CHARLOTTE CF FAMILIES
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  • 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
    • 2020 CF Education Day Recap
  • NEWS & UPDATES

CF Education ​Survey

Thank you for attending our CF Caregiver Education Night on February 26th. We welcome your feedback! Whether you attended virtually or in person, we want to know what you liked, what you didn't like, and suggestions for improvement next time.
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CF Education Night Survey

SUBMIT SURVEY

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Charlotte CF Families website and CF Family Advisory Board are operated by local CF families with the guidance of the Atrium Health Cystic Fibrosis Program. No advice or recommendations on this page should be taken above that of your CF Care Team. Every person with CF is different. The advice and suggestions on this page are simply a guide to help families feel connected and informed. 
Last Published November2020 
Site Design by Rebecca Preslar
  • 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
    • 2020 CF Education Day Recap
  • NEWS & UPDATES