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@hillcathyr 

Last reply

hillcathyr

Palliative Care

So I was diagnosed with RRMS "officially" in August of 2025. In April 2026, the Dr told me we were going to try Truxima. It took a month for the insurance to approve. Sadly, I had an allergic reaction. Then we tried Ocrevus and the same thing happened, an allergic reaction. So it's now July and we...

@chickenwizard 

Last reply

chickenwizard

Problems with my wife

I can't seem to get back to a good place with my wife. I feel like shes turned into a flatmate and honestly, im scared im pushing her away. She keeps trying to give me (bad) advice and gets upset when i say im not going to try it. Or she thinks im making an excuse when i cant do something. Its exhau...

@calliejade 

EditedLast reply

calliejade

Newly diagnosed

Hey everyone. I've just been diagnosed with RRMS. I had one episode of optic neuritis in November 2025, which led to numerous scans and a lumbar puncture, with my diagnosis being given on 3rd July. I have one area of demyelination on my brain, and one on my spine - neither of which were accompanied ...

@Felgi 

Last reply

Felgi

Numb and tingling legs up to hips

Hi, i just been diagnosed this month after a LP for the final results! I had tingling toes last November, when the whole adiagnosis process stated! I asked before, but didn’t get any answers! I am currently dealing with my legs being numb and tingling all the way up to my hips! I am not sure if the ...

@TiffOso 

Edited

TiffOso

MS fatigue hit me like a truck today.

I still had a full day of work, chased after my 2.5-year-old, and somehow managed to get my workout in. I’m definitely feeling it now, but I’m reminding myself that not every accomplishment has to look perfect. If today was hard for you too, give yourself some credit. Getting through the day with M...
Fort Myers, United States

@LanaGigi94 

Last reply

LanaGigi94

No one.

I’m currently dealing with a difficult conflict with my mother, and I want to explain why. When I was 13, I had early symptoms of MS. They were noticeable, but they were missed. At that age, I didn’t insist on medical exams because I felt sorry for her and for her financial situation. And her priori...

@Swannie 

Last reply

Swannie

How to get on MS trials?

Is there someplace to contact or stuff I need to do to be considered for trials? Or would I just need to contact my MS nurses?

@Pickle363600 

Last reply

Pickle363600

Heat

90 degrees here in Wisconsin. It's unbearable. My balance is super wonky and so many MS hugs 😭