Wednesday, December 28, 2011

VOR calls for moratorium on deinstitutionalization lawsuits

Concerned about deaths of intellectually disabled individuals, VOR, a national advocacy organization representing people with intellectual disabilities and their families, has asked Members of Congress in several states to call for a moratorium of federally-funded deinstitutionalization lawsuits.

“Protection & Advocacy and Department of Justice lawsuits have forced people with severe intellectual disabilities from their specialized homes and into smaller, unlicensed settings that are too-often not prepared to handle people with such severe degrees of intellectual disability,” said Tamie Hopp, VOR’s Director of Government Relations & Advocacy.

VOR’s call for a moratorium was prompted by the New York Times reporting of tragic preventable deaths of hundreds of people in New York group homes. Specifically, the Times found that “One in six of all deaths in state and privately run group homes [in New York], or more than 1,200 in the past decade, has been attributed to either unnatural or unknown causes. (“1,200 Deaths and Few Answers,” November 6, 2011).

“The silence by federal agencies in response to these deaths is deafening,” said Hopp. “Not only have P&A and DOJ done little if anything in response to these deaths, which numbered more than a 100 per year over 10 years, they have continued their ideological warfare on larger Medicaid-licensed and funded ICFs/MR.”

Since 1996, P&A have filed at least 17 lawsuits involving ICFs/MR for the purpose of “community integration.” In recent years, DOJ has also aggressively supported the closure of ICFs/MR in Georgia, Virginia, and Illinois, and is presently investigating similar facilities in Mississippi.

In Georgia, the DOJ settlement calls for the displacement of 10,000 people with mental illness and developmental disabilities.   “It’s a little like loading more passengers onto the Titanic,” remarked William Fischer, Professor of Psychology, Center for Mental Health Services Research, University of Massachusetts.

The Independent Reviewer’s first year implementation report, released October 5, cites serious problems associated with Georgia’s community-based care system, including access to health care, isolation and at least one death due to neglect.

Even P&A has recently acknowledged problems with health and safety in community programs in Alabama and North Carolina (National Disability Rights Network, “Keeping the Promise: True Community Integration and the Need for Monitoring and Advocacy,” December 1, 2011).  In Alabama, P&A was directly responsible for the closure of facilities, leading to the very health and safety problems it now condemns.

“Remarkably, P&A asks to receive more funding so it can better investigate problems in the community,” said Hopp. “VOR would rather they stop spending resources on lawsuits and other activities which serve to place these vulnerable people at risk in the first place.”

VOR’s call for a moratorium was sent to Members of Congress representing New York, Georgia, Virginia, and Mississippi, as well as the 66 Congressional cosponsors of H.R. 2032, federal legislation also which seeks to reform the way these lawsuits are handled.

Thursday, December 22, 2011

New York Times article highlights concerns for disabled in state care

Early last month a report in the New York Times brought attention to a crisis in care for developmentally disabled residents in many state homes. Exerpts from the article are reprinted below. At the end of November, VOR referenced the same article in urging Congress to pass H.R. 2032 and improve safeguards. We've included their letter below as well.

You can help by writing to your representatives asking them to support reform and reauthorization of the Developmental Disabilities Act and passage of H.R. 2032.

EXCERPTS: In State Care, 1,200 Deaths and Few Answers (NY Times)

In New York, it is unusually common for developmentally disabled people in state care to die for reasons other than natural causes.

One in six of all deaths in state and privately run group homes, or more than 1,200 in the past decade, has been attributed to either unnatural or unknown causes, according to data obtained by The New York Times. In deaths not resulting from natural causes there had been concerns about the quality of care in nearly half of the 222 cases.  Few states that release such data. [*see Note below.]

What’s more, New York has made little effort to track or thoroughly investigate the deaths to look for troubling trends, and did not take steps to prevent reoccurrence (such as alerts to all group homes), resulting in the same kinds of errors and preventable deaths in group homes, over and over. Responses were typically limited to the group home where a resident died.

