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The Byrd NestA couple's journey with their baby "Byrds."
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A couple's journey with their baby "Byrds."
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A couple's journey with their baby "Byrds."
The Byrd Nest: Memorial Day 2012
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A couple's journey with their baby "Byrds.". Sunday, June 10, 2012. We took our normal long weekend to the beach for Memorial Day and had a great time, as always. The trip really seemed to wipe Avery out. She took 3 hr morning naps and slept late every morning while we were there. She is normally an early riser, 5:45-6:00am every morning, so it was great to sleep in a little. Avery's 1st time playing in the sand. I love this one of Emma spinning. One happy little girl with her new "surf board". Chase HLH...
The Byrd Nest: October 2011
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A couple's journey with their baby "Byrds.". Monday, October 31, 2011. Avery's 1 week old check-up. I also asked the dr to look at this knot on the back of Avery's head and he seems to think its just skin and tissue but to have our pedi at home to watch it. It really reminds me of the staf infection my niece, Morgan had when she was 2 wks old so that is why I wanted him to look at it. He also said her jonduice looked a lot better and that she is free to fly home whenever we get permission. Chris has been...
The Byrd Nest: March 2012
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A couple's journey with their baby "Byrds.". Sunday, March 18, 2012. Yesterday was Emma's 1st Pee Wee (3-4 yr olds) soccer game/practice. They didn't really play a game just kicked the ball around and learned some rules of soccer which went pretty well. Now there was some tears shed by Emma, the coaches daughter and one other little girl but Emma recovered and enjoyed herself. Notice the girl to Emma's left, look how tall she is. She is almost 5 but not old enough to move up the the next age group. Play ...
The Byrd Nest: December 2011
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A couple's journey with their baby "Byrds.". Thursday, December 15, 2011. Yes, I know this is a bit late seeing how Christmas is next weekend, but I still want to share. We are especially thankful this year at Thanksgiving to finally be a family of 4 and to all be home together. It was a great Thanksgiving. We had lunch with Chris' family and dinner with my family. It makes for a lot of eating but we really enjoy spending time with everyone. Granny Ruth (Chris' grandmother) holding Avery for the 1st time.
The Byrd Nest: August 2012
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A couple's journey with their baby "Byrds.". Thursday, August 2, 2012. She still takes 2 naps a day, loves her paci and blankey Minnie while she is sleeping and maybe teething. She has been quite fussy this week and not sleeping well, so we shall see if any teeth pop thru. We lowered her crib mattress Tuesday since she started sitting up in her bed. She is also becoming more aware of strangers and strange places more attached me Mama. Wednesday, August 1, 2012. Now the buckets of water enter the scene.
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Because I Said So: July 2012
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Because I Said So. Wednesday, July 11, 2012. Subscribe to: Posts (Atom). View my complete profile. We're hanging out with Magnus in the recovery room. He's still fairly groggy from the anesthesia, but generally seems OK. He has to lie completely flat for. Wednesday, October 24th at 1:54 am Avery turned 1 year old. She really is one of the happiest babies we have ever met and we are not just saying that, she t. New update on Asher, and where my heart has been lately. Day Fifteen – discharge day! I figured...
Because I Said So: April 2013
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Because I Said So. Friday, April 19, 2013. Mother of the Year. And finally the third question that I totally flubbed.the one everyone asks and the one everyone wants the answer too, how do I do it all? Subscribe to: Posts (Atom). View my complete profile. We're hanging out with Magnus in the recovery room. He's still fairly groggy from the anesthesia, but generally seems OK. He has to lie completely flat for. Sadie Lou has left the House. Day Fifteen – discharge day! I haven't posted for a while, , um th...
Because I Said So: January 2012
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Because I Said So. Thursday, January 26, 2012. Getting Ready for #3. Within the next 6 months. Oh boy. Here we go. Yesterday C had her appointment with the interventional cardiologist, the doctor who does her heart caths. We knew this day was coming but knowing the day is coming sure does nothing to lessen the dread I feel in hearing the words, we are ready to schedule C for her next procedures. But, she is ready and that is what is important. Subscribe to: Posts (Atom). View my complete profile. I haven...
Because I Said So: September 2012
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Because I Said So. Friday, September 28, 2012. The fluid collection seems to be resolving as well. Even though she did have some fluid a month ago when we saw her cardiologist he did not feel he needed to do an echo when we saw him yesterday. I assume this means he feels her body is finally stopping with all the inflammation. She is still on the diuretics but hopefully for only a few more months. So, stable can in fact be a good thing. A great thing. Subscribe to: Posts (Atom). View my complete profile.
Because I Said So: What is Heterotaxy?
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Because I Said So. Tuesday, February 5, 2013. Http:/ www.heterotaxy.org/Pages/what is heterotaxy.aspx. Http:/ www.chop.edu/service/cardiac-center/heart-conditions/heterotaxy-syndrome.html. Is this a new diagnosis? Is this what they have decided is the reason they have been so puzzled? February 11, 2013 at 3:10 PM. Subscribe to: Post Comments (Atom). View my complete profile. Sadie Lou has left the House. Day Fifteen – discharge day! New update on Asher, and where my heart has been lately. I have learned ...
