I'm not really expecting replies I just needed an outlet.
I have suffered for 25 years but only just been diagnosed.
I had my laparoscopy on Monday morning, where they had to make 4 incisions.
Although I've been telling GPs for decades that I'm sure the pain and symptoms were due to endo, it was still a lot to come to terms with in reality.
I am due to have a pelvic MRI to check how deeply it has effected my organs. I was offered the injection that brings on menopause but I declined it, rather waiting for the next operation that I've been told that I will need. This next operation is to involve a colo/rectal surgeon. I'm 99% sure that it had spread beyond the pelvis and in to the thoracic area, if not further.
The relite of it all is slowly hitting me and I'm finding it difficult to cope with.
Due to my Mum dying from ovarian cancer 2 years ago, the surgeons looked around for signs of cancer during the laparoscopy. Fortunately they didn't find any but just hearing them saying that they had been looking for it in the first place is frightening.
I have several other health concerns going on and have upcoming referrals for those issues. It's just all getting too much to cope with and I needed an outlet; somewhere where others are suffering the same issues.
Ordinarily I would have discussed this all with my Mum but since she passed I have been a lost. My husband is pretty understanding, but nothing like my Mum was.
Thank you to anyone who has read this. It has helped to write it out.