ittybittyblog.wordpress.com
CDH-Info | Ittybitty Blog
https://ittybittyblog.wordpress.com/cdh
A place to share our life with family and friends and to help raise awareness and hope for babies born with Congenital Diaphragmatic Hernia (CDH). Many hospitals aren’t equipped to treat CDH babies. They either don’t have surgeons who can perform the hernia repair surgery or they don’t have an Extracorporeal Membrane Oxygenation machine ( ECMO. In Portland for our son’s birth and care. CDH Info from Children’s Hospital of Minnesota. CDH Info from Cincinnati Children’s Hospital. This website is for people...
ittybittyblog.wordpress.com
Grace’s Braces | Ittybitty Blog
https://ittybittyblog.wordpress.com/2014/01/16/graces-braces
A place to share our life with family and friends and to help raise awareness and hope for babies born with Congenital Diaphragmatic Hernia (CDH). January 16, 2014. Grace’s smile changed yesterday. She got braces. I’ve never seen anyone so excited to get braces on. She counted down for days and then in the last 24 hours all she said was “this is the last time I’ll do ‘. She already had such a pretty smile. Now it’s brighter and shinier…. Laquo; Previous post. Grandma Annie says :. Enter your comment here.
ittybittyblog.wordpress.com
Get Up. It’s Gameday. | Ittybitty Blog
https://ittybittyblog.wordpress.com/2013/10/26/get-up-its-gameday
A place to share our life with family and friends and to help raise awareness and hope for babies born with Congenital Diaphragmatic Hernia (CDH). October 26, 2013. Get Up. It’s Gameday. Laquo; Previous post. Next post ». Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. While we try to teach. Crook...
ittybittyblog.wordpress.com
Ittybitty Blog | A place to share our life with family and friends and to help raise awareness and hope for babies born with Congenital Diaphragmatic Hernia (CDH) | Page 2
https://ittybittyblog.wordpress.com/page/2
A place to share our life with family and friends and to help raise awareness and hope for babies born with Congenital Diaphragmatic Hernia (CDH). October 25, 2013. We went with Grandma and Grandpa to a nearby pumpkin patch…the same one that Danny and I used to go to as kids on class field trips. I think we hurried along the loose tooth that Owen has been working on for the past couple of weeks. It was a gorgeous day! October 23, 2013. Grace’s First Hunting Trip. October 21, 2013. October 20, 2013. The g...
colefamilymoments.blogspot.com
Cole Family Moments: A Most Awesome Day!!
http://colefamilymoments.blogspot.com/2010/07/most-awesome-day.html
It's the little things in our life that make it so special! Wednesday, July 14, 2010. A Most Awesome Day! Tom, Jaime, Sheryl, Jared, Beth, Katie, and Andy. The Trost family from Ohio is on a road trip to see family in Florida, and on their way south they stopped for a visit with us in NC. What a great time we had! Two Miracles on Wheels! July 16, 2010 at 10:28 AM. What an awesome visit! We so wish we could have made it. Tell us what you think! Subscribe to: Post Comments (Atom). View my complete profile.
jrgfoundation.blogspot.com
The Jack Ryan Gillham Foundation: It's Been Awhile
http://jrgfoundation.blogspot.com/2010/02/its-been-awhile.html
The Jack Ryan Gillham Foundation. To live in the hearts of those we leave behind is not to die." Thomas Campbell www.JACKRYANGILLHAM.ORG. Friday, February 12, 2010. It has been quite a while since we have updated the blog! We have lots of exciting things planned for 2010! We are hosting a poker run with a bit of a twist late this Spring that is sure to be lots of fun! In addition to those events we are doing a couple of new fundraisers this year. On March 1st we are launching " Every Penny Counts. Wyatt ...
jrgfoundation.blogspot.com
The Jack Ryan Gillham Foundation: February 2010
http://jrgfoundation.blogspot.com/2010_02_01_archive.html
The Jack Ryan Gillham Foundation. To live in the hearts of those we leave behind is not to die." Thomas Campbell www.JACKRYANGILLHAM.ORG. Wednesday, February 17, 2010. It's All About the Location. As I mentioned before, the Every Penny Counts fundraiser will kick-off on March 1, 2010. Our goal is to raise $2,000 in six weeks and I think we can do it! Here is a list of participating locations. Briar Patch Bridal and Formal Wear. Nationwide Insurance – Cheryl Gorton-Long. Clinique – NWA Mall. We are hostin...
jrgfoundation.blogspot.com
The Jack Ryan Gillham Foundation: June 2009
http://jrgfoundation.blogspot.com/2009_06_01_archive.html
The Jack Ryan Gillham Foundation. To live in the hearts of those we leave behind is not to die." Thomas Campbell www.JACKRYANGILLHAM.ORG. Monday, June 29, 2009. Golf Touney and Updates. I would like to take a minute to thank everyone involved in The 2nd Annual Jack Ryan Gillham Memorial Golf Tournament. It would not have been possible without the players, sponsors and volunteers! We also had a great silent auction and would like to thank the people/companies that donated items to that! We are so grateful!
jrgfoundation.blogspot.com
The Jack Ryan Gillham Foundation: CDH Awareness Day and Other Stuff
http://jrgfoundation.blogspot.com/2010/04/cdh-awareness-day-and-other-stuff.html
The Jack Ryan Gillham Foundation. To live in the hearts of those we leave behind is not to die." Thomas Campbell www.JACKRYANGILLHAM.ORG. Thursday, April 1, 2010. CDH Awareness Day and Other Stuff. A big thank you to everyone who wore turquoise in honor of CDH Awareness Day. A few of Jack's fans sent pictures of themselves wearing turquoise yesterday. And tons more sent sweet emails and messages on Facebook letting us know they were wearing turquoise. We truly appreciate it. We love them. :). The Jack Ry...
