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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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@slamminsammyms 

EditedLast reply

slamminsammyms

Teeth / nerve pain?

Hi all! I have had teeth pain get worse and worse over the months since being dxd. I thought it was the winter cold but here we are in nice weather and it is still happening. Could this be ms related or Trigeminal neuralgia? If the latter, how does one get diagnosed for something additional when ms ...
First posted on the Shift.ms app
18

@kala21 

EditedLast reply

kala21

I’m experiencing neuropathic nerve pain in my legs and feet 😔 Its so mentally draining I’m finding it hard to cope with because I got to stay active to keep my mind sane and because I can’t do that right now I’m not coping at all. I’m having bad thoughts and I don’t normally get this low or depressed. How do you all manage this?

Aberdare, United Kingdom
First posted on the Shift.ms app
9

@strengthinbloom 

Last reply

strengthinbloom

EMG Nerve Study

Has anyone had an EMG nerve study done before? What does it feel like? How did your nerves react to the test. Having issues with progression. It’s happening too fast dr said. Could be something else in my spine.
First posted on the Shift.ms app
7

@gigglehappy 

Last reply

gigglehappy

How to deal with nerve pain

My nerve pain is localized in my face. It makes smiling, laughing, talking, and listening to anything miserable. Anyone dealing with this? The pain is so bad I fight tears.
First posted on the Shift.ms app
10

@heebaw 

Last reply

heebaw

Nerve pain

Hello everyone! I’m not new here, but this is my first time posting. I was diagnosed with MS in 2022 and, after disease progression in 2024, I was switched to Ocrevus. About 2.5 weeks ago, I started experiencing nerve pain and numbness. It initially started in my right hand, then spread to my neck,...
First posted on the Shift.ms app
7

@jrk2023 

Last reply

jrk2023

SO STUCK RIGHT NOW!! Anyone have holistic remedies for nerve pain I might not have heard of before (I own 'Holistic Guide to Wellness' already though)?

I have had RRMS since 2023. I found out after losing feeling in my right foot that has progressed all the way up my leg, into my hip and lower back. It turned out, I have an 11mm sized lesion right at the base of my tailbone. I've been told that all the pain, numbness, etc., is all due to this lesio...
First posted on the Shift.ms app
3

@welshdragon 

Last reply

welshdragon

Has anyone tried Amitriptyline for nerve pain

I find it helps with my ms hug
First posted on the Shift.ms app
2

@megustaplantas 

EditedLast reply

megustaplantas

Does anyone else have a schwannoma/nerve sheath tumor in addition to MS?

I have a small nerve sheath tumor on my cervical spine. I was just diagnosed with both, so still figuring how life with both is going to look/how treatments for one will impact the other. Does anyone else have the MS/nerve sheath tumor combo? How has it impacted you if so?
First posted on the Shift.ms app
6

@deltalady284 

deltalady284

I’m dealing with MS-related foot drop and persistent nerve symptoms (tingling, cold sensation on the top of the foot). I appreciate the advice about keeping the dorsiflexor muscles active and using an AFO when necessary.My main issue isn’t just muscle weakness though — it feels like the nerve signals themselves aren’t fully getting through, which is causing the tingling and cold feeling.Has anyone actually restored the nerve signaling enough to get rid of foot drop?If so, what specifically helped — therapy approaches, electrical stimulation, medications, or other treatments that improved the nerve signal itself?

First posted on the Shift.ms app

@sarar0cks 

sarar0cks

nerve pain in hands

any tips or advice on nerve pain in hands? sometimes it gets so bad it’s difficult to sleep.
Haverstraw, United States
First posted on the Shift.ms app
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