I know I have said this before, but my life as a photographer has presented me with opportunities time and again to meet people that have a profound effect on my life. I’m amazed at how an ordinary day can be completely transformed with one phone call. That’s what happen last week with Ashley called inquiring about me photographing her 3 year old daughter for the holidays. As she began to tell me a little about Bayleigh I immedietaly went into crafting overload. I knew that I had to make her photo shoot as unique and special as her little girl is.
Bayleigh has a rare genetic disease named Dystrophic Epidermolysis Bullosa. Currently there are no cures, so Bayleigh continues to suffer from blisters internally and externally! She is one of three children in the state of Washington that has this rare disease. If you want your day to be transformed as mine was, you can follow Bayleigh’s story on Facebook at Bayleigh’s Butterfly.
https://www.facebook.com/bayleighsbutterfly?ref=stream&filter=1
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