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We are a charity and rely on donations

Charity Number: 1117194 (England and Wales)

Registered Company: 06000961

Registered address:
Shift.ms, Platform, New Station Street, LS1 4JB, United Kingdom

London office:
Shift.ms, Somerset House, Strand, West Goods Entrance, London WC2R 1LA, United Kingdom

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Sort 29 results by
Recent activityNewest posts

@MillarTestAdmin 

Last reply

MillarTestAdmin

unhappy post

I need help, worry, anxiety, depressed, depression
London, United Kingdom
1

@vecakep707 

Last reply

vecakep707

now an unhappy post

My last post unfortunately didn't get across how depressing and sad this is. I'm writing with an air of despondency. I can't stop crying. I can't think of any more ways to describe my negativity.
5

@martin 

Last reply

martin

Hello again 14/03/2022

My last post unfortunately didn't get across how depressing and sad this is. I'm writing with an air of despondency. I can't stop crying. I can't think of any more ways to describe my negativity.
6

@liamgrey1882 

Last reply

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...
2

@Adele_Barrow 

Last reply

Adele_Barrow

understanding

Ms is such a funny desease to have I use crutches to walk as my right leg is badly affected ive has surgery on my ankle to straighten foot, stop drop foot and waiting surgery on all toes now have clawing on right foot, people say was it worth having the surgery in first place . Well yeh I wouldn't ...
  • Health Conditions
  • People & Society
3

@angieH 

Last reply

angieH

Should I know if it’s a relapse?

I have been feeling so crappy. I am diagnosed with RRMS since 1998 at age of 28. No real problems until 2017! When I had a flare up main symptom dizzy and fatigue - severe. I recovered nearly complete, went on my first dmt copaxone. Annual mris were fine, a couple of small lesions even disappeare...
  • Health Conditions
6

@Alice352 

Last reply

Alice352

How long AE after pulse therapy?

Hello everyone! I was recently diagnosed with optic neuritis (and what apparently has been MS for several years now) and after long consideration I finally decided to opt for steroid pulse therapy (5 x 1000 mg methylprednisolone). The first few days were fine, I didn't experience any euphoria, slee...
  • Health Conditions
  • Drugs & Medications
1

@Henrietta 

Henrietta

Newly diagnosed - advice please!

I was dx (RRMS) over the phone on July 24th, a year after the symptoms which led to initial referral by GP to Neurology. Consultant said he was 'anxious to start treatment'. I was given two weeks to decide between Aubagio and Tecfidera. Told if I chose not to have treatment I'd be discharged back in...
  • Health Conditions

@Henrietta 

Henrietta

Newly diagnosed - UK MSers advice please

I was dx (RRMS) over the phone on July 24th, a year after the symptoms which led to initial referral by GP to Neurology. Consultant said he was 'anxious to start treatment'. I was given two weeks to decide between Aubagio and Tecfidera. Told if I chose not to have treatment I'd be discharged back in...
  • Neurological Conditions

@Henrietta 

Henrietta

Newly diagnosed - UK MSers advice please

I was dx (RRMS) over the phone on July 24th, a year after the symptoms which led to initial referral by GP to Neurology. Consultant said he was 'anxious to start treatment'. I was given two weeks to decide between Aubagio and Tecfidera. Told if I chose not to have treatment I'd be discharged back in...
  • Neurological Conditions
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