The state does not even collect statistics on specific causes of death, leaving many designated as “unknown,” even in cases where a cause is known.

The Times undertook its own analysis of 7,118 death records and found disturbing patterns: some residents who were not supposed to be left alone with food choked in bathrooms and kitchens. Others who needed help on stairs tumbled alone to their deaths.  Some died in fires. Still others ran away again and again until they were found dead.

The data from the state commission, which is responsible for overseeing treatment for the developmentally disabled, included only the broad “manner” in which people died — by homicide or suicide, accidents, natural causes, and “unknown,” the biggest category (10%), other than natural causes.  The average age of those who died of unknown causes was 40, while the average age of residents dying of natural causes was 54, which suggests problems in care.

At homes operated by nonprofit organizations, low-level employees were often fired or disciplined, but repercussions for executives were rare. At state-run homes, it is also difficult to take action against state employed caregivers.

New York relies heavily on the operators of the homes to investigate and determine how a person in their care died and, in a vast majority of cases, accepts that determination. And the state has no uniform training for the nearly 100,000 workers at thousands of state and privately run homes.
Group homes now care for a vast majority of the New York’s developmentally disabled. Staff training to avoid common mistakes which lead to tragedy (such as chokings, drownings, and fires) should be pursued. Providers are not inclined to make changes unless the state requires it; the state must act.

[*Note: Media reports from more than 30 states, however, indicate a widespread, systemic problem with assuring quality care in small group home settings. See, http://www.vor.net/abuse-and-neglect.]

---

VOR_bnr

November 29, 2011

Dear Members of the U.S. Senate and House of Representatives:

VOR is a national, nonprofit organization advocating for individuals with intellectual and developmental disabilities (ID/DD) and their families.

The disability community is quite diverse, ranging from people with some physical limitations to people whose cognitive and/or physical limitations are so significant that they function at the level of a newborn or an infant and require around-the-clock care.

Families of individuals with profound intellectual disabilities who receive life-sustaining care in congregate facilities (ICFs/MR) fear that the forced eviction of their family members will be a virtual death sentence.

A recent New York Times front page story, “In State Care, 1,200 Deaths and Few Answers," confirms their worst fears (see above). It exposes an unchecked system of group homes throughout New York where 1,200 deaths occurred during a 10-year period due to preventable tragedies such as drowning in bathtubs, fires, choking and wandering.  The Times attributes these deaths to a lack of system-wide reporting or staff training.

New York is not alone. There is widespread documented abuse, neglect and death of individuals with profound intellectual disabilities (most of whom are also medically fragile with physical disabilities) in small settings in more than half the states. [*1]

With apparent disregard for the impact on affected residents, many ICF/MR evictions and closures are due to lawsuits and other actions by federally-funded organizations, such as Protection and Advocacy (P&As)  and the  Department of Justice lawyers.

Congress must act. Legislative solutions are at hand:

A.    Pass H.R. 2032, a bill introduced by Reps. Barney Frank, Bob Goodlatte and Debbie Wasserman Schultz, to restore the decision-making authority of individual residents of ICFs/MR and their legal representatives in federally-funded legal actions by P&A and the Department of Justice.

B.    Reform and reauthorize the Developmental Disabilities Act to prohibit their programs from using federal funds for downsizing and closing of Medicaid-certified and licensed public and private ICFs/MR, actions which disregard of resident choice and safety, and fly in the face of federal law, including the Supreme Court’s Olmstead decision.

With documented tragedies, why are the federal agencies, which are charged to protect people with disabilities, closing ICFs/MR? Could these federal protectors be more concerned about their reputations than the lives of those Americans they are charged to protec? [*2] People are dying. Residential facilities are necessary and must remain open. Congress must act.

Please contact Tamie Hopp, VOR’s Director of Government Relations at 605-399-1624 or thopp@vor.net with any questions. Thank you for your consideration.

