Searching for Endometriosis Support Uk information? Find all needed info by using official links provided below.
https://www.endometriosis-uk.org/
About Endometriosis UK. Endometriosis devastates the lives of women and their families. Endometriosis UK helps them take back control by providing vital support services, reliable information and a community for those affected by endometriosis.
https://www.endometriosis-uk.org/get-support
Our Support Network is here to offer those affected by endometriosis the support and information they need to understand the condition and take control. Being diagnosed with endometriosis can be a daunting experience, but you don’t have to face it alone. You can call our helpline, join a local support group or join our online community.
https://www.myendometriosisteam.com/
MyEndometriosisTeam is the social network for women living with endometriosis. Get the emotional support you need from others like you, and gain practical advice and insights on managing treatment or therapies for endometriosis.
https://endometriosis.org/
Endometriosis.org is the global platform which links all stake holders in endometriosis - one of the most common causes of pelvic pain and infertility in women. We deliver up to date, evidence based, information and news about endometriosis, to provide the knowledge that empower women to make informed decisions about their treatment options.
http://endometriosis.org/support/
Support There are many sources of support for women with endometriosis, including: National support organisations. Contact details of all known endometriosis support groups around the world, which provide support, help, information, and advice for women with endometriosis and their families.. Online forums. Online support and chat forums may help you learn more about endometriosis and share ...
http://www.livingwithendometriosis.org/online-support-for-endometriosis/
Before I was diagnosed with endometriosis, I did not seek out much information online. I read the Endometriosis Association’s books, and other books I found on endo, but without the ‘official’ surgical diagnosis, I felt like I had no business popping up in forums and support groups to discuss my pain.
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