before and after of hemangioma before and after of PWS before and after of venous malformation before and after of AVM before and after of lymphatic malformation CMTC sturge-weber syndrome kts PHACE

Expert's Corner

Ask The Vascular Birthmark Expert
Dr. WanerVBF is proud to announce that Dr. Waner, the leading birthmark surgeon and treatment specialist will be answering emails regarding birthmark treatment.
Ask the PWS Expert
Dr.Nelson VBF welcomes Dr. Stuart Nelson of the Beckman Laser Institute as another one of our medical experts. Dr. Nelson will answer your questions concerning the diagnosis and treatment of Port Wine Stains.

Ask the Surgeon
Dr.LevitinMeet Dr. Gregory Levitin, partner to Dr. Milton Waner. Dr. Levitin will answer your questions regarding the surgical treatment of all vascular birthmarks and tumors. VBF's Ask the Surgeon!

Ask the AVM Expert
Dr. BerensteinVBF is proud to have the world renown expert, Dr. Alex Berenstein as its expert in AMVs. Send your questions concerning AVMs to him.
Ask the Wound Care Expert
Dr. SerenaVBF is proud to add Dr. Thomas Serena as our wound care expert. Please send Dr. Serena your questions regarding wound care for an ulcerated hemangioma or other vascular birthmark, tumor, or syndrome that requires wound care.
Ask the KTS Surgery Expert
Dr. GiangolaVBF is proud to welcome Dr. Giangola of NYC as our KTS surgical expert. If you have questions concerning the surgical treatment of KTS or other vascular lesions of the arms, legs, or trunk, contact him.
Ask the Lymphatic Malformation Expert
Dr. EdmondsVBF is proud to announce the addition of an expert who treats Lymphatic Malformations. Ask Dr. Edmonds your questions related to this vascular lesion.
Ask the Military Surgeon
Dr. ThompsonVBF is proud to welcome Dr. Steve Thompson as our Military surgeon to answer questions about vascular birthmarks to our military families. He is currently working with Dr. Waner in NYC.
Ask the Eye Specialist
Dr. FayDr. Aaron Fay joins VBF as our eye specialist VBF's Eye Specialist will answer questions concerning eye problems and birthmarks.
Ask the Research Expert
Dr.MihmVBF is proud to showcase Dr. Martin Mihm, Jr. as our Research Expert. Dr. Mihm is coordinating and directing research regarding vascular birthmarks and tumors.
Ask the AVM and Extremities Expert
VBF Welcomes Dr. Bob Rosen as our expert for all non-brain AVMs and vascular lesions of the arms and legs. Dr. Rosen welcomes your questions concerning these lesions.
Ask the Internal Lesions Expert
Dr. FishmanVBF is proud is welcome Dr. Steven Fishman of Boston Children's Hospital as our Ask the Internal Lesions Expert. Ask Dr. Fishman your questions about liver and other internal vascular lesions.
Ask the Doctor in Spanish, Portugese, or Italian
VBF is excited to have a multilingual expert. Dr. Piris is from Boston and can answer your questions in Spanish, Portugese, and Italian and of course English. Please send your questions concerning your vascular birthmark or tumor to Dr. Piris.
Ask the Interventional Radiologist
Dr. KonezVBF is proud to add Dr. Orhan Konez as our expert Interventional Radiologist. Questions regarding reading and interpreting films and treating malformations with sclerotherapy or embollization can be sent to Dr. Orhan Konez.
Ask the European Surgeon
Dr. TomrisVBF is proud to add Dr. Tombris as a European surgeon expert. He treats all forms of hemangomas, port wine stains and malformations.
