Info Just For You
- New and Expectant Parents
- Parents of School-Aged Children
- Brothers and Sisters
- Fathers (D.A.D.S.)
- Down Syndrome and Autism
- Families of Diversity
- K-12 Educators
- Policymakers and Advocates
- Research Opportunities
- Health Care Professionals
- General DS Information
Important Links and Documents
Visiting the State House
Find Your State Legislators
Join our Advocacy Efforts
(L to R) Katherine Craven, Jane Lane, Maureen Gallagher, John Anton,
Each year, the MDSC’s Legislative Advocacy Task Force reviews the scores of disability-related bills proposed by our friends in the Massachusetts legislature. From among them, the task force selects approximately a dozen pieces of proposed legislation that are the most consistent with our mission of ensuring that individuals with Down syndrome in the state are valued, included, and given opportunities to pursue fulfilling lives.
This slate of bills is approved by the MDSC Board of Directors and is known as our Legislative Platform. Each bill may be filed in the House, the Senate or both. Given limited resources, the MDSC chooses one or two “priority bills,” toward which the MDSC is able to devote significant resources. The MDSC also puts its weight behind the 10 “support bills” on our statewide platform, though to a lesser degree.
The late Massachusetts politician Tip O’Neill famously said that “all politics is local.” Indeed, we at the MDSC understand that the most effective method for getting our bills made into law is for you to reach out to your local state representatives and senators. Let them know what you care about and how they should vote. Even a single call from a single constituent can easily put a bill on a legislator’s radar that wasn’t before, transforming disinterest into advocacy.
To find your legislator, go here.
2015-2016 Platform Fact Sheets & Testimony
2015 Advocacy Day Fact Sheets
For Central Mass. residents:
2nd Annual Advocacy Day at the State House
The MDSC's 2nd Annual Down Syndrome Advocacy Day was held on June 4, 2015. It was an unbridled success as hundreds of self advocates and legislators gathered before the Grand Staircase of the State House to learn about and push for funding and policy priorities that allow people with Down syndrome to reach their fullest potential.
MDSC Executive Director Maureen Gallagher and MDSC Board Chair Steve Narey made a compelling case for our two new priority bills and funding for the MDSC line item and DDS line items to prepare folks for their meetings with legislators. These critical asks of the Mass. Legislature will provide access to organ transplants, more opportunities for higher education, and funding for MDSC's and DDS's many programs and initiatives.
The MDSC's House of Representatives Legislative Champion of the Year award was presented to House Ways & Means Chairman Brian Dempsey. The Senate Champion of the Year Award was presented to former Senator Richard Moore, who was introduced by Senate President Stanley Rosenberg. Both winners were presented with original works of art by painter Michael Avakian, who happens to have Down syndrome.
After the formal ceremonies, advocates fanned out throughout the building to meet with their legislators to tell their personal stories and lobby for Down syndrome priorities.
As Executive Director Maureen Gallagher said: "Without your active participation and advocacy, the MDSC would never have been as successful as we have been. With your help, the MDSC has become a strong voice for individuals with Down syndrome and their families."
The MDSC Makes Legislative History - June 2012
June 22, 2012 was an historic day for people with Down syndrome, their families and those who love them in Massachusetts. Just after noon, in the Governor's chambers of the State House, surrounded by more than a dozen legislative leaders, parents of people with Down syndrome and self-advocates, Governor Patrick signed landmark legislation that promises to bolster a bright future for the Down syndrome community in the Bay State.
An Act Relative to Down Syndrome Genetic Test Results (H3825), modeled on the national Kennedy-Brownback bill, will have a tremendous impact for decades to come.
The law mandates that new or expectant parents of children with Down syndrome are given the latest, culturally-appropriate information about what it means to have a child with Down syndrome and contact information for services to ensure they have access to the supports that every family in their position needs. The legislation specifically identifies the MDSC's Parents First Call Program as a key resource for these families, formally recognizing our signature outreach program, which is a national model in the field.
The bill, the broadest state legislation of its kind in the nation, was sponsored by Rep. Tom Sannicandro of Ashland, whose son David has Down syndrome and Senator Katherine Clark of Melrose. Both have been tireless champions of good disability policy. Given recent scientific developments around prenatal diagnosis, it was critical to get a bill like this on the books.
The future is indeed bright for the Down syndrome community in Massachusetts. See the complete communication about the passage of the Prenatal Bill from our Executive Director here.
2013-2014 Priority Bills (187th Session of Mass. General Court)
To find your legislator, visit the Massachusetts Legislature’s recently revamped website.
Testimony in support of bills on MDSC’s platform
An Act to require national background checks
For the most updated information on our priority bills or to get involved in the MDSC's advocacy efforts, please contact us at firstname.lastname@example.org.