Hi everyone! Found the community last month when I was searching for Endo support groups. From where I am, there seems to be very little known about the disease, or maybe I just haven't found them yet. Nevertheless, I am grateful to have found you and I hope to learn more about this unwanted disorder, its effects and developments towards a cure. Keeping my fingers crossed. Thank you for having me.

2 Replies

  • There are a number of charities around the world and they generally share information. I'll list a few.

    Endo Association of America

    Endometriosis SHE Trust(UK)

    Endometriosis New Zealand

    There are also lots of other information pages available such as endometriosis.co.uk

  • Thank you for the reply, I prolly made a mistake there, what I really meant was there are not a lot of support groups such as these from where I am. But I do appreciate the links you have listed, I'll check them out in a bit. I have been scouring the web for info on endo since I was diagnosed, and endoUK has been very helpful. :) Thanks again.

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