My school blog is working again, thanks to my wonderful friend Megan! She is basically a technology prodigy, and I feel so incompetent next to her! She basically hacked into my blog (with my permission!) and got it all squared away again. She thinks that blogger was the one that messed up the way I was used to doing links, but she showed me a different way to do it so that I can still add links. AND, she did it all over email from 20 minutes away! I was so thankful that I sent her a thank you card and candy through the Pony (school system mail service). My kids have really been bummed about the blog being down, so they will be thrilled to know it is working again! :)
If you happen to pick up the latest Reader's Digest, there is an article in there about Piper Breinholt , a four year old with CCMS. If you've been around here a while, you'll remember wayyyyyy back when we first received Abby's diagnosis that I was able to speak to Piper's mom, Reagan. The article is more about their story and not as much about the ins and outs of CCMS, but I think it's probably enough to get some people googling it and I'm hoping a few will end up here. Every once in a while, I give a blog post the title of Cerebrocostomandibular Syndrome so that it would show up in Google. My ever-present hope is that people will stumble across my blog and 1) be encouraged by the hope we have in Christ, 2) feel a connection with someone in a similar situation as them, or 3) get excited over the miracles that have been performed in Abby's life!! (a combination of all 3 is great too!) :) Notice that it's not to get famous and it ...
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