you are not alone


Many excellent resources are available to help you, or a loved one, if you’ve been diagnosed with ATTR‑CM.

Helpful resources

Get the Message brochure

Access a brief printable version of the key take-aways from this website for yourself or to share.


Descargar en español

Don’s brochure

Learn more about hereditary ATTR‑CM and how this disease has affected former NBA player and coach, Don Chaney.


Create your own customized doctor discussion guide

Simply answer these 4 questions to receive a guide that can help you prepare to talk with your cardiologist.
create discussion guide

Use the standard guide


Descargar en español

Watch our TV commercials about recognizing
ATTR‑CM signs and symptoms here.



Ver en español




Sign up here to stay connected

Voices for the Heart

Learn more about hereditary ATTR‑CM and Voices for the Heart community events.

About Hereditary ATTR-CM

Upcoming events

Register with Zoom

Learn more

How Faye found support


“I belong to an ATTR‑CM group on Facebook, where I look for advice, suggestions, and support. It means a lot.”
Watch Faye’s Story

Visit us on Facebook

  • Connect with others impacted by ATTR‑CM
  • Hear firsthand stories from patients who have been diagnosed
  • Learn more about the condition

Follow us

Find support from these trusted amyloidosis organizations

Check out the links below. They can help you find healthcare providers who are experts in the diagnosis and treatment of amyloidosis and connect you with other important resources.

Amyloidosis Support Groups

  • Provides education through support meetings, live in 30 cities
  • Provides education through virtual webinars, as well as support groups on Facebook

Learn more

Find a provider with ASG

Amyloidosis Research Consortium

  • Provides comprehensive support and information for patients
  • Accelerates development of and access to new and innovative treatments
  • Drives research that will have the greatest impact on patients

Learn more

Find a provider with ARC

Amyloidosis Foundation

  • Supports research for an earlier diagnosis
  • Educates medical professionals
  • Provides patients with a comprehensive range of services

Learn more

Pfizer does not sponsor, maintain, or confirm the accuracy of these resources, nor does Pfizer endorse any specific healthcare provider.

These websites are neither owned nor controlled by Pfizer. Pfizer does not endorse and is not responsible for the content or services of these sites. Pfizer is providing these resources for informational purposes only. The company does not sponsor, maintain, or confirm the accuracy of these resources, nor does Pfizer endorse any specific healthcare provider.

Together for Rare

Learn more about Pfizer Patient Affairs Liaisons—professionals dedicated to connecting patients and caregivers with Pfizer educational information and programs.​​​​​​​ Get in touch with the Patient Affairs Liaison in your area.

connect now

Learn about a treatment option