Expert's Corner
Ask The Vascular Birthmark
Expert VBF
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
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
Meet
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
VBF
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
VBF
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.
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Ask the KTS Surgery Expert
VBF
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 VBF
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
VBF
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.
Aaron Fay joins VBF as our eye specialist VBF's Eye Specialist will answer
questions concerning eye problems and birthmarks. |
Ask the Research Expert
VBF
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 VBF
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 VBF
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
VBF
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
VBF
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
VBF
is proud to welcome Dr. Delfanian as our Klippel-Trenaunay expert. Send
your questions concerning KT Syndrome to Dr. Delfanian. |
Ask the PHACES Expert
VBF
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
VBF
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
VBF
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
VBF
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
VBF
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 VBF
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
VBF
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 VBF
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
VBF
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
VBF
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
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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™
Our
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
I
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!
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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)
Please
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...

If you think you or your child has a port wine stain Click
Here...

If you think you or your child has a venous malformation Click
Here...
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
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!
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.
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