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The National Craniofacial Association |
| P. O. Box 11082 | * Chattanooga, TN 37401 |
| 800- | 332-2373 |
How do I pay the bills?
Dealing with the cost of medical treatment for your child can be overwhelming. The information below can help get you started.
There are several sources of funding available to cover the cost of medical care for your child.
- Health Insurance
- Public Programs
- Private and non-profit agencies
- Other alternatives
Health Insurance
Private and group health insurance will usually pay at least part of the cost of treatment
of craniofacial conditions. The following are important considerations when dealing with
health insurance companies.
- Does your child have a specific diagnosis?
- Does your health insurance plan address your child's needs?
- Are there limitations on services?
- Are there waiting periods for pre-existing conditions?
- If you are involved with a managed care (HMO or PPO)
organization, will they cover your child's doctors
if they are not in the group?
Always request a copy of your health insurance policy, not the
benefits summary brochure. The brochure is not specific enough.
Remember, the insurance company works for you. You pay them
to provide a service. When dealing with the insurance company, be sure to:
- get an 800 number; if they don't have one, ask them to call you back
- everytime you call, write down the date, the name,
position and telephone number of the person you
spoke with, as well as what you discussed.- ask to be assigned a case manager from the insurance company. This person will act as your advocate through the insurance maze, as well as become more familiar with your child's condition, in an effort to speak on his or her behalf to the company decision-makers.
Public Programs
There are a variety of federal and/or state funded programs that may be able to help your
child receive the care he/she needs. A few are:
- Medicaid
- State Children's Health Insurance Program
- Maternal Health & Child Health Block Grants
These programs are a good source of information. The following website is an excellent one that will take you to all of the programs available in your individual state: http://www.insurekidsnow.gov. They are required by the government to have "800" numbers. When dealing with public programs, be sure to:
- get a written list of benefits, restrictions, and eligibility criteria
- find someone within the program to help you through the process.
Make him or her aware of your child's needs- get involved on the advisory board for the program;
you will be able to more directly affect the program- get your legislator involved
Private and Non-profit Agencies
There are numerous private and non-profit agencies which may be able to help out. Many
organizations deal only with a specific disability or illness. Some organizations in your
community could be:
Shriner's Hospitals, Lions Clubs, Police Benevolent Associations, Civitan Clubs, Kiwanis
Clubs, Sertoma Clubs, Churches, Rotary Clubs, and Junior League Organizations.
If they cannot help you, always ask if they can refer you to another organization who
might be able to help.
Other Alternatives
There are several other things you can do to help pay for and/or reduce medical bills:
Finally, be proactive. Become an advocate for your child. Speak out; it is the only way in which health care reform will occur.
Am I Alone?
No! There are many families and organizations who will be glad to talk with you and help
you with information and support. Don't forget books, videos, and even websites. Listed
below are a few resources to get you started.
FACES: The National Craniofacial Association
P. O. Box 11082
Chattanooga, TN 37401
(800)332-2373
email: faces@faces-cranio.org
We provide financial support for non-medical expenses to patients
traveling to a craniofacial center for treatment. Eligibility is based
on financial and medical need. Resources include newsletters, information
about craniofacial conditions, and networking opportunities.
National Health Law Program
1444 I Street NW, Suite 1105
Washington, DC 20005
(202) 289-7661
Website: http://www.healthlaw.org
Provides extensive information on health care law affecting
families whose children have special healthcare needs.
Example of letter to write when your insurance company denies your claim.
Cleft Advocate
This website, under the direction of Deb Oliver, focuses on a number of financial issues
of cleft repair and treatment. She includes a number of example letters to assist parents
in appealing insurance decisions, as well as to assist with state Medicaid issues. Most of
the information on this website is very applicable to other craniofacial disorders and can
provide excellent assistance to parents making their way through the insurance maze.
American Speech-Language-Hearing Association
2200 Research Blvd
Rockville, MD 20850
800-638-8255
Click HERE for a
checklist developed by this organization outlining how to approach an employer to request
that health plan coverage for speech and hearing services be added or improved.
New England Serve
101 Tremont Street, Suite 812
Boston, MA 02108
(617) 574-9493
email: info@neserve.org
www.neserve.org/neserve/ptb.html
Visit the website or call to receive Paying the Bills: Tips for Families on Financing
Health Care for Children with Special Needs. Excellent resource!
Hill Burton Act
http://www.hrsa.gov/gethealthcare/affordable/hillburton/compliance.html
This legislative act provides funds for indigent care at hospitals where federal monies
were used for construction. The hospital admissions office has information on the
availability of these funds and the guidelines for eligibility.
National Association of Insurance Commissioners
444 N. Capital Street NW Suite 701
Washington, D.C. 20001
(202) 471-3990
Provides information on the Insurance Commissioner in your state. The state insurance
commissioner is the governing body that regulates the insurance companies doing business
in your state. This office can assist you in determining if your insurance company
is following all the rules and regulations as set forth in your policy.
Patient Advocate Foundation
421 Butler Farm Road
Hampton, VA 23666
(800)532-5274
email: help@patientadvocate.org
website: www.patientadvocate.org
Patient Advocate Foundation is a national, non-profit organization that seeks to safeguard
patients through effective mediation assuring access to care, maintenance of employment,
and preservation of their financial stability. Patient Advocate Foundation serves as an
active liaison between patients and their insurer, employer and/or creditors to resolve
insurance, job retention, and/or debt crisis matters relative to their diagnosis through
case managers and attorneys.
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Last modified on: Tuesday, February 08, 2011 04:38 PM
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