Little Girl With Pituitary Tumor Named Ambassador for Children’s Miracle Network

Katie WebbThe Lincoln Times in Lincolnton, North Carolina recently wrote about a young girl who has a nonfunctioning pituitary and a cleft palate named Katie Webb. Despite her many medical challenges, she and her family are big supporters of Levine’s Children’s Hospital in Charlotte, NC and organize a Christmas in July fundraiser to support them. Katie has been honored as the 2016-7 Champion Ambassador for North Carolina for the Children’s Miracle Network. She got to visit Washington D.C. for a week and will go to Disney World soon in that capacity. Learn more about it here or go to her Facebook page, called Katie’s Thousands.

Katie Webb (Facebook)

Print

Available Now!

PPRG6-500 Cover
The Pituitary Patient Resource Guide Sixth Edition is now available! Be one of the first to have the most up-to-date information. The Pituitary Patient Resource Guide a one of a kind publication intended as an invaluable source of information not only for patients but also their families, physicians, and all health care providers. It contains information on symptoms, proper testing, how to get a diagnosis, and the treatment options that are available. It also includes Pituitary Network Association's patient resource listings for expert medical care.

Buy Now