Learn about a new treatment option
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It’s time you enjoy
the little things.

ATTR-cardiac amyloidosis can make you miss out on the little things that
matter most. With new treatment options available, you and your
cardiologist can choose the one that may fit your way of life.

ATTR-cardiac amyloidosis is a serious heart condition also known as transthyretin amyloid cardiomyopathy, or ATTR-CM.

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Actor portrayals.

Take charge of your care, your health,
your life, your story.

ATTR-cardiac amyloidosis is a rare, but serious,
progressive heart condition.

There are 2 types of
ATTR-cardiac amyloidosis
  • Wild-type Wild-type

    Wild-type, which is caused naturally
    from aging

  • Hereditary Hereditary

    Hereditary, which is passed down

    through
    the family 

ATTR-cardiac amyloidosis is under-diagnosed.
Because the symptoms are similar to other heart
conditions, the average delay in diagnosis is
about 6 years

Common symptoms of ATTR-cardiac amyloidosis

  • Carpal tunnel syndrome Carpal tunnel syndrome

    Carpal tunnel
    syndrome

  • Digestive problems Digestive problems

    Digestive
    problems

  • Irregular heartbeat Irregular heartbeat

    Irregular
    heartbeat

  • Tiredness or weakness Tiredness or weakness

    Tiredness
    or weakness

  • Shortness of breath Shortness of breath

    Shortness
    of breath

  • Swelling in legs and feet Swelling in legs and feet

    Swelling in
    legs and feet

ATTR-cardiac amyloidosis disproportionately affects older adults and people of African descent. It is estimated that 1 in 25 Black Americans may be at risk of developing
ATTR-cardiac amyloidosis.

Learn more about ATTR-cardiac amyloidosis and a new
treatment option.

Learn More Learn more

Find a treatment option
that fits your life.

With new developments in ATTR-cardiac
amyloidosis care, now is the time to ask your
cardiologist about your treatment options.

Discover a new treatment option arrow
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