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@AWAYWITHMS 

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AWAYWITHMS

Doctors Appointments

Is it just me or can you relate? when I go to my appointments I like to listen. Im hearing what the dr is saying, registering what’s being said, I’m just not popping questions on the spot. My last couple appointments were shockers. I learned that my MRIs from last August showed lesions, even tho I ...

@carilyn1970 

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carilyn1970

I have been falling down.

I have been diagnosed since 1994. My past flare ups have involved going numb on the right side. Then vertigo, then opticneritis. (forgive the spelling) now. I don't know if what is happening is MS or something else entirely. But, I have fallen down twice in the last 6 weeks. I am going to see...

@KarenKay 

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KarenKay

Neuropathy

My neuropathy in my feet is getting really painful. The only thing I take for it is Gabapentin. It helps, but I can only take it at night because it makes me sleepy. Is there something else that will help?

@MichelleMM 

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MichelleMM

Locations

I am from Washington State and live in Louisiana where is everyone from? Anyone else in Louisiana? I was brought here due to military and can’t manage to leave this place it sucks you in and won’t let you leave!

@QBRAR 

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QBRAR

Feeling alone and forgotten

I'm 39 F and was diagnosed in my late teens.the neurologist at the time told me I had benign ms and that was it. For over 20 years I've had nothing that has hindered my way of life. I've gotten married had a child and basically forgotten all about it! This month I noticed my right leg was dragging a...

@shaunixxx 

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shaunixxx

MS and working out

Hey everyone, just wandering if anyone goes to the gym? I really need to lose some weight, this last year I really struggled to leave my house because of my MS and my anxiety. Ofcourse unless it was appointments, college ect. Apparently going to the gym is good for MS but can also cause alot of stra...

@tash221993 

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tash221993

MRI - annual MRI

Hi everyone! I live in West Yorkshire in England, and the nurse I will be transferring to says I won’t have an annual MRI - one of the reasons is that she has 700 people in the district and she is on her own. I’m a little confused as I thought people who were newly diagnosed with MS (diagnosed D...

@AWAYWITHMS 

EditedLast reply

AWAYWITHMS

Vision loss

Anybody experience vision loss at any point because of MS? I’ve been partially blind in my left eye since last year. I experienced optic neuritis late July 24’, did 5 days in the hospital on high dose steroids. Vision went from blurry to dim to dark. The iv steroid did little affect leaving my vi...

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