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davidandthegiant.wordpress.com

david and the giant

David and the giant. August 9, 2015. And now there’s today. Almost two and half years to the day after receiving our diagnosis. Every single thing has changed. We still have the loveseat, but it’s filled with joy. Our biggest surprise and sweetest blessing plays on that seat. It is truly a seat of love (yep, I went there). Click to share on Twitter (Opens in new window). Share on Facebook (Opens in new window). Click to share on Pinterest (Opens in new window). May 10, 2015. In Valentine, Nebraska. I...

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David and the giant. August 9, 2015. And now there’s today. Almost two and half years to the day after receiving our diagnosis. Every single thing has changed. We still have the loveseat, but it’s filled with joy. Our biggest surprise and sweetest blessing plays on that seat. It is truly a seat of love (yep, I went there). Click to share on Twitter (Opens in new window). Share on Facebook (Opens in new window). Click to share on Pinterest (Opens in new window). May 10, 2015. In Valentine, Nebraska. I...
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david and the giant | davidandthegiant.wordpress.com Reviews

https://davidandthegiant.wordpress.com

David and the giant. August 9, 2015. And now there’s today. Almost two and half years to the day after receiving our diagnosis. Every single thing has changed. We still have the loveseat, but it’s filled with joy. Our biggest surprise and sweetest blessing plays on that seat. It is truly a seat of love (yep, I went there). Click to share on Twitter (Opens in new window). Share on Facebook (Opens in new window). Click to share on Pinterest (Opens in new window). May 10, 2015. In Valentine, Nebraska. I...

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1

david and the giant | Page 2

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David and the giant. Newer posts →. November 29, 2014. For better or wors. E and truly, through the worse, it’s gotten better. I’m so grateful for this season, our lives and the continual surprises that keep coming our way. Keep the good ones coming! Baby number three – April 2015. Click to share on Twitter (Opens in new window). Share on Facebook (Opens in new window). Click to share on Pinterest (Opens in new window). November 25, 2014. Click to share on Twitter (Opens in new window). November 23, 2014.

2

Down syndrome | david and the giant

https://davidandthegiant.wordpress.com/down-syndrome

David and the giant. Http:/ www.ndss.org/. Http:/ www.rmdsa.org/. Click to share on Twitter (Opens in new window). Share on Facebook (Opens in new window). Click to share on Pinterest (Opens in new window). One thought on “ Down syndrome. Nick and Julia Cirbo. August 14, 2013 at 3:38 am. Jill you are a true inspiration and I am proud to call you my friend. You and your family are amazing and wish you the best on your new journey of life! Love you all,. Leave a Reply Cancel reply. Enter your comment here.

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The never-ending story | david and the giant

https://davidandthegiant.wordpress.com/2015/01/29/the-never-ending-stay

David and the giant. The motherhood →. January 29, 2015. I mean, who hasn’t been battling a cough and phlegm for weeks now? And I’m relatively healthy and have strong lungs. Poor David already starts at a disadvantage and has small, compact lungs. While he’s not regressing, he’s certainly not progressing and that leaves Jason and I feeling helpless. To be admitted.” But he’s his happy, giddy self. He’s flirting and smiling and winning hearts each day. We miss him! We want him home. January 29, 2015 at 8:...

4

The justification | david and the giant

https://davidandthegiant.wordpress.com/2015/01/25/the-justification

David and the giant. The never-ending story →. January 25, 2015. We’re on day four of a new hospital stay. It’s been over 280 days since the last time we were admitted. Long enough to get comfortable and a little cocky. Hospital stays are for the really young and “sickly”. David is bigger, stronger, healthier. He can handle anything! Or so we thought. Is this really just a common cold? Did the Botox move? Else I knew had a kiddo in the hospital, I would be freaking out for them. So why aren’t I? PS, if y...

5

Contribute | david and the giant

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David and the giant. Thank you, thank you! To everyone who has so generously donated to our family. We are so blessed by you all and can’t wait to share our completed puzzle with you! 8220;I prayed for this child, and the LORD has granted me what I asked of him.” (1 Samuel 1:27). One of the most difficult challenges of our diagnosis is the financial requirements that accompany an extended NICU stay, much of which is uncovered by insurance carriers. Click to share on Twitter (Opens in new window). Jill- W...

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neglectedkids.blogspot.com neglectedkids.blogspot.com

Neglecting My Kids: Surrender

http://neglectedkids.blogspot.com/2015/08/surrender.html

Finding new ways to ensure my children will need therapy, one day at a time. Tuesday, August 04, 2015. My shelf with my wips is getting a little out of control. Apparently I REALLY like pink project bags. My purple yarn is officially in a time out. It needs to learn to knit nicely. I've got a plan for it. I'm feeling fairly confident about the new course of action. It is a combination of all my previous techniques. But I haven't tried it out yet. I've been a little distracted. But that alpaca yarn. I loo...

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Our Journey Through Life... | Life is not measured by the number of breaths you take, but by the moments that take your breath away | Page 2

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Our Journey Through Life…. Life is not measured by the number of breaths you take, but by the moments that take your breath away. Newer posts →. A resolution to end hurtful words. I posted this on Facebook today. I thought I would share it here as well. I’ve seen a lot of people putting their resolutions and goals for 2014 on FB. This year, will you (my friends and family) consider a resolution of stopping the use of the words retard and retarded? By Melanie •. Posted in The 'R' word. The next setback ou...

