This topic contains 0 replies, has 1 voice, and was last updated by  Pulmonary Fibrosis News Moderator 10 months ago.

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    Since being diagnosed with IPF in 2016, Charlene has cherished the relationships she’s developed with other patients around the world, writing that for the most part, hearing others’ stories has given her comfort, hope, and encouragement.

    However, Charlene also acknowledges that there can be downsides to making connections as well. Read more from Charlene here.

    How has IPF connected you to other people? Can you relate to Charlene’s experience?

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