Honest Conversations: Adults with 22q November Meeting
Adults with 22q, we invite you to join us in a welcoming virtual space created for you to connect, share experiences, and build community with others who truly understand the journey. Whether you’d like to talk, listen, ask questions, or simply meet others navigating similar experiences, this casual conversation is designed to be supportive, relaxed, and judgment-free.
This is not a formal presentation — just an opportunity for real connection and honest conversation in a safe and welcoming environment.
Join Us!
When: Monday, November 2 at 7pm EST/4pm PST
Where: Virtual via Zoom
Who: Individuals with 22q differences ages 25+
This group is led by two adults with 22q. Learn more about them below.
How: REGISTER HERE
Based on interest and community feedback, we hope to continue offering these gatherings on an ongoing basis, while also creating additional virtual connection opportunities for other age groups and demographics within our 22q community in the future.
Meet Your Hosts:
Gracie Chavez
22q Young Adult Support Intern
Gracie Chavez was introduced to 22q community when she was diagnosed with 22q11.2 Deletion Syndrome at the age of two. Through out the years of never having any resources and not knowing anyone who could relate to her syndrome. So, after Gracie went to see a new geneticist with her mom. That's when they discovered a new name for VCF.
She educated herself about the syndrome. She connected with other 22q members. Since then she knew she wanted to help and share awareness. She loves spending time with family, blogging, and is a floral desginer and loves doing weddings /special events.
Gracie lives in Elmore, Ohio with her Mom and Dad. She has one sister and three brothers. Gracie is the youngest in her family and the only one with 22q. Gracie is always sharing awareness and constantly reaching out to young adults with 22q . Gracie is always saying "This is my journey and I love it!" That way she can always remember she can do it and never give up!
Peter Mason
Board Member
Peter is an adult individual with 22q deletion syndrome who lives in Connecticut. He is an artist, custom sneaker artist and collector, and a musician. Peter has been drumming since he was three years old. He shares his story with others in and out of the 22q community to help raise awareness for 22q. He enjoys being a part of 22q Family and helping to grow the 22q community. Peter hopes to inspire others in the community in a positive light