Fall 2003 Newsletter   click for links to other newsletter pages
 
 
 
Dr. Dynasaur Premiums Increased
Reorganization of the Agency of Human Services
Respite Program Appropriation Increased
 
 
 
Dr. Dynasaur Premiums Increased in the 2003 Legislative Session
Effective July 1, 2003, premiums paid by families for Dr. Dynasaur health insurance coverage for their children increased significantly.  These increases were part of a major restructuring of Vermont’s Medicaid system passed by the Legislature in 2003, including Dr. Dynasaur, Vermont Health Access Program (VHAP), pharmacy assistance programs, and coverage for working people with disabilities.  An additional change adopted by the legislature, scheduled for implementation in 2004, is that premiums will become prospective – that is, payment must be received in advance by the first of the month in order to have coverage that month.

Parent to Parent/Family Voices of Vermont worked diligently to get word of proposed changes out to affected families and professionals, and to help the legislators making the budget understand the impact of their proposals.  Initial premium increases on the table were as high as four times existing levels for some Dr. Dynasaur families.  There was great concern that families would not be able to pay the premiums, and be forced to drop their children’s medical coverage.

Working with other advocates, including the Vermont Coalition for Disability Rights and the Vermont Children’s Forum, we were able to get the appropriations committees to reduce the extent of premium increases and build in some other procedural safeguards.  Senator Dick Sears of Bennington, and others on the Senate Appropriations Committee, worked especially hard on behalf of families to contain increases in Dr. Dynasaur premiums.

Families with incomes below 185% of the federal poverty level will continue to pay no premiums for their children’s Dr. Dynasaur coverage. Beginning July 1st, premiums for families with incomes between 185% and 225% of the computed federal poverty level ($34,040 to $41,400 for a family of four) increased from $20 to $25 per month.  For families with incomes between 225% and 300% of the federal poverty level ($41,400 to 55,200 for a family of four) premiums increased from $24 to $35 per month for households with other health insurance, and from $50 to $70 per month for those with no other health insurance.

Parent to Parent’s staff was disappointed that nearly $84 million dollars of new federal fiscal relief money for Medicaid and other programs, scheduled to be received by Vermont over the next 18 months, was not used to offset premium increases.  Since the money came in very late in the legislative session—just a week before adjournment –the joint budget committee placed the vast majority of these extra funds into reserves for Medicaid and other General Fund programs.   While not providing relief to families this year, this action should help protect against additional cuts or premium increases in the coming year and beyond.

Following wrap up of the budget negotiations, legislative budget writers expressed hope that the changes passed would not result in significant disenrollment. Patricia House, Commissioner of the Department of Prevention, Assistance, Transition, and Health Access (PATH), which administers Medicaid programs in Vermont added: “We will work to implement the new premiums in a way that works for families, and we will very carefully evaluate their impact.”  ©

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Voices of Families Sought to Inform the Reorganization of the Agency of Human Services
A major initiative to reorganize the Agency of Human Services (AHS) was continued from the Dean to the Douglas Administration, and authorized by the Legislature in the 2003 session.  This restructuring will impact all departments and programs of AHS and their relationships to other state and nonprofit organizations, including schools. Parent to Parent/Family Voices of Vermont has been one of many groups providing testimony on the importance of including consumer voices in the planning process.

Eileen Elliott, Deputy Secretary for the Agency of Human Services, was present throughout the legislative hearings.  She concluded: “Many … complain about case coordination, program access, eligibility restrictions and administrative hurdles that appear illogical or even contrary to good public policy. Funding streams and the limitations they pose are frequently mentioned as frustrating good client service. Many … point out the shortsightedness of our lack of early intervention protocols in situations that clearly need them. Now begins the hard work of examining our programs and systems, working with our partners, and listening to our clients to decide where to make improvements.”
 
