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Contact Information
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If you have any questions or would like more
information about the CCS program:
County Office
1430 Freedom Blvd.
Suite 101
Watsonville, CA 95076
Open: 8am - 5pm
Mail Address: P.O. Box 962,
Santa Cruz, CA 95061
FAX: (831) 763-8410
From Santa Cruz:
(831) 454-2540
From Watsonville:
(831) 763-8000
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What
is the California Children Services Program?
California Children
Services (CCS) is a statewide program that arranges, directs, and pays
for medical care, equipment, and rehabilitation, when these services are
authorized by the program. Services can be authorized for
children and young adults under 21 years of age who have eligible
medical conditions and whose families are unable to pay for all or part
of their care. CCS defines eligibility and selects the most qualified
professionals to treat the child's CCS-eligible condition. However, it
is important for you to know that CCS is not a health insurance program.
It will not meet all of your child's health needs, only those
related to the CCS-eligible condition.
California
Children Services Benefits
What
you Should Know About CCS Appeals
What does the CCS program offer
children?
If your child's doctor thinks that your
child may have a medical condition that might be CCS-eligible, CCS may
pay for or provide a medical evaluation to find out if it is actually
covered.
If your child is eligible, CCS may
pay for or provide:
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Treatment, such as doctor
services, hospital and surgical care, physical therapy (PT) and
occupational therapy (CT), laboratory tests, X-rays, orthopedic
appliances, and medical equipment.
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Medical case management to help
get special doctors and care for your child when medically
necessary, and referral to other agencies, including public health
nursing and regional centers; or a
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Medical Therapy Program (MTP),
which can provide PT, and/or OT in some public schools for children
who are medically eligible for these special services.
How is the CCS program organized?
The California Department of Health
Services manages the CCS program. The larger counties operate their own
CCS program. Smaller counties share the operation of their program with
state CCS regional offices in Sacramento, San Francisco, and Los
Angeles.
How is the CCS program funded?
The program is financed from state,
county, and federal tax monies, along with some fees paid by parents.
Who is eligible for CCS?
Your child may be eligible if he
or she meets all four of the following requirements:
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Age -Your child
must be under 21 years of age.
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Residence -Your
child must be a permanent resident of the California county where
you apply. (Your child's residence is usually where you live.)
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Income -Your
family income must be less than $40,000 per year, according to the
adjusted gross income on your California income taxes. A child may
be eligible when the family income is more than $40,000 if medical
care for the child's CCS condition is expected to cost the family
more than 20 percent of the family's income. If your child is
adopted your income will not matter. There is no financial
eligibility requirement for diagnostic or therapy services.
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Medical Conditions
- Only certain conditions are eligible for CCS. In general, CCS
covers medical conditions that are physically disabling or require
medical, surgical, or rehabilitative services. Categories of medical
conditions that may be covered and some examples of each are shown
on page 4. There also may be certain criteria that determine if your
child's medical condition is eligible. Ask CCS if you have
questions.
Eligible Medical Conditions
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Conditions involving the
heart (congenital heart disease, rheumatic heart disease)
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Neoplasms (cancers,
tumors)
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Diseases of the blood
(hemophilia, sickle cell anemia)
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Diseases of the
respiratory system (cystic fibrosis, chronic lung
disease)
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Endocrine, nutritional,
and metabolic diseases (thyroid problems, PKU, or diabetes
that is hard to control)
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Diseases of the genito-urinary
system (serious kidney problems)
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Diseases of the
gastrointestinal system (liver
problems such as biliary atresia)
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Serious birth defects
(cleft lip/palate, spina
bifida)
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Diseases of the sense
organs (eye problems leading to loss of
vision such as glaucoma and cataracts, and hearing loss)
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Diseases of nervous
system(cerebral palsy, uncontrolled epilepsy/seizures)
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Diseases of the
musculoskeletal system and connective tissue (rheumatoid
arthritis, muscular dystrophy)
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Severe disorders of the
immune system (HIV infection)
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Disabling injuries and
poisonings requiring intensive care or rehabilitation (severe head, brain,
or spinal cord injuries, and severe bums)
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Complications of
premature birth requiring an intensive level of care
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Diseases of the the skin
and subcutaneous tissue (severe
hemangioma)
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Medically handicapping
malocclusion (severely crooked teeth)
Steps to CCS Services
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Child's condition found
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Referral made
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Application completed (if your
child does not have Medi-Cal, you must apply for it If your child
has Medi-Cal he or she may be assigned to a "Managed
Care"plan.)
