![]() Dawn Torrence Williamson Dawn is the mom of Shane Torrence (1/28/93-9/11/99). Shane was born with left-sided CDH, ASD, hypospadius, pulmonary sequestration, descended testes, and multiple other birth defects. Shane spent his first 10 months in the PICU at Duke University Medical Center and many more hospitalizations at the University of North Carolina at Chapel Hill. He had a trach for 3 years while he was on a ventilator for 2 years and oxygen for 2 and a half years. He also had a Mic-Key feeding tube, hearing aids, oral aversions, developmental delays and textile aversions. He suffered multiple complications including 6 CDH repairs, pulmonary hypertension, blindness for a year, hearing impairment, Cerebral Palsy, multiple blood infections and pneumonia and was lost to a very rare case of gastropleural fistula at age 6 and a half. Dawn is also the founder and President of CHERUBS. Having volunteered for 16 years until she quit her job as a web designer and graphic artist to become CHERUBS first full-time employee in 2011. Dawn works out of CHERUBS international headquarters in Wake Forest, North Carolina with 3 office volunteers; Shanon, Holly and Vicki. She is married to Craig, and they have 2 boys; 17-yr-old twins Braden and Garret. Going back to school to learn more about how to help our charity, she has a 4.0 in college while taking such courses as Biology, Anatomy, Medical Terminology, Business, Web Development, Public Speaking and more. She also is very active in her local community, belonging to several business and civic organizations as well as her local church. |
Showing posts with label Dawn Torrence. Show all posts
Showing posts with label Dawn Torrence. Show all posts
Thursday, March 28, 2013
MEET OUR BOARD - Dawn Torrence Williamson, President & Founder
Labels:
Awareness,
cdh,
Charity,
CHERUBS,
Congenital Diaphragmatic Hernia,
Dawn M. Torrence,
Dawn Torrence,
Dawn Torrence Williamson,
Dawn Williamson,
Research,
support,
Support group,
volunteer
Thursday, March 7, 2013
Washington DC Parade of Cherubs on April 19th!
Join us for April 19th, the International Day of Congenital Diaphragmatic Hernia Awareness on Capital Hill!!!!
Washington DC Parade
- Meet with Senate Offices on April 18th
- Reception the evening of April 18th
- Parade on April 19th
- On Facebook - https://www.facebook.com/events/401677689912783/
- Register on Eventbrite - http://cdhawarenessday-2013washingtondc.eventbrite.com/
- Set up your own Team Member page on Firstgiving - https://www.firstgiving.com/10125/cdhawarenessday2013
- 100% of money raised will go to the CDH Research Fund
- Contact Dawn Torrence Williamson with any questions about this event - events@cdhsupport.org
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