Ask the SWS Expert
Dr. ComiVBF is proud to announce that Dr. Anne Comi, one of the leading experts on Sturge Weber Syndrome will be responding to your questions concerning this syndrome. Read more about Dr. Comi and ask her expert advice on SWS.
Ask the KT Expert
Dr. DelfanianVBF is proud to welcome Dr. Delfanian as our Klippel-Trenaunay expert. Send your questions concerning KT Syndrome to Dr. Delfanian.
Ask the PHACES Expert
Dr. MetryVBF is proud to welcome Dr. Denise Metry as our PHACES expert. If you have any questions regarding this syndrome, please ask Dr. Metry.
Ask the Laser Doctor
Dr.AstnerVBF is proud to offer to our families a new service. VBF's Ask the Laser Doctor offers expert advice on laser treatments for all vascular birthmarks by Dr. Susie Astner.
Ask the Doctor's Expert
Dr. WilliamsVBF is proud to announce that Dr. Edwin F. Williams III will be answering emails from physiciansregarding the diagnosis and treatment of individuals with a vascular birthmark.
This form is intended for physicians ONLY. Parents who need assistance should ask an expert. Only physicians will receive a reply.
Ask the Pharmacy Doc
Helen FiggeVBF is proud to offer the services of a Pharmacy Doc who worked for many years at a Vascular Birthmarks Clinic. If you or your child has a vascular birthmark and you have a question regarding a prescription drug, please ask Doc Helen Figge.
Ask the Airway Expert
Dr. MouzakesVBF is proud to announce that Dr. Jason Mouzakes from Upstate New York has joined us as our airway expert. Email Dr. Mouzakes with questions regarding airway hemangiomas and other vascular lesions in the airway (throat area).
Ask Dr. Linda, VBF's President and Founder
Ask the VBF FounderVBF Announces "Ask Dr. Linda." Dr. Linda Rozell-Shannon is the leading lay expert in the world on the subject of vascular birthmarks.
Ask the CMTC Expert
Lex van der Heijden, Chairman, CMTCVBF is proud to have Lex van der Heijden, Chairman, CMTC, as our Cutis Marmorata Telangiectatica Congentica expert. If you or your child has CMTC, please contact Lex with your questions.
Ask the CMTC Doctor
VBF is proud to announce the addition of Dr. Marilyn Liang of Boston Children's Hospital as our Ask the CMTC expert. Send your questions regarding CMTC to Dr. Liang
Ask the Insurance Appeal Expert
Barbara JoyceVBF is proud to add Barbara (Basia) Joyce as our insurance appeal expert. Please send your questions regarding your appeal or request for out-of-network treatment to Basia.
Ask the Family Services Expert
VBF is proud to have Corinne Barinaga, our Administrative Director, to answer emails concerning family advocacy or treatment issues.
Ask the Developmental Specialist
Elissa Uretsky- Rifkin, M.Ed. CMHC is a trained developmental specialist and is on the board of VBF. Send questions concerning hemangiomas and this topic to Elissa  
Ask the Developmental Specialist
Leslie is a trained developmental specialist. Send questions concerning port wine stains and this topic to leslie    
Ask the Adult Rep in Spanish
AliciaVBF is proud to add Alicia as our Adult with an AVM who can translate your spanish questions to one of our docs and can answer back to you in spanish.
Ask the Makeup Expert
Ask the Makeup ExpertVBF is happy to provide you with an expert opinion regarding the use of make-up to cover a birthmark. Ask our expert Nancy Roberts, Co-Creator of Smart Cover Cosmetics (www.smartcover.com), your questions about make-up.

