He's here on The Plinth raising awareness of Congenital Heart Disease and adding to his walking total.
WELL DONE PAUL! YOU'RE A STAR!
Paul Willgoss - The Walker with Heart
Monday, 10 August 2009
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A life unlimited........
Originally this blog was all about my youngest child Emily, who was born with a rare congenital heart defect called ALCAPA. It began as a means of putting her story down on 'paper'. That part begins here but as often happens I went off on a tangent...............
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COPYRIGHT NOTICE
All original photographs on this site remain the property of IMAGEmily and the author.
Copyright IMAGEmily 2009. All rights reserved.
Copyright IMAGEmily 2009. All rights reserved.
1 comments:
Hi Jackie and Emily. Thank you, Jackie, for your comment on my son's blog (jerry's little heart). I have just finished reading your entire blog...oh my! I am aching, crying, and in shock for all that you have gone through. I am realizing more and more how detached I am from the horror of what we have been through with JJ. Although you must have been bored reading ours after all you have gone through. I feel like I was feeling so much more reading your blog than I have felt in our own situation...make any sense? I am so glad Emily is doing well..she is beautiful and the photos you girls take...amazing! I would love to email with a few questions I have if it is possible...mine is suezchi@comcast.net Thank you thank you thank you...you are the first person I have "met."
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