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

Contact Us

CF Family Advisory Board members are available to speak with families in our local community. Let us know a little about you and the types of questions you have by email or using the form below, and we'll connect you with someone who has children the same age as yours, experience with an area of care you have questions about, or just someone who lives near you and may want to meet and chat. ​You're not alone... we're on this CF journey together!
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CONTACT & FEEDBACK FORM

Do you have a question for the CF Family Advisory Board? Would you like to leave suggestion, comment, praise, or complaint for the FAB to share with the CF Care Team? Let us know!
    Please provide if you would like to receive our seasonal CF Newsletter by mail.
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1000 Blythe Blvd.
Charlotte, NC 28203
704-355-2000
Website
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MAIN HOSPITAL

1000 Blythe Blvd.
Charlotte, NC 28203
704-355-2000
​Website
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​SPECIALTY CENTER

Medical Center Plaza
1001 Blythe Blvd., Suite 200-E
Charlotte, NC 28203
704-381-8840
​Website
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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