Expert's Corner

 

 

Ask the Founder


VBF Announces "Ask The VBF Founder." Linda Rozell-Shannon is the leading lay expert (non doctor) in the world on the subject of vascular birthmarks.

 

Babies with Birthmarks™

Our newest program - guidelines for physicians to follow to diagnose and treat vascular birthmarks with the earliest intervention.

Recent Medical Papers and Research

New Research Out of Boston


Dynamic Cooling Paper by Dr. Nelson and Wangcun Jia


Arterio-venous Malformations Powerpoint Presentation


PWS paper by Dr. Mihm and L. Rozell-Shannon


SWS Glaucoma Facts by L. Rozell-Shannon and Dr. Fay

Test for Birthmarks

Psychosocial and Emotional Issues for Individuals with a Port Wine Stain

Simple things you can do to manage KTS (Dr. Delfanian and Linda Shannon)

Ulcer Care and Treatment (pdf)

The Vascular Birthmarks Foundation
along with the

Present the 2009 Port Wine Stain and Vascular Birthmarks Conference

VBF Celebrates 15th Anniversary October 2009

Meet Devion, VBF's Kid with KT
 
Diana, one of VBF's Orphans With Birthmarks

VBF is very excited to announce that despite the economy the Port Wine Stain and Vascular Birthmarks Conference will be held in Irvine, California on Friday, October 9th and Saturday, October 10th. This conference will take place at the Beckman Laser Institute in Irvine, and at the Island Hotel minutes away in Newport Beach, California. Families should fly into the John Wayne Airport (closest to the event). There is no shuttle to the hotel, but a bus or cab is only $20.

We are also very excited to announce that VBF will be celebrating its 15th Anniversary in California this year! Come join us for a piece of cake to help us celebrate that “We Are Making A Difference.”

Dr. J. Stuart Nelson, along with the Beckman Laser Institute will be co-sponsors of this year’s conference. A very exciting research announcement will be presented on Friday evening by VBF Co-Medical Directors Dr. Martin Mihm and Dr. J. Stuart Nelson.

This year, the first 50 families that register will have meals included and FREE lodging for the Friday night and a $100 discount on Saturday night (total cost is $208.09 so families only pay $108.09 if they choose to stay the second night). Lodging will be at The Island Hotel, www.theislandhotel.com. In addition, the conference fee is only $50 per family and the clinic fee is only $50 per family. Anyone who cannot pay the clinic or conference fee can request that the fees be waived. A $25 deposit is required for each family registering for the conference and this fee cannot be waived. This deposit is non-refundable.

Read more

You can now register on line or download the registration form from the links and send it in with your $25 registration fee as soon as possible to VBF, PO Box 106, Latham, NY 12110. Please direct all questions to Basia at the above indicated phone numbers or email address.

Download the registration form

Register online for the conference

Register online for the clinic

Physician's Registration


2009 Day of Awareness Launches with
VBF's First Annual Challenge - 1mile Walk and 5k Run
JOIN US - WALK/RUN FOR BIRTHMARKS

Ethan, before and after treatmentVBF is launching this year’s Day of Awareness with its first ever 5k Run and 1 Mile Walk on Friday, May 15th, 5:00pm, in Colonie, New York. VBF was founded in this area and it is fitting that the first run/walk would occur here. We are delighted to announce that The Center for Facial Plastic Surgery & University Ear, Nose, & Throat of Northeastern New York is our Event Sponsor.

May 15th is our international Day of Awareness. Families and individuals helped by VBF will be raising awareness about vascular birthmarks by telling their personal stories and some will help to raise needed funds as well. This walk/run is our kick-off event for this year’s Day of Awareness. If you have been helped by VBF, then now is your turn to help us. Please join us. Tell your story and host a mini-fund raiser. It’s fun and it is your way to give back and help other families affected by a vascular birthmark.

