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Health Insurance |
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CRUCIAL INFORMATION REGARDING AUTISM Attention All Families, Friends and Professionals From: Susan K. Goldstein (click name to e-mail) Vice President, Autism Society of Florida HEALTH
INSURANCE COVERAGE FOR AUTISM SPECTRUM DISORDER Senate President McKay will review the sales tax exemptions to find
more sources of revenue, however it is a difficult task in a shaken
economy. The intangibles tax repeal was delayed which contributed about
$130 million, however the state reserve fund for budget stabilization was
not utilized. There is almost
$1 billion in that reserve but legislators fear that if the State economy
does not improve there may be more potential shortfalls, possibly in the
$2 to $3 billion range. Although
your calls, letters and faxes were very effective, the cuts were
inevitable. The largest came from the Department of Education.
Autism CARD programs were cut by
$320,440 and overall FEFP was cut $250,264,821.
Another disappointing hit was $99,960 for the Centers for
Independent Living.
In
Health and Human Services, MediPass Services were cut $3,798,399,
which is an option that many of our families utilize.
Also hit was Community Mental Health Services by $215,567. A
huge debt of gratitude is owed to Senate Health and Human Services
Appropriations Chair, Senator Ron Silver! The Senate position was much
more palatable in terms of minimizing cuts to direct services for persons
with developmental disabilities. Senator Sanderson was also a very key
legislator contributing her support to $2.2 million in direct intervention
funding. Initially the House position was to cap waiver services.
If it cost more than $77,000 annually for care, that individual
would be directed to an ICF. Senator Silver was crucial in removing that
cap on cost plans and our friends at Florida ARF, Chairman, Dennis Haas
and lobbyist Max Bosman, worked tirelessly to eliminate it. Other
cuts came for the implementation of the Personal Planning Guide, which had
no significant impact and the Choice and Control Pilot Project that is
funded out of general revenue. The
approximately 150 people on the plan will not be affected to a great
degree as they will now be served in the Waiver, and no federal match is
lost. However, the Individual
and Family Support Program suffered a cut so services will be lost as will
federal dollars. The
Therapeutic Intervention Program remained intact, as did the Therapeutic
Residential Autism Care program, thanks to the efforts of our friend and
lobbyist Ron Book and his staff. Unfortunately,
the Inclusive Child Care Project lost it’s funding of $100,000 which was
only half of last year’s amount. This
is an issue we must let the legislature know is an important one.
Without quality childcare, we cannot earn a living.
As
many of you have been advised directly by Delmarva Foundation, they and a
company named Maximus have signed extended contracts with the Department
of Children and Families. Delmarva
was hired for quality control and assurance and Maximus for rate
utilization review and delivery consistency.
They offer, in my opinion, redundant services that the department
does and should be responsible to provide. Each contract is valued at
approximately $4 million over the term. These are dollars that should not
be tapped from direct services and duplicate the function of the support
coordinators, which are now costing $56.4 million annually.
Waiver support coordination helps consumers make informed choices
about services and assure they are cost effective.
They also monitor the programs and certify that services have been
received prior to payment to the provider. Each support coordinator must
not service a caseload of more than 36 individuals.
In addition, each district reviews and approves all cost and
support plans. They also monitor the support coordinators for performance
outcomes. In addition,
because of the budget crisis, many districts are reviewing each support
plan for cost efficiency. This
seems to be quite sufficient as far as a ‘checks and balances’ system
is concerned. Delmarva
held several public meetings across the state, however many got the notice
after meetings had occurred, or with only one days notice.
One parent, Holly Borfield, who did attend in Orlando, was very
upset that these companies would have access to our children’s medical
records and may override intervention prescribed by their regular
physician. Delmarva’s
doctors may do this without ever having seen the child. Such statements
along with the fear of cuts in program dollars created serious concern
over these contracts statewide. The concern of a ‘managed care’ effect
seems to be lurking in the shadows. It
appears to me that this is just another way to get around the ‘medical
necessity’ or ‘meaningful day activity’ that is required by law.
