@username
Write a post...
For a better experience get the Shift.ms app
Sort by

@skezz 

EditedLast reply

skezz

Aircon in the uk?

Hi, anyone in the uk got aircon? Built in or portable I’d like to know how much these are and which portable ones are decent as I know they cost less. I physically can’t stand this heat any longer I’ve never been so uncomfortable. Sleeping outside has become a genuine consideration and I’m at wits e...

@Lakiyah5555 

Last reply

Lakiyah5555

Job lose

. Since I’ve been diagnosed with relapsing Ms. my life has gotten worse. I kept brushing it off like I got this I’m fine.. BUT! The memory fog and speech slurr took over I worked from home answering calls . I forget the conversation I just had with clients when it’s time to enter notes . On June 11 ...

@Janenne 

Last reply

Janenne

Fumbling with my words

Anyone ever have a conversation and you try saying something and it’s like the words will not come out. It’s hard to explain I guess. I’ll be talking and I’m fumbling with my words and then nothing comes out. I get so frustrated with myself. I feel like people probably think I’m an idiot 🤦🏻‍♀️

@Zelda 

Last reply

Zelda

Sorry in advance

Okay I know this is probably not appropriate and I apologize on the get-go and if I need to take it down that is perfectly fine. Does anybody ever have the issue with having desires with your partner? Or sometimes no desire at all, and sometimes it just pops up at random times that are more likely n...

@Marjrscott 

Last reply

Marjrscott

Medical negligence!

Turns out I had non-specific lesions on my brain. I was having neuro symptoms when they found them, but they found them to be so “unimportant”…they LEFT IT OUT OF MY FINAL MED REPORT…..then slapped me with a psych diagnosis….now 2.5 years later my symptoms are worse and I’m disabled….im pissed. I’ve...

@msOrangepeel 

Last reply

msOrangepeel

Told my family about my diagnosis

I got diagnosed a couple weeks ago and have been sharing the news with my loved ones. My parents took it like a shot in the chest. They fully think my life is over, despite me trying to give them good information about treatment and outcomes and all. They’ve been calling me every day with more crazy...

@Juliapinkie1 

Last reply

Juliapinkie1

A "fait accompli"..my new reality?

Heya, Don't know if i have a question, statement or observation. Or all of the above. During these last 2 years, things really took a turn for the worse, ms wise. And subsequently, psychologically as well. No major relapses, but clearly a steady decline. And new meds, which cause side-effects that a...
Amsterdam, Netherlands

@lcritchl 

Last reply

lcritchl

@lllJlll 

Last reply

lllJlll

I think might be having a flare not sure

So I was diagnosed on May 28 had a 5 day steroid treatment and I'm currently on dimethyl fumarate. I was out late last night had me two beers and barely got any sleep so I'm wondering did I push my body or are this side affects from the meds. Started the meds about 4 days ago and took one last nig...

Welcome to Shift.ms

The global community for MSers