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@Cooper 

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Cooper

Divorce, illness payout she's going for

I have RRMS and its been slowish in development. Im now on ocrevus but things are happening with my cognitive behaviour - memory, focus, clarity of thought, problem solving. This has been getting gradually worse for a few years, but i knew my job inside out, so not too much of a problem. Of course i...

PPMS

I am new to this site and wondered how many people with PPMS used it? Really interested to hear other people's experience of PPMS. I was diagnosed three year ago after investigations into what was then a mild gait/drop foot problem. Over the past 18 months I have experienced significantly greater...

@McArthur82 

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McArthur82

MS?

Jan2004 is when my journey started

Falkirk Wobble SATURDAY 19th September

Morning all! Just a wee reminder about our next virtual meet up, 11am Saturday 19th September for Brunch and a blether about life in general with fellow MSers, since we're still restricted to only meeting 5 households outdoors. Please pm your email address to myself or @watsoncraig for us to send...

@Sarah_Williams 

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Sarah_Williams

The neverending story

Hi everyone :) I am getting close to an appointment with a general specialist physician to get the ball rolling for testing to get to the bottom of a big range of symptoms. Some I have been experiencing for a number of years, others have shown their face over the last few months. Due to Covid-19 it...

@liamgrey1882 

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liamgrey1882

I’m a newbie 😊

I usually kee things bottled up but here goes im struggling to let the fact I’ve been diagnosed with ms sink in I feel like guilty for putting my gf and family through it and my temper sometimes gets the better of me and I say stuff I don’t mean I’m on tysabri round 5 coming up soon and diluxatine f...

@Sammy33 

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Sammy33

New to MS

Hi everyone. I'm 33 years old and not so long ago I been diagnosed with RRMS. It took me a while to accept it and figured out what's happening with me. Still very new to it, trying to get as much information as possible. Thanks to everyone for sharing their stories, it's really helps.

@Paul_Tierney 

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Paul_Tierney

Helping with pains

Hi I have Ms for the last 8years , diagnosed at 21, I haven’t luckily had many pains up till now, basically haven’t been able to sleep due to spasm in feet , now given beclomec but don’t find it works , have any followers or volunteers heard of anything that does, nuisance as much as pain uncomforta...