Come Zoom with Us
Virtual Community Connections for People Affected by Scleroderma
Come Zoom With Us is SABC’s monthly virtual community connection space — a welcoming place to connect, share experiences, and stay engaged with others who understand life with scleroderma.
These peer-led sessions focus on conversation, connection, and shared understanding, creating space for people to check in, reflect, and learn from one another in a respectful, friendly environment. Participation is always flexible — you’re welcome to share, listen, or simply be present.
Questions or suggestions about these sessions? email: sabckelly@gmail.com
Upcoming Come Zoom with Us: Community Connection
Topic: Raynaud’s & Scleroderma
Date: Wednesday, February 25th 2025
Time: 7:00 – 8:00 PM PST
Format: Online via Zoom
Virtually all people living with scleroderma, approximately 95%, experience Raynaud’s Phenomenon. This Come Zoom With Us session will focus on shared experiences, challenges, and day-to-day realities of living with Raynaud’s in the context of scleroderma.
This is a peer-led, community conversation designed to create space for connection, understanding, and shared perspectives. You are welcome to participate in whatever way feels right for you — sharing, listening, or simply being present.
Who Should Attend:
People living with scleroderma, family members, caregivers, and supporters are ALL welcome.
👉 Register here: Raynaud’s & Scleroderma
After registering, you will receive a confirmation email with information on how to join the meeting.
We look forward to connecting with you virtually on February 18th.
About Come Zoom With Us
Come Zoom With Us is part of the Scleroderma Association of B.C.’s commitment to creating accessible, virtual community spaces for people affected by scleroderma across British Columbia.
These monthly online gatherings are designed to:
-
Foster connection and a sense of belonging
-
Encourage peer-to-peer conversation and shared experience
-
Reduce isolation through community engagement
-
Provide space for reflection, encouragement, and mutual understanding
-
Complement educational programming and other SABC resources
The virtual format allows participants to join from anywhere in B.C., making it easier to participate regardless of location, mobility, or energy levels.
Prefer in-person connections or looking for a local community of scleroderma warriors? Click here to Find support in your community
What to Expect When You Attend
Each Come Zoom With Us session includes:
-
A 60-minute facilitated virtual meeting
-
A welcoming, respectful, and inclusive environment
-
Opportunities to participate at your own comfort level
-
Peer-led discussion focused on shared experience
-
Monthly themes or open check-in conversations
-
Easy access via Zoom
You are never required to speak — many participants choose to listen and still find the experience meaningful.
Who These Community Connections Are For
These virtual community sessions are open to:
-
Individuals living with systemic or localized scleroderma
-
People who are newly diagnosed
-
Long-standing members of the scleroderma community
-
Family members, caregivers, and supporters
No prior participation or experience is required.
Guiding Principles
To ensure a safe, respectful, and welcoming environment for everyone, Come Zoom With Us follows a few important principles:
-
Sessions focus on connection, conversation, and shared experience
-
They do not replace professional medical care or advice
-
Promotion of treatments not approved by scleroderma specialists is not permitted
-
Facilitators help guide discussion to maintain a respectful and inclusive space
This approach reflects SABC’s commitment to evidence-based information, community wellbeing, and participant safety.
Ongoing Virtual Community Connections
Virtual Community Connections
Frequency: Monthly
Time: 7:00 – 8:00 PM (Vancouver time)
Format: Online via Zoom
Topics: Vary month to month and may include seasonal check-ins, shared experiences, and community-led discussions
Explore More Ways to Connect
SABC offers a range of virtual programs and resources designed to support people affected by scleroderma through education, connection, and community engagement.
👉 Explore:
The 20% – Men’s Virtual Support Group
Virtual Caregiver Support Group