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Registered Company: 06000961

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

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@Lovegod 

Last reply

Lovegod

Trying to find strength.need a little help, I’m experiencing the MS hug my fatigue is whipping me. and my depression is running rampage. I need a little help and I don’t think anyone understands, except those that are experiencing or have went through it

First posted on the Shift.ms app
14

@nexas 

Last reply

nexas

Jef, had MS for 40 + yrs. I was a social worker for 18 yrs. No I'm worthless. I have no wo wife no change ldren. Family but not liked by family members due to causing demize of f entire family as a result of me I think

First posted on the Shift.ms app
12

@Newtotheteam 

Last reply

Newtotheteam

Still trying to navigate things. Having a bad day. Worst in awhile and I feel like I haven’t been symptom free for weeks. Thinking about the emergency room. Any thoughts?

First posted on the Shift.ms app
12

@jamieerogers 

EditedLast reply

jamieerogers

I was diagnosed with MS in June 2025. Has anyone else found they catch everything that goes around? I work from home and honestly rarely leave as my MS is not controlled. But I literally am catching everything. Last month it was walking pneumonia and now bronchitis. I live in Iowa but we have had a mild winter. I am guessing my family is being the germs into our house. Has anyone else experienced this and if so how do you manage it? I eat very clean and already take a bunch of vitamins and drink a gallon of water daily. Would an air purifier help do you think?

First posted on the Shift.ms app
3

@Jeanettethomson 

Last reply

Jeanettethomson

Hi all, has anyone here once diagnosed started to get any eczema/ dermatitis too ? I’m 56 and was diagnosed with PPMS in 2023 and have never suffered with eczema until now ! My GP doesn’t think it’s related but I do , what do you guys think ? Thanks

First posted on the Shift.ms app
10

@melly777 

Last reply

melly777

Does anyone else think the Covid jabs have sped up their MS symptoms?

First posted on the Shift.ms app
33

@possum 

EditedLast reply

possum

As A former division, one wrestler and MMA guy, I think it a lot of times weights are my best therapy exercises that target mobility

First posted on the Shift.ms app
1

@shiftms-films 

EditedLast reply

shiftms-films

Do All MSers Think The Same? | Diagnosis: Part One

Join Roxy, Heather, Maytee, Katt and Dave as they agree and disagree with hot MS topics, opinions and share their multiple sclerosis diagnosis stories. Did you have a difficult diagnosis? Why not share the lessons you learned with the Community in the comments below 👇 https://www.youtube.com/watc...
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24

@Timothy_Little 

Last reply

Timothy_Little

I had another lumbar puncture and blood tests but I am cautious about taking meds especially since I have m.s and myeloma. No one has taken my symptoms seriously and I don't know what to think. I have lived with.s since December 2018 and I have treated it but not the cancer. I don't want to treat the cancer

First posted on the Shift.ms app
8

@dexter12 

Last reply

dexter12

I have a question. I had a check-up with a neurologist. I told him about all the symptoms I had last year. He still couldn't tell me what type of MS I had. But after an MRI analysis, he said I should switch to Orcevus instead of Kesimpta. Does this mean that I might have the type of MS I think he calls PPMS?

First posted on the Shift.ms app
17
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