I didn’t go through all your posts, just the initial threads created.
Diagnosing these kinds of things can be extremely hard and sadly often seems to be a lucky draw of either ending up in hospital where they can poke and prob or just happening to mention the right things to the right doctor who goes down the right avenue.
I was told I had “spastic colon” back in the old days and then later IBS when they gave it a new bullshit name for “we don’t actually know” and always have more fibre it will make it all better was the solution.
It took projectile vomiting and a full blown bowel obstruction at age 30 to put me in hospital and have every test, scan and X-ray done to discover I have Crohn’s Disease which also means fibre is absolutely the worst thing possible you can do.
So for years I was misdiagnosed and mistreating myself with completely the wrong remedies and just making it worse and then suddenly it with basically two weeks of nothing but liquids I was entirely reset and pain free (other than being ****ing hungry) for the first time in my adult life and then started the slow process of dietary change and life improvement.
Now some ten years later just knowing at least one part of the puzzle makes life so much easier even though I’m pretty sure there is another underlying issue I’m also not her aware of.
Some of it could be caused by my medication, but this has also been changed a few times over the years with little difference.
I have weird skin issues. At times I’ve had weird sunburn like sensations on the entire one side of my body without anything showing. I can hardly walk 1km in “plakkies” without socks on and I get these legions on my feet at all friction points.
I have constant bone and joint pain. When I say constant I mean just sitting dead still I can feel almost every joint in my body “creaking” or the bones straining, something normal people aren’t aware of. It’s similar to if you’ve broken bones before and it’s now a cold weather day. Then on bad days that flares up in my knees, ankles, wrists etc to the point it wakes me up at night and I can’t go back to sleep.
At times the muscles in my feet underneath where it joins your heel, can’t remember what it’s called now is so sore and tight that I basically can’t walk.
Then there is the actual bowel related pain. This is actually fairly controlled most of the time but can go off kilter and then it’s debilitating as I can’t really walk fully upright comfortably or sit at a desk, but this is where WFH has been an absolute blessing in disguise as I can still work happily without taking sick leave like in the past.
In between I have extreme bouts of fatigue and the as I’m getting older I have more and more uncontrolled spasms/twitches which will often see me throw my own coffee on myself or stuff like that which is where a family history of Parkinson’s and MS has me concerned, but I’m ignoring it until it becomes a daily problem.
I’m not saying any of this for sympathy, I’ve lived with it for a long time and built a bridge and gotten over it, but rather for illustration that chronic pain is a very real thing and I wouldn’t jump too quickly to assuming it’s all in her head because like I said I went undiagnosed while actively looking until I was 30.
That being said it can of course be all in her head and it would be a good idea to at the very least clear that up by having her seeing someone.
What medication is she on at the moment? How often? Does she exercise much?
What are the symptoms outside of the endo parts of the month?
Exercise was and still is the hardest thing on the planet for me to motivate myself to do, but it does help a hell of a lot once you fight through the initial pain of getting going.