Phantom smells? Anyone else experiencing issues with smells?

I’ve been having this weird issue with my sense of smell. Anytime I’m around a strong smell, like coffee or cooking, it seems to trigger this cigarette/smoky smell in my nose that I get stuck with for the rest of the day. Most of the time it doesn’t go away until the next day, and sometimes it can ...

@bigAlreeves 

Last reply

bigAlreeves

Bored

Sitting at home all day gets old and exhausting and now I’m bored out of my mind. If it weren’t for MS I could be riding my ATV but my right hand is totally ruined from Rheumatoid Arthritis and I am right handed so I really miss riding bikes and four wheelers

@BogWytch 

Last reply

BogWytch

NMSS in the US

I don't know who needs to hear this but the National MS Society in the US is absolute garbage! If I could share pics, I'd show the proof !! Over two years ago I was banned from the NMSS Facebook group over RELIGION*! When I talked to the group administrator, he spoke to me very disrespectfully, ref...

@laurapacino 

Last reply

laurapacino

Mayzent/siponimod

Had rrms for 25 years now diagnosed with spms. Due to start mayzent/siponimod after being on Tysabri for 20 years. Anyone gone through something similar? And what’s been your experience?

@Cassierae897 

Last reply

Cassierae897

Lonely

How does everyone deal with loneliness/unsupportive or emotionally absent partners? I’ve lost all my friends because of my diagnosis, I have no time to make new ones because every single day I have some kind of doctors appointment usually multiple. And I have no energy, when I need help with things ...