White House Highlights Costs of Treating Hemophilia With Special Guest at Joint Congressional Session

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On September 9, President and Mrs. Obama highlighted the costs associated with treating hemophilia by inviting Nathan Wilkes, father of a son with hemophilia, as a special guest to the Joint Congressional Session. Nathan's son, Thomas, was born with hemophilia in 2003 and over the past six years his family has encountered the problem of being under-insured and has endured sky-rocketing health costs.

The Obamas became familiar with the Wilkes family’s story when Nathan introduced the President in August at a Town Hall in Grand Junction, CO. When Thomas was first diagnosed, the Wilkes family had high quality insurance through the high tech telecommunications company that Nathan helped found, but when the insurance company saw Nathan's claims (ranging from a few thousand dollars to $750,000 a year for his son), they started to increase the premiums for all the employees and their families. The company tried to find other coverage, but no other insurance company would take them with Thomas on the policy. When Thomas neared the $1 million cap on his policy, Nathan searched for another option. This was just the start of the Wilkes’ long agonizing search through many barriers to finally attain health insurance coverage for their family. 

Read more about health reform on the ASH Web site.

To learn more about hemophilia and other blood disorders as well as how to become a hematology advocate, visit the Society’s public education site Blood: The Vital Connection.

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