supernash.blogspot.com supernash.blogspot.com

supernash.blogspot.com

Super Nash

Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero!!

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Super Nash | supernash.blogspot.com Reviews
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Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero!!
<META>
KEYWORDS
1 super nash
2 over halfway done
3 it was great
4 our address is
5 nash gehrls
6 cousin fun
7 friend time
8 our little swimmer
9 third x ray 38mm
10 hugs
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super nash,over halfway done,it was great,our address is,nash gehrls,cousin fun,friend time,our little swimmer,third x ray 38mm,hugs,pga park fun,playing at therapy,first x ray 12mm,second x ray 25mm,reactions,no comments,email this,blogthis,we're here
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Super Nash | supernash.blogspot.com Reviews

https://supernash.blogspot.com

Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero!!

INTERNAL PAGES

supernash.blogspot.com supernash.blogspot.com
1

Super Nash: May 2014

http://supernash.blogspot.com/2014_05_01_archive.html

Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero! Friday, May 16, 2014. This post is a little behind but we have been SUPER BUSY! The rest of the day was spent at the ZOO! The next ...

2

Super Nash: July 2014

http://supernash.blogspot.com/2014_07_01_archive.html

Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero! Tuesday, July 8, 2014. Well, the month of May went fast and so did June. Holy smokes its already July! We had some time to explore ...

3

Super Nash: August 2012

http://supernash.blogspot.com/2012_08_01_archive.html

Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero! Saturday, August 25, 2012. Movin up and out.and back home! Plus it was HUGE! We got back and both the kids were sleeping.yay! Dr Pa...

4

Super Nash: January 2013

http://supernash.blogspot.com/2013_01_01_archive.html

Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero! Sunday, January 13, 2013. Its been a while since I posted an update so here it is! Hattie just wanted to eat the wrapping paper :).

5

Super Nash: September 2012

http://supernash.blogspot.com/2012_09_01_archive.html

Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero! Tuesday, September 18, 2012. And the cast is off! They also said I had to MAIL (not email.snail mail! He was such a happy little gu...

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Chris and I have a wonderful son, Nash, who inspires and amazes us every day. Nash was born with a rare condition called PFFD or CFD. He is a strong little boy who will be going through a lot of surgeries throughout his life. We wanted to share our story to help people understand this condition and keep friends and family updated on his progress. He is our little Super Hero! Tuesday, July 8, 2014. Well, the month of May went fast and so did June. Holy smokes its already July! We had some time to explore ...

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