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Hi everyone! With my MS, I have intense chronic pain and I’m finding it difficult to meet people who have significant chronic pain who are around my age. Does anybody know of support groups in my area (Calgary, Canada), informal or formal, that targets young people with MS and who have chronic pain...

Dealing with chronic pain? Two shots of tequila amazing for leg pain.

Hi everyone! With my MS, I have intense chronic pain and I’m finding it difficult to meet people who have significant chronic pain who are around my age. Does anybody know of support groups in my area (Calgary, Canada), informal or formal, that targets young people with MS and who have chronic pain...

Hey guys I’m feeling pretty beaten down and frustrated, I live in Australia and work full time and deal with pain, fatigue and light sensitivity all the time. I’ve been researching help I can get from the government to support me in any way in terms of the cost of treatments etc and I’m not finding ...

Thought it might be of interest to fellow MSers Interesting BBC article about the therapeutic benefits of cooking for people with chronic pain and fatigue and a cookbook called ‘cookfulness’ which can be found on Amazon. The blurb says the recipe book focuses on cooking with a disability or chron...

I've avoided using the label "chronic pain" because my pain is not really a symptom of my disease. I'm slowly starting to realize I deal with almost constant pain, at least when walking...sometimes when sleeping or sitting, but it's not because of MS directly. My right knee is injured (sports inju...

hi all. So i was diagnosed with RRMS in 2017 following a supposed trapped nerve in my neck that has never recovered since December 2015: This is what lead to me requesting scans and eventual diagnosis. I'm really fortunate that the MS itself seems stable, but this nerve disturbance causes burning s...

I thought I knew #ChronicPain ( and I don't mean being unable to score some sticky Icky) Then, during a month long attack of #sciatica (not my first) I developed a fucked ankle (not a medical term) - presumably #MS #spasticity in the peroneal muscle (shin/calf - not per_I_neal!). Can't walk (got t...

Hello, I’m new here😃 I’m Callan and Im from Scotland. I have suffered with health issues mainly chronic pain since I was 15/16 years old. I was told I had fibromyalgia even when my symptoms worsened and I got more new bizarre symptoms I was reassured it was fibromyalgia and told to ‘stop searching...

Hi. My name is Kevin Toliver-Lyons and I seem to be on the verge of an ms diagnosis. I've had Bell's palsy twice, trigeminal neuralgia, and worsening neurological issues since 2013. I’ve been to the hospital several times for what they called "Brain Attacks," which include double vision, left-eye we...