CA
DISABILITY COMMUNITY ACTION NETWORK - Linking people to disability rights
CAPITOL NEWS
REPORT - ISSUE #61-2004 Website NOW up:
www.cdcan.org
APRIL 9, 2004
- Friday
DDS Releases New Draft
of Parental "Share of Cost" Plan Requiring Families to Pay Portion of
Regional Center Community-Based Services
SACRAMENTO -
The Department of Developmental Services released this morning a new draft
of an implementation plan to require parents of children with
developmental disabilities between the ages of 3-17, to pay some portion
of their regional center funded community-based services. The
controversial plan, as previously reported, now attempts to mitigate
several of the major concerns raised by families, with some advocates
praising the Department of Developmental Services for being "responsive",
though withholding final judgment on the new proposal. The plan requires
approval from both houses of the legislature and the Governor.
The new draft
proposal is still likely to be opposed by other advocates as a "trojan
horse" that they claim will eventually result in forcing families to pay a
greater portion of costs than what is currently proposed. The Department
of Developmental Services however has said it believes the new proposal
protects families while also implementing ways to help contain costs so
that "core services" needed by people with developmental disabilities can
be maintained.
The new plan,
would be implemented locally by the regional centers, and would cover
families whose incomes were at or above 400% of the federal poverty level
(about $70,000 for family of four) on a sliding scale. The plan would also
only cover certain specific services used by the family: respite, day
care and camping. All other services funded through the regional centers
are not included in the the current family share of cost plan. The new
plan does not call for any "enrollment fee" for regional center services.
Cost
Savings And New Regional Center Operations Positions
The Department of
Developmental Services projects only modest savings in the first year of
the plan, assuming it is approved as drafted, of $570,000 in the 2004-2005
budget year, though growing to $3.1 million 2005-06 and $3.5 million in
later years.
The Department
reported that an increase in funding for regional center operations would
be needed to implement the new plan:
* 2004-2005
budget year: $570,000 and 11 positions needed to perform assessments
needed at the regional centers, beginning January 2005.
* 2005-2006
budget year: $912,000 and 18 positions needed to continue initial
assessments and begin re-determination process for those families phased
in the year before
* 2006-2007
budget year: $770,000 and 15 positions (approximately) needed for on-going
functions
Who Is
Directly Impacted By Current Family Share of Cost Proposal
* Families at or
above 400% of the federal poverty level (though the actual financial
impact varies on a sliding scale), with children between the ages of 3-17
years (and who are not on Medi-Cal). The Department of Developmental
Services estimates that 48,000 persons with developmental disabilities
fall within that age group who receive regional center services - and of
that, about 26,000 children are covered by Medi-Cal and would be exempted
from the family payment requirement. The remaining 22,000 children would
- at least initially - fall under the requirements of the plan (many of
those would end up being exempted due to the family income requirements).
* Community-based
organizations who provide respite, day care or camping services for
children with developmental disabilities
* Direct care
staff who are employed directly by the family as their respite workers
Family
Income Level Targeted
* The current
plan would apply to families whose annual gross income is 400% or more of
the federal poverty level (about $70,000 for family of four), as adjusted
by family size - and would be on a sliding scale basis from 5% at 400% of
the federal poverty level to 80% participation at 1300% of the federal
poverty level and higher.
* The assessment
to determine who would be required to pay, would be adjusted to recognize
a family with two or more children in the home, receiving one more more of
the "targeted services" - by off-setting the cost for the second child by
50%, the third child by 75% and making no assessments against the services
for any additional children after that.
* A similar
off-set would be made for families with children in 24-hour, out of home
placement who also pay a parental fee to the State.
* The Department
of Developmental Services would develop "simplified" assessment tools to
be used by the regional centers in determining what families would be
required to pay - and at what level.
* The Department
would also establish audit tools to ensure compliance, including
procedures on collecting family financial information, computing the
contribution of families,
How This
Plan Would Impact Families
The Department of
Developmental Services outlined several scenarios on how the plan would
work - though this has not been verified either by advocates or others:
* Example 1:
A family of 4 persons (including parents, and two children ages 3-17) one
child with developmental disabilities residing in the home, is authorized
in their child's individual program plan (IPP) for 60 hours every three
months for "vouchered" respite services. The family's annual gross income
is $73,600 which is 400% above the federal poverty line.
What the
family would pay: this family would be obligated to pay for 5% of
those 60 hours (or 3 hours every three months). The regional center would
be required to fund the other 57 hours per quarter. Using current hourly
rates budgeted for vouchered respite ($8.57), the family would be required
to pay $25.71 every three months for that service - or $8.57 a month.
* Example 2:
Same family size and composition as in example 1, with same income level,
but is authorized for 72 hours of vouchered respite services every three
months, even though the family indicates it needs 90 hours per quarter.
The regional center determines that limiting the authorized hours at 72
would not be harmful to the health and safety of the child.
What the
family would pay: The family would be required to pay for 5% of the
72 authorized hours or four hours every three months of the vouchered
respite services, or $34.28 per quarter. The regional center would fund
the other 68 hours.
* Example 3:
Same family size and composition as in example 1, with same income level,
but is authorized for 90 hours per quarter for vouchered respite services.
