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hannahfaithmohn.com
This is a Blog about our daughter Hannah Faith Mohn who before birth was diagnosed with a very rare neuromuscular disease, so rare that they are calling it Hannah's disease right now. She also has Arthrogryposis Multiplex Congenita or AMC which is a stiffening of her joints. Please feel free to pass along as we are trying to keep it informational as well to help out other families who may be going with the same thing. Visit site »| Tweet |