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Sharing Your Diagnosis with Others

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  • #2297
    Jennifer K Chichka
    Site Admin

    We recently posted on the DCM Foundation Facebook and Instagram pages that sharing a diagnosis, like DCM, can be a challenging experience, but it can be rewarding as well. This post got some great feedback, so we thought we would continue the conversation here. For those of you who have shared a DCM diagnosis with family, friends, and coworkers, do you have any tips for someone who is still figuring it out?

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