Endometriosis and ME/CFS

I wonder how many women with Endometriosis and ME are suffering at home and don't know that they have it. There are the obstacles of getting a doctor to listen and agree to do a referral and then being well enough to go and have some tests. It too a MRI scan to dx mine and that was after 20 years. My niece has been diagnosed with Endo now and her parents went the private route.

 

It's a shame. It's really not rocket science to think of endometriosis when you have excruciating period pain and other cyclic symptoms

I got my diagnosis after googling for 2minutes and yet it took 4 years to have it formally confirmed.

 

I had a similar experience with diagnosis of rosacea. Although it was a person without medical training who told me it was rosacea. I had seen my doctor about something else. The spots were there plain as day, but no comment or dx was forthcoming.

 

I suspect the overlap is much higher than reported figures.

Typically Endometriosis only gets diagnosed fairly late, it's predominantly still seen as a middle aged woman's disease, though that attitude is slowly changing I believe.

I had the severe deep infiltrating type. I was told I'd had it since birth and it got triggered at puberty so I'd lived with the symptoms 25 years before my actual diagnosis. At first my worsening ME fatigue & malaise was blamed on it because it can cause fatigue.

I only got diagnosed with ME/CFS 14 months after contracting viral meningitis from the excision surgery which triggered disease progression to severe aided by a get like phased return to work (not the luckiest chain of events ) . So a similar diagnostic time lag assuming I actually first got ME age 20 after EBV/Glandular fever, rather than from the VM.