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@Davie 

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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 

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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 

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choco_daiquiri

Looking for Edinburgh/Central Belt MSers!

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

@julie1975 

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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 

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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 

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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 

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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 

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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 🤔

@Ddott 

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Ddott

MS and dating

Hey everyone, What has been your experience dating with MS? I’m having trouble “getting out there” because of my fatigue and I’m finding it tough to connect with people. And the couple of times when the chemistry was on point and I was excited about someone I was “second choice.” The first guy kne...