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Eligibility determined: age •
residency financial
medical disagree with the
decision you may appeal
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Services given:medically necessary •
prior authorization
How can my child receive CCS
services?
First, a referral and application must be
made. Anyone can refer a child to CCS, including parents. Ask your
child's doctor if your child has any of the medical conditions
listed on page 4. If so, either you or the doctor can call the CCS
office at your county health department to refer your child. The
referral will work best if medical information is given to CCS at that
time. If your child needs to be referred because he or she is in a
hospital, ask the attending doctor or hospital social worker to refer
your child within 24 hours after admission. After the referral to CCS,
parents must still fill out an application and/or financial eligibility
form and meet all four eligibility requirements. If CCS determines that
your child is eligible, your child can then receive services.
What papers should I bring?
To help
CCS determine if your child is eligible, you may need to bring papers to
the county CCS office to show your child's age, where you live, and how
much income you had in the past year. Examples of papers you might need
are your social security card, driver's license, rent and utility
receipts, paycheck stubs, birth or baptismal certificates, school
enrollment forms, military ID, health insurance information or Medi-Cal
card, and recent income tax forms. If you do not have some of these
papers, ask CCS what other papers you may bring instead.
Are there any costs to me?
There are some fees for CCS clients who do
not have Medi-Cal or who have Medi-Cal with a share of cost.The amount
of the fees is based on family income and size. Ask CCS if you have any
questions.
California
Children Services Benefits
What are CCS benefits?
Benefits of CCS are medical services that
the CCS program provides directly to eligible children or arranges to
pay for their cost. This section explains these services.
Case Management
Case management is
determining medical eligibility, deciding what your child needs, and
helping you get special doctors and services to meet your child's
special needs. This includes help to coordinate your child's medical
care and referral to other agencies, such as the county health
department, schools, and agencies that serve children and adults with
disabilities. Every CCS client receives case management.
If your child has Medi-Cal and a CCS
eligible condition, CCS can coordinate your child's medical care. This
way, decisions about who will provide care and payment can be made
faster by a person who is familiar with your child's needs. If you have
Medi-Cal and are enrolled in a managed care plan, case management
services may not be the same in all counties. In most counties, your
child's CCS-eligible condition is still the responsibility of CCS, but
in some counties it is the responsibility of the managed care plan. You
should ask your CCS office if the case management of your child's
CCS-eligible condition is covered by a managed care plan or the CCS
program.
Diagnostic Services
If CCS thinks that your
child might have an eligible condition, CCS will pay for diagnostic
services. These include examinations, laboratory tests, and X-rays.
Diagnostic services will be provided only until CCS finds out that your
child has a condition that is eligible for CCS.
Treatment Services
Treatment services include
medical services, medicines, equipment, or supplies that are medically
necessary to treat your child's CCS- eligible condition. Treatment
services are provided when they are a benefit of the CCS program,
prescribed by a CCS-approved doctor, and authorized by CCS. Most of the
time, these services can be provided in doctors' offices close to your
home, but sometimes CCS might refer your child to a special care center
if your child is eligible (see p. I 1). You should be sure to tell the
doctor everything you know about your child's condition and ask the
doctor about any services that might be available through CCS.
Doctor
Doctor services may include
consultations, office visits, surgery, anesthesiology, radiology,
and other medical services needed to treat the CCS-eligible
condition.
Emergency
Services
Emergency services,
including doctor, lab, or hospital services to treat a CCS-eligible
condition, may be a benefit of the CCS program. You, your doctor, or
other hospital staff must ask CCS for authorization on the first
working day after the service began. If your child is treated by a
doctor or admitted to a hospital that is not approved by CCS, your
child's treatment may be authorized for a short time, until treatment
by a CCS-approved doctor or hospital can be arranged or your child is
discharged.
