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Myofascial pelvic pain syndrome in females. Unrelenting pain in pelvic
Chronic Pain | Last Active: Jun 9 9:38pm | Replies (14)Comment receiving replies
@mackvogt13 thank you so much for replying. I also have IBS and some neuropathy issues as well. I understand completely about physical therapy as I did it for four years before I fell! I will get some info on Naltrexone. Thanks also for explaining about the wands although it sounds like I am not ready pain wise to even try it yet. It’s so good to talk to someone who understands about the pain from high tight muscles as most people have no idea what this condition can feel like and how to deal with it. Be well.
Replies to "@mackvogt13 thank you so much for replying. I also have IBS and some neuropathy issues as..."
@mshepard1 yes ofc! i totally know how you feel! it can be lonely sometimes.
@mshepard1 Nlatrexone changed my life because idk if i said in the previous oost but I had to drop out of ursing school, got excision surgery for endo, was on 10mg of birth control (normal dose 0.35mg), had and IUD and was in chemical menopause (i am 19) and nothing worked for my debilitating bed ridden cramps until I got on that and it took my cramps away but then all my other pain came through.
in pelvic therapy my therapis does ineranl massages and the pelvic wand is jsut so you can do that at home. there is multiple different kinds, like the one i have is bendable so easy to move around inside, there is one to put inthe freezer which apparently monopausal women like and and there is a vibrating one
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@mshepard1 a pelvic PT is your first step. Get an Rx from primary doctor - easiest. Also try a rheumatologist visit. They can order low dose naltrexone.
17 years of adhesions and 3 surgeries have taught me.
Also try ice, alternate heat. But do go see the specialists. I found it takes 2 years for injuries to stabilize. 🌸