#be - Shift.ms

@jbharris1356

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My first year with MS was horrid. I was going back-and-forth to the ER and I wasn’t getting help in the ER at first. Then I was hospitalized. Anyone experienced going back-and-forth to the ER the first year with being diagnosed with MS?

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2

@Prosp3rityfit

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To all my ocrevus MS warriors! Have you experianced being worse after the infusion then you were not on DMT? Lets talk about that

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15

@show

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I have some mild to moderate stenosis in my neck from degenerative arthritis that can produce the same symptoms . Has anyone else dealt with that combination of diagnosis before ?

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1

@PumaPie

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Scientists have been awarded the Nobel Prize for a major breakthrough in understanding how to stop the immune system from turning against the body itself.Their discovery explains key mechanisms behind autoimmune diseases, where the body mistakenly attacks its own healthy cells. This insight could transform how conditions like lupus, multiple sclerosis, and rheumatoid arthritis are treated in the future.By learning how to regulate an overactive immune response, researchers have opened the door to more targeted and effective therapies that may reduce suffering for millions of people worldwide. The discovery also holds promise for advancing treatments beyond autoimmune disorders, including potential applications in cancer research. The achievement marks a major milestone in modern medicine and offers new hope for long term disease control.THINGS

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2

@ReindeerAlaska

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FMLA, ADA, Teacher disability benefits

Hi, I’m looking to connect with others who are teachers or in public education and how did they do with intermittent FMLA, ADA accommodations and applying for teacher disability benefits because teachers don’t pay in to social security and do not qualify for SSDI

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1

@RMTH

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So am coming off Tysabri after five years. This is due to mental health issues. Tysabri was working fine. Now being asked if I want to go on Ubutuximab every six months intravenously or Ofatumumab (kesimpta) self injection at home. Anyone want to share their experiences with these treatments. TIA 🧡

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6

@jbharris1356

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When I first got diagnosed with MS and I left the doctors office got home reached in my pocket to get my keys and I couldn’t move. It took about three minutes before I could move again and it was really painful. Anyone go through that type of situation?

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4

@livvyluvs1

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Isolation and being judged.

I've recently learned I have MS in my brain and spine and the symptoms and pain, heavyness and the physical exhaustion it causes gets overwhelming. A lot of days I just want / need to stay in bed and be left alone. It makes me feel like a bad person because I'm not upholding the things that need to ...

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15

@mharris72

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