Hospital
Services
Overnight hospital care can be
authorized by CCS only if the doctor and hospital are approved by CCS
and your child's condition is severe enough to require overnight
hospital services. CCS must also authorize other services performed in
the hospital.
Home
Health Care Services
In some cases, home health care services such as nursing, occupational
therapy, physical therapy, or medical social services, may be provided
to treat your child's CCS-eligible condition. If your child's
CCS-authorized doctor prescribes the service and CCS agrees that your
child needs the service, it can be authorized.
High-Risk
Infant Follow-Up Services
CCS provides high-risk infant follow-up
services for eligible infants discharged from neonatal intensive care
units (NICU). The purpose of these services is to prevent or reduce
problems that may develop because of the child's medical condition.
Benefits include case coordination, home visits by nurses, and other
services that special care centers provide.
Other Medical
Services
Following are additional services that may be authorized only when CCS
determines that they are medically necessary to treat your child's
CCS-eligible condition. This list may not be complete. Ask CCS about
other services.
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Medicines, including
prescription drugs and special nutrition products
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Home infusion therapy
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Dental services
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Nutrition services
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Social work services
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Durable medical equipment (DME)
such as wheelchairs and braces
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Medical supplies
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Eyeglasses, prostheses, and
orthotics
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Dialysis
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Organ transplants and donor
services
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Audiology services and hearing
aid services
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Rehabilitation services,
including OT, PT, and speech therapy
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Medical transportation
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Genetic counseling service
Special Care Centers
A special care center is where
CCS can send your child to get the best medical care, using a team of
specialists, such as doctors, social workers, nurses, therapists, and
nutritionists. The team members will help you and your child manage your
child's medical condition, and you are expected to bring your child in
at least once a year. There will be evaluations to measure your child's
progress and team meetings, which include you and your child (if your
child is old enough) to discuss and/or change the treatments as your
child's needs change.
CCS special care centers
are not for every child enrolled in CCS. These centers are only for
children who have special medical conditions that require care from
many specialists working together. The CCS program requires that
children with certain medical conditions receive care through
special care centers. Examples of these conditions include:
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Complex congenital
heart diseases
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Inherited metabolic
disorders
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Chronic renal diseases
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Chronic
gastrointestinal diseases
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Chronic lung diseases
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Malignant neoplasms
(cancers)
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Blood problems such as
hemophilia, sickle cell disease Severe immunologic disorders
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Problems in the way
the skull and face were formed
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Spina bifida
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Endocrine disorders
including diabetes
If your child has any of
the above conditions, ask your doctor to explain what it means.
Medical Therapy Program
(MTP)
in Schools
The Medical Therapy Program (MTP)
is a coordinated program of medically necessary PT and OT services
provided to medically eligible children. These services are provided in
Medical Therapy Units (MTUS) located at certain public schools. PT and
OT may help your child to be independent in such areas as getting
around, getting in and out of a wheelchair, walking, feeding, dressing,
staying clean and neat, and home skills.
There is a separate
evaluation by the Medical Therapy Team (the doctors and therapists who
specialize in treating children with physical disabilities). The team
decides if your child would benefit from MTU services and meets with you
to discuss which services would best meet your child's needs. The team
can prescribe medically necessary PT or OT, as well as durable medical
equipment and any other medical services. These services are often given
in the MTU. However, they can also be provided by your child's health
maintenance organization or your child's health insurance provider.
Not every CCS client is
eligible for MTP services. Eligibility for the MTP is different than
for the CCS program. Residential eligibility for the MTP is the
same, but medical eligibility is different and there is no financial
eligibility. In other words, any child who is medically and
residentially eligible for the MTP can receive PT and/or OT at no
cost to the family. Two groups of children are served in the MTP:
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Children with a
neuromuscular, musculoskeletal, or muscular disease. Examples
include but are not limited to some types of cerebral palsy,
poliomyelitis, myasthenias, muscular dystrophies, osteogenesis
imperfecta, arthrogryposis, rheumatoid arthritis, amputation, and
contractures resulting from burns.
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Children under 2 years
old who have certain neurological findings that suggest a high
chance that they may have a physical disability that is eligible
for the MTP but who do not have symptoms.
