#no - Shift.ms

@Carlos

No

First posted on the Shift.ms app

@SugaBug1971

Last reply

These flare ups are the worse I notice when I turn my heat up I get one easily

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3

@Tcowart21

Last reply

No medicine

I have stop the zepoisa to treat the ms because my insurance wants 500 dollars for. That was 2 months ago. I have noticed some things happening. Now I’m worried

First posted on the Shift.ms app

9

@delki

EditedLast reply

I am not getting any thoughts about my situation right now. I cannot comprehend on what’s happening. It’s just scary and frustrating. I am so lost and I feel like no one understands me. I just had another episode of ON nearly after a year. I am just scared. I am an international student in WA and it’s so expensive. The tests and everything. I cannot keep going. I am just so so so lost.

First posted on the Shift.ms app

6

@greenmoose_

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does anyone in England know if having ms will entitle me to free prescriptions. I've been paying for years and nobody told me this was a thing!?

First posted on the Shift.ms app

12

@wigglestatic

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Hi I'm new here and I'm wondering if anybody's experienced eye issues this is the first for me. I've been diagnosed since 2007. Most of my lesions are in my brain and my spinal cord on the top. And I didn't have any eye pain but I had like lights sparkle flashing I had a blackout in my right eye for about 30 minutes the first day the second day it was only a few minutes and then the third day my eye was swollen shut. I went to the hospital for 3 days they put me on steroids ruled out a stroke. There was only a visiting neurologist because I was out of state and they had no answers so just curious if anybody can give me any feedback on that thank you..❤️

First posted on the Shift.ms app

2

@Jodikan

EditedLast reply

I’m losing my health insurance next month so I applied for medical but it looks like medical dos not cover kesimpta. Anyone have this happen?? I called the drug company and they said they will only help if someone has no insurance at all 😩 having medical makes me ineligible for medication assistance :(

First posted on the Shift.ms app

24

@Roman89

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Hi my name is Ramon I’m new here and I was recently diagnosed with MS and I’m still trying to learn more about it right now I’m doing infusions every 28 days and I still haven’t noticed any difference of feeling any better I’m going on my 4th infusion and I’m still feeling numbness in my side legs and feet along with a really bad pain like I’m walking on fire and pins at the same time has anyone else experienced this

Gardiner, United States

First posted on the Shift.ms app

10

@FredT77

EditedLast reply

Shortness of breath... has anyone on here have had this come out of nowhere? It happened to me lastnight went to the hospital they did chest x-rays and CT scan with dye bloodwork.. and nothing showed at first they believed I may have either the flu or pneumonia but nothing... can this be from the MS?

UPDATE: Just seen my primary doctor she says that I have an enlarged heart and the start of pneumonia... So gonna get started on antibiotics for the pneumonia and now have to call to set up to see a cardiologist for my heart..

First posted on the Shift.ms app

18

@jlucret71

EditedLast reply

How long did it take to get started on Kesimpta once your doctor put in the order? Been a week and insurance needs a prior authorization so called the doctors office to make sure they send it in but have not heard back. Does it take some time to process and then waiting for a nurse to call me to schedule the first dose so been waiting to get started already to see if it helps especially since been going through rough symptoms and therapy!

First posted on the Shift.ms app

3

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