Skip to main content
Williams Syndrome Association logo.
Donate
  • Events
  • Join
  • Shop
  • Español
  • Forums
  • About Us
    • Overview
    • Position Statements
    • Strategic Plan
    • Structure & Administration
      • Board of Trustees
      • Medical Advisors
      • Executive Director and Staff
    • eNewsletters
  • 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
    • Gastrointestinal Concerns
    • Neurodevelopment & Behavioral Health
    • COVID-19 Vaccine Recommendations
    • Williams Syndrome Clinics
    • renovascular hypertension collaborative
    • Resources
    • Research
      • Overview
      • Current Studies
      • Grant Opportunities
      • Collaborative Registry for WS
      • 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
      • WS In the News
      • Frequently Asked Questions
    • Adult Life
      • Overview
      • Transition Strategies - High School to Adult Life
      • Life Skills & Post Secondary Programs
      • Housing
      • Employment
      • Adventure Seekers
    • Family Support
      • Overview
      • Family Support Network
      • Connect with Others
      • Available Aid and Assistance
      • Financial Planning
      • Grandparents
      • Siblings
      • Resource Organizations
      • International Organizations
      • Attend an Event
    • Programs
      • Become a Member
      • Virtual Programs
      • Conferences & Convention
      • Camps
      • Adventure Seekers
      • Financial Aid & Scholarships
      • Grant Opportunities
    • Webinars
    • Resources
    • Frequently Asked Questions
    • eNewsletters
    • Blog
    • Convention
  • Get Involved
    • Overview
    • Become a Member
    • Make connections
    • Volunteer
    • Friends of the WSA Spotlights
    • Share Your Story
    • Events
    • Awareness Month
    • Fundraise
    • Donate
    • Your Contributions at Work
    • Shop our Merch
    • Contact the WSA

You are here

Home » WSA Blog

Science and Motherhood Collide: Journey to the WSA

01/29/2019 - 12:01 pm |

Jocelyn Krebs, PhD Jocelyn Krebs, PhD

I Didn’t Think My Career Path was Going to Prepare Me This Way for Motherhood…

 

joclyn and rhys.From an early age, I knew I wanted to be a biologist.  I quickly discovered that I was most interested in genetics, and in cells and molecules…so I became a molecular and cell biologist, specializing in epigenetics.  (Wait, don’t stop reading!)  I followed my interests along the circuitous path that scientific inquiry tends to take, until I found myself studying the role of a gene called BAZ1B, that encodes a very interesting protein called the Williams Syndrome Transcription Factor (WSTF).  “What is Williams syndrome?” I asked myself, and starting reading about it, both the scientific literature as well as the information I found on this very website—my first encounter with the WSA.  My initial reactions were “what a fascinating syndrome,” and “wow those kids are adorable!”  Then I was off to the lab with my students, studying how WSTF is needed for the early development of the brain and other tissues, how it might contribute to the complex clinical picture of WS.

We studied WS for several years and were getting exciting results…but my time on the research was soon getting balanced by time spent with my son Rhys.  I had Rhys in 2009, and he greeted the world with big surprised blue eyes and nine months of terrible colic.  Soon, we were encountering health issues and missed milestones…and eventually, genetic testing and a diagnosis of WS when Rhys was 19 months old.  On the phone, the geneticist got as far as “We found a deletion on chromosome 7,” when I interrupted with “Are you kidding?  It’s Williams??”  The coincidence was mind-boggling. I entered into the WS community with the unusual perspective of a deep understanding of the genetic basis of WS and of the current research—but new to the world of early intervention, IEPs, ST/OT/PT…  So it was back to the WSA, now as a parent, to try to understand the new circuitous path to follow with Rhys!

At our first convention (Boston 2012), I gave a talk on my research in the professional conference, then attended the convention with my family—and it was life-changing.  I’ll never forget that first time seeing so many individuals of all ages with WS, so many different life paths—and the feelings of connectedness and shared experience.  It has been wonderful to be able to give back to the WSA as a member of the board of trustees. I begin my term as board president looking forward to helping the WSA grow and continue its work sustaining research and providing resources and support for more and more families from all walks of life—helping us all along on our winding paths.  

--Jocelyn Krebs

President, WSA Board of Trustees

Member Spotlight

Featured posts

No Better Way to Celebrate
In Memoriam: Dr. Ursula Bellugi
Our 40th Anniversary…A Year of Transition for the WSA
Finding Answers, Changing Futures…Our Community Makes All the Difference

Categories

  • Ask the Expert
  • Awareness
  • Education
  • Employment & Community Involvement
  • Housing
  • Medical
  • Member Spotlight
  • Message from the Executive Director
  • Miscellaneous
  • Parent Perspective
  • Programs
  • Regional News and Events
  • Research
  • Technology
  • Volunteer Spotlight
  • Year-end wrap-up

Monthly archive

  • November 2020 (1)
  • September 2020 (1)
  • August 2020 (3)
  • June 2020 (1)
  • April 2020 (3)
  • March 2020 (1)
  • January 2020 (2)
  • September 2019 (1)
  • August 2019 (1)
  • July 2019 (2)
  • May 2019 (2)
  • March 2019 (2)
  • ‹ previous
  • 2 of 5
  • next ›

Contact us

560 Kirts Blvd. Suite 116
Troy, MI 48084-4153

info@williams-syndrome.org

248.244.2229
800.806.1871
248.244.2230 fax

Follow us

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 that 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
  • media & press center
  • 501(c)(3) organization
Copyright © 2023 Williams Syndrome Association | Web design
Enter our Disney Dream Sweepstakes!

Wishing for a dream vacation to Disney? Every $100 entry gives you a chance to win an unforgettable trip to a Disney destination of your choice, while supporting a great cause.  

enter the sweepstakes now