Read more

Sign up to do a Day of Awareness Event (sign up from the Day of Awareness site)
Sign up to do the Day of Awareness Walk/Run (online registration)
Download walk/run registration form (pdf format)
Download walk/run brochure (pdf format)
Sponsor a Family (online)


VBF Day of Awareness Events

VBF Board Members

  • VBF Parent Rep Natalie and Treasurer Brian Bolinger – Texas, October 2009 – Silent Auction and Texas Hold ‘Em – Annual event and largest Day of Awareness fundraiser. Their daughter Nicole had a hemangioma.
  • VBF Secretary/SWSC Co-Director - Tiffany Ethington and son Glen Ethington. Tiffany and Glen have an annual interview on noon news to raise awareness. Glen has Sturge-Weber syndrome/facial Port Wine Stain, and organized a newsletter and pen pal group for kids with birthmarks and their siblings/friends called “Glen’s Gang”. VBF Chapter Director/SWSC Co-founder Glenda Ethington also helped organize this annual event.
  • VBF Executive Assistant Basia Joyce – VBF Walk/Run organizer. Basia’s daughter Anna had a hemangioma.
  • VBF Director of Musicians with Birthmarks Jenny Legary – Jenny is putting on a show in NY. Jenny has port wine stain.
  • VBF Parent Rep Danielle Vlahos – Each year Danielle hosts a “Jeans Day” at her workplace. Danielle’s son Cole had a hemangioma.
  • VBF Parent Rep Lianne Chase – Team running in the VBF Walk/Run in NY. Lianne’s son Cody has a lymphatic malformation.
  • VBF Legal - Barbara Rothaupt – VBF Walk/Run organizer
  • VBF President Dr. Linda Shannon and daughter Christine Shannon – VBF Walk/Run organizer. Christine had a hemangioma on her lip and was the inspiration for the organization of VBF.
  • VBF Parent Rep Elysa Baron and her daughter VBF Student Rep Saige Cavayero – Selling VBF Kids Who Care bracelets and organizing a team for the VBF Walk/Run. Saige was the inspiration for the bracelets. She designed them as a fundraiser for the first VBF Day of Awareness. Glen’s Gang and the VBF Kids Who Care program used Saige’s original design for adult bracelets and designed a blue/white swirl bracelet for children. Saige had extensive facial hemangioma.

Family and Volunteer Events

  • Donna Ducker and Evan Ducker – International Event - Buddy Booby Read-Along – Buddy Booby is the mascot for VBF. Mother and son authored the “Buddy Booby’s Birthmark” book about a booby bird with PWS. Evan Ducker has a facial PWS
  • Lisa Burdick – Saegertown, PA Collection Box
  • Allen Stotler – Sunrise, FL - Collection Box and VBF Starter Kits
  • Arlin Diaz – Hopelawn, NJ - Collection Box
  • Mike Jackson – Newton Centre, MA – VBF Starter kits
  • Rita Jones - Grand Saline, TX - Collection Box
  • Kate Steele – Dekalb, IL – Collection Box and VBF informational materials - In Honor of Aliyah Steele and VBF
  • Karenina – Advance, NC - in Honor of daughter, Juliana Grubb – VBF informational materials
  • Bianca Shemper – Hattiesburg, MS – VBF Stickers
  • Kathy Wyrick – Lake City, FL – Article in local paper and informational pamphlets
  • Jan and Andrew Dreger – 3rd annual Awareness Day Event at family
    owned/operated restaurant- Campbell's Boat House in Media, PA. Percentage of sales donated to VBF
  • JoAnn Campbell – Media, PA - Buddy Booby Birthmark Read Along to students at St. Cornelius School. JoAnn is a teacher in Chadds Ford, PA. Also, video montage shown to students of grandson Owen Dreger.
  • Rabbit Hill Nursery School – Springfield, PA - Buddy Booby Read Along to Owen Dreger's Pre-school class.
  • Vanessa Beall – Aptos, CA – Collection Box – In honor of Lillie Nichols
  • Christine Sylvester – Milwaukee, WI – postcard and sticker campaign to friends and family
  • Kathleen Miller – Slingerlands, NY – Lunch and Learn, collection box – In honor of Camryn Shea Miller

VBF Chapter Events

  • VBF Latin America - Andrea Domingues - São Paulo, Brazil - Medical Lecture – Each year Andrea hosts a meeting of People with Hemangioma and Linphangioma Brazil. The conference is organized by ABRAPHEL, a Brazilian association for people with Hemangioma and Lynphangioma. Andrea’s daughter, Gabrielle, has Proteus syndrome.
  • VBF India - Santo Banerjee – Kolkata, West Bengal, India – Writing an article in the local newspaper. Santo’s son, Sumangal, has SWS.
  • VBF Poland – Ewelina Ochab – plans pending
  • Sturge-Weber Syndrome Community (SWSC) – Lexington, KY - Tiffany and Glen Ethington – Tiffany and Glen have an annual interview on noon news to raise awareness. Glen has SWS/PWS and organized a newsletter and pen pal group for kids with birthmarks and their siblings/friends called “Glen’s Gang”.
    • Glenda Ethington , SWSC – distributing informational pamphlets to local hospitals/doctors.

