I have to fellow endosisters in South Africa and one responded with
"For endometriosis I have been told Prof van der Merwe at Vincent Palotti Hospital."
Still waiting for the other to respond and I will also check somewhere else. I'll be back soon
im sorry its south africa thank you very much for ur responce
I just want to confirm where SA is. South Africa? Sacramento? Sorry I am from canada not sure what that abbreviation is . Let me know and I can find you one :)
hi ticked do u know of any endo specialist in SA bcz im having all the symptoms for endo bt my gyn stil insist that he doesnt c anything and i'v jst had miscariage and i think its bcz of my endo.....i realy want another child plz help
Well you are in luck if you can go to either of these doctors. They are the best of the best and you have an option to go to either which is like winning the Endo surgery lottery to be honest. There are only a handful of Endo specialists around the world and you are situated near the best of the best.
Dr. Andrew Cook
Vital Health,
14830 Los Gatos Blvd,
Ste 300,
Los Gatos, CA 95032
T. (408) 358-2511
Specialisation: GYN only
Bowl/urinary tract surgery: Does some bowel/urinary tract work.
*Dr. Cook's practice offers a functional approach to treating endometriosis.
He also has a book called "Stop Endometriosis and Pelvic pain" which is an amazing amazing book.
Dr. Camran Nezhat
Center For Special Minimally Invasive & Robotic Surgery,
900 Welch Rd
Ste 403
Palo Alto, CA 94304
T. (650) 327-8778
Specialisation: GYN only
Bowl/urinary tract surgery: Does some bowel/urinary tract work.
I have had terrible cramps since I was about 14 (I got my period at 11) they have gotten more debilitating as the years have gone by. I'd say the pain before in after is a kind of new or maybe just much more noticeable. I live in Novato, California!
I don't think you are being over dramatic at all.
It took 14 yrs to diagnose me with stage IV Endo and it was only due to the fact I grew an endometrioma after the birth of my daughter.
I also had rectal pain and I had rectovaginal endometriosis.
You will not see Endo on a scan unless you have an endometrioma. Also if the bcp isn't working it's possible you have moderate to severe disease as usually hrts will not work at that stage.
You really need to find yourself an Endo specialist. Let me know where you live and I can find you one in your area .
If you are interested you can read my journals there is on there called endometriosis and migraines which might help.
Did this pain just start or have you always had it? When did it start?