CF Get Loud 1/26/21 CF Get Loud 1/26/21

Health Technology Assessment

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CF Get Loud 1/19/21 CF Get Loud 1/19/21

#WEGOTLOUD Spotlight on Ted Falk

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CF Get Loud 1/12/21 CF Get Loud 1/12/21

#WEGOTLOUD Spotlight on Jim Wilson

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CF Get Loud 1/7/21 CF Get Loud 1/7/21

#WEGOTLOUD Spotlight - Elected Officials Edition

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CF Get Loud 12/30/20 CF Get Loud 12/30/20

PMPRB guidelines delayed until July 1st, 2021

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CF Get Loud 12/22/20 CF Get Loud 12/22/20

Trikafta formally accepted for review by Health Canada - Part of ‘aligned review’ with CADTH/INESSS

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CF Get Loud 12/21/20 CF Get Loud 12/21/20

Letter from pCPA to Jim Wilson MPP regarding current negotiations

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CF Get Loud 12/18/20 CF Get Loud 12/18/20

Court rules PMPRB does not have unlimited jurisdiction

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CF Get Loud 12/9/20 CF Get Loud 12/9/20

All-Party Emergency Access to Trikafta Caucus

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CF Get Loud 11/16/20 CF Get Loud 11/16/20

Sickboy Podcast Interviews our very own, Stephanie Stavros

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CF Get Loud 9/25/20 CF Get Loud 9/25/20

Junior Advocates Program, Back to School Workbook Released

It all begins with an idea.

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CF Get Loud 9/10/20 CF Get Loud 9/10/20

Beth Vanstone sits down with Living with Cystic Fibrosis Podcast. “CF Get Loud, the Canadian perspective.”

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CF Get Loud 8/24/20 CF Get Loud 8/24/20

RESEARCH STUDY: PROJECTING THE IMPACT OF DELAYED ACCESS TO TRIKAFTA

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CF Get Loud 8/4/20 CF Get Loud 8/4/20

Letters for Lives Campaign - PMPRB Submission

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CF Get Loud 6/3/20 CF Get Loud 6/3/20

CF Get Loud Townhall

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CF Get Loud 5/27/20 CF Get Loud 5/27/20

Canada, Don’t Give Up on Us.

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CF Get Loud 2/24/20 CF Get Loud 2/24/20

CF Families GET LOUD for Access to Medicine at Queen’s Park

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CF Get Loud 1/23/20 CF Get Loud 1/23/20

After ‘getting loud’, the First CF Patient in Canada is approved for Compassionate Care for Trikafta

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