You don’t have to go it alone with Pilonidal Disease! There are hundreds of other patients going through the same thing you are right now, and thousands more who’ve already been there and stick around to help. It’s easy to feel like you’re the ONLY one with this awful cyst on your butt, but you aren’t.
Not only does this website provide comprehensive information on the disease, we also host the largest community of patients suffering from Pilonidal Disease. Join our forums, read the stories of other patients, add yourself to our map, then stop by the humor page for a little chuckle.
The gang is all here, ready to help and provide the support you need as you make your journey from discovery to fully healed. We have forums for both patients and doctors.
Stories are our shared legacy and bring us together. Add your story to help the next patient who needs support.
Having an abscess on your butt shouldn’t be funny, but it can be. Entertain yourself for a little bit with the wit from our forums.
Add Yourself to the Map!
Google users! If you want to add your own pushpin to the community map, click on the top right corner icon of the map. Another window will open with the map, you’ll need to be signed in to a Google account in order to “Edit” the map and add a “marker” . Once you have placed your marker, refresh this page to see your pin on this map.
Add yourself to the map!
Thanks for Sharing!
Personal Blogs and Websites
UK Patient https://pilonidal.wordpress.com/
French Patient (in French) http://pilonidal.fr
This page last updated: January 2, 2019