Hello, my name is MaKellee Kathryn Doty-Robinson, but to make it way easier, everyone just calls me Kellee. I have suffered from HS since I can remember, but was finally diagnosed in March of 2013, the day before my 13th birthday. My birthday present was a giant excision of HS out of the center of…
Hope for HS is pleased to share exciting news! A documentary team from PBS will be doing a spot on Hidradenitis Suppurativa for the 2019 season of Medical Stories, to highlight the true impacts of living with HS and raise awareness among the general public. This is slated to air in the summer of 2019.…
This year HS School will take place on Saturday, October 13th and Sunday October 14th, from 1:30pm to 3:30pm, with an afternoon meet-and-greet on Friday, October 12th. The SHSA takes place at Women’s College Hospital Conference Centre, Toronto, Canada. Join us by registering on the SHSA website. Prices go up after August 21st.
Saturday, August 11th. Ann Arbor, MI. Super Hero 5k for Hidradenitis Suppurativa Awareness. Register to Walk or Run: Click here to register as a walker or runner. Use the code “HOPE4HS18” for $5 off of your registration fee! HS Hero T-shirt: To purchase an HS Hero shirt on Amazon, click here – please order this…
Join us on Saturday, June 9th for a candlelight vigil to raise Hidradenitis Suppurativa awareness. MEMORIAL PARKROYAL OAK, MICHIGAN8PM People affected by Hidradenitis Suppurativa (HS) around the world will be lighting candles on Saturday, June 9th, during #Hidradenitis Suppurativa Awareness Week, to #BrightHStoLight Hope for HS, a national 501(c)(3) nonprofit patient organization based in Detroit, will…
