CHARLOTTE CF FAMILIES
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  • WHAT IS...
    • Cystic Fibrosis
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    • Oral Glucose Tolerance Test (OGTT)
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    • Pulmonary Function Test (PFT)
    • Pulmozyme / Dornase Alfa
    • Sputum Cultures
    • Sweat Test
  • EVENTS
    • 2022 CF Education Day Recap
    • 2021 CF Education Day Recap
    • 2020 CF Education Day Recap
  • NEWS & UPDATES

Resources for Families

The Charlotte CF Family Advisory Board and CF Care Team have compiled a list of helpful hints and suggestions, including recommended products and our favorite websites. The list is always growing, so check back often! 
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UNIQUE OPPORTUNITIES

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SEASONAL
​NEWSLETTER

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FINANCIAL ASSISTANCE

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mental health

MENTAL
​HEALTH

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NUTRITION & SUPPLEMENTS

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SUPPORT
​GROUPS

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LEGAL
​AID

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The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.
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About CFF  •  Charlotte CFF Chapter
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  • HOME
  • ABOUT
    • MEET THE CF CARE TEAM
    • CONTACT
  • RESOURCES
    • COVID-19 Mental Health Resources
    • Virtual Care
    • Programs & Opportunities for CF Families
    • Financial Assistance
    • Support Groups
    • Mental Health
    • Legal Aid
    • Nutrition & Supplements
    • Newsletter
  • WHAT IS...
    • Cystic Fibrosis
    • Antibiotic Resistance
    • Bronchodilator
    • Chest X-Ray
    • Hypertonic Saline
    • Inhaled Antibiotics
    • Labs / Blood Work
    • Mucus Thinners
    • Oral Glucose Tolerance Test (OGTT)
    • PEP Device
    • Pulmonary Function Test (PFT)
    • Pulmozyme / Dornase Alfa
    • Sputum Cultures
    • Sweat Test
  • EVENTS
    • 2022 CF Education Day Recap
    • 2021 CF Education Day Recap
    • 2020 CF Education Day Recap
  • NEWS & UPDATES