What the
family would pay: The family would be required to pay 5% of the 90
authorized hours or 5 hours every three months (amounting to $42.85 per
quarter). The regional center would be required to pay the remaining 85
hours per quarter.
* Example 4:
A family of five (parents, with three minor children), one child with
developmental disabilities residing in the home, is authorized for 72
hours per quarter for vouchered respite services. The family's annual
gross income is $280,000 which is 1300% over the federal poverty level.
What the
family would pay: The family would be required to pay for 80% of the
72 hours (or 58 hours and amounting to $497.06 per quarter). The regional
center would be required to fund the remaining 14 hours per quarter.
Accessing
the Full Report on The Web
The fulll report
can be found at the Department if Developmental Services' website at:
http://www.dds.cahwnet.gov/0405proposals/Proposals_Home.cfm
or at the
Caliufornia Disability Community Action Network (CDCAN) website at
www.cdcan.org
Background
* Last year,
January 2003, former Governor Davis initially proposed a plan for parental
co-payments that would have required families at or above 200% of the
federal poverty level (about $36,000 for a family of four) to pay 100% of
their regional center funded services up to $5,000. There was no sliding
scale or other mitigating factors, and the plan was fiercely opposed by
families and other advocates in hearings last year that drew thousands of
people last April.
* As a
compromise, the Assembly later approved the general concept of a parental
co-payment or share of cost plan, to take effect July 1, 2005, that would
require parents with a child with developmental disabilities between the
ages of 3-17 years, and with incomes at or above 200% of the federal
poverty level (about $36,000 for a family of four) to pay some portion of
their regional center funded services. The Senate later agreed to the
plan, which also required the Department of Developmental Services to
submit to the Legislature on April 1 this year, a draft implementation
proposal, with specifics details. The Legislature reserved the right to
modify, reject or accept the plan.
* The Department
of Developmental Services held one statewide community meeting to hear
input and comments on the proposed concept, on December 2. They also
heard additional public comment in a California Disability Community
Action Network Townhall Telemeeting, held on December 12. In additional
the Department of Developmental Services received many written comments
from advocates and families.
* The Department
of Developmental Services released an initial draft plan in early March,
though without the specific income level requirements - and specifics on
what services would be impacted. The draft plan was met with initial
opposition from many advocates. A final draft plan to the Legislature was
due on April 1 - but was delayed until April 9 due to the time needed for
review within the Schwarzenegger Administration.
NEXT STEPS
* A special panel
of the Assembly Budget Committee is scheduled to meet April 15, Thursday
morning upon adjournment of the Assembly floor session, to continue its
look at the broad oversight issues relating to regional center funded
services - including the parental/family share of cost plan and its
implications in savings for the state. Other issues will be reviewed at
that special meeting, which is not a hearing - and follows up on an
earlier meeting held on March 11. The meeting will also review the
current draft of proposed statewide limits on regional center funding for
community-based services and supports, regional center operations, and
regional center director salaries. In addition, the Department of
Developmental Services is required to report back on specific questions
raised at the March 11th meeting - including specifics on costs savings
and cost shifting of several of the proposed reductions.
* Budget hearings
on developmental services - including the parental/family share of cost
plan are scheduled for April 19th (Monday afternoon at 1:30 PM) by the
Senate Budget Subcommittee and April 26th (Monday afternoon at 4:00 PM) by
the Assembly Budget Subcommittee.
URGENT -
CONTRIBUTIONS NEEDED TO CONTINUE EFFORT
As of 4/8/04,
many many, thanks again, to the friends, people with disabilities and
their families, community organizations and others who have sent in
generous and needed contributions and donations. As mentioned before,
individual thank you letters are now being sent out (due to workload have
been delayed!). However, until grant funding is finalized, contributions
from people and organizations is still very urgently needed to keep the
advocacy efforts going for the next several months. Please make check or
money order to: California Disability Community Action Network (or
abbreviate CDCAN). CDCAN is not yet a non-profit organization (work on
this will have this happen in within the next few months) Send
contributions to: California Disability Community Action Network, 1225
8th Street Suite #480, Sacramento, CA 95814. A method to contribute by
credit card (through Paypal) is NOW set up on our website, at
www.cdcan.org.
FOR MORE
INFORMATION ABOUT THE CDCAN CAPITOL NEWS REPORTS
* This is a
news report of the non-partisan California Disability Community Action
Network, a link to thousands of Californians with developmental and other
disabilities, their families, community organizations and providers,
direct care and other workers, and other advocates. These reports is for
all of them. In addition it also goes to news organizations, state and
local government officials and staff.
* If you would
like to get on this distribution (and conversely, get off of it) please
send an email with that request to:
martyomoto@rcip.com. Sharing
information is part of our organizing effort. Please feel free to forward
or copy this (attribution is nice). We're all in this together!
Marty Omoto,
director/organizer
California
Disability Community Action Network
1225 8th
Street Suite 480 Sacramento, CA 95814 VOICE PHONE: 916/446-0013
FAX number:
916/446-0026 email:
martyomoto@rcip.com
INFO HOTLINE
TOLL FREE NUMBER: 1-877-260-0267 (cannot leave messages)
SAME INFO
HOTLINE FOR SACRAMENTO AREA: 486-4652
WEBSITE:
www.cdcan.org