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X-WR-CALNAME:Hemophilia Alliance
X-ORIGINAL-URL:https://hemoalliance.org
X-WR-CALDESC:Events for Hemophilia Alliance
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DTSTART:20240310T070000
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DTSTART;TZID=America/New_York:20240821T130000
DTEND;TZID=America/New_York:20240821T140000
DTSTAMP:20260515T165611
CREATED:20240807T200904Z
LAST-MODIFIED:20240816T140453Z
UID:67941-1724245200-1724248800@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Presents - Genetic Testing Program
DESCRIPTION:Date: Wednesday\, August 21\, 2024\nTime: 1:00pm – 2:00pm ET \n \n \n  \nTitle:\nHemophilia Alliance Genetic Testing Program \nHemophilia Alliance has introduced a new Genetic Testing Program as of August 1\, 2024. This initiative offers genetic testing for individuals with Hemophilia A\, Hemophilia B\, and von Willebrand’s disease. The program is specifically designed for patients receiving care at Hemophilia Alliance Member Treatment Centers who either lack insurance coverage\, are ineligible for other free genetic testing programs or studies\, or face prohibitive out-of-pocket costs. The testing will be conducted by Bloodworks in Washington state and Versiti in Wisconsin. \nWho will be eligible for free testing? \n\nPatients receiving care at a Hemophilia Alliance Member HTC who are not eligible for other available genetic testing free programs or studies AND meet one or more of the following criteria:\n\nPatient does not have insurance coverage.\nPatient does not have coverage for genetic testing under their insurance plan\, i.e. not a covered benefit.\nPatients who cannot afford the out-of-pocket expenses associated with the testing and are at\, or below\, 400% of the Federal Poverty Level.\n\n\n\nAdditional information on the program and how to get started can be found here.
URL:https://hemoalliance.org/alliance-events/hemophilia-alliance-genetic-testing-program/
CATEGORIES:Members Only,Webinar
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