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A Very Special Journey: July 2010

http://veryspecialjourney.blogspot.com/2010_07_01_archive.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Tuesday, July 20, 2010. Tomorrow, July 21, is the one-year anniversary of when we found out about Markos from our agency! Links to this post. Subscribe to: Posts (Atom). The kids with their cousins. Beach Week, 2010.

veryspecialjourney.blogspot.com veryspecialjourney.blogspot.com

A Very Special Journey: November 2009

http://veryspecialjourney.blogspot.com/2009_11_01_archive.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Saturday, November 28, 2009. He's experiencing many firsts today, and he's clearly eager to keep the string alive leading his mom all over the airport while I type. This is gonna be fun. Links to this post. Friday, November 20, 2009. Roxie turns ...

veryspecialjourney.blogspot.com veryspecialjourney.blogspot.com

A Very Special Journey: May 2011

http://veryspecialjourney.blogspot.com/2011_05_01_archive.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Friday, May 20, 2011. School Placement for Roxie. When I think of moving Roxie to another school I feel some excitement, but I also have many reservations. Will the school be 30 minutes away and begin at 7:30? If a typical school doesn't work out...

veryspecialjourney.blogspot.com veryspecialjourney.blogspot.com

A Very Special Journey: January 2011

http://veryspecialjourney.blogspot.com/2011_01_01_archive.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Sunday, January 23, 2011. Roxie on a rocket. Links to this post. Subscribe to: Posts (Atom). The kids with their cousins. Beach Week, 2010. United Mitochondrial Disease Foundation. Easter Seals UCP North Carolina. Roxie on a rocket.

veryspecialjourney.blogspot.com veryspecialjourney.blogspot.com

A Very Special Journey: August 2009

http://veryspecialjourney.blogspot.com/2009_08_01_archive.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Tuesday, August 18, 2009. Court Date: Oct. 5". Links to this post. Saturday, August 15, 2009. Ugh, just when we thought we might be in the clear . Links to this post. Tuesday, August 11, 2009. In the morning, she is likely to have serious "matter...

veryspecialjourney.blogspot.com veryspecialjourney.blogspot.com

A Very Special Journey: DC charter school organized around inclusion

http://veryspecialjourney.blogspot.com/2011/08/dc-charter-school-organized-around.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Friday, August 12, 2011. DC charter school organized around inclusion. More social entrepreneurs, schools, and school systems need to move in this direction. Where can one find a school like this. Subscribe to: Post Comments (Atom).

veryspecialjourney.blogspot.com veryspecialjourney.blogspot.com

A Very Special Journey: Roxie at the pool

http://veryspecialjourney.blogspot.com/2011/08/roxie-at-pool.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Saturday, August 06, 2011. Roxie at the pool. Subscribe to: Post Comments (Atom). The kids with their cousins. Beach Week, 2010. United Mitochondrial Disease Foundation. Easter Seals UCP North Carolina. DC charter school organized around inclusion.

veryspecialjourney.blogspot.com veryspecialjourney.blogspot.com

A Very Special Journey: August 2011

http://veryspecialjourney.blogspot.com/2011_08_01_archive.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Friday, August 12, 2011. DC charter school organized around inclusion. More social entrepreneurs, schools, and school systems need to move in this direction. Where can one find a school like this. Links to this post. Saturday, August 06, 2011.

veryspecialjourney.blogspot.com veryspecialjourney.blogspot.com

A Very Special Journey: July 2011

http://veryspecialjourney.blogspot.com/2011_07_01_archive.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Thursday, July 28, 2011. Vacation with Abridged Family. Links to this post. Wednesday, July 13, 2011. Don't Be Jealous: We Saw the Wiggles Live. Links to this post. Subscribe to: Posts (Atom). The kids with their cousins. Beach Week, 2010.

veryspecialjourney.blogspot.com veryspecialjourney.blogspot.com

A Very Special Journey: Vacation with Abridged Family

http://veryspecialjourney.blogspot.com/2011/07/vacation-with-abridged-family.html

A Very Special Journey. This blog is dedicated to discussing the ups and downs of a family with a child who has Mitochondrial Disease. A blog seems to be a good way to share our experiences as a family and to hopefully connect to others with similar experiences. Thursday, July 28, 2011. Vacation with Abridged Family. Subscribe to: Post Comments (Atom). The kids with their cousins. Beach Week, 2010. United Mitochondrial Disease Foundation. Easter Seals UCP North Carolina. Vacation with Abridged Family.

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