New blog to share

Thanks to little miss mayhem, i've had the privilege of meeting this wonderful, very supportive and always helpful lady named Debi. Debi and Taylor both have congenital upper extremity amputations. Taylor's on the left and Debi's on the right. We first met when Taylor was about 4 months old, minutes after Taylor received her first prosthetic arm. Debi shared a glimpse into her life from birth to present and I left that day knowing without a single doubt that Taylor would grow up strong and always be able to do anything and everything she put her mind to. I love being able to get her feedback on things. Generally I really only have the insite of other parents of children like taylor who have been in my shoes, I don't often, or ever usually, get to hear and see things from the amputee's perspective. Debi has shared her experiences as a child, teen, adult, mom and now grandma. She's been through it all and then some i'm sure. With '1/2 a century' of knowledge and experience, Taylor will always be in great hands with Debi around. That said, Debi has started a blog so that she can reach out and help and educated even more people. She just started it a few days ago so there are only a couple posts so far but i'm truly looking forward to her posts to come. Her blog is called
Single-handed Solutions and the site link is:
 www.singlehandedsolutions.blogspot.com 

Enjoy!

-- Sent from my Palm Pixi