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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...

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...

Hi, What I love about this forum is the wealth of experiences and empathy! I really need some advice folks. Some background: I've had RRMS for over eight years. My last treatment was Lemtrada five years and I had a really good response to it. My old symptoms are now returning: chronic pain is worse...

A friend's clearly struggling with symptoms which range from tingling, numbness, heat patches to pain, cognitive impairment and fatigue, spasticity to trigeminal Neuralgia bladder and bowel issues recently too. Athough she has had an MRI, which a muscosceletal doctor has said looks normal, she is s...

Hi everyone, first time posting and I can’t seem to find if anyone has discussed this before, so thought I would ask! I’ve not been offered any DMTs for my MS, and I’m really struggling to understand why. I haven’t met anyone else who hasn’t been put straight on a DMT, so I really don’t understand ...