VM and Dr. Levitin - 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 > AVM Help > AVM Help and Resources

Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 07-06-2012, 09:11 PM
mom s mom s is offline
Junior Member
Join Date: Feb 2008
Posts: 7
Default VM and Dr. Levitin

hello, we are scheduled to go and see Dr. Levitin for surgery for my daughter who has a VM on her right cheek and lower lip in a few weeks. I was hoping maybe someone could share their story about Dr. Levitin and if you were happy with how things went and where you are now. Being that it is getting closer I am freaking out a little bit, but I know it is the right thing to do for our daughter.

I am also struggling with insurance and what will be covered. Dr. Levitin's part will be but she will also be having sclerothearapy injections first by Dr. Niimi and this part will not be covered. Does any know about insurance and how I can go about getting this part covered as well??

Thank you in advance for any advice and sharing of stories
Reply With Quote

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