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.
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 email@example.com.
We are so privileged to have Erin Martinez, LMSW, speak with us in April on the topic of Chronic Disease and the Impacts on Sexual Health. With Hidradenitis Suppurativa inwardly affecting our self-esteem and outwardly affecting the skin in intimate areas, this presentation and Q&A session will be vitally illuminating! Please join us in Detroit at New Center One. Location information is available at on our website and video simulcast with Q&A will be live on our Facebook page.
We hope to see you there!
Hello, and welcome to the website of Hope for HS of Southeast Michigan. We are a support group for Hidradenitis Suppurativa that meets in Detroit, Michigan. We have an active Facebook group for daily discussion and support. Members also participate as a group in community events to spread awareness of HS.
If you have questions about the group or HS please use the Contact Us link above, connect with us on Facebook, Youtube or Twitter, and please join us at a regular meeting if you are in the Detroit area.