Even before Breanna was born, we knew she was special. The first time we laid eyes on her, we knew she was the greatest gift that God could ever give us.

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

After almost a year of consulting doctor after doctor, we received devastating news, words that no parent would ever want to hear: "I’m afraid I have bad news. Your daughter has a rare, neuro-muscular disorder called Dystonia."

This site was created to bring understanding and awareness about Dystonia, and about the efforts to find a cure for Breanna and the thousands of others like her.

Throughout its pages, you’ll hear Breanna Rose’s story, the challenges she has faced (and many which she has overcome), as well as the continued struggle for the "freedom to move."

We welcome your interest! Blessings, Dave and Kim Strange