This is a personal blog for Chrissy and her friends to share their HS story and continued HS journey.
We are awareness activists and HS patients who volunteer our time to spread Hidradenitis Suppurativa awareness and education online and in our local community. Our goal is to educate the public and medical professionals so that more patients can be accurately diagnosed and receive proper medical treatment. Most HS patient’s are not properly diagnosed for many years and suffer needlessly. We’d like to see this change.
We also advocate for more HS research to be conducted to find better treatments and a possible cure.
Lastly, we are here to help others with HS. Feel free to contact us for help.
We are not an organization or business, we’re just long time patients with HS who want change.