Groin muscle discomfort and endometriosis?
Answers:
Yes, you should still see the gynecologist to rule out endometriosis (which this sounds close to what it is) as a possibility.
Endometriosis can cause agony to go and refer to the groin nouns. When this happens the spasm can irritate the nerves in that nouns.
Also, some women can have as their totally first symptom related to endo that of thinking it's a pulled muscle when it's not. This is exactly what happened to me during the Spring of 1997 even though I have already had some problems near the exam being raw to the point of jumping past its sell-by date the table the way you did when the PT touched the nouns. What made my situation so strange when it came to the symptoms be that my mom and I were living beside friends for a while when this happened. We be in our room watching tv. I be leaned up against the wall and when I started to try to move I felt this really strange discomfort. And because of that pain I thought that I have pulled a muscle. So I tried to lie on my bed thinking that would reorganize things and it did not. It was worse.
Then a bit after that that afternoon when I went to carry up from the bed I felt my uterus and ovaries spatter forward. When I told a few drs about this symptom they laugh at me which basically expected that they thought I was crazy.
Well, the twinge that I had contained by part because of that and it staying adjectives the rest of the month (with the exception of the week before my time of year, and then own my period come and the spasm issues start all over again). It stayed this channel for 9 months. What was even worse is that for most of that 9 months the throbbing was so bleak that I was bedridden. I also discovered that not solitary could I not lie on my side still (had a problem next to this for years before I know I had endo) but I discovered that whenever I tried to cut into my toes on my left foot my uterus hurt. So I pretty much could not even gash my toes.
It took me several drs to find one that could help me (and did so next to the help of a friend who is a surgical technologist). Then when she and another dr get involved in the case and took me to surgery (yep, laparoscopy an outpatient procedure is the just definitive way to diagnose endometriosis) they found out I have endometriosis.
But yes, please see the gynecologist any way. Also, my problem beside the pain a well brought-up part of it settled around my disappeared side too, and causing misery of ovulation (even when I wasn't supposed to yet) occurring at other times during the month and many times vastly sharp when it came to intensity of aching.
To learn more roughly speaking endometriosis please check out: http://www.endocenter.org
I be diagnosed with endometriosis 10 years ago when i be 17. It started with agony and irregular bleeding for me. My gyno suspected it right away and monitired me for 6 months. Then he said the only agency to diagnose was visually beside an operation. I had that done and own had endo ever since. The discomfort you described is right for endo, along with bloody intercourse and irregular periods. It also affects my bowel, because i enjoy deposits of endo all through me. Best entry you can do is go to your gyno and make clear to them you are concerned it could be endo and demand that further invetigations be done. If you do own it, it can be lasered off and at hand are treatments available. Just because they dont work for everyone doesnt mean they wont work for you.
Take charge of your own robustness a little more so you can bring to the bottom of it!
Good luck
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