 

It's never too late to register for the 2009 VBF International Day of Awareness. Our annual celebration for Awareness is on May 15, but events can be held at any time during the year. Join these dedicated families in supporting VBF and raising awareness for vascular birthmarks. Visit the VBF Day of Awareness website today for more details and to register your event. With your help, we are making a difference!
http://birthmark.org/awareness


Bags for Birthmarks

You can help to “Sponsor A Family” so that they can attend the VBF annual medical conference and receive a treatment plan. Donate a new or gently used high-end, vintage, or designer handbag or bid on one at www.birthmark.org. Both ways help! Tell your family, friends, or colleagues that they can help too by donating or bidding on a handbag

To donate a bag, click here, fill out the form, and mail it to us.

To get a bag, click here.


Welcome to the Poland Chapter of the Vascular Birthmarks Foundation, VBF Poland!

Hemangioma - informacje
Naczyniak „Plama wina port“- informacje (Port Wine Stain, naevus flammeus)
Znieksztalcenie zylne- informacja (Venous Malformation)
pokrewny warunki

Nasze Dzieci

Every year in the United States, 40,000 children are born with a vascular birthmark, 85% of which are in the head and neck area. Statistics show us that the incidence is the same in other countries. These birthmarks include:

No one knows why vascular birthmarks occur, but treatment guidelines are changing.


VBF Mark of Beauty Gala and 2008 Conference
a HUGE success

VBF took on a big task this year. It was our first ever gala in NYC (Mark of Beauty) at the Hudson Theatre in Times Square on Friday evening, November 14th. We also held our annual international conference the very next day at the Beth Israel PACC at Union Square. The responses from those who attended the gala and/or the conference were similar. Comments included such descriptors as “fantastic” and “phenomenal” and “one of the best galas I have ever attended” and “the most informative conference on vascular birthmarks” and so on. Almost overnight, we received over 30 thank you notes from families attending the conference and almost as many from individuals who attended the gala.

There were 285 attendees at the gala and 240 at the conference. We were privileged to have two “phantastic” performers – Gary Mauer and Beth Southard, stars of the Phantom of the Opera. They brought the house down with the finale song (Phantom), especially when they were joined in the finale with Christine Shannon and Stephen Dale.

Gary Mauer, Stephen Dale, Christine Shannon, and Beth Southard Barbara Rothaupt, VBF Ex. Asst. Basia Joyce, and VBF President 
              Dr. Linda

Gary Mauer (star of Phantom of the Opera) Stephen Dale, Christine Shannon and Beth Southard (wife and co-star of Phantom) after their spectacular performance at the gala

Barbara Rothaupt, VBF Ex. Asst.
Basia Joyce, and VBF President Dr. Linda

To read the entire story click here: http://www.birthmark.org/08gala.php


Dr. Roy Geronemus, VBF 2008 Physician of the Year

Dr. GeronemusRoy G. Geronemus, M.D., Director of the Laser & Skin Surgery Center of New York, graduated from Harvard University and pursued his medical education at the University of Miami School of Medicine.

He trained in Dermatology at the New York University Medical Center where he was the Chief Resident and subsequently underwent a fellowship training in Mohs Micrographic Surgery and Cutaneous Oncology. He is a Clinical Professor of Dermatology at the New York University Medical Center where he has founded its laser program and served nine years as its Chief of Dermatologic and Laser Surgery. He is also the Director of the Skin/Laser Division in the Department of Plastic Surgery at the New York Eye & Ear Infirmary. He is Past President of the American Society for Dermatologic Surgery and the American Society for Laser Medicine and Surgery. He has received the Ellet Drake award for outstanding contributions to laser medicine and the Leon Goldman award for excellence in clinical laser research. Dr. Geronemus has been a featured speaker of the American Academy of Dermatology, American Society for Dermatologic Surgery and the American Society for Laser Medicine and Surgery for many years, as well as speaking to other national and international audiences. He has published over 200 medical articles, chapters and books, including the most recent 2nd Edition of Illustrated Cutaneous and Aesthetic Laser Surgery.

