Alba tull biography of william

Our singular goal is to find cures for Rett syndrome as efficiently and quickly as possible. We will not rest until our children have them. Twelve of our board members have a child, grandchild, or sibling with Rett. We are driven by the most profound motivator — love for our children and an unwavering commitment to change their lives and the lives of all with Rett.

Our scientific staff are equally dedicated. Their track record, integrity, and combined experience is unparalleled amongst Rett non-profits. Our track record speaks for itself.

Based in Los Angeles,

Built on decades of scientific advances Roadmap to Cures will select and drive three genetic medicines that attack the root cause of Rett syndrome to clinical trials by Monica launched the Rett Syndrome Research Trust in late to pursue the next steps from that milestone. As chief executive officer she oversees all aspects of the organization, including day-to-day operations, strategic direction, fundraising, and communications.

Together with her colleagues and with input from advisors and the scientific community at large, Monica sets and executes RSRT's research agenda. She is a founding trustee of the American Brain Coalition. In Monica was featured in a New York Times article. Monica has two honorary doctorate degrees, one from the University of Massachusetts Medical School , received in , and one from the University of Edinburgh , received in Monica was born in Italy and immigrated to the US in her childhood.