
H.R.1255 |
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H.R. 1255 is a federal disability rights bill aimed at advancing the rights of individuals with profound cognitive disabilities whose care needs are often best provided for in Medicaid-licensed homes where high quality, compassionate supports are provided. Introduced by Rep. Barney Frank (D-MA), H.R. 1255 has now has 87 cosponsors, both Democrats and Republicans. This legislation addresses the injustice of federally-financed class action lawsuits filed with the ideological purpose of moving vulnerable individuals with profound developmental disabilities from their homes into community settings, despite the fact that most residents or their guardians oppose the move. Such displacement violates the civil and human rights of the affected residents to maximize their development potential in safe and specialized residential homes where they are very much integrated in the surrounding community. H.R. 1255 INTRODUCED BY BARNEY FRANK ORGANIZATION SIGN ON LETTERJOIN 100 ORGANIZATIONS About H.R. 1255 H.R. 1255, if passed, will require that before federally-financed class action lawsuits against Medicaid-certified and funded ICFs/MR can proceed, residents and guardians must receive notice of the lawsuit and be given a time-limited opportunity to opt-out of the proposed lawsuit, or do nothing and join in. Why H.R. 1255 is needed and supported by families of ICF/MR residents Class action lawsuits have closed many ICFs/MR and reduced options for those who need fulltime care Fifteen of these cases have led to the closure of ICFs/MR, affecting thousands of individuals with mental retardation (see, http://www.vor.net/classactions.htm). Bizarrely, despite the fact that ICFs/MR are a residential option created by federal law and funded and monitored by HHS, most of these lawsuits are filed under the Protection & Advocacy (P&A) program, whose lawyers are also funded by HHS. These ideologically-driven suits are essentially HHS v. HHS. H.R. 1255 could help prevent tragic outcomes and preserve residential choice H.R. 1255 is consistent with federal law; specifically, the Developmental Disabilities Assistance and Bill of Rights Act (DD Act), which authorizes funds for P&A attorneys, embraces the policy that individuals and their families/guardians are the “primary decisionmakers” regarding the services and supports they receive (see, DD Act, 42 U.S.C.15001(c)(3)(2000)). Individuals and their families/legal guardians should make fundamental care decisions, not lawyers. |