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Stories From the Heart: A Mother’s Day Tribute (link to view) | Our Journey Through Life...

https://mellbugg.wordpress.com/2014/05/08/stories-from-the-heart-a-mothers-day-tribute-link-to-view

Our Journey Through Life…. Life is not measured by the number of breaths you take, but by the moments that take your breath away. Coming soon to your television screen – Eli! Stories From the Heart: A Mother’s Day Tribute (link to view). Here it is – Our family’s television debut! Our family thanks you! Watch Stories From the Heart: A Mother’s Day Tribute HERE. I can’t say it enough – Thank you! Thank you for your continued support of our family. Thank you for loving our boys. By Melanie •. May 9, 2014.

neglectedkids.blogspot.com neglectedkids.blogspot.com

Neglecting My Kids: The Return Of Boyd

http://neglectedkids.blogspot.com/2006/02/return-of-boyd.html

Finding new ways to ensure my children will need therapy, one day at a time. Friday, February 17, 2006. The Return Of Boyd. Legal Disclaimer: The Greatest formally protests the pictures in this post. I have assured him that everyone has a spot like this in their home. Having said that, here I go. I have a confession to make. I lost Boyd. I know he was hanging out in the Christmas Tree. Then we took the tree down and he just disappeared. Was I sad to have lost Boyd? What's he been up to? Boyd seemed rathe...

lifewiththequeenbean.blogspot.com lifewiththequeenbean.blogspot.com

Life With Lily: The Hard Times

http://lifewiththequeenbean.blogspot.com/2015/07/the-hard-times.html

Tuesday, July 28, 2015. So we have had a rough week with Lily. I wasn't kidding when I said that she is an angel unless she is teething. And she is teething hard right now. Working on that last "hippo tooth.". She is crabby, and won't eat and won't sleep and is generally making life horrific for everyone in the house. And she isn't eating. Because her mouth hurts. We did take our Sweet Lily Bean to the pediatrician to be sure it was only teething and not something more serious. I slept through the night ...

lifewiththequeenbean.blogspot.com lifewiththequeenbean.blogspot.com

Life With Lily: Selected

http://lifewiththequeenbean.blogspot.com/2015/08/selected.html

Monday, August 10, 2015. T he 2015 NDSS Times Square Video will play in the heart of New York City on the. Clear Channel Spectacolor screen. In Times Square on September 19, 2015 at 10 am ET. They are people. With feelings, ideas, hopes and dreams. They are worthy of dignity and respect and love. And they are loved. So very loved by people who hope and dream for their acceptance and safety in this world. I'm so excited Lily was selected. I just wish I could remember which picture I submitted. Our three l...

lifewiththequeenbean.blogspot.com lifewiththequeenbean.blogspot.com

Life With Lily: July 2015

http://lifewiththequeenbean.blogspot.com/2015_07_01_archive.html

Friday, July 31, 2015. Our little Queen is anemic. We get to add another specialist to our team. It is totally fun to call the Hematologist and have the recorded message say "Thank you for calling The Children's Hospital Pediatric Oncology Department." And by fun I mean not fun at all. It makes your heart stop. I hung up the phone and double checked the phone number. I was in the right place. And Lily is anemic. He prescribed some heavy duty iron drop to be given twice a day. What he didn't tell me was t...

lifewiththequeenbean.blogspot.com lifewiththequeenbean.blogspot.com

Life With Lily: Rule #3

http://lifewiththequeenbean.blogspot.com/2015/07/rule-3.html

Tuesday, July 21, 2015. Lily loves her bathtime! We have two rules for the tub. 1) We do not stand in the tub. 2) We do not poop in the tub. Lily likes to play fast and loose with both rules. Tonight bathtime was provided by her oldest sister. Afterward I found Pork Chop.my children would like their anonymity preserved, so with the exception of The Queen they will all be referred to by the nicknames given to them on my other blog. But it was too late. She was trying to be helpful? So then I cleaned the t...

courtney-heartofbeauty.blogspot.com courtney-heartofbeauty.blogspot.com

Heart of Beauty: His Hand

http://courtney-heartofbeauty.blogspot.com/2014/03/his-hand.html

Thursday, March 6, 2014. When in the darkness of life,. I cry out to Him. I beg for wisdom,. I moan for relief,. I search for hope,. As we were in Corban's pediatrician's office for the ump-teenth time the summer of 2012, and Corban was wasting away and in terrible pain, I prayed for supernatural knowledge for the doctor so that we could help Corban. It didn't happen. God did not tell the doctor what was going on. The Lord's hand did not move to answer my cry. The Lord's hand did not move to answer my cry.

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david and the giant

David and the giant. August 9, 2015. And now there’s today. Almost two and half years to the day after receiving our diagnosis. Every single thing has changed. We still have the loveseat, but it’s filled with joy. Our biggest surprise and sweetest blessing plays on that seat. It is truly a seat of love (yep, I went there). Click to share on Twitter (Opens in new window). Share on Facebook (Opens in new window). Click to share on Pinterest (Opens in new window). May 10, 2015. In Valentine, Nebraska. I...

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