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
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.

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:

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:

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:

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
1101 14th Street, NW, Suite 405
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.

Example of letter to write when you disagree with the amount the insurance company pays on your claim.

Example of letter to write to your state insurance commissioner to lodge a complaint against your insurance company.

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
10801 Rockville Pike
Rockville, MD 20852
800-498-2071
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
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
www.hrsa.gov/hillburton/compliance-recovery.htm
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 309
Washington, D.C. 20001
(202) 624-7790
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
700 Thimble Shoals Blvd. Suite 200
Newport News, VA 23606
(800)532-5274
email: info@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: Wednesday, September 09, 2009 05:03 PM

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