Because I Said So: We Did A Parade
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Because I Said So. Monday, February 11, 2013. We Did A Parade. On a side note, we took third place in our division (yay! And even more impressive, my husband was personally asked by the parade chairman to participate in the big parade this Saturday. Over 200,000 people to reach out to.lets keep spreading the news. C is just one of the 1 in 100. You guys did a fantastic job! So good that you have been invited to the big parade. Thanks for the updates, always praying! February 11, 2013 at 3:15 PM. I picked...
Because I Said So: August 2012
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Because I Said So. Wednesday, August 22, 2012. Yesterday C had a follow up cardiology appointment. She is still being seen pretty frequently as she continues to have lots of post Fontan issues. We had actually gone 4 weeks between visits but alas, that did not last as we will be going back to cardiology next Tuesday. Monday, August 20, 2012. August 19, 2012. Happy birthday to my big 3 year old! Subscribe to: Posts (Atom). View my complete profile. Sadie Lou has left the House. The Hester House Blog.
Because I Said So: A New Year
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Because I Said So. Friday, January 11, 2013. Yesterday we met with the cath cardiologist. I really dread the appointments with this doctor. Not because I dislike him, actually quite the opposite, I simply adore him but I dread these appointments because once we see him I know we are looking at doing some kind of procedure, most likely a heart cath. Ugh. Thanks for updating us. I think of you guys often. Prayers still going up on your behalf. January 12, 2013 at 3:05 PM. January 18, 2013 at 6:42 PM. Wedne...
Because I Said So: March 2012
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Because I Said So. Friday, March 30, 2012. Follow Up Story by Local News. Http:/ www.fox4now.com/news/local/145009465.html#.T3UqP0lfjFE.facebook. Thursday, March 29, 2012. Prayer Vigil and Bake Sale. Subscribe to: Posts (Atom). View my complete profile. We're hanging out with Magnus in the recovery room. He's still fairly groggy from the anesthesia, but generally seems OK. He has to lie completely flat for. Sadie Lou has left the House. Day Fifteen – discharge day! The Hester House Blog. Surgery #3 for o...
Because I Said So: Stability
http://kyleandtodd.blogspot.com/2012/09/stability.html
Because I Said So. Friday, September 28, 2012. The fluid collection seems to be resolving as well. Even though she did have some fluid a month ago when we saw her cardiologist he did not feel he needed to do an echo when we saw him yesterday. I assume this means he feels her body is finally stopping with all the inflammation. She is still on the diuretics but hopefully for only a few more months. So, stable can in fact be a good thing. A great thing. Praying for you, C and the whole extended family.
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BYRDS FLYGHT
Friday, March 16, 2018. Sweetheart Of The Rodeo by Lloyd Green and Jay Dee Maness. Pedal steel guitar players Lloyd Green and Jay Dee Maness both played on The Byrds' "Sweetheart Of The Rodeo" album in 1967. Their new CD (to be released on April 22nd, 2018) is called "Journey To The Beginning - A Steel Guitar Tribute To The Byrds Sweet Heart Of The Rodeo". It features 10 tracks from these Spring 1968 sessions, recently re-recorded by the duo. Tuesday, March 13, 2018. You can get it from. SIDE TWO 1. ...
The Byrd Nest
A couple's journey with their baby "Byrds.". Sunday, October 28, 2012. Wednesday, October 24th at 1:54 am Avery turned 1 year old. She really is one of the happiest babies we have ever met and we are not just saying that, she truly is. She is always smiling, laughing, babbling/talking, squealing in joy and playing. She does have a bit of a temper and we are working on that with her. Playing with the blocks she got from Emma for her birthday. Sharing with her big sister. Emma feeding the sheep. She still ...
Byrds For A Cure
Byrds For A Cure. Saturday, October 30, 2010. New Wheels for the Byrd Household. I am thrilled to inform you that we accepted delivery of our new wheelchair accessible van yesterday. We will be forever grateful to the Clara Abbott Foundation. Who among the many requests for financial assistance from Abbott Labs employees selected ours to grant. Their generosity strikes us almost speechless and we feel forever indebted to them for such an expensive, lifestyle changing gift. There was no luxury spared....
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Byrds for a Cure. Welcome to Byrds for a Cure. We are the proud parents of three wonderful kids: Jenna, and twins Kyle and Lauren. We are determined to fight this disease, and with your help we can find a cure. We are passionate about increasing awareness of SMA and funding cutting-edge, critical research in hopes of finding a treatment and a cure. Our Initial Message to Loved Ones. Yesterday, the pediatric neurologist confirmed that both twins do have Spinal Muscular Atrophy (SMA), type II.
虫歯はそのままにしないで歯医者に行こう
Byrds for a Cure. Welcome to Byrds for a Cure. We are the proud parents of three wonderful kids: Jenna, and twins Kyle and Lauren. We are determined to fight this disease, and with your help we can find a cure. We are passionate about increasing awareness of SMA and funding cutting-edge, critical research in hopes of finding a treatment and a cure. Our Initial Message to Loved Ones. Yesterday, the pediatric neurologist confirmed that both twins do have Spinal Muscular Atrophy (SMA), type II.
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