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Home » Make Connections » Connect with your Local Community

Colorado

The Williams Syndrome Association is organized into 19 regions across the United States. Colorado is part of the Rocky Mountain region. Each region works to provide resource information and social and educational opportunities to its members. Volunteers are standing by in each state within the regions (parents and grandparents who can provide resources and information) to speak with new families or any families needing support. They are joined by many other volunteers who work hard to facilitate gatherings such as picnics, conferences, and fundraisers. 

Below you will find the name(s) and contact email addresses of your state's Family Support Network volunteer(s).

Blog author, Family Support Specialist:
Jen Keeton of Timnath, Colorado
Email

Areas of focus: children, teens, WSA camp

Local Facebook Group:
Family Support Volunteer, WSA Board:
Bill Palmer of Lyons, Colorado
Email

William Palmer (Bill) is a semi-retired engineer, and has worked for several nonprofit organizations in the building/infrastructure design and construction industry. He was executive director of two nonprofits and then spent 20 years as editorial director of a group of magazines and websites for construction contractors. Bill has also served on several volunteer boards, including the Williams Syndrome Association board of trustees, where he served and was president in the late 1990's during a critical growth period. During his term as president of his local library board, he helped raise several million dollars for a new library. Bill and his wife, Wynne live in Colorado with their 31-year-old daughter Autumn, who has WS.

Family Support Network area of focus: adults

Local Facebook Group:
Family Support Volunteer:
Lecia Walker of Castle Rock, Colorado
Email

Area of focus: adults

Local Facebook Group:

Upcoming Events in CO

FSN - Only Child Family Support Group

Wed, 11/29/2023 - 8:00 pm EST

FSN - December Support Parent/Caregiver Meet-up #1

Mon, 12/11/2023 - 8:00 pm EST

FSN - Grief Support for Parents/Caregivers who have lost someone with WS

Wed, 12/13/2023 - 8:00 pm EST

FSN - December Support Parent/Caregiver Meet-up #2

Wed, 12/27/2023 - 8:00 pm EST

FSN - Parents/Caregivers of Adults & Children with WS and Anxiety Meeting

Wed, 01/03/2024 - 8:00 pm EST

FSN - Parents/Caregivers of Children 4 and under with WS

Mon, 01/08/2024 - 8:00 pm EST

FSN - Parents/Caregivers of Teens & Tweens with WS

Tue, 01/09/2024 - 8:00 pm EST

FSN - Parents/Caregivers of Adults with WS and Challenging Behaviors Meeting

Wed, 01/10/2024 - 8:00 pm EST

FSN - Grandparent Family Support Group

Thu, 01/11/2024 - 8:00 pm EST

FSN - Complex Communicators and Feeding Challenges Group for Parents/Caregivers

Mon, 01/15/2024 - 8:00 pm EST

FSN - Grief Support for Parents/Caregivers who have lost someone with WS

Wed, 01/17/2024 - 8:00 pm EST

FSN - Parents/Caregivers of Individuals with WS-Autism Dual Diagnosis

Thu, 01/18/2024 - 8:00 pm EST

FSN - Only Child Family Support Group

Wed, 01/24/2024 - 8:00 pm EST

Contact us

243 Broadway #9188

Newark, NJ 07104

info@williams-syndrome.org

248.244.2229
800.806.1871
248.244.2230 fax

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Inclusion statement

The WSA upholds the following positions on inclusion.  We believe that:

  • everyone benefits when individuals with WS are meaningfully included in educational, work, and community settings
  • individuals with WS should receive all necessary supports and services to fully participate in their family lives, communities, and society as a whole
  • high expectations should be the norm, and individuals with WS and their families should decide how they best learn, work, and enjoy social settings
  • “inclusion” is not one-size-fits-all, and will look different for each family based on each individual’s desires and needs
  • inclusion creates a sense of belonging in society, meaningful relationships, and opportunities to achieve dreams

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Project WellCAST is now enrolling for the next wave!

Now recruiting legal guardians of 2 to 35-year-olds with WS for a clinical trial focused on caregiver well-being. 

Eligible participants are assigned to receive a FREE 12-week virtual support program delivered 100% online.

Programs vary and may include self-guided resources, live individual or group therapy, and/or peer coaching with another rare disorder caregiver.

Complete the WellCAST Screening Form