I have been diagnosed with endo for 13 years and have had my fourth laporoscopy in August this year.
The Gyno now believes I may have Adenomyosis and possibly Endo in the bowel.
If my symptoms persist til Feb 2012 I will have to go and see a colorectal (??) surgeon.
I'm looking for advise, help, support from anyone who has had endo in the bowel?
Have you had to have bowel surgery?
Did it relieve the pain?
How long does it take to recover?
What type of pain did you have?
I'm just hoping to get some support and answers as I have been dealing with the return of bad endo pain since April this year and it is not showing signs of getting better.
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