An original forerunner in the application of the pulse dye laser for the treatment of port wine stains and other vascular birthmarks, he has been involved with the development of several new laser systems and therapeutic techniques, which are now commonly used throughout the world.

Dr. Geronemus is also the Chairman of the Board of the New York Stem Cell Foundation.

To make an appointment with VBF's 2008 Physician of the Year, please contact Jamie Giangrande, Executive Assitant at the Laser & Skin Surgery Center in New York by calling 212-686-7306 (Ext. 255) or by email at jgiangrande@laserskinsurgery.com Please visit their website at

www.laserskinsurgery.com


Port Wine Stains: Clearance, Cure, and Recurrence
To Treat or Not to Treat

The following rebuttal by Dr. Stuart Nelson and Dr. Roy Geronemus was published in the New England Journal of Medicine in response to an article about the recurrence of Port Wine Stains (PWS) after pulsed dye laser treatment. At this year’s conference in Irvine, several physicians spoke about the pathology, progression and treatment of PWS. To summarize what was presented, after a PWS is treated using the pulsed dye laser, the vessels that are targeted by the laser will not necessarily come back, but rather new, deeper vessels will work their way up to the top of the skin thus making “some” stain appear. It is important to understand this because many people believe that PWS will always come back and, therefore, they should not have laser treatment. This is not true. While the laser does not “cure” the PWS, it offers the most hope for clearance, for keeping the skin from thickening and cobbling and for maintaining the best aesthetic outcome for the patient (comment by Linda Rozell-Shannon, President and Founder of the Vascular Birthmarks Foundation, 11/8/07).

Comments from Dr. Stuart Nelson and Dr. Roy Geronemus:

"We reviewed “Redarkening of Port-Wine Stains 10 Years after Pulsed-Dye-Laser Treatment” by Huikeshoven et al (NEJM 2007;356:1235-1240) with great interest and would offer our comments.

Read more here


 

 

Parent's
Corner



Information for Parents

DOA Logo
Don't Forget!
Every Day is a Day of Awareness for VBF!
Visit the VBF International Day of Awareness Website:
birthmark.org/awareness


Good Search

What if the VBF earned a penny every time you searched the Internet? Now it can! GoodSearch.com is a new Yahoo-powered search engine, with a unique social mission... every time you use GoodSearch, money is generated to support the mission of VBF. Just go to www.goodsearch.com and be sure to enter the Vascular Birthmarks Foundation as the charity you want to support. The more people who use this site, the more money we'll earn so please spread the word! Go to http://www.goodsearch.com

If you think your child has a hemangioma Click Here...
hemangioma
If you think you or your child has a port wine stain Click Here...
Before and after of port wine stain
If you think you or your child has a venous malformation Click Here...
Before and after of venous malformation


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Publications for Parents:

  • VBF Vascular Birthmarks Brochure - Download and Print - A comprehensive brochure describing all vascular birthmark types, syndromes and treatment options. To print, click here (you will need the Acrobat Reader to view and print this document).
  • Doctor Visit Survey Have you been seen by a doctor to assess a vascular birthmark? Please click here and complete our survey. This survey will be used to provide feedback to the doctors about the information and treatment they provide to families affected by a vascular birthmark. Complete your survey and mail to Corinne Barinaga, VBF Director of Information Services, 17309 NE 29th St., Vancourver, WA 98682.
  • Before you visit, email, or speak to a birthmark specialist, be sure to read our Checklist for Parents!
  • Dr. Rosen's Vascular Birthmark Information for Parents
  • Simple things you can do to manage KTS (Dr. Delfanian and Linda Shannon)

You will need Adobe's Acrobat Reader to open and print the pdf documents. If you do not already have it installed, you can find it here.

You will need Microsoft's Word to open and print the Word Documents.

RECRUITING SUBJECTS FOR A RESEARCH STUDY ON FACIAL BIRTHMARKS