#mpps

I also do wanna ask, or google but i'm curious about iuds and if they cause mpps too? I mean I have physical trauma and sexual trauma. I did smack the back of my head against a slightly submerged "floating" dock when I was a kid. All of that can be counted as trauma and can create pain issues. (my neck often has flareups.) But I'm curious about iuds because the way they insert them, it's not uniformly done , cutting strings seems to be different from person to person who inserts, even advice on strings seems to be different. (I recall first time it being inserted, after it was, the person putting it in tugged on it asking 'can you feel that?' ... the amount of pain with that was so unpleasant. I was also told by that one you should tug on the string monthly to ensure it doesn't go to close to the walls... But a different person who put my second one in, left the strings way longer and said 'don't touch them. iuds don't go for uterus walls. thats a myth.' first lady also said 'oh no' 'shoot' 'give me a second' when she inserted, meanwhile second person who put my second one in was more confident, and seemed less panicky... both hurt but the second one as less painful in a way.) and also the way they remove the IUD is with a strong (SUDDEN) tug in both cases. So I'm wondering if iud insertion techniques and removal could also lead to development of MPPS? Like another cause to pelvic floor pain. I wanna ask the physio dr about it.

So I think one of the reasons why i got that advice of "Go to a different gyno, call around, find someone who will give you surgery, and don't mention you have MPPS" (... we are going to ignore you can't self refer or call around in canada. & that MPPS was found out by pelvic exam.) - But I think this also comes down to people not knowing what MPPS is (Myofascial pelvic pain syndrome) Even saying "Myofascial pelvic pain syndrome" or "Myofascial pain syndrome" people are like: 'whats that?' 'yeah but what is it?' "why does that matter for fibroid surgery?" "Shouldn't whatever that is, go away with surgery?" "Can't they remove that too?" "I've never heard about that in my lifetime and I'm (age here). are you sure? is this a thing I need to now be worried about having?" I think chronic pain illnesses are hard, and when its one people don't hear about it's uh... interesting? Because it seems like if its not discussed people have there own ideas to what it is. I've been told (In support groups) to NOT mention it to drs, or 'just ask for it to be removed too' or "Can't you just go find someone else and like make sure it doesn't happen?" or "A dr can't deny you surgery and say you need physio first. NEXT DR. He's not qualified!" (He didn't "deny" we are booked for oct to re-see him. after pelvic floor therapy has started, because he said if I get surgery prior it would be unfavorable patient outcome with recovery.... because lower abdomen surgery would be cutting thru muscles and causing more tension and trauma... My lower abdomen is already under a lot of tension. Its unable to relax. hints the jolts of sudden pain that feels like lighting.) I really do think tho its apart people don't know what MPPS is, and the other part is this thought you can dr shop and drs can't just tell you "no", and maybe there's a thought too that surgery is the cure-all. But like lets see, I've had post Postmastectomy pain syndrome (PMPS) after a lumpectomy was done to remove a tumor growth in my breast close to my nipple, which caused a really painful flare up and cramping and burning /stinging sensation with random stabbing after surgery. So I honestly prefer the slow and steady route. But I don't think this means my dr is unqualified cause he won't give me surgery right away.