Introduction:
Last updated on:
Monday 23rd January 2012 at 7:49pm
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Welcome to Endometriosis in the UK - You're NOT Alone!
This site was originally created back in 1999 to help give free and unbiased support to women like myself who suffer from this horrible disease, there just seemed to be hardly anything in the UK for us then. Whilst there is so much more support available now, we feel that we can still make a difference by keeping this site going, we are not or affiliated with, any company or charity and my husband and I run the site in our own time with the help of voluntary donations from the now well established community that use this website.
I wrote my story, posted it up to the site and added a form to allow others to share their experiece of living with endometriosis. Slowly but surely, more stories have been sent in and now in total there are 1,454 EndoStories published on this site many of which are updated from time to time. Maybe you would like to share your story, a great many women find it is good to get it off their chest and it provides a valuable resource for proving that you really are not alone with Endo.
Over the past 13 years the site has grown massively and changed dramatically to accomodate all the information, we have added a message board - The EndoLounge - and here you will find our EndoFamily, which is getting larger and friendlier by the day, a great place to get support from and also your chance to provide support to women who know exactly what you are going through and also to have a natter in realtime as there is a chatroom available for registered members. It is a good idea to register for membership as you will get access to all areas and features on the board which include a community based calendar and a blog for each registered member.
There is a Partners support page. Living with someone with Endo is not easy, this is a chance for the men in our lives to put their point of view accross and maybe chat to each other, they could probably do with some support aswell.
If this is your first experience with Endo, check out the EndoGuide for a few pointers and there is a Links page to help you on your way to other related sites. Finally, the Goodies section (no not the comedy from the seventies) is a place to share your poems, jokes and funnies, check this section out for some light hearted humour and deep prose.
Any feedback about the site is always welcome. With your input, this site can only get bigger and better, and hopefully bring greater awareness of this crippling disease to more and more people. <Click Here> to send us your comments.
Getting Around Our Site:
Our site is best viewed at a resolution of 800 x 600 pixels or even a higher resolution.
To go to another page or section, you will need to use the Menu. This can be found at the top of every page.
All the links on this site are coloured GREEN and change to purple when hovered over. Clicking on these will take you where you want to go. If you find a broken link, please help by contacting us and letting us know.
Disclaimer: All of the information on this website has been gathered since my diagnosis with Endometriosis and is presented for information purposes only. The material is in no way intended to replace professional medical care or attention by a qualified practitioner. The information on this website cannot and should not be used as a basis for diagnosis or choice of treatment. I do not claim to be an expert, medical or otherwise. I have tried to keep the information simple and it is basically a fellow sufferer's view of what Endometriosis is all about. I hope you find it useful. To view our Privacy Policy, Click Here
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