Ask CCS whether your child
may be eligible for this program.
Click
here for more information about the MTP program
Other Services to Help
Parents and Children
The CCS program understands that you and your child may require more
than just medical services. For instance, skilled nursing services in
your home may be necessary for your child. Possibly you or your child
could benefit from talking to someone about stress and worries. Or, you
might need financial help in taking your child to a special care center.
It is important to remember that these specialized services are only
available on a limited basis. Some of the services you or your doctor
may want to ask CCS about are listed below.
CCS sometimes provides
nursing services in the home by licensed nursing personnel. Since
there are rules about when this can be provided, you should ask CCS
whether it can be authorized.
Counseling
to
Help With Stress and Worry
Being the parent of a child with special health care needs or being a
child with special health care needs can cause anger, worry, or
sadness. Sometimes the worry or sadness gets to be too stressful and
you or your child might need help with these feelings. Talking to a
professional trained to help with these problems can make you or your
child feel better. This kind of help may be a CCS benefit when CCS
agrees that the stress and worries are connected to the CCS-eligible
condition and that they affect the child's treatment. If Medi-Cal or
another insurance program covers your child, you should ask the other
insurance program for the help first.
Transportation,
Lodging, and
Meals
Services that provide the
kind of special help that your child may need might not be available
near your home. Sometimes, CCS may authorize help with travel expenses
(mileage, bus transportation, food that you have to eat out, and the
cost of staying at a motel) if you cannot afford them and no other
resources are available. This help is available when the distance from
your home to the provider that CCS authorized is so far that you
cannot make the trip in one day or if you have to stay at the hospital
to learn how to care for your child. To have CCS pay YOU back, you
must have prior authorization and save all your receipts. CCS will
usually authorize the closest appropriate provider. If you prefer to
take your child to a provider farther away than the one CCS
authorized, you may have to pay for the travel expenses.
What are the rules about CCS
benefits?
Benefits may be authorized only
from CCS-approved doctors, hospitals, OTs, PTs, etc. These people or
groups are called "providers." Only services determined by
CCS to be medically necessary to treat the CCS-eligible
condition will be authorized. CCS must also have enough money to pay for
the benefits.
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Services
must be medically necessary
"Medically
necessary benefits" means that the service, equipment, test, or
drug
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has been ordered by
the doctor approved to provide care for your child;
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is a benefit of the
CCS program; and,
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according to a CCS
medical consultant, is the most effective way to treat the
CCS-eligible condition.
Prior Authorization is
Needed for CCS Services
Authorization by your local CCS program must happen before a service
is given. Authorization means a written approval by the CCS program for
a specific provider to give specific service(s). The
authorization will name the service, the provider, and when the service
must be provided. Each service
requires a separate CCS authorization. For example, if CCS authorizes a
provider to treat your child, the provider may decide that additional
services are needed. You should be aware that other authorizations are
required for the additional services. It is especially important to know
this when your child is receiving services at a hospital. Additional
authorizations are needed when your child is sent to different
departments or doctors, even if it is in the same hospital. Before any
service is given, you should ask if CCS has authorized the service. If a
service is provided without authorization or it is not exactly the same
as what was approved, CCS may not pay for it. You may then have to pay
for the service yourself.
If the doctor or hospital
cannot get authorization for emergency or urgent services because the
CCS office is closed, CCS should be contacted for authorization on the
next working day. Parents can call the doctor or CCS to be sure this was
done.
You Must Use A CCS
Provider
CCS wants to be sure that your child gets the best possible care.
Therefore, hospitals and other medical providers must meet strict
standards before they may treat CCS clients. Providers must be
specialists in the care of children with special health care needs.
Doctors must be experts in their specialty and members of the staff of a
CCS-approved hospital. They must also agree to coordinate the care
related to the CCS-eligible condition, to accept CCS payment as payment
in full, and to keep the CCS program informed about your child's
progress.
When CCS Will Not Pay For
a Service
CCS will not pay for services for your child if any of the following
things happen.
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The service was not
authorized or the authorization has expired.
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You did not use a
CCS-approved provider.
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It is not a CCS benefit.
