WWDACT is planning to contribute to the
Inquiry into endometriosis and other chronic pelvic pain conditions.
You can read the terms of reference for the inquiry
here.
We want to hear from members about their experiences.
This survey is for
people with disabilities who experience
chronic pelvic pain conditions (including endometriosis, adenomyosis, polycystic ovarian syndrome (PCOS), or other chronic pain condition and who
live or access care in the ACT. If you have any experience of pelvic pain, we encourage you to respond, including if you are undiagnosed.
We have suggested some prompts for you to respond to. You can give as much or as little detail as you like.
All questions are optional. You don’t need to respond to all the prompts or all the questions. If you prefer, you can skip to the last question which is a free text box, and tell us about your experience in any format that works for you.
You can also share any thoughts and experiences directly with our policy officer Pippa via email policy@wwdact.org.au.
Please note that your responses to the survey are saved and submitted to us after each page of the survey. You can come back and edit them at any time.
This survey is anonymous. We will be collecting all the stories we hear through this survey to make general comments in a submission. We won't use any specific details you have told us unless you give us permission at the end of the survey.
Please email Pippa policy@wwdact.org.au if you have any questions or if we can make this survey more accessible for you.
The survey will close on Monday 23rd March.
