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alone

I am victim of domestic abuse due to having ms it sucksseems I cannot post this here

@Vicki_Fielder 

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Vicki_Fielder

Ocrevus

A couple of people in another MS group I'm in have been told they can have their next infusion but they will have to self isolate for 12 weeks after. Anyone else had this ?

@pinkie100 

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pinkie100

Tysabri - few symptoms but new lesions

I was diagnosed in June 2019 having woken up with pins and needles in my hands in January. No previous symptoms. Pins and needles extended to whole body from chest down and I experienced MS hug a few times. After a couple of months things seemed more or less back to normal and although the pins and ...

@Ralee 

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Ralee

Paddle Boarding

Happy Tuesday everyone! So I was really chuffed yesterday, I went out on the board for the first time in a year. The family and I love going to Sandbanks and we had a good day in the harbour. I was nervous, because last year, my brother and I (Identical twin) went for a swim and I realised very qu...

@Rosie_Paolo 

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Rosie_Paolo

Feel a bit deflated and stupid

So I’m waiting for a diagnosis of various symptoms. I had an appointment via video link at home with a neurologist and I just feel like I messed it up. I’ve been waiting for 6 months , in pain , and I couldn’t articulate my symptoms . He asked me if it’s there all the time or now and again - I an...

@UpsandDowns 

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UpsandDowns

Relapse Symptoms

Hi everyone, I am abit frustrated.. I can not find what l am looking for in any MS related sites. Do i have to have a relapse to get steroid injection in other words can i have steroids to dampen down the symptoms I have been experiencing? Thanks

The coronavirus and MS – updated

From the International MS Federation. June 2020 - https://www.msif.org/news/2020/02/10/the-coronavirus-and-ms-what-you-need-to-know/ - Just the latest, that is all.

@Dawson.McWatch 

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Dawson.McWatch

Am I the only one?

I think it’s time I just take a step back an re-evaluate everyone that I have in my life.. having ms literally makes my day to day living hard for me, an none of the ppl I have in my life can understand that. They say they do but actions speak louder than words. It’s tough living this life being ove...

Any one want to talk?

I'm 24 and find it hard to cope with M.S.

@Erusha 

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Erusha

Life expectancy

Hi guys I just read the average life expectancy of someone with ms is 25 to 35 years after diagosis Anyone with any thoughts?