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Charity Number: 1117194 (England and Wales)

Registered Company: 06000961

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Shift.ms, Platform, New Station Street, LS1 4JB, United Kingdom

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Shift.ms, Somerset House, Strand, West Goods Entrance, London WC2R 1LA, United Kingdom

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@hopki007 

Last reply

hopki007

I know a lot of people will laugh, but a daily afternoon warm tea does good for the body

First posted on the Shift.ms app
9

@PepperMS 

Last reply

PepperMS

I would love some feedback from people who have had RRMS and have progressed to SPMS. I was recently rediagnosed. I know MS is different for each individual but I’m wondering what I might expect the future to be like for me.

First posted on the Shift.ms app
10

@sango 

sango

Anyone had to switch from Kesimpta?

Did any of you have to switch from Kesimpta to another DMT following a relapse?
First posted on the Shift.ms app

@binkii 

Last reply

binkii

4th Kesimpta Injection

I'm currently onboarding onto an MS treatment and I had my fourth injection last night. My body has taken quite a hit from it, it's been trembling and I'm feeling really fatigued, weak and in pain. These effects haven't subsided since last night. Is this normal or has anyone else experienced this?...
First posted on the Shift.ms app
3

@KylieMarie89 

Edited

KylieMarie89

Help and ramble about kesimpta.

Hi everyone, this is my first post on here. I have been diagnosed with spms since may 5th of 2013,at that time I wasn't able to walk as I barely could move my arms and my right eye was having a hard time seeing. Spent a month in the hospital with that to come home as after 6 months of that I stoppe...
First posted on the Shift.ms app

@giovanac 

Last reply

giovanac

My neurologist recommended Briumvi / Kesimpta / Ocrevus — how do I choose between them?

I had my second appointment, and they recommended those three treatments. What should I base my decision on? Is there anything in favor of or against any of them that you guys can share with me? I was diagnosed a month ago — any help or advice is very welcome. Also, is there anything that can help...
First posted on the Shift.ms app
9

@Semms 

Last reply

Semms

Keeping strength

As title has anyone managed tho keep their strength many years after diagnosis? If so how have you managed this ? By going to the gym of just by luck , I’ve been ill with other issues last few months and looking to get back into gym loss of strength is one of my big ms concerns so will be good to ...
First posted on the Shift.ms app
12

@Jeremi 

Last reply

Jeremi

Dating is a real issue for me my MS has made me so lonely. I don’t even know what to do anymore.

First posted on the Shift.ms app
6

@JohnMacV13 

JohnMacV13

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

@Timothy_Little 

Last reply

Timothy_Little

I had another lumbar puncture and blood tests but I am cautious about taking meds especially since I have m.s and myeloma. No one has taken my symptoms seriously and I don't know what to think. I have lived with.s since December 2018 and I have treated it but not the cancer. I don't want to treat the cancer

First posted on the Shift.ms app
8
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