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@Markae 

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Markae

Crap gap

Crap gap amd this heat is royally kicking my arse end of month Infusion time and hopefully cooler weather

@Diandra 

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Diandra

Learning to have patience

I know I’m pretty early in my MS diagnosis even though I’ve probably had it for the past 3 to 4 years but this is the most frustrating thing ever. They keep saying the first year is the hardest cause you’re learning how to live your new life with your diagnosis . It is also very lonely regardless o...

@Donnalew 

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Donnalew

Heat

This heat is knocking me for six honestly I can't do anything I feel like I have no energy and feel dizzy is this normal

@claudiamonique 

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claudiamonique

Looking to talk to someone

Just looking to talk to someone who can understand what I’m going through. My family and friends they don’t listen. They brush it off so I need to talk to someone just as friends someone who can understand what I’m going through and I can be there for someone who might need an ear to listen.

@Tiffcorpus 

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Tiffcorpus

Magic mushrooms

OK guys so I am basically guinea piging Myself with magic mushrooms. I’ve heard a lot about people micro dosing to help them with all kinds of stuff, but I do have a high Tolerance so I will not be micro dosing. This is my first time and it’s all in hopes that it helps with neuroplasty. Has anyone ...

@deano 

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deano

After PIP review , i was awarded 6 more years

No phone interview , just based on the form and evidence I submitted Decision was made within 8 days of form being scanned at the DWP. Then a further 2 weeks before I knew the outcome via post. I have SPMS

@jackieo66 

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jackieo66

Uncaring

I’m not sure if uncaring is the title I really want for this rant/observation but I started thinking of the years since my diagnosis (2002) my family members even my grown children I don’t think any one of them has really been curious enough to read about my symptoms the things I deal with daily and...

@serenawolf 

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serenawolf

Occupational therapy

So my doctor recommended I try OT again for my hands. I have a lot of numbness and tingling and weakness has been increasing. Since I still have to work full time and am waiting on an actual diagnosis put in my chart, I need my hands. Orthopedic OT said it's nerve issues, suspicions of MS, so Im to...

@Donnalew 

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Donnalew

Vitamin d

My neurologist said I need to take vitamin d tablets alongside my treatment, do you take vitamin d tablets and if so which ones 😊

@DeSelby 

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DeSelby

Story about the start of my MS journey

I don't know if I'd call it a funny story, but it's certainly a bit odd. So I had my first relapse in 2012 (although I think I had symptoms predating that with hindsight). Anyway it's 2012, I'm on a year out from university, and when I'm not studying Physics in preparation for my final year I was r...