thevinjefamily.blogspot.com thevinjefamily.blogspot.com

thevinjefamily.blogspot.com

Our Life ♥

A blog about a family of 7, and their journey with Hypoplastic Left Heart Syndrome(HLHS).

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Our Life ♥ | thevinjefamily.blogspot.com Reviews
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A blog about a family of 7, and their journey with Hypoplastic Left Heart Syndrome(HLHS).
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Our Life ♥ | thevinjefamily.blogspot.com Reviews

https://thevinjefamily.blogspot.com

A blog about a family of 7, and their journey with Hypoplastic Left Heart Syndrome(HLHS).

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thevinjefamily.blogspot.com thevinjefamily.blogspot.com
1

Our Life ♥: January 2015

http://www.thevinjefamily.blogspot.com/2015_01_01_archive.html

My family of 7, and our journey in the world of Congenital Heart Defects. Thursday, January 1, 2015. Dear Parents of children with heart defects,. I am a mother that understands. I pour my love and energy into being someone you can trust. Because I want to be your friend. If you're hurting, I dont want you to feel alone. I do not play doctor and preach medical advice. But I do seize every opportunity to educate and empower another parent if it strengthens their role as patient advocate. Links to this post.

2

Our Life ♥: August 2014

http://www.thevinjefamily.blogspot.com/2014_08_01_archive.html

My family of 7, and our journey in the world of Congenital Heart Defects. Thursday, August 28, 2014. The Super Sibling Celebration. Children's Hospital of Philadelphia, and INOVA Fairfax Hospital for Children. We throw the occasional " ♥Moms Night Out", or other similar themes, and those of us in Anne Arundel County frequently meet for weekly play dates at the park. Our very first dinner together. ♥ Being a part of. Community has been so profoundly rewarding for my soul. We are a family. And all of the o...

3

Our Life ♥: November 2013

http://www.thevinjefamily.blogspot.com/2013_11_01_archive.html

My family of 7, and our journey in the world of Congenital Heart Defects. Saturday, November 2, 2013. Dear family and friends that are wondering what's going on since the last bomb I dropped about Cecilia's MRI results and outcome prediction consult:. So, to be honest, I'm having some difficulty coping with what I know now. I'm so thankful to know it all because like I said, ". Should I request them anyway? And who/ what centers am I interested in if. I'm not confident in the opinion/plan we receive back?

4

Our Life ♥: March 2014

http://www.thevinjefamily.blogspot.com/2014_03_01_archive.html

My family of 7, and our journey in the world of Congenital Heart Defects. Sunday, March 30, 2014. Please visit Never Forget Lily Grace. On facebook to learn more about Lily Grace and her mother Amy. These headbands will be donated to little girls in the hospital, along with the hair bows that Amy makes. She's also asking for donations of supplies, and crocheted hats. You can find more information about this on the link above. Links to this post. Subscribe to: Posts (Atom). View my complete profile. So gl...

5

Our Life ♥: April 2014

http://www.thevinjefamily.blogspot.com/2014_04_01_archive.html

My family of 7, and our journey in the world of Congenital Heart Defects. Wednesday, April 30, 2014. Cath (Day 3 4). I'll add in description later. Links to this post. Monday, April 28, 2014. After we left, we had lunch. We stopped by the park and had a blast until Cecilia fell and scraped her face. :(. Family to Cecilia, and we can't imagine our journey without her love, because it definitely was the bright spot in a lot of bad times. Links to this post. Sunday, April 27, 2014. Some pictures from today:.

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