Dr. Jay Burns - Vascular Birthmarks Foundation Forum
  Vascular Birthmarks Foundation Hemangiomas  |  Port Wine Stains  |  Vascular Malformations  

1994 - 2014 Celebrating 20 years with 75,000 networked into treatment, over 3,000,000 views monthly on our world wide websites, virtual chapters on 6 of the 7 continents in the world, 500 families provided free lodging while seeking a medical opinion or treatment,over 400 conference scholarships awarded, 200 Day of Awareness events, 15 conferences, 12 programs (including our Ask/Accept Anti Bullying Program),10 walk/runs, 6 research projects funded, 4 physician education grants awarded, 4 college scholarships awarded, 3 Galas, and 2 International Missions Trips with over 300 treated by our international team.
Donate to VBF

Go Back   Vascular Birthmarks Foundation Forum > Port Wine Stain Help > Port Wine Stain Help and Resources

Reply
 
Thread Tools Display Modes
  #1  
Old 06-30-2003, 05:43 PM
hismommmy
 
Posts: n/a
Default Dr. Jay Burns

???Hi, I wanted to see if anyone had ever used Dr. Burns in Dallas? We were accepted to Children's Medical however things are not going very smoothly there so we're looking for someone new. My son has a PWS on his left cheek. I'd appreciate any help you can give.
Thanks so much,
Erin
Reply With Quote
  #2  
Old 07-11-2003, 07:03 PM
mamalamb
 
Posts: n/a
Default Re:Dr. Jay Burns

Hi Erin,

We use Dr. Burns and have nothing but good things to say about him.
If you would like to speak to me privately with any questions and concerns I would be
happy to speak with you. Contact me at: mamalamb@hotmail.com

Reply With Quote
Reply


Thread Tools
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
Newborn with PWS/Dallas area momtotrips+1 Port Wine Stain Help and Resources 12 03-15-2011 12:36 AM