Even before Breanna was born, we knew that she was special; and the first time we laid eyes on her, we knew that she was the greatest gift that GOD has ever given us.

Within a few months of her birth we noticed that she was not reaching her milestones, and something major was wrong. For months and months we searched to find out why she was unable to do the simplest things.

After almost a year of searching, we received those words that no parent ever wants to hear..."I am afraid I have bad news. Your daughter has a rare neur-muscular disorder called Dystonia."

This site is dedicated to the effort of creating awareness for Dystonia in an effort to find a cure for Breanna and the thousands like her.

Throughout its pages, this website will tell The Breanna Rose Story and the challenges she has been forced to overcome, as well as the continued struggle for the "Freedom to Move."

Please join us!