Sign In | Sign Up

 

> Cohen Syndrome

browse all Diseases & Topics

News

Submit News

PINELLAS PARK — In 2006, Mikayla DeMarco had one wish — a red tricycle like the one she rode in class. That wish was granted by the Kids Wish Network, a national nonprofit that grants wishes to children with life-threatening illnesses. Beth DeMarco, however, just wanted to know what afflicted her daughter. After nearly 14 years, with the help of a doctor at All Children's Hospital, she learned that her daughter has a rare disease — so uncommon that only about 1,000 people in the world have been diagnosed with it.

Free Health Risk Guide

Talk to a Genetic Counselor

Discussion comments and posts are provided by individuals and reflect their personal opinion only. Under NO circumstances should you act on any advice or opinion posted in this forum. We have no obligation to monitor any comments posted on this website nor do we in any way endorse the views of any user. > More Info

Content on this website is for informational purposes only and is not a substitute for professional medical advice, diagnosis or treatment.
You should always seek the advice of a physician regarding any questions you have about your specific medical condition. More info

This website is certified by Health On the Net Foundation. Click to verify. This site complies with the HONcode standard for trustworthy health information: verify here.

© 2008-2010 AccessDNA, Inc. All rights reserved.