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Hello everyone, I'm a Respiratory Therapist and wanted to check in.

Good afternoon,

I'm a long-time therapist in middle TN, and I've had the privilege of taking care of many patients with cystic fibrosis over the years. My first experiences with it were as a student at the Vanderbilt Children's Hospital in Nashville, and I was overwhelmed with how tough my young patients were, and just how much they had to deal with. I've recently spent a lot of time thinking about you all.

I would love to ask those of you with CF, or with loved ones with CF, how are we doing as your care team? What can we do better? Where are we falling short? What do you like about the your current care partners and program? What do you dislike?

I would love to find out how we can improve things for you. I can't promise I can change anything other than how I operate, but I can and will pass along your feedback to my coworkers. Please share your thoughts if you have time.

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