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@Donnalew 

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Donnalew

Upset

So having to do a mandatory reconsideration for my pip but I requested my PA4 form that has just come today and basically the reason I cant do things is because I'm overweight not because I have ms. This has really upset me because I have to get my head round this life long illness that as changed m...

@laurapacino 

Last reply

laurapacino

Mayzent/siponimod

Had rrms for 25 years now diagnosed with spms. Due to start mayzent/siponimod after being on Tysabri for 20 years. Anyone gone through something similar? And what’s been your experience?

@NTKhasMS 

Last reply

NTKhasMS

MS and Mother Nature, you owe me a summer. ☀️

This summer was supposed to be sunshine, fresh air, and making memories. Instead, I spent most of it fighting my own body, pain, inflammation, spasticity, fatigue, and one thing after another. And now, as we head into fall, I’m still not feeling 100%. I have another MRI coming up, and I’m waiting t...

@FarahN 

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FarahN

Forgot how much I missed the gym

I couldn't go when I was relapsing but I've started again and forgot how it cheers me up. Not only because gym does that but because I'm well enough to actually go Yayyyy :))))

@PJR57 

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PJR57

Infusion side affects???

My Doctor has talked about potentially moving to an infusion treatment. Is anyone willing to share any side affects they have experienced after infusion? Heard 2 weeks of flu like symptoms, head exhaustion...wondering what others have felt.

@bertugk 

Last reply

bertugk

Boosting the Immune System

Hello everyone, I take Fingya, an immunosuppressant medication; I take one pill daily. Because of this, I really can't handle the cold—I get sick very easily. What do you do to support your immune system? Besides eating winter fruits rich in Vitamin C, I also drink turmeric mixed into hot water. I...

@abrhym1 

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abrhym1

Hello everyone,

♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️♥️ I am writing to you as a fellow community member from North Africa (Libya). Since I am not fully fluent in English, I often find myself having to constantly copy posts, search on Google Chrome, and switch back and forth just to translate content. It has become quite tire...

@Mephi 

Last reply

Mephi

Do you feel lonely with MS?

Hi everyone, how are you all doing? I was diagnosed with MS in 2024, when I was 22, and I’m 25 now. As I mentioned in the title, I’ve been feeling really lonely since my diagnosis. I know MS is considered a relatively common disease, but I don’t know anyone my age who has it. Sometimes it feels li...

@Bramble1 

Last reply

Bramble1

Making new friends

Hi all, I was diagnosed 2001 RRMS tried Avonex for 3 years but could cope with the injections, no further contact with Neurologist and decided just to live life taking LDN. Now back in the system and am SPMS. I use an active manual wheelchair but can't blame the ms entirely for that - I have drop ...