Regional Meeting Schedule – For more details, contact Regional Advisory Groups through the AHS Reorganization website at http://www.ahsnet.ahs.state.vt.us/council/ 
September 17: 
Middlebury: People of Addison County Together 
Barre: Central VT Community Partnership  
September 18: 
St. Johnsbury:  St. Johnsbury Community Coordinating Council  
St. Albans: Franklin/Grand Isle Community Partnership  
September 24: 
Morrisville: People in Partnership  
Rutland: Rutland Regional Board for Family Services 
September 25: 
Burlington: The Champlain Initiative  
Springfield: The River Connection Regional Stakeholder Meetings 
October 1: 
Hartford: Community Partnership of Orange/Windsor 
Bennington: Catamount Partnership for Community Health, Inc. 
October  02: 
Brattleboro: Alliance for Building Community  
Newport: Orleans/Essex Community Partnership 
At a recent meeting of advocacy groups with AHS Secretary Charlie Smith, Smith pledged that the process is being designed “to try to get complete consumer input.  We will work together to rethink the way the Agency of Human Services can best serve Vermonters.”  Based on consumer, advocate, employee, and other stakeholder views gathered from July through October 2003, AHS will prepare a report for the legislature by January 15, 2004.

Secretary Smith described a four part process to gather information: surveys, regional and statewide meetings, focus groups and task forces on specific topics, and a web site. As a first step, information is being gathered from surveys distributed to AHS employees; advocates, providers, and contractors; consumers; and educators.  These surveys were distributed in July and early August and collected by August 29, 2003.

Next, 12 large regional meetings are scheduled for September and early October that will gather together all the regional stakeholders, including the schools.  The purpose of these meetings is to collect local perspectives, share indicators about the health of the region and other quantitative data from surveys; gain qualitative data from participants; and summarize and prioritize messages to be represented at a Statewide Conference scheduled for late October.  These meetings are a wonderful opportunity to provide testimony about what works and what doesn’t for families.  (See schedule at left):

Peter Youngbaer of the Vermont Coalition for Disability Rights (of which Parent to Parent/Family Voices is a member) commented, “We cannot urge consumers and family members enough to get involved with their regional partnerships and planning councils (a subset of the partnerships).  These local discussions and forums will inform the statewide discussion and send representatives to the state advisory group.  Get involved with your partnership - contact them, if they haven't contacted you - and soon.”
A statewide conference is scheduled for October 28-29 with participants from the regional partnership forums and other statewide organizations.  The purpose is to share and understand data gathered; find common ground; understand differences; and produce preliminary recommendations. AHS is also planning to assemble a number of task forces to examine problems and recommend solutions, including one to continue the work of the Long Term Care Policy Cluster and Respite Summits Parent to Parent has co-sponsored.
In addition to the regional meetings, topic specific focus groups to gather information from targeted groups of consumers will be scheduled in September and October.  It is highly likely that some of these groups will include topics related to children with special needs (for example autism, or services like nursing and personal care), but as this newsletter goes to press the topics and dates have not yet been determined. Anyone potentially interested in participating in a focus group should contact Kay Van Woert at 985-5668 as soon as possible.
Finally, the AHS will solicit comments via a web site devoted to information on the reorganization.  The address is http://www.ahsnet.ahs.state.vt.us/council/ This site contains up-to-date information on the reorganization process, as well as providing an opportunity to leave public comment.
It is critically important that the Agency of Human Services hears family voices as the agency plans and implements this reorganization. Add your voice today!  ©

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Children with Special Health Needs Respite Program Appropriation Increased Significantly
The Children with Special Health Needs respite program has long been Vermont’s most under funded respite program.  Parent to Parent/Family Voices of Vermont has worked with the Vermont Coalition for Disability Rights for several years to gradually increase the level of funding for this program for families with children with significant health challenges.  This year, thanks in large part to the efforts of House Appropriations Committee member Representative Martha Health, the legislature made a significant enhancement by adding $80,000 to the program’s prior year funding of $170,000.  ©
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Fall 2003 - In this Issue:
From our Director
Board & Staff Update
Thank you, Richard Tarrant!
Family Support Report
Supporting Parent Honor
Vermont Medical Home Update
Family Voices of Vermont
Partners In Care Conference '03
Inn Raffle #2!
Family Story Update: Demeritt
Our Calendar | News & Note 

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