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Your child is not or is
no longer eligible for CCS.
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You or your child did
not follow the treatment plans or keep scheduled appointments.
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The service is not for a
CCS-eligible condition.
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You have not paid the
required CCS fees.
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The medical treatment
has been completed.
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The service your child
needs is fully covered by your health insurance plan or Medi-Cal.
Family
and CCS Program Expectations
What can our family expect
from CCS program staff?
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All families
and children should expect to be treated with respect and dignity,
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able to get information
about other resources that may be helpful to them,
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assured of the
confidentiality of their personal records and information, and able
to have their child's eligibility determined and authorizations
processed in a timely way.
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Able to have their child’s
eligibility determined and authorizations processed in a timely way.
What about confidentiality?
Confidentiality means that your
records are private and can generally only be given to you or someone else
with your permission. However, CCS program staff and other authorized see
your records, but they must maintain confidentiality. The CCS program will
also allow you to see your child's records. A copy of your child's records
may be available for free or at little cost. You can see the record as
long as you schedule a meeting in advance and when there is a person that
the county CCS office believes can interpret the medical terms for you.
What is Family-centered
care?
Family-centered care means that
families are involved as equal partners in the care of their child with
special health care needs are more likely to receive this type of care if
they let ram know that they want to be involved.
Family-centered care is based
on an equal relationship between family members and service providers. The
following describes what all service providers should provide in the
context of family-centered care.
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Service providers should
recognize that you are the only ones who are there all the time in
your child's life. The people who provide services are
always changing, but your child is your responsibility all the time.
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Service providers should
share all information with you about your child's treatment in a
caring way. You have a right to know what the provider is
recommending, what good will come of it what the possible
risks are, and why the provider thinks it is the best choice. You
also have the responsibility to ask questions until you
understand what the provider is
saying.
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They should respect
different ways of dealing with health problems. When providers tell
you what they think is best for your child, they should
also listen to what you think, too.
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They should invite you to work
together with doctors and other staff in the care of your child. This
means that you should be included in planning the treatment
for your child before decisions are made, not just be
given a consent form to sign.
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Service providers should ask you
what you liked and disliked about the care your child received and how
to improve it.
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They should use their understanding
of the special needs of children of different ages in how they provide
health care. They should explain to you and your child what will
happen and why. Your child should also be asked his or her opinion and
feelings about their treatment. Your teen should generally receive the
full explanation that you get. You have the right to ask the
provider to talk to your child and the responsibility to do
it if the provider is not able to do
so.
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They should invite you to talk to
other families of children with similar conditions. Parents can
help other parents in a way that no doctor can. No one knows
what you are going through better than another parent who has
gone through it. Information should be
available about how to contact other parents like you.
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And all service providers should
try to make health care flexible, convenient, and meet the family's
changing needs.
We hope that giving you this
information will help you get family entered care for your child and to
ask for it if you don't get it.
What does the CCS program expect from
families?
Following is what the family, legal
guardian, or emancipated minor must do to receive CCS services.
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Complete and sign CCS program
forms, including the application form, program services agreement,
the yearly financial eligibility redetermination, and medical
Release of Information forms. (if you have difficulty filling out
these forms, CCS staff will be happy to assist
you.)
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Be determined eligible for CCS
services and comply with program requirements, policies, and
procedures.
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Notify CCS program
representatives and providers of any health insurance at the time of
application and agree to ask your insurance to pay for a service
before asking CCS. Apply for and cooperate with Medi-Cal when asked
to do so by the CCS program.
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Inform CCS within 15 days about
any changes that might affect eligibility, such as health insurance/Medi-Cal
coverage, residence, income, employment status, or a child's legal
guardianship.
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Pay any required program fees.
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Keep appointments or call the
provider if you need to change the appointment.
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Follow treatment plans.
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Notify the CCS program
immediately about any financial settlements, payments, or awards
received in connection with the child's CCS-eligible condition.
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Repay CCS for money spent for
your child when required to do so.
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Promptly inform CCS of any
emergency or nonscheduled hospitalization.
You should also remind the provider
to request prior authorization for all services, to notify CCS of any
changes in the treatment plan or termination of medical treatment, and
to send reports of the services to CCS.
