sayaboutthat.blogspot.com
And That's All I Have To Say About That: And Then There Were SIX!
http://sayaboutthat.blogspot.com/2012/04/and-then-there-were-six.html
And That's All I Have To Say About That. Tuesday, April 3, 2012. And Then There Were SIX! As in six WIPs! I finished Diamond Delights 9 by DebBee's Designs over the weekend. While Dana, Wendy, and Melissa GTG'd at my house, I finished the "squiggles" and started beading. And kept beading, and beading, and then decided more bling was called for. What can I say, my inner crow must be heard! I also have an updated photo of Egypt Garden to share. But, I am getting there! April 3, 2012 at 11:14 PM. And, ewww,...
stitching-for-jaxon.blogspot.com
Stitching for Jaxon: Life is back to normal
http://stitching-for-jaxon.blogspot.com/2014/11/life-is-back-to-normal.html
Jaxon was diagnosed with Fibrodysplasia Ossificans Progressiva (FOP) 5 days after his second birthday (Feb 2011). His mother told me that Jaxon is the seventh (7th) child in Canada to be diagnosed with this rare disease. I am his great-aunt Louise and I come up with the idea of this blog to keep people informed, and to use my passion for stitching to raise money for the FOP organizations. How can you help? Wednesday, November 26, 2014. Life is back to normal. Subscribe to: Post Comments (Atom). Life is b...
stitching-for-jaxon.blogspot.com
Stitching for Jaxon: July 2014
http://stitching-for-jaxon.blogspot.com/2014_07_01_archive.html
Jaxon was diagnosed with Fibrodysplasia Ossificans Progressiva (FOP) 5 days after his second birthday (Feb 2011). His mother told me that Jaxon is the seventh (7th) child in Canada to be diagnosed with this rare disease. I am his great-aunt Louise and I come up with the idea of this blog to keep people informed, and to use my passion for stitching to raise money for the FOP organizations. How can you help? Tuesday, July 29, 2014. Tuesday, July 1, 2014. Subscribe to: Posts (Atom). Fibrodysplasia Ossifican...
stitching-for-jaxon.blogspot.com
Stitching for Jaxon: I'm Back!!
http://stitching-for-jaxon.blogspot.com/2015/04/im-back.html
Jaxon was diagnosed with Fibrodysplasia Ossificans Progressiva (FOP) 5 days after his second birthday (Feb 2011). His mother told me that Jaxon is the seventh (7th) child in Canada to be diagnosed with this rare disease. I am his great-aunt Louise and I come up with the idea of this blog to keep people informed, and to use my passion for stitching to raise money for the FOP organizations. How can you help? Friday, April 3, 2015. Subscribe to: Post Comments (Atom). We raised over $700. Rare Disease Day - ...
stitching-for-jaxon.blogspot.com
Stitching for Jaxon: To 2015 - hopefully a better year
http://stitching-for-jaxon.blogspot.com/2015/01/to-2015-hopefully-better-year.html
Jaxon was diagnosed with Fibrodysplasia Ossificans Progressiva (FOP) 5 days after his second birthday (Feb 2011). His mother told me that Jaxon is the seventh (7th) child in Canada to be diagnosed with this rare disease. I am his great-aunt Louise and I come up with the idea of this blog to keep people informed, and to use my passion for stitching to raise money for the FOP organizations. How can you help? Friday, January 2, 2015. To 2015 - hopefully a better year. Subscribe to: Post Comments (Atom).
stitching-for-jaxon.blogspot.com
Stitching for Jaxon: April 2014
http://stitching-for-jaxon.blogspot.com/2014_04_01_archive.html
Jaxon was diagnosed with Fibrodysplasia Ossificans Progressiva (FOP) 5 days after his second birthday (Feb 2011). His mother told me that Jaxon is the seventh (7th) child in Canada to be diagnosed with this rare disease. I am his great-aunt Louise and I come up with the idea of this blog to keep people informed, and to use my passion for stitching to raise money for the FOP organizations. How can you help? Sunday, April 20, 2014. Back from Branson, Missouri. Tuesday, April 1, 2014. Toy Shop is finished.
stitching-for-jaxon.blogspot.com
Stitching for Jaxon: A Very Successful Craft Fair
http://stitching-for-jaxon.blogspot.com/2014/11/a-very-successful-craft-fair.html
Jaxon was diagnosed with Fibrodysplasia Ossificans Progressiva (FOP) 5 days after his second birthday (Feb 2011). His mother told me that Jaxon is the seventh (7th) child in Canada to be diagnosed with this rare disease. I am his great-aunt Louise and I come up with the idea of this blog to keep people informed, and to use my passion for stitching to raise money for the FOP organizations. How can you help? Saturday, November 22, 2014. A Very Successful Craft Fair. Subscribe to: Post Comments (Atom).
stitching-for-jaxon.blogspot.com
Stitching for Jaxon: April 2015
http://stitching-for-jaxon.blogspot.com/2015_04_01_archive.html
Jaxon was diagnosed with Fibrodysplasia Ossificans Progressiva (FOP) 5 days after his second birthday (Feb 2011). His mother told me that Jaxon is the seventh (7th) child in Canada to be diagnosed with this rare disease. I am his great-aunt Louise and I come up with the idea of this blog to keep people informed, and to use my passion for stitching to raise money for the FOP organizations. How can you help? Monday, April 6, 2015. Rare Disease Day - February 28, 2015. Http:/ ottawa.ctvnews.ca/video? Fibrod...
stitching-for-jaxon.blogspot.com
Stitching for Jaxon: May 2014
http://stitching-for-jaxon.blogspot.com/2014_05_01_archive.html
Jaxon was diagnosed with Fibrodysplasia Ossificans Progressiva (FOP) 5 days after his second birthday (Feb 2011). His mother told me that Jaxon is the seventh (7th) child in Canada to be diagnosed with this rare disease. I am his great-aunt Louise and I come up with the idea of this blog to keep people informed, and to use my passion for stitching to raise money for the FOP organizations. How can you help? Sunday, May 18, 2014. Some pics of the goodies from Nashua. Sunday, May 11, 2014. Hello wonderful p...
stitching-for-jaxon.blogspot.com
Stitching for Jaxon: January 2015
http://stitching-for-jaxon.blogspot.com/2015_01_01_archive.html
Jaxon was diagnosed with Fibrodysplasia Ossificans Progressiva (FOP) 5 days after his second birthday (Feb 2011). His mother told me that Jaxon is the seventh (7th) child in Canada to be diagnosed with this rare disease. I am his great-aunt Louise and I come up with the idea of this blog to keep people informed, and to use my passion for stitching to raise money for the FOP organizations. How can you help? Friday, January 2, 2015. To 2015 - hopefully a better year. Subscribe to: Posts (Atom). Stoyanka Iv...
