Waner Children's Vascular Anomaly Foundation

 

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!

 

 

 

SAVE THE DATE!!

 

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" 

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Media

Two-and-a-half-year-old Canadian Maddox Flynn and his life-changing surgery - May 21, 2010

NEWYORK - ABC 7

"Changing Faces" - March 8, 2010

In this special, "Changing Faces," Dr. Milton Waner is profiled as he treats two patients: a baby girl born with massive hemangioma and an older female patient from Iran who has lived with her vascular anomaly for years but  finally crossed paths with Dr. Waner who will treat her condition.