It has been a very personal decision to focus this website to a Community of our peers, to know that One in every ten children is born with a birthmark (vascular anomaly) and between fifty and sixty percent of them will require some form of treatment.  

Boston is one the leading comprehensive medical centers for such diagnosis and treatment in the world.  

We are committed to providing a valuable source for patient/family resources and focuses on treating all aspects of the patient’s problem.  

And remember, this site is all about hope and healing.

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creating awareness - providing support - uniting families with hemangiomas, port wine, Klippel Trenaunay & Sturge Weber

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  • New Member
    Suzanne Davies Suzanne Davies joined
    January 21 at 6:53 PM
    Suzanne Davies
    "I am the mother of a 14 year old daughter with Klippel-Trenaunay. She is in the 10% with a smaller affected limb rather than larger. Lauren's arm, chest and back are affected. We recently moved to Oregon from Minnesota."
  • New Discussion
    Kelly Meyers Kelly Meyers started Pictures
    June 17, 2011 at 10:30 AM
    Kelly Meyers

    "Hi, I'm Kelly, and I'm a photographer. More importantly, I'm also the mom to a daughter with a facial vascular malformation...."

    Read more…

  • New Member
    Kelly Meyers Kelly Meyers joined
    June 2, 2011 at 12:35 AM
    Kelly Meyers
    "Hi, I'm Kelly. My daughter, Addison, is 14 months old (born 4/2010) and has a complex vascular malformation. We also have a 10 year old daughter named Chloe."
 
Boston Birthmarks Awareness & Support http://photos4.meetupstatic.com/photos/event/7/8/d/1/global_17250929.jpeg
Founded May 4, 2009
20090504
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