Contact the Oral and Dental Experts


Physician to Physician Case Study Forum created by Dr. Orhan Konez

High Risk Pregnancy Expert

If you are pregnant and have a vascular birthmark, tumor, or malformation, and have any concerns about your pregnancy, contact Dr. Rebarber.

Dr. Andrei Rebarber
70 East 90th Street
New York, NY 10128 (Corner of 90th and Madison) 2nd Floor
(212) 722-7426
(212) 722-7409

 

VBF NEEDS LANGUAGE TRANSLATORS - SPANISH, PORTUGESE, AND ASIAN LANGUAGES

Babies with Birthmarks™

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

Recent Medical Papers and Research

VBF has a great deal of research available, including a bibliography for offline research.

Ask the Adult Rep in Spanish

 

AliciaI was born in Cuba on June 14, 1950. I took more than a month before my father and mother noticed the big red mark I had on my left ear and scalp.

Suddenly the great happiness of having their first child turned into worry and sorrow. I had been born with a malformation they did not know what it really was. My mother cried every night in the bathroom hiding from my father. She was totally devastated.When my dad found out and told my mother it was a birthmark that is was a benign tumor and that at the moment science did not know how to treat it , just had to be left alone and that eventually it will go away. Years went by and it did not go away, it grew and changed color. My father, as a doctor, consulted every dermatologist, and every pediatrician he could reach in Cuba and Spain, and they all told him the same; ‘Watch and See’ for my dad this meant NO HOPE!I became an overprotected child by my father, when we went to the beach, he put a hat on my head and I had to stay under a palm tree. I could only get into the water early in the morning or late in the afternoon when the sun was milder. I watched my friends play in the water and shed many tears, many times. I guess that is the reason why I now hate the beach.As a young child and teenager I refused to comb my hair up in a ponytail because everybody stared at me and asked, with a terrible pitiful tone, if I had been burned or hurt, sometimes they asked too many questions that made me cry and even hate the world!
My dad combed my hair in a ponytail and forced me to face the situation, responding to those questions that it was a birthmark, that it was given by God so I would not get confused if lost with another similar girl with the same name and looks. I believed him and for many years to come I responded in the same manner. Now is different, the years and the cruel attitude of people made me tougher and indifferent to their curious questions about this red and bulky stain I was born with and which I hated with all my soul. I prayed for years and made promises and Novena and so God will make it go away. My dad in a way became my hairstylist, he had to approve of the ribbons, rubber bands or anything that I used on my hair, no direct sun to hit me, I had to wear a hat, etc.

As I grew up and my permanent teeth were coming out I bled during the night and many nights I woke up to a bed soaked with blood, because I had some of this malformation on my gums. When I bled, I was taken to the doctor and they ran lab. tests for internal bleeding but they all came back negative. Doctors, including my Dad, could not believe the great amount of blood it usually came out of my ‘Hemangioma’.In 1961 when I was 11 years old and my brother seven we were sent alone to the United States with the Catholic Church to escape Communism. We came without our parents, the group was known as "PETER PAN" My father was a physician, a Pediatrician and my mother a Pharmacist and a Registered Nurse.

They could not leave Cuba at the time for political reasons, they were opposed to the New Revolution’s lack of freedom and declared atheism also Castro did not let any professional in the Medical field to leave the island either, so we really believed we will never see our parents again. They were desperate not only because we were away in a strange land but mainly because of my Birthmark condition.We were taken care by Dr. Novak and his wife of Alexander City, Alabama while our parents were trapped and trying to escape the island. We did not speak any English. It was truly traumatic. We were being temporarily adopted by a really rich, caring and good-hearted family that I could not tell them of my ear and scalp and the bleeding, because they spoke no Spanish and we Spoke No English. A nightmare! My brother cried all the time. I did too when he felt asleep. The more I cried the more the 'Hemangioma' on my scalp and ear became deep red, and dilated, it became very hot with fast pulsations. I thought it was going to explode and I will bleed to death.Through my life I have suffered episodes of bleeding, but this time not of the birthmark on the ear and scalp, but of my throat and gums, that is when we found out the birthmark extended to the right side of the throat and left side of the gums in the back.
In 1971 I was a student at the University of Puerto Rico, and while on a study trip of Modern Art to New York City, blood came out of my throat I had to return to San Juan, because I was bleeding so much it became a hemorrhage. The doctors in Puerto Rico did not know what to do. The ENT doctor, my dad and the Emergency room doctor were amazed at the great amount of blood coming out of my throat. The cans stop the bleeding with a coagulant injection direct to my throat, something the Doctor has never done before.

By this time I was a traumatized young woman with is a terrible feeling of being alive with the uncertainty that next day I could be soaked in blood and dead, before my time.
I learned how to live fast and passionately, The AVM ruled my life, deep down inside I was always sad and anxious, as waiting for something bad to happen at any moment, not knowing where to go, whom to talk to or what to do. It was a desperate feeling of impotence and frustration.

In 1981 I had my only son, he was 9 pounds 15 ounces, a really big baby for me. He had to be born by C-section. The last month of my pregnancy I had terrible pain in my throat. Nothing helped me. The doctors did not know why. Ten months later, I started to bleed from the right side of my throat, the blood came out with a lot of strength and it was constant. As I had to swallow all that blood, my stomach became very upset, I felt like I was having or rocks inside, I coughed and the bleeding became worse. I lost 26 pounds in three weeks, I cried every day, I did not have the energy to open my eyes, I thought I will die.
I started to pray and pray, and one morning I had the impulse to open the Phone Directory
Under Ear, Nose and Throat doctors for the University of Miami School of Medicine there I found listed an ENT Professor Dr. Antonio Jose Maniglia. I went to see him. He treated me with Lasers. He was successful and the bleeding stopped.


