A Guide to Hidradentitis Suppurativa: Living with HS aims to help individuals with Hidradenitis Suppurativa (HS) to learn more about HS and how to effectively manage this condition. In conjunction with patients, this book is suitable for family members and friends of HS patients, as well as generalist healthcare practitioners who would like to increase their understanding of HS and the challenges associated with this condition.
Note: Deadline for application as of September 24, 2024
The Canadian Hidradenitis Suppurativa Foundation (CHSF) is offering travel grants for Canadian dermatology residents to attend the HS Academy from December 6-8, 2024, in Irving, Texas. Four grants are available, providing up to $1,250 in reimbursement.
The application deadline is October 23, 2024.
Hidradenitis suppurativa (HS) is a painful, long-term skin condition that causes abscesses and scarring on the skin. The exact cause of hidradenitis suppurativa is unknown, but it occurs near hair follicles where there are sweat glands, usually around the groin, bottom, breasts and armpits.
THE PAIN IS TO THE CORE, TO THE POINT WHERE IT IS DEBILITATING. AS A RESULT, I LEARNT TO LANCE MY LESIONS.
WE REALLY NEED MORE DISEASE AWARENESS AND SUPPORT.
Joshua
A PERSON LIVING WITH HS, SHARED
We couldn’t be prouder of the first certified dermatologists of the Canadian Hidradenitis Suppurativa Foundation’s national Higher Standards for Hidradenitis Suppurativa Deroofing Program!
Dr. Chris Keeling and Dr. Lauren Lam led a weekend hands-on workshop for dermatologists and nurses from all across Canada, including Prince George, Kelowna, Kamloops, Red Deer, London, Toronto, and Scarborough!
The goal of the CHSF was to provide a standardized training program for dermatologists to become confident enough to incorporate deroofing in their own practices so that our rural patients no longer need to drive 6 hours to see us for deroofing.
We hope to run this program on an annual basis. Stay tuned for more information.
This event is being hosted be HS & Me and is a chance to bring together individuals living with Hidradenitis Suppurativa, their loved ones, and healthcare professionals to raise awareness, build community, and enjoy a relaxed, supportive afternoon.
Event Details:
📅 Date: Saturday, May 31, 2025
📍 Location: Erindale Park – Area C, 1695 Dundas St W, Mississauga, ON L5C 1J4
⏰ Time: 11:00 AM – 3:00 PM
🍔 Activities: Awareness walk, BBQ, guest speakers, and community connection
Registration Link: https://www.eventbrite.ca/e/3rd-annual-hs-awareness-walk-and-bbq-tickets-1307449389319?aff=oddtdtcreator
HS & Me would also love your help in spreading the word about a second event—an in-person HS Support Group on Tuesday, June 3, 2025 at 7:00 PM. This gathering offers a safe space for individuals living with HS to connect and share. Check out the website for more details.
Helene Veillette – President (Quebec), Lauren Lam – Vice-President (Alberta), Chris Keeling (Alberta) – Secretary/Treasurer, Susan Poelman – Past President (Alberta)
Pat Coutts (Ontario), Ralph George (Ontario), Danielle Marcoux (Quebec), Simon Wong (British Columbia), Helene Veillette (Quebec), Rochelle Tonkin (Alberta), Raed Alhusayen (Ontario), Marni Wiseman (Manitoba), Jessica Asgarpour (Ontario), Lima Hermenio (Ontario)
Proud Supporters
Copyright © 2022 Canadian Hidradenitis Suppurativa Foundation
