theshaws6.blogspot.com
The Shaw's: Stride & Ride 2010: Ryan's Hope
http://theshaws6.blogspot.com/2010/07/stride-ride-2010-ryans-hope.html
Wednesday, July 28, 2010. Stride and Ride 2010: Ryan's Hope. Stride and Ride 2010: Ryan's Hope. Today, Ryan cannot do anything for himself as the only extremity muscles left working, albeit weak, are his fingers, so he can still play his video games. There is currently no cure…and it can happen in any family. Ryan is the joy of our lives and keeps us laughing along this journey with him. He is one of thousands of boys with Duchenne's that is fighting for the right to grow up. View my complete profile.
sarahhisprincess.blogspot.com
His Princess: May 2015
http://sarahhisprincess.blogspot.com/2015_05_01_archive.html
Where a daughter of the King shares pieces of His work in her life. Wednesday, May 6, 2015. About a month ago, my cleaning lady surprised me by planting purple petunias in my backyard. This is the first time I've ever had anything growing back there except weeds! I can't tell you how much difference it's made to walk through and see these flowers, whom I call my Purple Ladies, each time I come and go from the carport to the house. Friday, May 1, 2015. Subscribe to: Posts (Atom). He does it not by pushing...
sarahhisprincess.blogspot.com
His Princess: My littlest sunshine
http://sarahhisprincess.blogspot.com/2015/03/my-littlest-sunshine.html
Where a daughter of the King shares pieces of His work in her life. Thursday, March 19, 2015. It's been a hard week so far (yes, I know, first world problems).finding out I sprained my neck in accident and perhaps pinched a nerve and being told by doctor to go down to 30 hrs/wk (from 45-55). Lots of pain from overdoing it the past three days. Wednesday, April 1, 2015 at 8:36:00 PM CDT. Oh my gosh, she is so cute! What an adorable little baby! Subscribe to: Post Comments (Atom). Glory to God in the church!
sarahhisprincess.blogspot.com
His Princess: Five Di's plus one
http://sarahhisprincess.blogspot.com/2015/07/five-di-plus-one.html
Where a daughter of the King shares pieces of His work in her life. Monday, July 27, 2015. Five Dis plus one. Because six di's (dianthus) doesn't really have the same ring to it. Their friends the Purple Ladies are gone (fungus). Trying to water and will my girls through the brutal next two months. Subscribe to: Post Comments (Atom). 8220;God can do anything, you know—far more than you could ever imagine or guess or request in your wildest dreams! Glory to God in the church! Glory through all millennia!
sarahhisprincess.blogspot.com
His Princess: August 2014
http://sarahhisprincess.blogspot.com/2014_08_01_archive.html
Where a daughter of the King shares pieces of His work in her life. Saturday, August 9, 2014. 2 Weeks from now. I will be with "the redheads", as we're fond of calling them, with this tiny one being the newest:. She's two weeks old in that picture. First smiles. I love that and that her little cheeks are starting to get chubby. Apparently her big sister is giving her Daddy a run for his money:. And the migraines will be more under control. Subscribe to: Posts (Atom). Glory to God in the church! Though I'...
theshaws6.blogspot.com
The Shaw's: Saying Goodbye is Hard to Do
http://theshaws6.blogspot.com/2010/02/saying-goodbye-is-hard-to-do.html
Thursday, February 4, 2010. Saying Goodbye is Hard to Do. We have had to say goodbye to Jumper this week as she was hit by a car and killed in the early morning hours of January 31, 2010. As much as our pets cause aggravation. Void in the family. It is amazing how much these four legged friends become such an integral. February 7, 2010 at 6:44 PM. Subscribe to: Post Comments (Atom). Saying Goodbye is Hard to Do. Ryan and Jumper shortly after we brought her home. Ryan with Nana and Jumper 2002.
sarahhisprincess.blogspot.com
His Princess: Happy First Birthday
http://sarahhisprincess.blogspot.com/2015/07/happy-first-birthday.html
Where a daughter of the King shares pieces of His work in her life. Monday, July 13, 2015. There is so much to write about when my neck and shoulder heal. But first things first. This happy redheaded darling turns one today. She is our little peanut. What she lacks in size, she makes up for in personality! Her big sister cried when Mommy gave her birthday cake. Pretty sure this one will shove it in with both little fists. Happy birthday, Alyssa Jane! Subscribe to: Post Comments (Atom). Living Proof Minis...
theshaws6.blogspot.com
The Shaw's: May 2009
http://theshaws6.blogspot.com/2009_05_01_archive.html
Monday, May 25, 2009. The Now Newest Addition to the Family. Stephanie (Shay) will be giving us our first grandchild. Kahlia Ryan is due to make her appearance sometime around July 26th. We are all very excited to make her aquaintance. Here is a shot of Mama Stephanie and an ultra sound picture of Kahlia. Hey, Hey the Gangs All Here! This was a day that we took a trip to Lake Erie. It was very beautiful! Here is the Birthday boy. It is hard to believe he is 13. A teenager! Subscribe to: Posts (Atom).
theshaws6.blogspot.com
The Shaw's: February 2011
http://theshaws6.blogspot.com/2011_02_01_archive.html
Monday, February 21, 2011. The Love of a Grandchild. I came home from work one evening to something that brought back some memories for me. I always come in through the garage and step up into our kitchen. One night in particular as I stepped up into the kitchen, peering around the refrigerator was my granddaughter Kahlia. Our paternal grandparents lived in a small village called South Bloomingville. As I watched Kahlia. That night and hearing her say Papa with such excitement and joy I also remembered t...
theshaws6.blogspot.com
The Shaw's: July 2010
http://theshaws6.blogspot.com/2010_07_01_archive.html
Wednesday, July 28, 2010. Stride and Ride 2010: Ryan's Hope. Stride and Ride 2010: Ryan's Hope. Today, Ryan cannot do anything for himself as the only extremity muscles left working, albeit weak, are his fingers, so he can still play his video games. There is currently no cure…and it can happen in any family. Ryan is the joy of our lives and keeps us laughing along this journey with him. He is one of thousands of boys with Duchenne's that is fighting for the right to grow up. Subscribe to: Posts (Atom).