In 1995 the AVM on my left ear started to grow, it bled sometimes. I started to see every six months Dr. Goodwin at the University of Miami, and ENT oncologist, Chief Doctor of the University Sylvester Center, he said nothing could be done, just watch and see. The growing continued and by 2005 it bled so much again I lost my mattress and pillows. I began to worry a lot. I felt miserable.

One afternoon in 2005 I was reading ‘SELECCIONES’ that is READERS DIGEST in Spanish and found out about Dr. Waner and his miraculous surgeries on Hemangiomas and AVMS, I started to look for him on the Internet and found the VASCULAR BIRTHMARK FOUNDATION. Immediately I sent Dr. Gregory Levitin an Email
With some pictures of my ear and scalp. Days later he mailed back telling me. S I did not have a HEMANGIOMA that
It was an ARTERIOVENOUS MALFORMATION. Wow! was I confused, he explained that they were related but they had different treatments and that I needed a plan. His words finally gave me hope.
On June 26th. 2006 I arrived in New York City with an MRI and my heart full of joy and sorrow at the same time, it was a difficult feeling to express, I wanted to tell the Dr. Waner and Dr. Levitin before they said anything, if they could help me or not, how much I have suffered, how my father died in 1991 with the immense worry of not being able to help me find a cure, of how this Birthmark had ruled my life and how much it had affected me emotionally, socially and spiritually. They told me they could help me, that they could remove the AVM with minimal risk. I felt I was given back the opportunity to be born again normally this time, a last chance, a final solution to all my life worries. I will never forget Dr. Waner and Dr. Levitin faces, their smile, their support, specially from Dr. Levitin, since then, I guess I am bonded to them for life. On November 14, 2006, I went to surgery at Roosevelt Hospital with a unique team of doctors, it was difficult for me and for them too, but I went with faith in God and in all of them, they knew I trusted them 100%.
First Dr. Waner told me he will not open my scalp, that he will only remove my ear growth but a different story was when in the surgery room they saw that my arteries where so dilated that they had to open my scalp and fix them. if I was to live longer, my heart could not tolerate for many years the big effort to pump all the blood in the condition my arteries were.
I became a challenge at that point, entubation was also another delicate problem, since I had an Experimental repaired done with lasers to my airways in 1983 nothing could disturb it because there was a high risk that my throat could bleed again. Seven days later I was on a plane back to Miami.
Well I made it, the doctors made it, I am now cured !
My heart is full of gratitude to all the doctors, nurses, and Dr. Waner’s office staff for all their love, their caring, their patience and tolerance with me and my condition.

My eyes fill with tears when I remember Esma, Cheryl, Sonya, Dr. Alejandro Berenstein, Dr. Waner and most of all Dr. Gregory Levitin. I am compromised because of them, because of what they did for me, because of my life suffering. I need to give something back of what God and they gave me and the best way is to help others have hope, and strength to find a cure to fight back any obstacle; because it is the only way to finally be FREE!

Notes: For any of our medical experts to give you an expert opinion, please give details such as age of person you are inquiring about, location of lesion, when it first appeared, any treatments, if it has grown or if it has shrunk in size since it first appeared. Also include any previous treatments and if it has bled or ulcerated.

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Make Your United Way Pledge to VBF


Go GREEN and Support VBF! Vascular Birthmarks Foundation is partnering with Recycling for Charities, a non-profit organization aimed at reducing electronic waste. By donating your old cell phones, pagers, and other electronic devices you have the unique opportunity to help keep the environment clean and support VBF at the same time! Please click here to learn more about this exciting program and remember to designate VBF as your charity of choice.
Visit www.CaringBridge.org CaringBridge is a free, nonprofit web service that connects family and friends to share information, love and support during a health care crisis, treatment and recovery. Tell a Friend about CaringBridge.

VBF NEEDS LANGUAGE TRANSLATORS - SPANISH, PORTUGESE, AND ASIAN LANGUAGES

If you can volunteer your time to translate VBF's key informational pages into one of the above mentioned languages, or in any other language not indicated, contact VBF President and Founder Linda Rozell-Shannon at hvbf@aol.com. There are approximately 24 key pages. Please put "Language Translation" in the subject line. This is very important for our families all over the world to be able to have the highest quality of information and to have it in their own language. We can make a difference, but we need your help to continue to help families all over the world that are affected by vascular birthmarks.

