Hemophilia Medical CoverageHemophilia medical coverage can be very expensive. Hemophilia treatment is among one of the most expensive chronic diseases in the United States. New technology like recombinant dna technology improves the safety of new blood products, but new technology is really expensive. Healthcare is expensive nationwide, however, research and development for many of the specialized products used by people with hemophilia come with a huge price tag. Currently, hemophilia therapy is among the most expensive in the world with a total annual cost per person ranging from $60,000 to $150,000. Complications such as undergoing immune tolerance for an inhibitor, major surgery, HIV/AIDS and/or hepatitis treatments, can increase the costs of hemophilia medical coverage exponentially. Methods of insurance reimbursement are changing constantly and patients and hematologists alike find the system difficult to manage and confusing. Private insurancePrivate insurance companies vary a lot from state to state. It is hard to know what they can do for you without asking specifically for information about your hemophilia medication. We are happy to help you with this. Over the years we have developed a talent for asking the right questions of the insurance companies - and getting answers. We can contact your insurance company for you and work out an arrangement. If you would like us to talk with your insurance, just contact us and we will get with you as soon as we can. Many insurance plans have lifetime caps. Sometimes this is a worry for people with hemophilia. I can understand why. The very idea that your insurance will ever stop is a frightening concept. We can answer your questions regarding this also. Just call any time at (877) 836-7832 or email me using this form with questions about your hemophilia medical coverage. Government ProgramsFederal ProgramsSocial Security Disability or Medicare is sometimes used by people with hemophilia. Especially older and disabled people. State ProgramsMost state’s medical aid programs are called Medicaid. In California it is called “Medi-Cal” in Tennesee it is called “Tenn-Care”. In addition to these “Medicaid” programs, most states have other programs for people with genetic disorders. California has “Genetically Handicapped Persons Program” GHPP for adults and California Children’s Services” CCS. Most states have high risk insurance pools but these are usually expensive to join. Financial AidThere are non-profit organizations that help people with chronic disorders pay their insurance. We donate to these organizations so that they can assist people suffering from hemophilia with their hemophilia medical coverage. We can help introduce individuals to these organizations. They are doing a wonderful work and we are happy to introduce you to them if that is what you need. Links and ResourcesThe following are some great resources for people with hemophilia having medical coverage difficulties. If you have any questions or need any assistance please contact us we are here to help. MEDICARE MEDICAID SSI - SOCIAL SECURITY INCOME SSDI - SOCIAL SECURITY DISABILITY INCOME CHIP - COMPREHENSIVE HEALTH INSURANCE PROGRAMS SCHIP - STATE CHILDRENS HEALTH INSURANCE PROGRAM TITLE V CSHNP - CHILDREN WITH SPECIAL HEALTHCARE NEEDS PROGRAM HIPP - HEALTH INSURANCE PREMIUM PROGRAM
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We have been dealing with insurance companies since our oldest son was born and we have gotten pretty good at it. I can totally eliminate the stress of dealing with your insurance company. You don't shouldn't have to bear that burden. You have enough to deal with. All you need to do is 