#k - Shift.ms

@bighammo69

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Im a RRMSer, who's recently been diagnosed as a diabetic T1. The symptoms are very much similar fatigue and balance problems. I haven't had a relapse for over 15 years. How do I know what causes my fatigue. Is it my MS or diabetes.

First posted on the Shift.ms app

2

@JohnMacV13

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Want to introduce my self. My names John. I have SPMS. The first event was in 1986, paralyzed On the left side. I was missed diagnosed as something else. In 2019 MS hit me like a bomb! Finally know what I have. Pretty damn awful for the last 39 years, especially curren condition. Looking for connections.

First posted on the Shift.ms app

2

@jamoranto

Be happy for this moment. This moment is your life. Omar Khayyam

💯

@lulagm2001

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I was diagnosed with MS 6 months ago. Because the neurologists said it was an aggressive type they stared me on B-cell therapy 2 months later. I know that because I’m in the middle of treatment it’s very unlikely that I’m having a relapse. It’s so hard to know what is happening with my body because it’s all so new. I feel like there is something definetly wrong with my body but it feels mole like aches that the fist episode which was mainly numbing of the legs. It’s so hard to know when to seek medical attention. I feel like my symptoms seem so random now but I feel like something is not right. How do you all decide when you just let it run it course or when to go to the hospital

First posted on the Shift.ms app

1

@buck82

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PPMS and needing a knee replacement

I’m new here I was diagnosed with PPMS in 2019. I work full time changing oil, tires, headlights and batteries. I was told in 2024 I needed a knee replacement on my dominant leg and that I was too young to have it done I needed to strengthen it and received pt. I receive Ocrevus infusion every 6 mon...

First posted on the Shift.ms app

2

@show

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Experiencing numbness hands fingers and legs mostly left leg . Anyone else deal with this ? My mri says no new lesions do I don’t know what’s going on . MS truly truly suckssss!

First posted on the Shift.ms app

29

@meanna

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Has anyone been on or is Aubagio(teriflumonide) if so please let me know what to expect as far as side affects?!? Thank you

First posted on the Shift.ms app

2

@nanny82

EditedLast reply

It's been so hard these past couple weeks, last week I was moving something lift it and my back snapped. Its getting better now thank God. Then the heat, I though I was ok because after been diagnosed last winter I realized I had cold sensitivity so I was hoping the summer wouldn't be a problem. Now the heat is here and I'm STRUGGLING. I feel heavy, like I'm walking through wet cement or sand. They say exercise helps with fatigue and we need the sun for vitamin D. I'm so tired...I feel like just crying, I really dont know what to do to help with these feeling. This disease sucks real bad, I'm so tired. What are some things you guys do to help with the fatigue.

First posted on the Shift.ms app

14

@juwa52

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Covid on Kesimpta

I got a bad cold and took an at home test for Covid after a few days because it was getting worse even though I started an antibiotic. The test came back positive. I were I get Covid more than anyone I know and I am careful. Anyway, my doctor wouldn’t prescribe an antiviral and it’s been like 7 days...

First posted on the Shift.ms app

13

@GRACIOUS

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What do I do if I can't afford to keep getting MRIs and everything and they diagnosed me with possible Ms a year ago but I can't afford to get more tests done and I'm having a lot of side effects

First posted on the Shift.ms app

3

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