The problem is that these interpretations are currently in
litigation and still undecided. It
is my experience with the health care industry that their definition of
“medical necessity” means: Is it a matter of life or death? This is
the same argument the industry uses in committee when they try to gut our
insurance bill every year. If you are ever the victim of this circumstance
or experience a disregarding of vital services, remember that you have the
right to a hearing and due process. We will need all our parents who are
attorneys to step up to the plate and form a committee to address what
could potentially become a significant and frequent issue. These
and other funding concerns prompted a teleconference call, which took
place last Thursday that included a group of parents and providers, with
Carl Littlefield, who is in charge of the DC&F, Mike Hanson from the
Governor’s office, Shelly Brantly the Medicaid Bureau Chief and Susan
Dickerson, Medicaid Budget Supervisor.
Carl Littlefield stated that the contracts were designated language
by the legislature and specific proviso in SB 2000, special appropriation
377, Home and Community Based Waiver, referring to quality assurance.
Their function, as he explained, is a ‘checks and balances’ system.
Delmarva comes in up front and Maximus follows as a backup.
He also stated that it was a 25/75 match meaning that 75% of the
dollars were federal, however, this was inconsistent with earlier reports
I received. Susan Dickerson stated that quality assurance is required by
ACHA contracts and it is ‘Medicaid protocol’ when federal dollars are
drawn. Suggestions
given in the conference call were to bring stakeholders to the table
before decisions are made that affect the lives of our children.
When budget cuts are eminent, preferably administrative redundancy
is considered for a cut before the direct services to our precious
children. A better dissemination of information was also suggested and
requested. Mr. Littlefield
said that a $90,000 grant from the Development Disabilities Council is in
the works to fund an information liaison. I’d like to know how to apply
for that job! Better yet, lets spend the $90,000 on those that need it and
try e-mail or a web page. This
situation is far from being over; we will work hard to prevent additional
cuts in services. Remember,
when an alert is sent, please respond promptly, it can make a big
difference in the life of your children.
Happy Holidays and a better New Year! Any questions, e-mail me at skgoldstein@hotmail.com. I am pleased and proud to announce that THE AUTISM INSURANCE BILL STILL ALIVE AND KICKING and will never go away! The status of the Autism Insurance Bill is an important issue this 2002 session as many who are wait-listed for the waiver will not be receiving the services that Mr. Littlefield promised would come in March. Representative Crow and Senator Geller have already filed and we must not give up this fight for insurance coverage. Please contact your legislators and ask them to sign on as sponsors. Now more than ever the State must require the insurance industry to accept some of the financial burden they have abandoned and written off for so long. Premium-paying policyholders with autistic children are discriminated against and we must not let it continue. Insurance is a mutually beneficial concept. Our premiums pay for treatments of other children, as theirs should pay for treatment of autism. Call you House member and Senator. Go to your delegation and sign up to speak at the public hearings. Take your child to their district offices and let them meet in person. Tell them we must pass the insurance bill! Let’s do it this year! SENATE Bill
110 and HOUSE
Bill 43 SPONSORED BY Senator
Steve Geller and Representative Larry Crow Representative Larry Crow, who has a brother with autism has made this his number one priority this session. He is a powerful and seasoned Legislator. We have a much better chance to pass in the House this year. Let Rep. Crow know we appreciate his efforts by working this Bill. Senator Steve Geller has also made our bill a priority. Senator Geller is on the Insurance Committee and also Chairs the Agriculture Committee. We must help them both to build momentum by getting everyone (especially leadership) to sign onto to our Bill. Call write and call your legislators and ask them to sign on. Then call Speaker Feeney and Senate President McKay and ask them to sign on and help move the Bill because the lives of our children are at stake. They have waited far too many years for coverage of critical intervention and we are tired of the finger pointing in Tallahassee. Something must be done now!!! If anyone says "no" to your request for sponsorship, PLEASE E-MAIL ME IMMEDIATELY AND LET ME KNOW! WE NEED EVERYONE'S HELP TO GET ALL LEGISLATORS TO SIGN ONTO THIS
BILL!!! |
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Don't take no for an answer. Remember...if they say
"no" they just don't have enough information to say
"yes." Lets get busy!!! |
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