@username
Please wait...
Sort by

Ppms

I've been diagnosed with primary progressive MS I'm 45 was very active. I know it's a question everyone will ask. I have a young family and need to try and support them by continuing to work. Is it likely I'll work until I retire. Am I likely to walk without crutches?I can't walk very far anymore. R...

@Davie 

Last reply

Davie

Relationship

After been diagnosed last year my wife keeps telling me that ms is not a real illness and to suck it up I told her to have a day in my shoes dose anyone get this response of there partners cos Iam really debating after 22 years of marriage of ending it cos can’t cope with stress which make my sympto...

@Burton9923 

Last reply

Burton9923

Depression not wanting to be here anymore

I was diagnosed a few years ago after a long process of many years and a missed diagnosis. I am really struggling. I feel so sad all the time, crying all the time. Everything is getting on top of me. I feel this deterioration is related to a relapse I had due to location of the lesion. Struggling at...

@BillySmith 

EditedLast reply

BillySmith

A question about other people with MS

I think being diagnosed with MS is like being dropped into a new country and not knowing the language. All of a sudden we’re expected to know the MS lingo, pick a treatment, tell our friends, look at our diet, notify our employers etc. For me, there’s no way I could’ve confidently done any of it w...

Do you think finding other people with MS makes it easier for you to make further health decisions with MS?

Total answers: 555

@choco_daiquiri 

Last reply

choco_daiquiri

Looking for Edinburgh/Central Belt MSers!

Hoping to build some new friendships and a support network! 🤞🏾
Edinburgh, UK

@julie1975 

Last reply

julie1975

Being called 'lazy'. Need to vent 😡

I've been told by someone I work with what someone called me before they left and it hurt me quite abit. Apparently I was lazy. To think someone thinks of me in that way just shows that they haven't a clue what MS is. I work 3 days a week with stiff legs half the time, never ring in sick and I'm laz...

@SkyCc 

Last reply

SkyCc

Support groups

Does anyone know of any support groups in the Glasgow area? In some serous need of speaking with people who get it!
Glasgow, United Kingdom

@Dtoste77 

Last reply

Dtoste77

First time post.

Hi everyone, First time poster. In late 2021 I was diagnosed with Relapsing Remitting Multiple Sclerosis. This is a very new diagnosis for me, and I’m learning every day. I learned is that connecting with people in the MS community is a powerful thing and I’ve decided to get out of my comfort zone ...

@BULLMAN 

Last reply

BULLMAN

Todays post

I’m so old that when I was a kid you actually had to win something to get a trophy
Leeds, United Kingdom

@SkyCc 

Last reply

SkyCc

Carnival rides

Is anyone unable to go on rides at the carnival? I loved the carnival rides but not long after doing diagnosed any time I went on one. The speed and the turning can really upset my head. I can't walk in a straight line afterwards or focus my eyes on anything in particular 🤔