reflectingonthemoment.blogspot.com
Reflecting on the Moment: November 2014
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Reflecting on the Moment. Waiting is not just the thing we have to do until we get what we hope for. Waiting is part of the process of becoming what we hope for. - Ben Patterson. Saturday, November 29, 2014. This is So Not Okay. Ten years ago this month we started building our house. And we I say "we", I mean my husband, his father, and our builder. Not really in that order. Against all odds, we have been here 4 months shy of 10 years and have not had even one mouse in the house. Not even ONE. I know tha...
reflectingonthemoment.blogspot.com
Reflecting on the Moment: August 2014
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Reflecting on the Moment. Waiting is not just the thing we have to do until we get what we hope for. Waiting is part of the process of becoming what we hope for. - Ben Patterson. Saturday, August 30, 2014. The first "week" of school is in the books. And by "week", I mean two-and-a-half days. Two-and-a-half great days of seeing smiling students, talking with families, spending time with teachers, and hanging out for a few hours at high school retreat. I had been taking pictures one by one, so I had to up ...
reflectingonthemoment.blogspot.com
Reflecting on the Moment: January 2015
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Reflecting on the Moment. Waiting is not just the thing we have to do until we get what we hope for. Waiting is part of the process of becoming what we hope for. - Ben Patterson. Friday, January 2, 2015. My youngest son's teacher asked him to work on his multiplication facts over Christmas break. I can totally see why. This is taking every ounce of patience I have, and I typically have a fairly strong reserve of it! But math details.they just don't stick right now. Me: Okay, let's practice our 3's again.
reflectingonthemoment.blogspot.com
Reflecting on the Moment: October 2014
http://reflectingonthemoment.blogspot.com/2014_10_01_archive.html
Reflecting on the Moment. Waiting is not just the thing we have to do until we get what we hope for. Waiting is part of the process of becoming what we hope for. - Ben Patterson. Sunday, October 12, 2014. A Day in the Life. Tonight I was studying with my 8 year old for his history test. It was going something like this. Me: What were the leaders who people chose to act or speak for them called? Me: (Eyebrows raised in surprise that he knew that.). Me: (Impressed. I didn't know that.). I know this one!
celebratingsamantha.blogspot.com
Celebrating Samantha: September 2011
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Our family's attempt to cope with mitochondrial disease. Tuesday, September 27, 2011. No news is good news. Obviously, I am a horrible blogger as it has been over two months since my last post. Or, something like that. I am not sure why it's been so long. We always do feel busy, but that is nothing new. I know there are a few of you out there who have expressed an interest and actually do use the blog to get your Samantha updates. Samantha continues to be her funny, loving, smart, adorable self. Val ...
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Celebrating Samantha: August 2012
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Our family's attempt to cope with mitochondrial disease. Friday, August 24, 2012. There is never a stagnant moment when it comes to Samantha. Things are usually going up, or down. I am sorry to say that within the last few weeks we have seen yet another slow up in terms of Samantha's motor skills. Sam has stopped walking again. And, we aren't really sure why. We have a follow up appointment with Dr. C in Ohio again in mid-September- so perhaps he will have some additional insight. Until next time,. The D...
celebratingsamantha.blogspot.com
Celebrating Samantha: December 2012
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Our family's attempt to cope with mitochondrial disease. Monday, December 31, 2012. Until next time,. Subscribe to: Posts (Atom). The Special Needs Blogger Weekend Link-up: Le place for le posts. Last gasps of summer. A Day in the Life of Reagan Leigh. Carrot 3 car seat take 2! Happy Birthday, Alex! Life with the Ferrells. 2016: Up To Speed. The Martin Family and Mito. Will health update Q4 2015. All the Marletts, Our Life as a Family. It's a Girl . The House of DeStephano. The Dyeds vs. the Whites.
celebratingsamantha.blogspot.com
Celebrating Samantha: October 2013
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Our family's attempt to cope with mitochondrial disease. Friday, October 18, 2013. 10 months worth of updates in one post. Or, at least I will try. Today it doesn't feel as hard. So, here is my attempt to try to catch up to where we are now. 2013 has been an interesting year. In February we were able to go on Samantha's Make a Wish trip. As our girl likes everything princess (that is nature and NOT nurture! Here is a pic of the three of us at Epcot:. Due to our fear of germs and Sam's general clingyness,...
