conandrob240 said:
There isn't really much treatment for endometriosis other than surgery. The BC pills are one option to stop/ reduce tissue growth and reduce symptoms. Severe cases need surgery. So, what are you hoping they will / would have done?
lisat said:
Sorry that happened to you, Chicagonative. I'm not sure what the symptoms of endometriosis are. I recall pain. Is heavy bleeding also?
You might want to call your internist and enlist his/her help in getting an appointment with another gynecologist quickly.
What testing is usually done to determine whether a person has endometriosis? Can any of the testing be ordered by your internist?
You might take the low dose estrogen just to see what impact it has. That way you'll have more information for the next doctor you see about this. By the way if heavy bleeding is one of your symptoms, then it may be caused by perimenopause. The supplement Oona worked for me, and is available at Whole Foods.
I liked the Avalon practice but am not sure if they are right for this.
I didn't love Klatchko because I found her a bit dismissive of my hot flashes, but over zealous about my heavy bleeding. She even said the 'C' word which freaked me out. I decided to never return, but I think she would do more testing than less and might be good for you. I personally decided to find a female internist who would also do the gynecology stuff. I figured that even if she sent me to a specialist, I could rely on the internist to take the lead and be a calming influence. So I went to Dr. Karen Young, and found her to be perfect for me.
I hope you are able to feel calmer about this. Do you have an internist whom you like?
carolanne said:
Do you symptoms wax and wane with your cycle? Or are theymore constant? I agree its worth exploring endometriosis because of your family history, but if have had many abdominal surgeries and now are having abdominal pain and cramping, its also possible that its scar tissue and adhesions from past surgeries. I hope you can figure this out and find relief.
calliope said:
Find a new doctor ASAP, @Chicagonative. A few years ago I was explaining my complicated medical history to a physician, who told me "That is historically interesting, but has no bearing on what you are dealing with now" HUH??? That sort of dismissive, LAZY@$$ attitude has no place in any medical community, I don't care how much alphabet soup appears after his/her name,and how expensive the medical education is, it is all for naught if there is no respect for the patient.
I wish I had a recommendation for you--- I truly do. I hate most of my doctors.
conandrob240 said:
But there really aren't conclusive tests for endiometriosis. The only true test is surgery and finding it when they go in.X-rays and standard tests like sonograms are of absolutely no use in finding endiometriosis. It can only really be seen invasively through surgery. What did you suggest she do?
If there is endiometriosis and the symptoms of heavy bleeding and cramping, the BC pills may give some relief without having to put you through another surgery. So, it sounds like her approach may be the right one.
Now, her not listening to your complicated history and being dismissive aren't acceptable. And certainly there are doctors out there who may be more compassionate. Just do your homework, ask the right questions and know what your options are.
giner said:
Aw Chicagonative, I'm sorry that happened to you. I do like my ob gyn nurse practioner at Summit Medical Mary Alice Saporito. She may not be quite right considering your diagnosis but I've found her to be great at being normal in this weird world of perimeni-whatever. She also has a terrific haircut that I admire every time I see her. Hope all works out for you.
So glad I stumbled onto this long standing conversation. Thanks for sharing all this from the bottom of my moody, recently irregular mid-40s heart that now worries about an unexpected pregnancy like a college sophomore. Happy to report that my hair stopped falling out in unusually large amounts in the shower a few months ago. Not sure why it started and not sure why it stopped.
Looks like there is more fun waiting around the next bend.
conandrob240 said:
Yes, I understand, I had similar ( maybe not as severe). The BC pills helped a little. Try them. That last thing I want is surgery especially when they can't even be sure endiometriosis is the cause. Terrible that there is so little that can be done for a very common problem.
leighan said:
Chicagonative, I believe you told me that you've had uc for years when I was asking for advice about my daughter who was recently diagnosed with it. She was sent to a new gyno last month after a colonoscopy didn't explain the scope of her pain. She does have uc, but her pain was also in areas of her abdomen where there wasn't ulceration seen. Her new gyno suspects she has endometriosis as well and wants to start her on hormonal bc to see if it helps. He says that the common thinking is that if the symptoms improve while on hormonal bc, then it is endometriosis. It's that....or exploratory laparoscopic surgery.
In doing some research, my daughter came across a statistic that said that 80% of women with uc also have endometriosis.
Best of luck finding a doctor who will listen!!
conandrob240 said:
Not bad. Not like the ones from 20 yrs ago. Give them a try. Good luck. I think maybe you ( we) were hoping for a cute that doesn't exist with endiometriosis. Surgery or the pills is really all we've got bet if men got it, it would have all kinds of treatments.
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Thanks, Joanne!