Aa
doctors said i hve endometriosis r endomentrium.
I hve been in pain for very longtime now. Im 28 years old with no kids i need help. Please. K im in pain lot of pain pelvic pain lower back. Pain. Nausea hurt when i intercourse with my bf . Etc. I hve been to many obgyn they can't seme to tell me one thing r give me one awser. Why? I dnt . Im actually in pain can't do anything im getting to the point were im like enough is enough. Nd awsers and want kids in the future it really hurts .im bloated blood in urine hurts when im abt to use bathroom. Anything i hve been bleeding fora month . Help me plz . Please. Anything to get ths pain away.
Okay here they are. Dr Orbuch I met a couple weeks ago at the Endometriosis symposium in Toronto, she is great and also treats co-morbid diseases such as Pelvic floor dysfunction and IC.
Dr. Iris Orbuch
202 Spring Street, 2nd Floor,
NY, NY 10012
T: (212) 343-3040
F: (212) 343-3036
Specialisation: GYN only
Bowl/urinary tract surgery: Unknown
Dr. C.Y. Liu
NYC Women’s Robotic and Minimally Invasive Gynecology,
872 5th Ave,
NY. NY. 10065
T: (212) 988-1444
F: (212) 988-1755
E: ***@****
W: http://www.cyliu.com/
Specialisation: GYN only
Bowl/urinary tract surgery: Does some of own urinary tract and bowel work
.
Dr. Iris Orbuch
202 Spring Street, 2nd Floor,
NY, NY 10012
T: (212) 343-3040
F: (212) 343-3036
Specialisation: GYN only
Bowl/urinary tract surgery: Unknown
Dr. C.Y. Liu
NYC Women’s Robotic and Minimally Invasive Gynecology,
872 5th Ave,
NY. NY. 10065
T: (212) 988-1444
F: (212) 988-1755
E: ***@****
W: http://www.cyliu.com/
Specialisation: GYN only
Bowl/urinary tract surgery: Does some of own urinary tract and bowel work
.
There is a great one in New York he is one of the best. I am not on my computer but I will come back tomorrow to give you all the details. I know women have had surgery with him I can ask about the insurance too. What is te name of your insurance? Maybe they will know :)
I wll hope tht they tke my insurance. I really nd help my fibroids are nt tht big they sd bt i bleed too much even am on bc shot. And stll in pain. I live in the USA .
Thanks for coming to the Endometriosis Forum. I can help you the best I can.
The reason that they don't in most part is because they are not listening to you and are in the dark ages when it comes to Endometriosis.
If you tell me where you live I can tell you where to go to as there are only a handful of Endometriosis surgeons around the world for 200 million women so most people end up with reg OBGYN with them pushing them off.
I have many journals in my profile if you are interested in reading them.
It took 14 yrs to diagnose Endo for me because I could not exactly tell them where the pain was as I ended up getting diagnosed with IBS at 15 and Fibro at 17yrs old. I wasn't diagnosed until I was 27 which is the average age unfortunately. Unless there is an endometrioma (blood filled cyst) and they are not listening to you then they wouldn't put two and two together.
Its a really frustrating disease hence why I do this because I suffered in silence for way too long and it destroyed me mentally.
I had painful bowel movements and sex, and periods were unreal and heavy. Not regular either. I had migraines all the time.
Let me know and I can help you out and guide you in the right direction
The reason that they don't in most part is because they are not listening to you and are in the dark ages when it comes to Endometriosis.
If you tell me where you live I can tell you where to go to as there are only a handful of Endometriosis surgeons around the world for 200 million women so most people end up with reg OBGYN with them pushing them off.
I have many journals in my profile if you are interested in reading them.
It took 14 yrs to diagnose Endo for me because I could not exactly tell them where the pain was as I ended up getting diagnosed with IBS at 15 and Fibro at 17yrs old. I wasn't diagnosed until I was 27 which is the average age unfortunately. Unless there is an endometrioma (blood filled cyst) and they are not listening to you then they wouldn't put two and two together.
Its a really frustrating disease hence why I do this because I suffered in silence for way too long and it destroyed me mentally.
I had painful bowel movements and sex, and periods were unreal and heavy. Not regular either. I had migraines all the time.
Let me know and I can help you out and guide you in the right direction
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