Skip to main content
Williams Syndrome Association logo.
Donate
  • Join
  • Events
  • Shop
  • Español
  • Forums
  • About Us
    • Overview
    • Structure & Administration
      • Board of Trustees
      • Medical Advisors
      • Executive Director & Team
      • Consultants & Partners
    • Position Statements
    • Programs
    • Strategic Plan
    • Newsletters
    • Media & Press Center
    • Executive Director Search
  • Education
    • Overview
    • Getting Started in School
    • Creating an IEP
    • Creating a Vision Statement
    • Education Strategies
    • Testing & Evaluation Strategies
    • Therapeutic Strategies for Education
    • Transition Strategies - High School to Adult Life
    • Life Skills & Post Secondary Programs
    • Featured Education Resources
    • Virtual Education Resources
    • Convention
    • Resources
  • Medical
    • Overview
    • Diagnosing Williams Syndrome
    • Healthcare Guidelines
    • Anesthesia Concerns
    • Cardiovascular Concerns
      • Cardiac and Sudden Death information
    • Gastrointestinal Concerns
    • Neurodevelopment & Behavioral Health
      • WS and Sexuality
    • Williams Syndrome Clinics
    • Collaborative Registry for WS (CReWS)
    • renovascular hypertension collaborative
    • Resources
    • Research
      • Overview
      • Current Studies
      • Grant Opportunities
      • Renovascular Hypertension Collaborative
  • Life with WS
    • Overview
    • What is Williams syndrome?
      • Overview
      • General Information
      • Diagnosing WS
      • New Diagnosis: First Steps
      • Therapeutic Interventions
      • Talking to Children about WS
      • Frequently Asked Questions
    • Family Support
      • Overview
      • Family Support Network
      • Support Groups
      • Connect with Others
      • Available Aid and Assistance
      • Financial Planning
      • Grandparents
      • Siblings
      • Resource Organizations
      • International Organizations
    • Adult Life
      • Overview
      • Transition Strategies - High School to Adult Life
      • Life Skills & Post Secondary Programs
      • Housing
      • Employment
      • Adventure Seekers
      • Voting Resources
    • Programs
      • Become a Member
      • Convention
      • Camps
      • Adventure Seekers
      • Financial Aid & Scholarships
      • Grant Opportunities
    • Media and Entertainment
      • The Starry-Eyed Podcast
      • News Items
      • Blog
    • Frequently Asked Questions
    • Attend an Event
    • Convention
    • Resources
  • Get Involved
    • Overview
    • Walks for Williams
    • Awareness Month
      • 2024 Awareness Month Social Media Toolkit!
    • Become a Member
    • Donate
    • Fundraise
    • Volunteer
    • Event Calendar
    • Host a Social/Connection Event
    • Vendor Network
    • Share Your Story
    • Your Contributions at Work
    • Shop our Merch
    • Contact the WSA

You are here

Home » File

Family Discussion Guide Workbook_2023_REV 2.pdf

PDF icon Family Discussion Guide Workbook_2023_REV 2.pdf

Contact us

243 Broadway Unit 9188
Newark, NJ 07104

info@williams-syndrome.org

248.244.2229
800.806.1871
248.244.2230 fax

Follow us

Position on Inclusion

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

Funding priorities

Funding priorities pie chart.

  • Privacy Policy
  • Disclaimer
  • Non-discrimination statement
  • dei statement
  • media & press center
  • 501(c)(3) organization
Copyright © 2024 Williams Syndrome Association | Web design