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  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.
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Search: Posts Made By: lorenzo1977
Forum: Port Wine Stain Help and Resources 02-01-2010, 12:07 AM
Replies: 7
Views: 8
Posted By lorenzo1977
Thank you Missy for clearing up some doubts I...

Thank you Missy for clearing up some doubts I might have had.

I greatly appreciate what VBF does. I currently live with a pws on the right said of my face, so I can relate very well with the...
Forum: Port Wine Stain Help and Resources 01-29-2010, 04:14 PM
Replies: 7
Views: 8
Posted By lorenzo1977
Is there any reason why VBF cannot offer...

Is there any reason why VBF cannot offer financial assistance?

Just trying to figure out why VBF would be a good charity to donate and raise money for?

Thank you for your quick response and time.
Forum: Port Wine Stain Help and Resources 01-29-2010, 02:20 AM
Replies: 7
Views: 8
Posted By lorenzo1977
More Information on VBF..

Hi, I would like more information on VBF. Mainly I would like to know if this foundation also supports Canadian families, and is support limited to information only or does VBF also support the...
Forum: Port Wine Stain Help and Resources 01-27-2010, 04:10 AM
Replies: 62
Views: 6,101
Posted By lorenzo1977
Hi mine is on the right side of my face.. I'd...

Hi mine is on the right side of my face..

I'd just like to say that this forum is pretty amazing.. I'm 32yrs old & for most of my life I thought I was the only one with a PWS.. I know sounds...
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