Linda Taylor wrote -
Imagine the symptoms of autism, cerebral palsy, Parkinson's, epilepsy, and anxiety disorders…all in one little girl.
Now imagine these symptoms vanishing ... one by one.
This is the work of the Rett Syndrome Research Trust
Rett Syndrome is the most physically disabling of the autism spectrum disorders. It strikes at random in early childhood, affecting little girls almost exclusively. Many girls live into adulthood, requiring total, 24-hour-a-day care. There is no treatment beyond supportive, and often ineffective, measures such as feeding tubes, bracing, orthopedic and GI surgeries, and medications for anxiety and seizures.
Loss of speech and motor control
Functional hand use replaced by compulsive hand movements
Severe digestive problems
Orthopedic abnormalities including scoliosis and fragile bones
Disrupted sleep patterns
Impaired cardiac and circulatory function
The Rett Syndrome Research Trust is a 501(c)(3) organization (tax ID: 26-0687439).
Our numbers reflect RSRT’s commitment to our current and future supporters: In 2010 96% of every dollar donated was channeled directly to our program services - and RSRT has only one program service: research.
We believe passionately that Rett Syndrome is reversible. Everything we do, every day, stems from this belief. The scientists, technologies and ideas are in place. Our next steps are clearly defined. We need your support to continue our work.
If healing your child would heal your heart, we invite you to join our effort.
Whether you are the stunned and grieving mother and father of a newly diagnosed baby, or the seasoned parents of a thirty-year-old whose potential has been locked in by Rett Syndrome since she was a small child, our message to you is that this fate is unacceptable.
Taking this stand is not a simple task for a parent while doing all that daily nurturing requires, rejoicing in each small step our child can accomplish and grateful for any amelioration of pain and stress. But visionary leaps are not achieved through acquiescence or passive hope.
The Rett Syndrome Research Trust is a determined and highly focused research organization engaging the most brilliant scientific minds. The task of unlocking the mechanisms of Rett Syndrome and related MECP2 disorders is difficult and important. The restoration of normal human function in such a complex syndrome has enormous implications for a much greater population. Twenty-first century science is moving very rapidly; a new paradigm of what is possible has already been established for Rett Syndrome, and that is the starting point of the Rett Syndrome Research Trust.
If healing your child would heal your heart, we invite you to join our effort. For information on how you can make a meaningful contribution to this work, please contact us.
Help us REVERSE Rett Syndrome.