Hello ladies,
I am 2 days post lap after having a patch of endo removed. I have found the whole thing very emotional and exhausting both mentally and physically. I’ve found the gas ( used to blow your stomach up during the op) to be more painful and un-comfortable then the 3 incisions I’ve come away with. I can barely breath , pain through my back , shoulders and chest 😣. I’ve been drinking peppermint tea but it doesn’t seem to be shifting yet . I waited 13 months for the op after being continually told my symptoms where ‘just’ my IBS. So to have found out it was endo too was a mixture of both relief and upset. Like so many other posts I have read I was disappointed with the after care; I wasn’t told until the next day how my surgery had gone(so I had no idea if they had found anything or not) I was told at my ‘discharge brief’ there were patches of endo that had to be removed the gynaecologist ( male ) put it to me very bluntly and you could see the female junior next to him offering a smile and squirming(that was not sexiest lol but the genuine situation) . The things he was saying and the way he put it out I just feel was so direct and heartless he said off the cuff “you wouldn’t be considered for IVF as you already have a child”. That was the only ‘fertility’ remark I was given and said I would need to go back on the contraceptive pill to manage the pain. I wouldn’t even say it was all matter of fact it was just very direct and quite odd. There was no other aftercare advice given so I’m presuming I make an appt with my GP? I really don’t mean to sound dramatic but I think the aftercare is appalling for a condition that is potentially life long?
Just feeling upset and overwhelmed.