How to Appeal an Insurance Denial or
Request Out-of-Network Treatment
(pdf)

The Catalanotto FamilyPlease join the VBF and Texas Rangers outfielder Frank Catalanotto and his wife Barbara as we team up to strike out vascular birthmarks!

Donna and Evan Ducker and Buddy Booby Make it Big...

CBS Early Show

VBF Gets Referenced in Buddy Booby Birthmark Articles

CBS Early Show

Information for Parents

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

Information on syndromes associated with vascular birthmarks

Multifocal Lymphangioendotheliomatosis with Thrombocytopenia
Read about Jadyn's Journey with this rare vascular syndrome

Multifocal Lymphangioendotheliomatosis With Thrombocytopenia
A Newly Recognized Clinicopathological Entity

Article Located at Archives of Dermatology

Multifocal Lymphangioendotheliomatosis With Thrombocytopenia:
A Rare Cause of Gastrointestinal Bleeding in the Newborn Period

Article Located at Pediatrics

Please Note:
Dr. Waner's Office Has Moved To:
Vascular and Birthmark Institute of New York
126 West 60th Street
New York, NY 10023
Contact Clinical Coordinator directly at:

Corey R. Tournay, R.N., Clinical Coordinator
Vascular Birthmark Institute of New York
126 West 60th Street, Ground Floor
New York, NY 10023
Tel: 212-636-3977
Fax: 212-636-3979
CTournay@chpnet.org

If you have an appointment or are trying to make an appointment please make sure you know that he is now at a new location but still in Manhattan.

VBF is Making a Difference

What Our Families Are Saying



75 Minute Miracle - Anna before and after surgery done by Dr. Waner in 75 minutes

Chapters of the VBF

VBF
VBF Europe
VBF Latin American
VBF New Zealand
VBF Australia
VBF India
VBF Africa
VBF Asia
Sturge-Weber Syndrome Community
SWSC-Canada

Partners

Anomalie Vasculaire Site for French speakers worldwide, and friend of VBF that offers support and information about vascular birthmarks

Participate in our Annual Day of Awareness
Pariticpate in our Annual Book Reading of Buddy's Booby Birthmark Book
Participate in our Kids Who Care Program
Participate in Glens Gang newsletter for kids with birthmarks

See Dr. Waner in Europe
If you are a patient of Dr. Waner's, we are in need of before and after photos. Click here.

YOU CAN HELP - PARTICIPATE IN VARIOUS VASCULAR BIRTHMARKS STUDIES
Research Studies

New! Our list of research studies for vascular birthmark related research.

Low-Dose Aspirin Study for people with SWS

NEW PHACES Study

PWS Study

Use of the Atkins diet for children with Sturge-Weber Syndrome

PHACE Syndrome Registry. Parents of children with PHACE Syndrome registry

The Effect of Facial Hemangiomas on Psycho-Social Development

 

Publications for Parents
Find helpful documents for families

MAKE UP FOR BIRTHMARK COVERING
Nancy Roberts of www.smartcover.com will send anyone who wants to cover a birthmark a gift certificate. Write directly to our Ask the Make-up Expert on our experts corner and receive a free gift certificate for $15.00 towards the purchase of any Smart Cover make up product.


Read Kay's Story (VBF Europe Rep)
Kay before SmartCover and Kay after SmartCover
Make-up by Stacey Craven
Aesthetician/Makeup Artist

Do you have any suggestions to improve the services we offer to our VBF families? Send us your comments and suggestions!

Christine, today Linda Rozell-Shannon and her daughter Christine- The Founder of VBF Tells Her Personal Story

Meet the Webmistress
Missy Scott
Missy has worked with VBF for seven years and is responsible for all technical and design issues of this site. If you have a question or concern about VBF's website, please contact her.

Nevus Clinic (Non-Vascular Birthmarks) Starts at Mass. General Hospital
Dr. Martin Mihm and his team will be seeing patients with congenital nevus (giant hairy, moles, pigmented lesions, etc.) and all other non-vascular birthmarks (Mongolian spots, Spitz Nevus, etc.) in addition to Vascular Birthmarks, at the Saturday clinics at the Mass. General Hospital in Boston. Dr. Mihm is combining the Vascular Birthmarks Clinic with the Congenital Nevus clinic to form the first combined vascular and non-vascular birthmarks clinic. Linda Shannon will be the clinic coordinator at these combined clinics. This clinic is for adults and children. To schedule an appointment, call Andrea at 617-724-1350.