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***JEREMY'S CDH BLOG***

The story of how we learned about Congenital Diaphragmatic Hernia from our son Jeremy.

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***JEREMY'S CDH BLOG*** | jeremycdh.blogspot.com Reviews
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The story of how we learned about Congenital Diaphragmatic Hernia from our son Jeremy.
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***JEREMY'S CDH BLOG*** | jeremycdh.blogspot.com Reviews

https://jeremycdh.blogspot.com

The story of how we learned about Congenital Diaphragmatic Hernia from our son Jeremy.

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1

***JEREMY'S CDH BLOG***: September 2011

http://jeremycdh.blogspot.com/2011_09_01_archive.html

JEREMY'S CDH BLOG* *. The story of how we learned about Congenital Diaphragmatic Hernia from our son Jeremy. Jeremy @ 20 weeks. At 20 weeks we found out about CDH on April 19 2011. Wednesday, September 7, 2011. Took Isaic to see Jeremy's grave. We love and miss you so much! Subscribe to: Posts (Atom). To donate in the memory of Jeremy R. Nolan it will go to the research on CDH and EA/TEF. Https:/ www2.glennon.org/Waystogive07/memgft newdesign.aspx. View my complete profile. Took Isaic to see Jeremys grave.

2

***JEREMY'S CDH BLOG***: Recieved a call a few days ago

http://jeremycdh.blogspot.com/2012/01/recieved-call-few-days-ago.html

JEREMY'S CDH BLOG* *. The story of how we learned about Congenital Diaphragmatic Hernia from our son Jeremy. Jeremy @ 20 weeks. At 20 weeks we found out about CDH on April 19 2011. Sunday, January 15, 2012. Recieved a call a few days ago. The hospital in St. Louis SSM Cardinal Glennon. Subscribe to: Post Comments (Atom). To donate in the memory of Jeremy R. Nolan it will go to the research on CDH and EA/TEF. Https:/ www2.glennon.org/Waystogive07/memgft newdesign.aspx. View my complete profile. A Very Tha...

3

***JEREMY'S CDH BLOG***: Wanting to do a fundraiser in the memory of Jeremy

http://jeremycdh.blogspot.com/2012/01/wanting-to-do-fundraiser-in-memory-of.html

JEREMY'S CDH BLOG* *. The story of how we learned about Congenital Diaphragmatic Hernia from our son Jeremy. Jeremy @ 20 weeks. At 20 weeks we found out about CDH on April 19 2011. Thursday, January 26, 2012. Wanting to do a fundraiser in the memory of Jeremy. Subscribe to: Post Comments (Atom). To donate in the memory of Jeremy R. Nolan it will go to the research on CDH and EA/TEF. Https:/ www2.glennon.org/Waystogive07/memgft newdesign.aspx. View my complete profile. Recieved a call a few days ago.

4

***JEREMY'S CDH BLOG***: August 2011

http://jeremycdh.blogspot.com/2011_08_01_archive.html

JEREMY'S CDH BLOG* *. The story of how we learned about Congenital Diaphragmatic Hernia from our son Jeremy. Jeremy @ 20 weeks. At 20 weeks we found out about CDH on April 19 2011. Thursday, August 18, 2011. Information on Jeremy's other birth defect EA/TEF. There are five different variations of a TEF. The one that Jeremy had I think it was this one. Esophageal Atresia with Tracheoesophageal Fistula. Information from this website http:/ www.chw.org. Today I stopped by to see Jeremy's grave. I love you s...

5

***JEREMY'S CDH BLOG***: January 2012

http://jeremycdh.blogspot.com/2012_01_01_archive.html

JEREMY'S CDH BLOG* *. The story of how we learned about Congenital Diaphragmatic Hernia from our son Jeremy. Jeremy @ 20 weeks. At 20 weeks we found out about CDH on April 19 2011. Thursday, January 26, 2012. Thank you to all the followers and vistors to Jeremy's CDH blog. Wanting to do a fundraiser in the memory of Jeremy. Tuesday, January 24, 2012. The Band Perry - If I Die Young. Friday, January 20, 2012. Poems that I found online about a child dying. You are a Precious Child. Created out of love,.

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