Thank you to The Oakland Press for bringing awareness to Hidradenitis Suppurativa by highlighting the story of Sandra Guilbault, one of our key volunteers that struggled with her condition for years. Now that it is well-controlled, she donates a tremendous amount of her time to advocating for patients and advancing Hidradenitis Suppurativa causes with Hope for HS.
Join us on Saturday, June 9th for a candlelight vigil to raise Hidradenitis Suppurativa awareness.
ROYAL OAK, MICHIGAN
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 host a LIVE candlelight vigil, commencing at 8 p.m. in Memorial Park in Royal Oak, MI. Please join us in lighting a candle in the darkness, and take an important step toward bringing #HidradentisSuppurativa out of the shadows.
We want to help raise global awareness of HS, a common and painful skin disease by lighting a candle in solidarity to support all people with this disease, foster compassion and understanding in order to shed light on this affliction. We will also honor those who have succumbed to HS-related complications.
Hidradenitis Suppurativa: a painful autoinflammatory skin disease that dramatically affects quality of life. Not contagious. No known cause. No cure. There are many unknowns about Hidradenitis Suppurativa. Many of these unknowns lead us to hide the disease from the world. Many of these unknowns lead to a lot of us not even having a diagnosis. HS has a terrible effect on us, our families and the community. We stand in the same darkness as the medical profession. In hope, we believe our actions may encourage increased public interest that will help doctors find a cure.
Please join us in lighting a candle in the darkness, and take an important step toward bringing Hidradentis Suppurativa out of the shadows.
Hope for HS is proud to host this live #BringHStoLight vigil in support of a global campaign for 2018 HS Awareness Week, created by Penny White of Atlanta, Georgia. For further information about how you can host a vigil near you and a list of global participants please visit https://penspen.wixsite.com/bringhstolight/
Tune in on Facebook live on Tuesday, April 24th at 7:00 PM Eastern to view our presentation on disability benefits for Hidradenitis Suppurativa from attorneys at the law firm of Benjamin Levine – disability specialists based in Michigan but serving clients nation wide.
If you have any questions for the attorneys before the presentation begins, comment here or e-mail them to firstname.lastname@example.org.
Governor Rick Snyder has proclaimed a week for Hidradenitis Suppurativa Awareness in Michigan for the second year in a row. June 4-10, 2018 will be recognized to raise awareness in the state of Michigan, hopefully reducing the time to diagnosis and increasing the quality of care for everyone affected by HS.
There is still time to get HS Awareness Week recognized by your state government! Use the contact form to tell us what state you’re in and we’ll send you all the information, letters, and whereas clauses you’ll need to ask your governor to recognize HS Awareness Week in your state!