This month is, super-coincidentally, an awareness month for 2 conditions I have – a craniofacial condition (Moebius syndrome) & alopecia, a much more common autoimmune disease.
Besides the fact that I’m a bit bewildered by the fact that there are two different craniofacial months each supported by different organizations, I think it’s great to see what various organizations are doing and how they incorporate other organizations to spread the word.
The American Girl company posted a great photo of their “wigless” dolls – perfect for young girls with alopecia or who are undergoing cancer treatments. I loved that it was important enough to feature.
I seeing RJ Palacio, who wrote the children’s book Wonder – about a boy with a craniofacial condition – speak tonight and I really think she does a lot to spread the word about craniofacial conditions. Or at least I think it could, so I hope it continues to spread both her message about kindness and about awareness for craniofacial conditions.
Those American Girl dolls are so inspirational. Thanks for sharing.