Hi everyone,
I have recently been told that my consultants (who have suspected endometriosis for quite a long time) want to perform a laparoscopy to investigate and potentially treat what they find. This has come as a slight surprise after years of unresolved symptoms.
Few questions for all you lovelies:
(1) Do any of you have an autoimmune condition too? (I have systemic lupus and am intrigued about whether there is a link)
(2) How long should I take off work? I was provisionally told 1 week if they find nothing, and 2 weeks if they do have to treat. Literature so far seems to say this is a bit quick.
(3) Any tips for recovery and what to have stocked at home or take to the hospital with me?
Thank you in advance to anyone who responds.
Heather xx