Newly Diagnosed Endometrioma - where does... - Endometriosis UK

Endometriosis UK

70,655 members52,130 posts

Newly Diagnosed Endometrioma - where does it go from here?

MsDiagnosed profile image
3 Replies

Hi All, new to all this so bear with me :0)

Admitted on Saturday to local hospital with severe abdominal pain - after an ultrasound, X-ray and bloods I've been told I have an endometrioma on my right ovary. Bit of a shock really, led to believe for the last 20 + years I had IBS - but the more I read about the symptoms of endometriosis the more I think I never had IBS in the first place. Also becoming increasingly painful to have my smears done over the years - could this be related?

Have to go back as an out-patient for further scan and gynae review soon but would be grateful for your experiences of what I can expect next?

Written by
MsDiagnosed profile image
MsDiagnosed
To view profiles and participate in discussions please or .
3 Replies

I have had endometriomas on both ovaries and had them excised via a laparoscopy at a BSGE centre where they specialise in treating endometriosis which has helped me. You could ask your GP to be referred to a BSGE endometriosis centre if you aren't already going to one. I think it's best to have a diagnostic laparoscopy where the excision treatment for the endometriosis can be done at the same time. By the way, I have always had painful smears and IBS symptoms so I do think they are related to the endometriosis. I have found a gluten free diet has helped as well. I hope it works out for you and you get the treatment that you need.

MsDiagnosed profile image
MsDiagnosed in reply to

Thanks for the reply. Thankfully my local hospital is a BSGE centre so I guess I'm lucky in that regard. Will look into gluten free diet - willing to try anything that helps.

in reply to MsDiagnosed

I'm glad your local hospital is a BSGE centre. Just to say they also will probably suggest you go on hormone treatment. I would research the different types of hormone treatment for endometriosis before your consultation. It's best to make an informed decision when they go through all your different options. I am about to go on progesterone only pills so at the moment I am unable to say if it's any help. From what I have seen different treatments work for some people but not others, it's about finding out the best treatment to suit you. I hope this helps.

You may also like...

Where do I go from here?

pointing towards endometriosis and so many doctors saying that it probably is endo, I have been...

I am so upset and don’t know where to go from here…

bladder pain? Anyway, she explained that I should go on this pill for to “dissolve endometriosis”,...

Where do I go from here!

though if my pain and symptoms aren't endo related, that my pain would be different to the pains I...

Hi is anybody on here from the coventry area? Newly diagnosed and worried.

1 for 7 years but had it taken out in hospital after I was taken in with severe abdominal pain....

Endometrioma: The process of being diagnosed!

everything? Are ultrasound really reliable and I definitely have Endometrioma/endometriosis? What...