The legislation, approved by the Finance Committee, includes funding for systems to enhance school safety by providing direct communication between school personnel and first responders.
This bipartisan working group will be designed to evaluate the implementation of safety and security measures the state mandated following the events of Sandy Hook, and to produce new recommendations to ensure school security and safety going forward.
Sen. Fasano also spoke to the group about bipartisan efforts in Connecticut to craft legislation that supports students, including Hispanic students, working towards earning a college degree if they are on a path to citizenship.
Rep. Yaccarino Meets with Individuals from Connecticut Department of Developmental Services (CT DDS) Families First
The mission of CT DDS Families First is to secure all opportunities and support Connecticut citizens with intellectual and developmental disabilities (I/DD) so that they may live full and productive lives in their communities.
Quinnipiac University presents town of North Haven with $700,000 check, which will be used for two elementary school playgrounds
Freda said, the money will be used to build a new playground at the Montowese Elementary School, and an inclusive handicapped accessible playscape at Ridge Road School.
The event highlighted the importance of the Bioscience sector in Connecticut – including taking steps towards urging that new improvements be made to bring Connecticut successfully into the future.
Fasano, Lawmakers Call for Public Hearing, Full Transparency on State’s Inmate Medical Care Failures
In recent months, a pattern of cases has come to light in which inmates in the state’s correction department were reportedly not provided proper medical care.
Read Across America is an annual event held on Dr. Theodor Seuss Geisel’s birthday, March 2nd, to commemorate his life’s work and his ability to captivate young audiences with his unique children’s books.
Sen. Fasano and Rep. Yaccarino are both long-time advocates for individuals who suffer from rare diseases and have worked on legislation to raise awareness and help people access treatment and research.