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.
Wednesday, November 9, 2011
Di from Arkansas
Hello tis me again, I must apologize to Di, I have not posted very much since Janice and I got back from Ohio. We were down there with some wonderful ladies who we met at another retreat in Canada and when they had their own retreat in October, I invited myself down. Of course they said yes, and that they would love to have us (Janice and I). While we were there, Di had stitched up a lovely fingertip towel for our project and she was working on another one that weekend. And silly me had not posted her work. So finally, here it is.
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