CYSTIC FIBROSIS PARENT EDUCATION
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As CF Parents, We Share A Mission:
Caring For Someone With Cystic Fibrosis

Continuing Education Workshops

We provide CF Education Workshops to Cystic Fibrosis parents, caregivers, and individuals living with CF. Our various topics all pertain to current CF research and technology, so CF families can stay in-the-know on current therapies, resources, and opportunities available.

All our meetings are held virtually and available to all CF parents/caregivers regardless of your location.

To participate in an upcoming workshop. please click here to register and we will provide ZOOM login information after you RSVP. We will add you to our mailing list and inform you of future workshops. Be sure to also check out our archive of past workshops.

We look forward to connecting with you!

U P C O M I N G   W O R K S H O PS


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Managing Practical Matters

Focus on the practical things required to manage family life with CF. Discover tips for managing time, storing medication, record keeping, and getting organized, so you have more time to focus on your family and yourself. In this workshop, you will learn how to increase balance in your life, improve your quality of life, and become more efficient with your time and energy
Sunday, November 16, 2025
6:30pm ET   |   5:30pm CT   |   4:30pm MT   |   3:30pm PT
REGISTER
Sponsored by CF Parent Education, in collaboration with Bright Beginnings. Bright Beginnings is supported by an Impact Grant from the CF Foundation. Presented by Lisa Greene, M.A., CFLE, an author, speaker, educator, coach, and mother of two adult children with CF. Lisa is dedicated to helping parents raise healthy, happy families since 2003. She inspires families to believe in their strength, no matter the hardship.

Recent Workshops

New Diagnosis

Speaking Up and Asserting Your Expertise

September 2025
There will be times when you need to speak up for your child's rights or care needs. It can be difficult to challenge what medical professionals are telling you. This workshop teaches a process for developing an advocacy plan and develop skills in speaking up for your child and family.
NACFC

Coping with the Emotional Rollercoaster

March 2025
The emotions of dealing with CF have been described as being on an "emotional rollercoaster." Learning how to accept and cope with the ups and downs of life with CF as early as possible will help you build resilience.
CF Story

Your CF Story: How to Talk About CF

January 2025
When you are new to the CF journey, you will receive many questions from family, friend, and other about what you are going through. It's important to have a plan about what you want to share. This workshop helps you reflect on your story and decide who, how, and when to tell others about your child's diagnosis.
BROWSE ARCHIVES
DISCLAIMER: The information published on this website or in any connected material is the opinion of Jennifer Webber and CF Parent Education Group only, and is not meant to replace professional medical or mental health care. Persons should always seek the advice of a medical professional when making decisions about personal healthcare or treatment.

We Look Forward To Connecting With You


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  • HOME
  • ABOUT
  • CONTACT
  • UPCOMING WORKSHOPS
  • ARCHIVES
  • CF BLOG