I've been officially diagnosed with Asherman's Syndrome today. I went into hospital for a second endometrial ablation only to be told when I came round that it had been impossible to perform because of the amount of adhesions blocking the way.
I've had no noticeable symptoms since my first ablation, which was done in May last year. It had improved things a little but not to a point I was happy with (hence going in for another) but I've had less pain than previously and there's clearly no issue with it obstructing my periods themselves.
The majority of information I'm finding online is geared towards treating it with a view to having children but I'm more interested in how it's dealt with when fertility isn't a concern.
I'll be seeing my consultant in a few weeks to discuss where we go from here but I just wondered if any MNetters have had experience of Asherman's, particularly either post-children or if you didn't want them.
I'm still a tad squiffy from the GA and morphine so be kind if I've missed any glaringly obvious sources of info 