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Charity Number: 1117194 (England and Wales)

Registered Company: 06000961

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

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

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@AWAYWITHMS 

EditedLast reply

AWAYWITHMS

Vision loss

Anybody experience vision loss at any point because of MS? I’ve been partially blind in my left eye since last year. I experienced optic neuritis late July 24’, did 5 days in the hospital on high dose steroids. Vision went from blurry to dim to dark. The iv steroid did little affect leaving my vi...
First posted on the Shift.ms app
27

@Gracie690 

Last reply

Gracie690

Worried i have MS

Hi all I hope you don't mind me posting here. Apologies if this is long but if i dont share my worries somewhere i might explode! I have suffered migraines all my life, however about 6 weeks ago I had a cluster and on the 3rd day started to get blurred vision as opposed to the usual aura and began t...
First posted on the Shift.ms app
13

@Johnwayne 

Last reply

Johnwayne

Hi Everyone... I have had 14 months of unusual undiagnosed symptoms such as neurological pain, falling down episodes, pre syncope, blurred vision, stroke like Sensations, can't walk a straight line ever, Etc my doctor prescribed me pregabalin 100 mg a day to start.. I was wondering if anybody out here has taken pre-gablin for MS and or epileptic seizures.. and I was wondering if it worked for them and if there's any side effects please touch base back with me if you have thank you so much

First posted on the Shift.ms app
9

@anniespencer 

Last reply

anniespencer

Eye pain

Anyone suffer with eye pain but not optic neuritis? My eye goes through stages of pain on movement but the opthalmology clinic says it's not optic neuritis it's happened a few tea for a few weeks at a time in different eyes but after scans and tests they say my optic nerve is fine and my eyes are he...
First posted on the Shift.ms app
4

@Lauren21 

Last reply

Lauren21

Retrobulbar neuritis

If you've experienced retrobulbar neuritis before, can you share what symptoms you had and how it was diagnosed? I've visited the optician after having had pain in my left eye when moving my eye. No blurred vision or colour vision loss. The optician has suggested RN as a possibility and made an urge...
3

@farky 

Last reply

farky

I keep hearing about leeshions hod yoy know you have then and what are they l have had blurred vision once lasted about 3 hours still nor shure if it was ms related I'm out of work and that's hard for me I fear I may struggle to find a job was self employed builder but I can no longer do that feeling defeated

First posted on the Shift.ms app
4

@Brookaroo 

EditedLast reply

Brookaroo

Diagnosis not through MRI?

I now have three doctors (including my MS neurologist’s opinion) that I may have MS. My brain and cervical spine MRI appear normal but my symptoms and physical assessments show MS symptoms and all doctors say CNS difficulties. Experienced some mild symptoms for years but in July my right arm went se...
First posted on the Shift.ms app
13

@ChrissyD46933 

Last reply

ChrissyD46933

New to the Fourm. Was recently diagnosed with MS last September. I get to see a Neurologist in June. Dealing with Face numbness, blurred vision, muscle pain, vertigo, headaches and chronic fatigue as well. It's starting to interfere with my ability to walk. I work as a case worker for Family and Social Services so I often have a heavy work load but my MS is causing me to fall behind due to days I can't get out of bed. I could really use some support. I'm not very educated about MS but I'm learning. Any information and tips would be very helpful! TIA!!

First posted on the Shift.ms app
11

@Puppypower2304 

EditedLast reply

Puppypower2304

MS OR ME/CFS

My GP has diagnosed me with ME/CFS but I don’t think it is to be honest. I get a lot of tingling in my arms and legs My hands jerk a lot especially at night Pain in my legs and arms is horrendous but I’ve also got pain everywhere else but the pain in my arms and legs are much worse. I’m exhausted al...
Launceston, United Kingdom
First posted on the Shift.ms app
5

@MakkaC 

MakkaC

Noob here, hi 😁

Hello everyone, I'm a nooby to this site and i have joined because I'm worried i might have MS or possibly something else that's affecting me this way. My story is quite long so i don't want to bore you all. But i just wanted to know if any of you have suffered with sudden onset of stuttering, tre...
First posted on the Shift.ms app
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