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Hear from patients taking VYNDAMAX
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Jump ahead to
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Hear from people and their loved ones living with ATTR-CM, transthyretin cardiac amyloidosis
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Meet Raymond
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“ATTR-CM is a rare, progressive condition, and it's important to receive an accurate diagnosis as soon as possible. Learn more about it, and don't wait.”
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Raymond, a real patient with ATTR-CM taking VYNDAMAX
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Meet Alan and Kathy
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“I told my doctor how I was feeling and he told me it’s ATTR-CM. He told me there is no cure but VYNDAMAX slows it down and helps you live longer.”
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Alan, a real patient with ATTR-CM taking VYNDAMAX
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Create a discussion guide to talk to your doctor and start your own conversation about ATTR-CM
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I told my doctor how I was feeling and he told me it’s ATTR-CM. He told me there is no cure but VYNDAMAX slows it down and helps you live longer.
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Alan
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a real patient with ATTR-CM taking VYNDAMAX
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You have to advocate for yourself. Knowledge is power. You have to look into all the things you can do about ATTR-CM.
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Kathy
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Alan’s partner and caregiver
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Meet Stan
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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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Stan, a real patient with ATTR-CM taking VYNDAMAX
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I was glad to find out that there is treatment available…so that gave me some hope.
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Stan
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a real patient with ATTR-CM taking VYNDAMAX
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Once I learned that VYNDAMAX can help to slow the progression of ATTR-CM, I was eager to begin the treatment journey.
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Stan
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a real patient with ATTR-CM taking VYNDAMAX
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Hear about Jack Nicklaus' ATTR‑CM Journey
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Listen to Jack discuss ATTR-CM and VYNDAMAX.
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Get to the heart of what matters
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Stay informed with educational materials about ATTR-CM and VYNDAMAX.
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Check out share your story
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