I understand your concerns, as I have also had some similar situations. It is your RIGHT to get healthcare that you are comfortable with. If you feel that your doctor doesn't know enough about your condition (which isounds to be the case) INSIST on another doctor who knows what they are talking about. Remember also that just because a doctor is female does not mean she knows more about endometriosis because she has a uterus! If any doctor dismisses anything you say, it means they aren't doing their job properly and it is your right to get another doctor. If your insurance is problematic, then ask to speak to a manager and explain the situation and tell them you need another doctor. I'm afraid I had to go through MANY doctors before I found one that actually knew what they were talking about but once I found him, it was awesome (then we moved, coz we are military so I had to start the process all over again :-( so I KNOW how trying this is for you!)
The best advice I can give you is to keep plugging away at your doctor situation until someone LISTENS to you. I had to put up with some medical professionals treating me like a drug addict because I have to take pain medication, some of them telling me absolute bullcrap about endometriosis and about my OWN body, because they THOUGHT they knew what they were talking about but they really didn't!
Don't hesitate to ask me any more questions and I will try my best to answer them if I can, from my own experience. I have dealt with a lot of stuff with this condition and am very willing to share my experiences if I think it will help anyone else!
Good luck! Virginia
I have had endometriosis for most of my life (23 years). I have found that the treatments from my natropathic doctors seem to work best for me. I have had 3 laporocopies over the years, and took various forms of birth control until the year 2003. I refused to go for a hysterectomy because I wasn't done with my female organs yet. I hope this helps many of you.
I am now 11 weeks pregnant, and having intermitant issues with my left ovary that feels like my endometriosis. The funny thing is that it occuring every 2 weeks. The MD that is part of my OB treatment (due to insurance issues) said that the pain must be because I'm constipated. That is not consistent with how my body has been functioning. My ND is using bowen and acupuncture and it seems to be helping. Maybe this will help some of you too.
Best of luck with your syptoms, and remember, you are your own best advocate.
Hello Ladies,
I am not pregnant, but am trying. I have a sister and cousin with endo-sister, zero baby and cousin, infertility drugs and twins! Anyway, I have been experiencing, for couple years now, dizzy spells, light headedness, and nausea off and on about a week prior to my cycle-good days and bad days. I too have an upcoming appt as to "convence" my doctor that I need to go ahead with a lap to see if I have it. I'll be 36 soon and don't have time to wait for 6 months-1 year to try. So, my question is did y'll have these symptoms? I know pelvic pain seems to the the primary, but I don't really have "pain"....it's more like, friction and aching...enough to finally get up out of bed and take three motrin around the clock.....I also have heavy bleeding, lower back pain, really bad cramp when I have a bowel movement, oh lets see, and my bowels slow down.
Did y'll have any of this?
Thanks for the input!!
Best wishes.