What
you Should Know About CCS Appeals
General Rules About the CCS Appeals Process
Once you have applied for CCS services, you will get a written decision if
your eligibility or a service has been denied, reduced, or stopped. This
decision is called a "Notice of Action" (NOA). The NOA explains what
action has been taken and why the action was necessary. If you do not agree with
the decision, you have the right to appeal it. Before you ask for an appeal, you
should call the CCS office at the number listed on the NOA to talk about your
complaint. Often, complaints can be resolved without asking for an appeal.
However, do not wait too long because there are time limits for appeals. If you
decide to ask for an appeal, you must show that the decision by CCS was not
right for your child.
The appeal process begins when a family requests an appeal of a
decision. The process has two steps. Both steps give applicants or clients a way
to share information and settle differences. The first step is the First Level
Appeal. If you do not agree with the result, you may go to the second step and
request a Fair Hearing. You must make a request in writing for each level of
appeal.
What is the difference between a First Level Appeal and a
Fair Hearing?
A First Level Appeal is an informal review of all information about
your complaint by experienced health care professionals.
A Fair Hearing is a formal meeting where you are given a chance
to present evidence to a hearing officer. A hearing officer is an attorney
required by the state to make a fair decision about your complaint. To do this,
the hearing officer will review your child's records and keep all information
confidential.
Will services be continued during the appeal process?
Your child's services may continue during the appeal process if all the
following things have taken place.
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The service was already authorized by CCS.
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You requested (in your written appeal) that the service
continue.
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Your request was determined to be medically necessary by a
CCS authorized physician.
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The length of time that services can be continued will vary,
depending on the length of the appeal process.
Where can I get help with my appeal?
The best way to find out about getting help is to contact your local CCS
program.
CCS can help by explaining the complete appeal process and allowing you
to review the information in your case file. Copies of your records and the
regulations and policies upon which decisions are made will be made
available to you upon request for little or no charge.
OTHER RESOURCES
You are not required to have legal representation. However, help or
representation may be available through private attorneys, legal clinics, and
nonprofit legal organizations if you need it. You may also have an advocate
from another organization that knows your child, such as a regional center for
developmental disabilities, a family resource center, or an organization that
gives information about your child's CCS-eligible condition. They may be
listed in the white or yellow pages of your telephone book.
How do I ask for an appeal or a Fair Hearing?
If you must make either request in writing within 30 days of receiving an
NOA. The appeal must tell CCS what your complaint is about, why you disagree
with the decision, and what you want CCS to do about it. Your request for a Fair
Hearing must be made within I 5 days of receiving the appeal decision and must
include a copy of the First Level Appeal decision. Both types of requests must
be signed by you and should provide enough information to show exactly why you
disagree with the CCS decision. You may wish to write the appeal in a personal
letter, get help with it, or have someone write it for you.
Can I have an interpreter at the Fair Hearing?
If you need an interpreter for the Fair Hearing, CCS will provide one for
you at no cost. You must ask for an interpreter and tell CCS what language you
speak when you make your Fair Hearing request.
Are there services that can’t be appealed?
Sometimes a CCS-approved doctor will not prescribe a service
that you want for your child. Also, the doctor may refuse to continue
prescribing a service. You cannot appeal either decision. For example, medical
therapy services can be stopped by a private CCS-approved physician or by a
physician in the Medical Therapy Program. If this happens and you disagree with
the decision, there is a different process that you can use to settle the
disagreement. You may request a second medical opinion from an expert physician.
You will be able to choose the doctor from a list of three experts that CCS will
give you. The opinion of that expert is final.
What are the laws relating to CCS?
California state law and regulations govern the CCS program. The
state laws are found in the Health and Safety Code, Welfare and Institutions
Code, and the Government Code. The regulations are found in the California Code
of Regulations. These laws and regulations can be found in a county law library.
All written decisions will tell you which laws and regulations apply to your
child's case.
Is there more information about the appeal process?
The CCS appeals process has more requirements than described
here. For a complete description of the appeal
process, you may contact your local CCS program. A copy of the appeal
regulations may be available for free or at little cost.
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