Do you have a rare genetic skin disease or care for someone who does?
Are you a clinician, scientist, or industry representative working on rare skin diseases?
Do you want to learn more about the latest research, treatments, and challenges in this field?
If you answered YES to any of these questions, then you are invited to join us April 5, 2024 for a one-day meeting on rare skin diseases, hosted by the SickKids. This event will bring together patients, families, clinicians, scientists, and industry partners to share their experiences, insights, and vision for the future of rare skin diseases.
The meeting will feature:
- Keynote speakers from leading experts in rare skin diseases
- Panel discussions on topics such as diagnosis, management, advocacy and innovation
- Breakout sessions for networking and collaboration
Location: PGCRL Building
SickKids Research Institute
686 Bay Street, Toronto, M5G 0A4
Registration
The meeting is free to attend, but registration is required! Scan the QR code or visit this link https://www.eventbrite.ca/e/inaugural-canadian-genodermatoses-network-meeting-tickets-800024553977 to register.
If you are an industry representative and would like to sponsor a family to attend, please email: This email address is being protected from spambots. You need JavaScript enabled to view it.
If you are a parent/patient and would like to be sponsored for attending the event, please email: This email address is being protected from spambots. You need JavaScript enabled to view it.
Space is limited, so register early to secure your spot.
Let’s work together to improve the lives of people with rare, genetic skin diseases. See you there!
