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Sharing your journey as a CF caregiver?
CF News Today has welcomed a new columnist, Jennifer Chamberlain! In her first column titled Exposing the Outside World to Our Family’s Cystic Fibrosis Journey, Jennifer describes what the experience of opening up about CF and caring for her daughter, Claire, has been like. I appreciate Jenn’s perspective as a caregiver and her column got me thinking about parents and caregivers here on the forum.
A friend called Claire’s care routine “intense.” How would you describe your role as a caregiver? Do you feel comfortable talking about CF/your loved one’s care around others? How much of your experience do you share with friends and family?
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