This guide was made from Michelle and Leilani’s own painful personal experiences and they would love for this document to be a tool and resource for others who are living in silence with chronic pelvic pain. Their hope is to empower and help shorten other’s journey so that they can get the answers and care needed to begin healing sooner, rather than later.

What does your contribution to the creators of the pelvic pain resource guide do? 
1. Your contribution will help expand future goals and initiatives that can deliver sustainable pelvic health awareness, ensuring everyone can receive the correct education and integrated care they need no matter their circumstance.

2. A portion of each contribution will be given to organizations that focus on pelvic pain conditions such as the Pudendal Neuralgia Association, The National Vulvodynia Association, and a Canadian endometriosis charity: Endometriosis Events

3. Your contribution will allow us to connect with more people living with pelvic pain using in-person and online support groups, local events, and social media.