by Ashley Kus | Oct 4, 2024 | Media Room, Uncategorized
Mark and Lyndsee F., Cambria’s Grandparents Cambria is 14 years old, 3’10″, and 40 pounds. The doctor who delivered her was the first to mention CdLS. She was medevacked to Tucson Medical Center, where they formalized her diagnosis, gave her a feeding tube, and...
by Ashley Kus | Oct 3, 2024 | Media Room, Uncategorized
Adapted from: Udservices.org Adults with disabilities make up nearly 20% of the American workforce. Still, they often face more significant challenges in finding and maintaining employment. In most cases, this is because they don’t have the opportunity to develop...
by Ashley Kus | Sep 26, 2024 | Media Room, Uncategorized
Lisa T., Dorian’s Mom On January 17, 2001, Dorian was diagnosed with CdLS after her pediatrician noticed that she had only gained four pounds since birth despite being breast-fed. Despite not showing any limb abnormalities, Dorian’s slow growth raised...
by Ashley Kus | Sep 25, 2024 | Media Room, Research News, Uncategorized
If you’re new to the CdLS Family you’re probably very interested in learning whether your child with CdLS is mildly, moderately, or severely affected. The following article, written by Dr. Antonie Kline, CdLS Foundation Medical Director focuses on the genetic...
by Ashley Kus | Sep 23, 2024 | Media Room, Uncategorized
Medically reviewed by: Carolyn Sewell-Roberts, LCSW, Cerebral Palsy (CP) Care at Nemours Children’s Health As a parent, you want to give equal attention to all your children. But when parenting a child with special needs, that can be hard. It may feel like there is...
by Ashley Kus | Sep 19, 2024 | Media Room, Research News, Uncategorized
By: Julia O’Connor, Ph.D., Psychologist, Kennedy Krieger Institute and CdLS Foundation Professional Development Committee (PDC) Member Individuals with CdLS experience significant challenges including behavioral health concerns, such as anxiety, depression, and...
by Ashley Kus | Sep 17, 2024 | Media Room, Uncategorized
By: Family Services Whether the words “Cornelia de Lange Syndrome” are new to you or have been the focus of many hours of exploration/investigation/contemplation, we welcome you to our Foundation. However you choose to contact us — by phone, letter or email...
by Ashley Kus | Sep 12, 2024 | Media Room, Uncategorized
By: Sharonza P. Elijah may be smaller than other nine-year-old kids, but he is big in personality, energy, wit, kindness, and snacks. Elijah is a great help to his classmates at school. He is very observant and quite mischievous. He enjoys getting into anything and...
by Ashley Kus | Sep 5, 2024 | Uncategorized
By: Gabriella, Kalani’s mom Kalani just turned 1 in July! We recently got his diagnosis in June. He has several GI issues, growth restrictions, and slightly delayed development. We are learning more and more about CdLS every day. We often contact the foundation,...
by Ashley Kus | Sep 4, 2024 | Research News, Uncategorized
By: the CdLS Foundation Family Service Team Cornelia de Lange Syndrome (CdLS) is a genetic disorder present from birth, which causes a range of physical, cognitive, and medical challenges. While there have been many advances in the diagnosis and treatment of CdLS,...
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