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Go Back   Vascular Birthmarks Foundation Forum > Hemangioma Help > Help and Resources for Hemangiomas

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  #1  
Old 04-23-2009, 09:56 AM
asya asya is offline
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Join Date: Dec 2007
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Hi,

I have a son ,20 months old,has a Hemangioma on his hand.

I would like to ask if there is any link/thread in the forum about sharing websites or blogs.
I would like to read other moms/dads writings about their lifes and experiences

Thanks

Last edited by asya : 04-23-2009 at 10:06 AM.
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  #2  
Old 04-23-2009, 12:29 PM
jgoodman0814 jgoodman0814 is offline
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your more than welcome to see our site. click on the link below.
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Jessica Ball
www.caringbridge.org/visit/avaball
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  #3  
Old 04-23-2009, 07:37 PM
madison'smom madison'smom is offline
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I just made a slideshow of my daughter's Hemangioma journey. You can check it out. http://picasaweb.google.com/szander4...78571155758642
Stacey
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  #4  
Old 04-24-2009, 04:38 PM
nickbar nickbar is offline
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On the msnvb support group site, we have a section (under links) that have personal website, stories.

www.msnvb.org
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