Today I am joined by Jodie Hughes, the founder of Endometriosis South Coast and the Chair of Trustees.  She has also started her PhD at University of Roehampton London, that is researching the differences in care of Endometriosis patients. 

I connected with Jodie recently and her passion for what she does and her story is so inspiring. We talk about symptoms, types, treatment for Endometriosis and living with the condition. As you know I am passionate about hormonal health and have my own journey with loss of cycle and stress, I hope you enjoy todays conversation. 

Endometriosis South Coast is an inclusive charity set up to support people who are going through the diagnosis stages of Endometriosis and Adenomyosis or have been diagnosed with the conditions. There  for people that feel they may be suffering with the conditions without starting the process of diagnosis, friends, family and cheerleaders of the people that have to jump through hoops to get started on the diagnosis pathway.
· Spread awareness of a crippling condition.
· Research the condition.
· Provide online support and educate members with monthly support group meetings.
· Fundraise
1 in 10 people are diagnosed with Endometriosis.

This condition is an under funded and under treated area of health, and that needs to change.

You can make contact with Jodie;
https://www.endometriosissouthcoast.com/about
Facebook page:
https://www.facebook.com/endosouthcoast/?ref=bookmarks
Instagram: https://www.instagram.com/endosouthcoast/
App we mentioned:


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