
careforcoby.blogspot.com
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME)This blog is dedicated to following Coby's journey with Granulomatous Meningoencephalitis (GME).
http://careforcoby.blogspot.com/
This blog is dedicated to following Coby's journey with Granulomatous Meningoencephalitis (GME).
http://careforcoby.blogspot.com/
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Care for Coby - our journey with Granulomatous Meningoencephalitis (GME) | careforcoby.blogspot.com Reviews
https://careforcoby.blogspot.com
This blog is dedicated to following Coby's journey with Granulomatous Meningoencephalitis (GME).
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME): March 2014
http://careforcoby.blogspot.com/2014_03_01_archive.html
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME). This blog is dedicated to following Coby's journey with Granulomatous Meningoencephalitis (GME). Monday, March 10, 2014. Happy belated birthday Coby. WowI didn't even write on Cobys birthday! He turned 5 on February 18th! I'm so blessed to still have my little guy here with me despite his GME diagnosis at age 1. He's still a happy, healthy boy! Subscribe to: Posts (Atom). Happy belated birthday Coby. View my complete profile.
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME): Pictures
http://careforcoby.blogspot.com/2013/06/pictures.html
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME). This blog is dedicated to following Coby's journey with Granulomatous Meningoencephalitis (GME). Monday, June 17, 2013. Subscribe to: Post Comments (Atom). View my complete profile.
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME): January 2013
http://careforcoby.blogspot.com/2013_01_01_archive.html
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME). This blog is dedicated to following Coby's journey with Granulomatous Meningoencephalitis (GME). Sunday, January 6, 2013. Tuesday, January 1, 2013. Another year has come and gone without any health problems for little Coby! Subscribe to: Posts (Atom). View my complete profile.
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME): November 2012
http://careforcoby.blogspot.com/2012_11_01_archive.html
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME). This blog is dedicated to following Coby's journey with Granulomatous Meningoencephalitis (GME). Thursday, November 29, 2012. 2 years Prednisone Free. It's official, Coby has been prednisone free for TWO years now! Thursday, November 22, 2012. Today (& every day during the year), I am so very very thankful for Coby's excellent health! Labels: Alaskan Klee Kai. Monday, November 19, 2012. Subscribe to: Posts (Atom).
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME): December 2012
http://careforcoby.blogspot.com/2012_12_01_archive.html
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME). This blog is dedicated to following Coby's journey with Granulomatous Meningoencephalitis (GME). Wednesday, December 5, 2012. AKC Canine Health Foundation and GME research. To help donate to GME research, please check out the link below to see my Heroes for Health Research page I created. Http:/ k9hf.convio.net/site/TR/Events/General? Below is a new research project for. Dr Nick Jeffery, BVSc, Iowa State University. Coby had a holi...
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Care for Coby - our journey with Granulomatous Meningoencephalitis (GME)
Care for Coby - our journey with Granulomatous Meningoencephalitis (GME). This blog is dedicated to following Coby's journey with Granulomatous Meningoencephalitis (GME). Monday, March 10, 2014. Happy belated birthday Coby. WowI didn't even write on Cobys birthday! He turned 5 on February 18th! I'm so blessed to still have my little guy here with me despite his GME diagnosis at age 1. He's still a happy, healthy boy! Friday, January 3, 2014. Coby is doing GREAT! Wednesday, August 7, 2013.
Care for Cody - careforcody.com
We need your help and can use volunteers of time,. Work, information and monetary contributions. Will you help us please? Whoever heard of Gaucher's disease. The vast majority of people probably haven t. Yet Cody has it. It is an incurable, genetic liver disorder. That affects only some 10,000 people world-wide. And Cody has it. Cody requires infusions every two weeks for the rest of his life. But brace yourself the infusions alone currently cost over $8,218. Have we got your attention? Dedicated to Cody...
Care for Cody - careforcody.com
We need your help and can use volunteers of time,. Work, information and monetary contributions. Will you help us please? Whoever heard of Gaucher's disease. The vast majority of people probably haven t. Yet Cody has it. It is an incurable, genetic liver disorder. That affects only some 10,000 people world-wide. And Cody has it. Cody requires infusions every two weeks for the rest of his life. But brace yourself the infusions alone currently cost over $8,218. Have we got your attention? Dedicated to Cody...
Care for Cody - careforcody.com
We need your help and can use volunteers of time,. Work, information and monetary contributions. Will you help us please? Whoever heard of Gaucher's disease. The vast majority of people probably haven t. Yet Cody has it. It is an incurable, genetic liver disorder. That affects only some 10,000 people world-wide. And Cody has it. Cody requires infusions every two weeks for the rest of his life. But brace yourself the infusions alone currently cost over $8,218. Have we got your attention? Dedicated to Cody...
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