Join us on September 18th, 2010 for a sand VOLLEYBALL TOURNAMENT Benefitting the Waner Children’s Vascular Anomaly Foundation in support of Lil’ Miss Ella Musalek.

CLICK HERE FOR MORE INFORMATION on www.ellapalooza.com

Click below to watch the inspiring story of Maddox Flynn that ran on FoxNews.com. Wonderful story!

Our First Annual Picnic in the Park was a huge success! Click here for pictures!

Thank you to all our wonderful patients and participants - volunteers and friends for making the Picnic in the Park such an incredible event. 500 attended the event... an incredible turn-out for the very first one. I had the opportunity to listen and watch parents hug, cry and laugh together - children played together and new friends were made. We will post photos as soon as they are available. The drawings from the children are so wonderful and we will have them up and ready for your votes soon. Please join our discussion forum at www.wanerkids.org/forum and continue the community and support. Mark your calendar for June 5, 2011 - it is sure to be another wonderful picnic. It was an incredible day and emotional day for everyone. We truly have the very best parents... hope to see you all soon.

Waner Children's Vascular Anomaly Foundation

Waner Children’s Vascular Anomaly Foundation was established in 2007 by co-founders Milton Waner, M.D., Edward Foster and Sherri Foster. The vision of the foundation is set out in three parts; to provide financial assistance to families with children afflicted by these vascular anomalies, to provide or fund research directly related to understanding and treating vascular birthmarks and to support the activities of the Vascular Birthmark Institute of New York in their efforts to educate the medical community through seminars and a fellowship for training other physicians.

Waner's Vascular Birthmark Support Group
Next Meeting will be held July 19th, @ 6:30pm
No support meeting in June due to the
Patient Reunion "Picnic in the Park"