This blog is intended for Bardet-Biedl grandparents and other family members, although friends and BBS folks are welcomed, too. I want this blog to help family members with the challenges and victories that are a part of having a loved one with BBS. See previous articles, research and other helpful links below right side.
Blog Author
Teresa Scruton
Sunday, November 6, 2011
PS
I just realized... I have 2 blogs: this one, and another for my condition: Hereditary Angioedema Type III, and my signature on that one is now used on this site... so if that seemed confusing, that's why. I'm no techno-whiz, that's for sure!
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