We share a lot about our medical. But I wanted to take a moment and share our joys! The kids have a LOT of bad days, but they have really good days too!! This is one of those days!!! 
We took these
pictures with our first big snow this year. The kids don't endure long to be in the cold or running around, but when they get a chance too, they make the most of every moment!
Snow balls!! Snow men!!! Snow angels!!!!
We have tons of fun together! Mito is tough but we remember every day that we may have Mito but Mito certainly doesn't have us!!!
On a quick note regarding the van...
We just got another $500!!! So We are still coming right along! This gift brings our total to $2,574.38
We are so excited! Please continue to share our story for many reasons... YES we need a van and we need people to continue to gather around to meet this need, but also, people need to begin understanding more and more about Mito. Just this weekend, another precious Mito baby went to be with Jesus! There just isn't enough knowledge! Please help us teach others about Mito so that kids can be diagnosed early, treatment started sooner and more research to take place on how to find a cure or better treatments! Worth a cure! Every child!!
We doctors know little about this unless we HAVE a good REASON to LEARN about it, such as an afflicted patient or family member, or if they have or know someone with a condition in a similar category, such as autoimmune conditions. Even tho I'm close to the Pfohl family, since I'm not directly involved in their care, I learn most from Mindy herself. She is very bright and able to keep each child's needs straight. I would trust ANYTHING she tells me is wrong with one of her children or what needs to be investigated. I'm actively trying to help them obtain funds to get a van to transport the family and their supplies. I hope anyone reading this will consider giving ANY sized donation. They all add up.
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