Rett Syndrome Awareness Month

WHEREAS, Rett syndrome is a devastating neurodevelopmental disorder caused by a sporadic, genetic mutation of the MECP2 gene on the X chromosome and mainly affects females; and

WHEREAS, every two hours a girl is born with Rett syndrome, but its symptoms usually do not appear until six to 18 months later; and

WHEREAS, girls with Rett syndrome are generally born healthy, then begin to show signs of regression or stagnation of milestones that would otherwise be routinely accomplished; and

WHEREAS, those with Rett syndrome lose their ability to speak, walk, and control their hands and may develop seizures and scoliosis; and

WHEREAS, due to the genetic mutation, apraxia is one of the most severe handicaps associated with Rett syndrome, causing an inability to carry out learned, purposeful movement; and

WHEREAS, in advance of finding a cure for Rett syndrome, researchers and scientists from around the world are working to find treatments; and in 2007, scientists discovered the reversal of Rett syndrome symptoms in mice; and

WHEREAS, increased awareness of Rett syndrome is essential to providing the necessary funding for those who are dedicated to finding a cure:

NOW, THEREFORE, I, Robert Bentley, Governor of Alabama, do hereby proclaim October 2011, as

Rett Syndrome Awareness Month

in the State of the Alabama, encourage all citizens to gain a greater understanding of this disease, and support education and the funding of research programs to find a cure.

 

Given Under My Hand and the Great Seal of the Office of the Governor at the State Capitol in the City of Montgomery on the 18th day of October 2011.

 

                                                                                 Governor Robert Bentley