I had a laparoscopy in May and was told I've got endometriosis... This explains my ongoing battle with pelvic, back and leg pain. It was performed by an Endometriosis specialist (gyne). I am still having pain and my GP has told me its around the area my bowel/intestine is... I've tried anti-spasmodic meds which don't do much to help!
What I want to know is... Will the specialist have looked at ALL organs or only the gyne ones when she did my lap?
I'm fed up of not knowing what's going on in my body and why I'm in pain every day
Written by
Jodiex
To view profiles and participate in discussions please or .
If you've had a diagnosis what is the plan of action to make you better ! Why aren't you having it removed ???? Once that is achieved you then need to manage your periods with possibly hormone therapy etc
I have the mirena fitted already and I have tramadol for the pain. They offered me zoladex but I was advised not to have it if I want a family in the next 2 years (I'm 25 with no children).
With my diagnostic laparoscopy they looked at everything they could reach without making a large incision. So bowel, liver, kidneys etc. Most like they did the same for you, post op I tried a series of contraceptive pills (they said this would prevent it from returning so aggressively) this was unsuccessful as I had a 4 and half month bleed and the pain was worse than it was before.
I now take nothing, and my cycle is regular. Diet is crucial ! I suffer with endo on the bowel so suffer in that area too 😳 I suggest at least 2 litres of water a day to ensure hydrated muscles and minimise fatigue in your legs. I mainly use the anti candida diet, it's not a weight loss thing it's purely to minimise any fungus/yeast build up that effects hormonal conditions such as endo !
I really hope this helps .. Sorry it's a long reply !
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.
Anyone fed up with the pain?
Fed up!
Pain specialist says it's not endo
Fed up and tired
Is it possible to have endometriosis that can't be found/seen?
