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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

 

Come Zoom With Us

Upcoming Community Connection

Winter Check-In

Date: Wednesday, January 7

Time: 7:00 – 8:00 PM PST

Format: Online via Zoom

Join us for a seasonal Winter Check-In, designed to bring the scleroderma community together for conversation and connection during the winter months. This session offers an opportunity to reflect on how you’re doing, hear from others, and stay connected in a supportive, peer-led space.

Sharing is always optional, and all are welcome.

Who Should Attend:

People living with scleroderma, family members, caregivers, and supporters are ALL welcome.

👉 Register here: Winter Check-In

After registering, you will receive a confirmation email with details on how to join the Zoom session.

We look forward to connecting with you in the new year.

 


 

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:

Scleroderma Resource Hub

The 20% – Men’s Virtual Support Group

Virtual Caregiver Support Group

 Virtual Yoga for Scleroderma

 

 

 

 

 

 

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