FCS Foundation – Patient Worthy

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Familial Chylomicronemia Syndrome Foundation Announces Support for HEART Act

Post author:Jessica Lynn
Post published:July 13, 2020
Post category:Familial Chylomicronemia Syndrome Rare Disease

In a July 9 press release, the Familial Chylomicronemia Syndrome (FCS) Foundation announced its support for a bill introduced by Congressman Paul Tonko (D-NY) and David B. McKinley (R-WV).…

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