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REPOST: from our lovely friend, Stephanie. @supersaltysteph is one who is in the ten percent who does not have a modulator available, she recently shared this post on her personal page and is allowing us to share a bit from her admission. As grateful and ecstatic as we are for Trikafta, we have a lot of work to be done, so let’s stand in solidarity with those who don’t yet have a modulator (or who’s country hasn’t approved them).

A post shared by CFNewsToday (@cfnewstoday) on Jan 15, 2020 at 10:13am PST

Cystic Fibrosis Canada launched its fourth annual holiday fundraising effort, with a focus last year on the very special…

Posted by Cystic Fibrosis News on Monday, January 20, 2020

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