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@Terauda 

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Terauda

Dealing with Chronic Facial Nerve pain

Hi everyone 👋. Hope each and everybody is having a good day. Question.. can anyone suggest tips to ease the pain you get from facial pain, my right side has been hurting more than usual this recent week 😔. Thanks

@kaylouise 

EditedLast reply

kaylouise

PIP assessment last week

Good morning all, I had my pip assessment on Thursday it was around an hour long over the telephone - the assessor then called me back a few hours later and told me she had spoken with her manager and my case is quite complex and that they wanted to get it right for me - I’m guessing complex becaus...

@Treesa52 

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Treesa52

Humble

Yesterday I took a walk with my daughter, because of my balance I used my cane for the first time. What a humbling experience. Is using a walking aid embarrassing for any of you?

@shellyEd 

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shellyEd

Working Fully Remote

Asking if anyone has ever asked their employer to grant working fully remote because of health issues and was denied. Even though everything done on site can be done at home. Please Share experiences or laws concerning disability in the workplace that you are aware of. I am in the state of MA.

@Mcfly 

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Mcfly

Responding to friends

I'm finding that I am getting quite frustrated and upset that friends dismiss my symptoms, say I'm doing well and tell me they can't see I have any issues at all when inside I'm struggling with fatigue, tingling, loss of sensation and symptoms like vertigo, eye pain and balance issues. How do people...

@josielouisemat 

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josielouisemat

Help deciding which DMT

Hello! I am new here. I got diagnosed with MS two days ago and just taking it all in. It’s very overwhelming and emotional. I am in the process of learning everything I can about this disease as 3 months ago (before my first symptoms/flare) I didn’t even know what MS was really! I have been given ...

@DudeCrewMama 

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DudeCrewMama

Kesimpta expectations vs reality?

Hi everyone, I’m Robin. I was diagnosed with MS in November 2024 and started Kesimpta in November 2025. My neurologist (who specializes in MS) has told me that on Kesimpta I basically won’t know I have MS—that I shouldn’t get new lesions, my body will start healing, and possibly in 15–20 years I ...

@Swannie 

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Swannie

I am so tired..

I am so tired of this heat. I’m in serious pain and the fatigue is a killer. I just cannot do anything. I save all my energy to look after my pets and to shower/bath (because of how hot it is I’m sweating buckets) Cooking is not an option. Climate change and global warming sucks.