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I am collecting information in an attempt to contact those that are making our laws about opioid addiction. I have already contacted some law makers. When the new proposals are announce, I want to be very ready to get active in trying to be sure that those of us in chronic pain are not ignored in the process. Please be very specific if you feel that you have already been affected by new state laws or the national CDC Guidelines for pain managers and their use of opioid. Thanking you all in… read more
I really enjoyed your comment. Exactly how I feel.
Iv recently had some trauma in my life I started meditation.15 mins a day.you know it helps more visual.though I go through my pains my diet.etc try it . Helps me I'm self taught.🤗🤗
Back pain from DDD, goes down my legs and I cannot sleep.
I take cbd oil with a bit of the for bed time. During the day 3 times I take a half a gummy and oil with no thc 3 times a day. Cold pack for back and Dr ho vibrator for neck. Manageable
I have fibromyalgia and have had it for at least six years( have been diagnosed).This is an awful disease, I also have other issues to go along with it.
I have insomnia because of my pain. I don't know what to do. I have tried aromatherapy and relaxation techniques but they don't help. I don't want to take sleeping pills because I'm afraid of getting addicted to them. Any ideas? Please help!!!
My grandma drank warm milk and honey when she couldn’t sleep. I do it and it’s helped me. Also try melatonin. It’s all natural and no addiction.
I'm off it now but when my ears started I took my High Blood Pressure tablets and it helped a lot ! Now off the HBP so I just try to I live with it
I am in the same boat every one else is in. But what can we do about it. I have 5 fused disc in my neck. Gone thru two surgeries. The ppl that need pain meds can’t get them. But ppl that don’t need them gets all kinds of meds. How can that be. And what can we do about it ?
I get it really get it.
I have suspected EDS and am awaiting official diagnosis, but I am coming to find that I feel extremely alone in this as even my partners don't quite understand what I am dealing with. This has been a wonderful community of caring, understanding people, but I would very much like to connect with people who have been diagnosed with or suspect they may have EDS and perhaps learn more about living with it as even regular chronic pain tricks don't always help.
Leigh'
There is no cure
Make sure that you avoid lifting weight.
To protect your skin, make sure that you are using the right type of sunscreen.
Make sure to avoid soaps that are harsh and can… read more
My pain level is ok at the moment but the burning in my foot is so intense, specially if I try to sit with my foot up, does anyone else have this. It has never been this bad, could Tramadol make it worse, as I have had to take it twice today for the pain. I have only been on Tramadol for a couple days so really would like to hear from anyone that is also on it. Thanks in advance
I'd be interested in any holistic meds that work too.
On your limited access to your health records via your multi or Franciscan mychart,the conditions listed on your current health conditions/past conditions diagnosed on legal record health conditions?iron clad enough ,legal,real,etc info?info you could realistically put down on any medical forms,etc as yes these are my health conditions?
@A MyChronicPainTeam Member I have been on ssa for many years,I was born with aspergers and some psychiatric conditions.yet I was very physically healthy,even getting a mild flu was extremely seldom.i… read more