If you're the parent of a child with cystic fibrosis, you probably know the worry that comes along with sending your kid away to summer camp. To ensure that my own kids with CF were cared for at camp, I wrote the following letter outlining their special medical needs.
- Social Life and Relationships
- Parents & Guardians
- Emotional Wellness
- Get Involved
- Lung Transplantation
- Care Team
- CFTR Modulators
- Coronavirus (COVID-19)
- Adult Care
- North American CF Conference
- About the CF Foundation
- Fertility and Reproductive Health
- CF Related Health Conditions
- Clinical Trials
- Infection Prevention and Control
- Our Research Approach
- Teen Care
- Traveling with CF
- Drug Pipeline
- Care Centers
- Family Planning & Parenting
- In Memoriam
- Clinician Resources
- Mental Health
- Our Advocacy Work
- Great Strides
- Patient Registry
- Working with Your Child's School
- In the Spotlight
- Researcher Resources
- Airway Clearance
- Diversity, Equity, and Inclusion
- Infant Care
- Patient Assistance
- Aging with CF
- Choosing Coverage
- Cystic Fibrosis Foundation Therapeutics (CFFT)
- Therapeutics Development Network
- CF-Related Complications
- Health Care Reform
- Treatment Plan
- Clinical Care Guidelines
- (-) Caring for a Child With CF
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