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Celebrating Samantha

Our family's attempt to cope with mitochondrial disease.

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Celebrating Samantha | celebratingsamantha.blogspot.com Reviews
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Our family&#39;s attempt to cope with mitochondrial disease.
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Celebrating Samantha | celebratingsamantha.blogspot.com Reviews

https://celebratingsamantha.blogspot.com

Our family&#39;s attempt to cope with mitochondrial disease.

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1

Celebrating Samantha: August 2012

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

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...

2

Celebrating Samantha: October 2013

http://celebratingsamantha.blogspot.com/2013_10_01_archive.html

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,...

3

Celebrating Samantha: 10 months worth of updates in one post

http://celebratingsamantha.blogspot.com/2013/10/10-months-worth-of-updates-in-one-post.html

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,...

4

Celebrating Samantha: September 2011

http://celebratingsamantha.blogspot.com/2011_09_01_archive.html

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 ...

5

Celebrating Samantha: December 2012

http://celebratingsamantha.blogspot.com/2012_12_01_archive.html

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.

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Celebrating Samantha

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,...

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