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


Building Strong Relationships With Your Healthcare Team

Your medical care team plays a crucial role in your life—some with CF even describe them as "like family." Building strong relationships takes time and effort. This workshop will explore patient- and family-centered care, culturally respectful care, and partnership in care while boosting your confidence in working with you CF team.
Sunday, June 1, 2025
6:30pm ET   |   5:30pm CT   |   4:30pm MT   |   3:30pm PT

Sponsored by CF Parent Education, in collaboration with Bright Beginnings.
Guest speaker, Lisa Greene, M.A., CFLE, is an author, speaker, educator, coach, and mother of two adult children with CF. She is dedicated to helping parents raise healthy, happy families since 2003. Lisa inspires families to believe in their strength, no matter the hardship.
REGISTER

Future Workshops

September 21, 2025
Speaking Up and Asserting Your Expertise

November 16, 2025
Managing Practical Matters (Time, Storing Meds, Record Keeping Tips, etc.)

Recent Workshops

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.
New Diagnosis

Newly Diagnosed with CF

October 2024
An overview and deeper dive into topics for parents and caregivers of those newly diagnosed with CF (discussion geared for age 3 and younger)
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