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Lifetime Caps Bill Introduced
Date:2/19/2009

NEW YORK, Feb. 19 /PRNewswire/ -- On Friday, February 13, 2009, Anna G. Eshoo (D-CA) and Jim Langevin (D-RI), along with Senators Byron Dorgan (D-ND) and Olympia Snowe (R-ME) introduced the Health Insurance Coverage Protection Act (H.R. 1085; S442). The legislation, introduced in both houses in 2008, will set a $10 million minimum lifetime cap on health insurance, with future increases based on inflation.

The National Hemophilia Foundation (NHF) played a vital role in encouraging the legislation and assembling a coalition of more than 50 patient advocacy and health organizations currently working for its passage. "However, nothing could happen without the critical leadership of the members of Congress who recognized this problem and decided to do something about it," said Val Bias, NHF CEO. "We applaud these leaders for identifying this critically needed piece of healthcare reform and moving it forward." On Thursday, February 26, 2009, more than 350 people affected by bleeding and clotting disorders will gather on Capitol Hill for our annual Washington Days advocacy event. We will express our support for this important legislation and discuss other key healthcare issues with members of Congress and their staff.

"Having an inadequate lifetime cap defeats the purpose of health insurance and forces those with disabilities and chronic illnesses into an impossible situation," Dorgan said. "Low caps also end up costing the taxpayer because once people with illnesses hit their cap, they often turn to government programs for their care. This legislation will raise lifetime insurance caps and allow those with illnesses to focus on recovering--not worrying about how they are going to pay for their treatment."

"This bill addresses a critical lack of coverage for those with disabilities or chronic illnesses," said Eshoo. "It's a travesty to think that people are job-hopping in order to switch insurance plans or quitting
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SOURCE National Hemophilia Foundation
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