In-active endometriosis : I had laproscopy... - Endometriosis UK

Endometriosis UK

73,026 members53,343 posts

In-active endometriosis

Lovehearts- profile image
3 Replies

I had laproscopy 4 days ago, they removed a chocolate cyst and found in-active endometriosis by my ovary. They didn't remove this inactive endometriosis, what is in-active endometriosis and will that reactivate?

I'm currently on the pill for symptoms but concerned when I come off the pill symptoms will start again.any advice would be helpful 😊

Written by
Lovehearts- profile image
Lovehearts-
To view profiles and participate in discussions please or .
Read more about...
3 Replies
TogetherWeAreStrong profile image
TogetherWeAreStrongModeratorEndometriosis UK

Oh, Lovehearts- welcome to the forum and for contibuting to the discussion. I honestly could not of answered you question, with such conviction prior to joining the forum.

I am very lucky to have had some extended pain free years, as a result of the medications that I was taking. I discussed with with my GP and we both agreed that I would stop taking them, but unfortunatley this is when the inactive endo started. I had not had a period in years, but after a few months of not takintg the meds, my pain started, so this was a case of inactive endo resurfacing.

Do what feels good for you meds or no meds and we are all here to support you x

Lovehearts- profile image
Lovehearts- in reply toTogetherWeAreStrong

Hello, Thank you for replying, ahh ok so did you have in active endo as a result of medication suppressing it? How did they know it was inactive? Is it because symptoms suppress?

Did you go back on the medication because your symptoms started again? Sorry for all the questions.

I was quite surprised they didn't remove the inactive endo when they did my op on Monday, just in case it activates again when I come off the pill which I'm planning to do

X

TogetherWeAreStrong profile image
TogetherWeAreStrongModeratorEndometriosis UK in reply toLovehearts-

Make sure to ask your consultant why this decision was made as I really don't know what would be behind that. It was inactive as I had not had a period for approx 8 years, the meds did work that way, my pain came back quite quickly as it does take sometime for you cycle to start regulating. So it was always there, in a kind of remission and when my hormone balance changed, it was back to where I had been before I started the treatment.

No apologies please, to be able to communicate with others about this subject is great for me. In a nutshell, I took a position working in India for 6 months (tramadol is available to buy, co codamol is not) and I then had to relocate back to the UK, so that's when I started from scratch, visit with GP to start the refferal process and my consultant was amazing!

Not what you're looking for?

You may also like...

Cerazette / Bowl Endometriosis

Hi All! I was diagnosed with endometriosis many moons ago and they put me on the pill levest....
Felicity91 profile image

Endometriosis and Emotional

Hi All, I was just wondering if anyone else feels really emotional when their endometriosis...
Vw28 profile image

Endometriosis & Me.....Please sign my Endometriosis petition!

http://epetitions.direct.gov.uk/petitions/39032 The petition is about changing the protocols so...
Sofiekirsten profile image

Stage 4 endometriosis - new diagnosis

Hello Ladies 💛 For context, I’m 28 years old, never had kids, been suffering with...
Everdeenxx profile image

Endometriosis diagnosed

Can u lovely ladies help me ?? I was referred for a scan at hospital then to the gynaecologist, the...
Joolzrich profile image

Moderation team

See all

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.