February 2022 Issue
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Next Webinar: February 16th*

"Ask a Heart Failure Specialist"

Date: Wednesday, February 16, 2021
Time:  6:00-7:00 PM ET

Click HERE to Register

Join us as we learn about DCM from a heart failure specialist. Have an opportunity to ask questions during the Live Q&A.

Webinar topics include:

  • DCM Overview – No 2 patient paths are the same
  • Is your cardiologist a DCM expert?
    • Questions to ask your cardiologist
    • How to find DCM specialists
  • The genetics of DCM and the need to be genetically tested
  • Live Q&A
*NOTE: All registrants will receive a webinar recording after the event. 

Virtual Heart Failure Patient & Caregiver Day
hosted by the Heart Failure Society of America (HFSA)

Date: Sat., February 12
Time: 10:00 AM - 1:15 PM ET

Click HERE to register for this FREE event!

The program will give patients and caregivers the opportunity to participate in interactive educational discussions with leading heart failure experts and features a heart-healthy cooking demonstration by Dr. Richard Collins, the ‘cooking cardiologist.’ Click here to view the event FLYER.

Also, HFSA's Patient and Caregiver Day will be followed by Heart Failure Awareness Week, a week of virtual activities, education, and community, starting on Sunday, February 13. We hope you can join us for these informative events!

January Webinar Recap: 
"Living with DCM - A Patient's Perspective"

We'd like to say a huge thank you to Stephanie Fallon, Steve Fietek, and Sarah Schaff, for sharing their DCM journeys and tips for living with DCM. To view a recording of the "Living with DCM" webinar, please click here.

Looking forward to seeing you all at on our next webinar: "Ask a Heart Failure Specialist."

Did You Know? 

You can view all past DCM Foundation webinars and newsletters by going to:
Learn about various aspects of DCM including:
  • Living with DCM
  • Heart Transplant
  • Gene Therapies in Development
  • Navigating Financial and Insurance Issues
  • Living with a Pacemaker or ICD
  • and many more topics!
Thank you to our generous sponsors:

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About Us

Founded in 2017, the DCM Foundation is a non-profit organization with a mission to provide hope and support to patients and families with Dilated Cardiomyopathy (DCM) through research, advocacy, and education. 

To view past monthly DCM webinars and DCMF newsletters, please click here.

Medical Providers: Please forward this newsletter to your DCM patients & their family members.

Event Reminder:

February 16th 6:00-7:00 PM ET

Ask a Heart Failure Specialist

Recently Diagnosed with DCM?  Click here to learn more.
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