We originally started this blog (years ago) to keep track of the every day things in our lives that we didn't want to forget but knew that we would in time. As life got in the way, we posted less and less until March 2010 when Matthew's arrival rocked our world. Now we use this blog to let everyone know how Matthew is progressing and the big events going on at the Hoy House. We are so appreciative of everyone who has read our story and has thought and prayed for Matthew and for us.
Today is World Rare Disease Day-- and though Matthew is alone in his diagnosis, he is far from alone being rare. We are thankful for those that have paved the way before Matthew and we stand beside those that are walking the rare journey.