Sybil Finken, Co-President       Ann Knighton, Co-President  

[*2] See, “Neglect for Sale, The American Prospect (November 30, 2000) http://prospect.org/article/neglect-sale (“Because the P&As were so instrumental in closing state institutions, several advocates told us, they fear divulging anything, particularly to the media, that might reflect negatively on community-based programs.”)

Wednesday, December 14, 2011

Former SDC summer camp yields clues to Valley history

Senior State Archaeologist Breck Parkman
stands in what's left of Camp Butler
photo: Beth Schlanker/Press Democrat
There's an interesting story in the Press Democrat this week that includes a bit of Sonoma Developmental Center history. (see Archaeologists examining 1930s-era summer camp at Sugarloaf state park, 12/11/11, by Bob Norberg.)

Back in 1920, when the Sonoma Developmental Center (SDC) was known as Sonoma State Hospital, the Center acquired property along Adobe Canyon in the northern part of Sonoma Valley to build a dam to create a reservoir. Plans were ultimately stopped by neighbors, and in 1964, the land became a state park.

But while SDC still had the property, a summer camp for children was operated there, providing an outlet for Boy Scouts and Camp Fire Girls during the years of the Great Depression. Staff of the California Department of Parks and Recreation are now documenting what remains of the camp site.

According to the PD article, the camp was built in 1931 and named after Dr. Frederick Butler, who was superintendent of the Center from 1917 to 1948. It was closed at the advent of World War II and never reopened.

Breck Parkman, Senior State Archaeologist is quoted as saying, "What is not apparent is whether the campers were wards of the state center, children of the staff or both."

Do you have any stories about or experience of the camp -- or know anyone who attended outings there? You can email Parent Hospital Association at info@parenthospitalassociation.org. It would be great to know more and pass the information on.

Friday, December 9, 2011

SDC residents create ornaments for official state capitol holiday tree

Residents of the Sonoma Developmental Center (SDC) created over forty ornaments for the annual State Capitol Tree Lighting Ceremony in Sacramento, which was held on Wednesday, December 7th, on the west steps of the State Capitol. This year marked the 80th year for California's official tree lighting ceremony.




The tree was decorated with approximately 900 hand-crafted ornaments created by children and adults with developmental disabilities who receive services and support from the state’s developmental centers and twenty-one nonprofit regional centers. The sparkle factor was amped up by the illumination of 10,000 ultra-low wattage LED lights.



Sonoma Developmental Center residents have participated in creating ornaments for the state tree for more than twenty years. This year the Center's ornaments included colored glittery pinecones, foamed windsocks, decorated cd’s, handmade Christmas trees, and many individualized ornaments made from paper and paper plates that were laminated to protect them from rainy weather.

Merry Christmas California, from everyone at Sonoma Developmental Center!

Tuesday, December 6, 2011

Sonoma Developmental Center Holiday Craft Faire -- Dec. 6 and 7, 2011

The annual holiday craft fair held at the Sonoma Developemental Center is happening now -- today and tomorrow -- December 6th and 7th, from 10 a.m. to 4 p.m. both days, in the Center's gymnasium.

More than twenty local vendors will be displaying their crafts and handmade goods. Items available for purchase will include knitted hats, pottery, bags with your name embroidered on them, handmade dog bowls, beauty products, ornaments, holiday baskets, handmade jewelry, baked goods, handmade toys, potholders, body lotions, candles, ceramics, one of a kind gifts -- and much, much more.

It sounds like you could do all your holiday shopping with just one visit to the SDC Craft Faire!
Proceeds from the event raise funds for client activities that are not funded by the State.

Entrance to the Craft Faire is free and the event is open to the public.  For directions to the gymnasium, located on the corner of Wilson and Sonoma roads, go to http://www.dds.ca.gov/Sonoma/Directions.cfm.

For more information about the Holiday Craft Faire, contact Becky Zyskowski, Coordinator of Volunteer Services at (707) 938-6713.
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