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VYNDAMAX is used to treat adults with wild-type or hereditary ATTR-CM to reduce death and hospitalization related to heart problems.
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ATTR-CM impacts your body and your life

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In addition to the heart, the signs of transthyretin cardiac amyloidosis (ATTR-CM) can show up in other parts of the body

In fact, people may experience symptoms and conditions that seem unrelated to the heart.

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These symptoms and conditions may include:

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Carpal tunnel syndrome

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Lower back pain

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Stomach issues

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Strange tingling or pain in toes or feet

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Find a heart specialist

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See a heart specialist when you start experiencing symptoms. If you think you may have ATTR-CM, it may be time to find a heart specialist near you.

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By clicking "Search", you acknowledge and agree with the Terms and Conditions. This directory is updated regularly. Search results may not include all information about every doctor who treats and diagnoses ATTR-CM. Please see the  Terms and Conditions  for more details.

If you are a provider, please contact us to  update your information  or to opt in/opt out.

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Tips if you’re newly diagnosed with ATTR-CM:

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  • Understand that ATTR-CM is a rare, life-threatening, progressive heart condition, which means it will get worse over time
  • Discuss treatment options with your doctor as soon as your diagnosis is confirmed. The sooner you start treatment, the sooner you can begin to slow disease progression
  • It can be helpful to connect with other people diagnosed with ATTR-CM
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Early diagnosis is important so that treatment can begin as soon as possible

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Learn about Stan's early symptoms

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“My journey to diagnosis was fairly long...I had symptoms for at least 10 years before the final diagnosis was made.”
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Learn how VYNDAMAX may help

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