November 17th is SMS awareness day. A day for us impacted by this genetic disorder to try to get the word out. Not that I don't talk about it all the time on here anyways. Because I do.
But, I don't talk about it much to those who actually spend time with Finleigh on a regular basis. So this year, we're going to try to spread the word at Finleigh's school. They all know who she is. They all know that she's different. But I'm not sure they know much about this syndrome that affects an estimated 1 in 15,000 to 25,000 people.
So. I guess. That's about all I have to say about that.
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