Support VBF's International Medical Missions Teams (iTEAM)

Vascular Birthmarks Foundation	Hemangiomas \| Port Wine Stains \| Vascular Malformations
1994 - 2018 FAMILIES GIVEN NEW HOPE Dr. Linda Rozell-Shannon, PhD President and Founder
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Every week, children and adults with vascular birthmarks around the world seek VBF's support.

In response, the Vascular Birthmarks Foundation aims to spread knowledge and equip doctors wherever there is a need. We organize an international trip each year to provide free treatments and educate physicians outside the USA regarding the latest developments in the diagnosis and treatment of vascular birthmarks.

These medical missions trips are life changing. We bring a team of vascular birthmark experts to each country and co-host a conference which focuses on the latest in the diagnosis and treatment of vascular birthmarks. In some instances, the experts are also able to do free treatments. After our visit, local doctors continue to help families affected by a vascular birthmark.

In 2013, our iTeam went to Russia and treated over 125 children for free. The clinic they established has already treated over 400 children. In 2014, we traveled to India and treated over 30 patients. In February 2015, we presented to over 100 specialists at a vascular anomalies conference in Tel Aviv, Israel. Our next trip for training and treatments will be in Parma, Italy in July 2016. We have a waiting list of countries seeking the expertise of our iTEAM.

We invite you to show your support of our international outreach with $100 donation.

The smiles of the 125+ children we treated in Moscow, Russia shows just how meaningful your contribution is.

Contribute today.

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VBF
PO Box 106
Latham, NY 12110

Mission Statement:An international charitable organization that networks families affected by a vascular birthmark, tumor, or syndrome to the appropriate medical professionals for evaluation and/or treatment, provides informational resources as well as sponsors physician education, mobilizes medical missions trips, and supports research and programs that promote acceptance for individuals with birthmarks.

Here you will find information and resources for patients and families affected by hemangioma, port wine stain, arteriovenous malformation, capillary malformation, lymphatic malformation, Sturge Weber syndrome, Klippel-Trenaunay syndrome, and any other type of vascular birthmark and syndrome.

Social media links: https://www.facebook.com/VascularBirthmarksFoundation https://twitter.com/VBirthmarks https://www.instagram.com/vbirthmarks/ https://www.youtube.com/user/VBFchannel?feature=watch

Translations of the VBF website: Español | Deutsch | Français | Italiano | Português

DISCLAIMER
Information accessed through the VBF is presented in summary form in order to impart general information relating to the diagnosis and treatment of vascular birthmarks. Such information is not complete and should not be used as a substitute for a consultation or visit with your physician or other health care provider. Information accessed through VBF is not exhaustive and does not cover every aspect of vascular birthmarks. VBF makes no warranty as to the information's completeness, reliability or accuracy. Should you have any health care related questions regarding this matter, please see your physician or other health care provider promptly. Information accessed through the VBF is provided "AS IS" and without warranty, express or implied. All implied warranties of merchantability and fitness for a particular use or purpose are hereby excluded. VBF shall not be liable under any theory or indemnity. In no event shall VBF be liable for any damages, direct or indirect, and all other damages, direct or indirect, special, incidental, consequential or punitive, are hereby excluded even if VBF has been advised of the possibility of such damages.

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Dr. Linda Rozell-Shannon (PhD), President and Founder
Vascular Birthmarks Foundation, PO Box 106, Latham, NY 12110
© Dr. Linda Rozell-Shannon, All Rights Reserved.
Federal Tax ID 16-1515227

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