Read Imogen's story of survival at www.imogendyson.co.uk - Imogen was born on 9th April 05 with a Congenital Diaphragmatic Hernia. Against the odds, Imogen defied the challenge set before her and to the amazement of many people is thankfully with us today. Imogen's site is aimed at parents diagnosed with CDH or other conditions causing uncertainty, with the hope of offering optimism and encouragement to others. We always welcome mail to lindseyandimogen@aol.com
WOW. I cannot beleive just how grown up she is now! Going to school and everything! Looking back at those photos of her as a tiny dot, really does remind me just how poorly she was. What a fighter.. all the staff from NNSU still refer to Imogem as the miracle baby. And they love to get the updates from you. Thank you for those... keep them coming. Its fantastic to see her doing so well. Alison. S/N @ NNSU
3 comments:
What a big girl in her school uniform!
A beautiful redhead! I am also a redhead, so I am naturally drawn to that spirit. :)
I ran across your blog from another CDH blog. My son, Carter, was born Oct. 7, 2008 in the U.S. with a left sided CDH.
Reading stories of older CDH children and seeing how well they are doing is very encouraging.
-Kellie
WOW. I cannot beleive just how grown up she is now!
Going to school and everything!
Looking back at those photos of her as a tiny dot, really does remind me just how poorly she was. What a fighter.. all the staff from NNSU still refer to Imogem as the miracle baby. And they love to get the updates from you. Thank you for those... keep them coming.
Its fantastic to see her doing so well.
Alison. S/N @ NNSU
Post a Comment