
In choosing a Managed Care Organization for a child in
foster care, social service professionals if given a choice of plans may wish to consider
a number of factors. Understanding both the specialized services a child will require, the
geographic location of the childs residence and who will provide primary care are
all important matters to bear in mind. A plans description of benefits and a list of
primary care providers can be found through the plan service representative or, the plan
ombudsman. The State Social Services and or Medicaid office may also have information
about benefits.

Therapies/Home Care/Planning Services
Speech and language therapy
Physical therapy
Occupational therapy
Nutrition counseling services
Home nursing services
Personal care attendant
Home health aide
Counseling/mental health services
Genetic services
Hospice
Case Management
Diagnostic testing
Durable Medical Equipment
Ventilator
Suctioning equipment
IV stands and equipment
Air compressors
Feeding pumps
Monitor
Wheelchair
Braces
Casts
Prosthetic devices
Medications and Supplies
Tracheostomy tubes
Gastrostomy tubes
Feeding bags
Specialized dietary products
Dressings
Prescription drugs
Adaptive Equipment
Prone standers
Corner tables
Specialized car seats
Bath aids
Van adaptations
Ramps
Corrective shoes
Eyeglasses
Specialized orthodontics
Prosthetic devices
Communication equipment

- Which providers contract with this plan?
- Does the child currently have a Primary Care Provider?
- Would the child benefit from staying with the same Provider?
- Is the provider accessible from where the foster family lives?
- Are the specialists the child uses available through this plan?
- Can the child get direct access to the specialists for some services?
- Where are the hospitals and clinics located? --Are they physically accessible?
- Does the Primary Care Provider have privileges at nearby hospitals and clinics?
- Will transportation funds be covered through the managed care organization?
- Are the specialists and therapists trained in pediatric care?
- What is the procedure for authorizing urgent or emergency care?
- What is the procedure for authorizing urgent or emergency care if the child is traveling out of state?
- Are translation services available to families at the providers offices, or clinics?
- What coverage is offered for equipment and medical supplies? Where is equipment and supplies available? Who is responsible for repairs and replacements? Who has to approve requests for equipment and supplies?
- How are prescription drugs covered, and where can they be obtained? Are there any restrictions on the drugs that can be prescribed and paid for?
- Is there a clinic in the plan that specializes in the childs diagnosis/disability? Are there classes or informational materials that address parenting and health care issues for our childs diagnosis/disability?
- What process or alternatives are available in the event that there is a complaint?
- How easy is it to change plans if the plan is not meeting the childs needs or the childs needs change?

In choosing a primary care provider you are looking for
someone who will value you as an expert on your child and acknowledge you as a competent
partner. You want your Primary Care Provider to:
- Help you find and continually update the information you
need to understand your childs condition.
- Not withhold or omit any information concerning the
severity or extent of your childs condition. Also, not hesitate to use medical terms
when necessary.
- Agree to routinely provide you with copies of any medical
records and reports.
- Help you to understand the range of possibilities and tell
you the worst and best possible prognosis.
- Acknowledge your sense of urgency by responding quickly to
requests for medical information, referrals, etc., so that appropriate services can begin
or continue.
- Remind you of your childs strengths from time to
time.
- Collaborate with other professionals providing care for
your child.
- Take time to talk with you about your concerns.
Some practical questions you might want to ask before thedoctor has seen your child.
- Do you see children with disabilities in your practice?
- Do you have experience with children who have (childs
disability)__?
- Would you be comfortable working in a medical team
situation with other professionals who will be seeing my child?
- Can you schedule extra long appointments?
- Who sees your patients when you are not available?
- Which staff person is responsible for following up
pre-authorizations or approvals for specialty care? What is your protocol for getting
pre-authorizations?
- Which hospital do you use for patients who require
hospitalization or hospital tests?
- What are the facilities of this hospital for children and
families like mine? If my child were hospitalized, would I be allowed to stay with
him/her?
- How do you handle a childs fear, discomfort, or pain
when preparing him/her for invasive procedures?
- After youve examined my child, can you arrange for
one of your staff to watch him/her for a few minutes so we can talk alone?
- Would there be any additional charge for any of these
arrangements?
*Adapted from Health Care Connections: A Guide for
Families of Children with Special Health Care Needs; Produced by Bay Area Family
Health Links, CARE, Family Resource Network, Matrix Parent Network & Resource Center,
Support for Families of Children with Disabilities
** List is adapted from "PASSPORT: For Children with
Special Health Care Needs" from University affiliated Program, Child Development
& Rehabilitation Center, Oregon Health Science University.