Hey everyone! Hope you all made it through this week ok. Everyone managing quarantine life?
So I wanted to share Wendy’s latest column with you all. I found this piece to be both enlightening and relatable. When the first FDA-approved treatment for my disease went on the market, I had similar feelings as Wendy did about Trikafta. She writes about everything from survivor’s guilt, to the wave of emotions that come with starting a new treatment.
It’s like you spend your entire life surviving and managing your CF symptoms. Then suddenly, a treatment comes along, and your perception of where your life is headed changes drastically. It’s a lot to take in!
Do you agree with Wendy? Do you have any other thoughts regarding Trikafta?
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