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  <title>The Lipid Lens: Bringing Lipid Health Into Focus</title>

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  <copyright>© 2026 The Lipid Lens: Bringing Lipid Health Into Focus</copyright>
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  <description><![CDATA[<p><b>The Lipid Lens Podcast: Bringing Lipid Health Into Focus</b> is a patient-focused podcast from the Foundation of the National Lipid Association, designed to help you better understand your lipid health and what it means for your heart, metabolism, and long-term wellness.</p><p><br></p><p>Building on the science and expertise behind the National Lipid Association’s clinician education, the Lipid Lens series translates complex lipid topics into clear, practical conversations for everyday people. From cholesterol and triglycerides to lipoproteins, genetics, lifestyle, and treatment options, we break down what you need to know—without the medical jargon.</p><p><br></p><p>Each episode empowers you to be a more informed advocate for your own health, ask better questions, and understand the “why” behind your care.</p><p><br></p><p>For trusted patient education, resources, and tools to continue learning, visit <b>learnyourlipids.com</b>.</p>]]></description>
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    <itunes:title>Episode 1 | In Their Shoes: Caregiver Voices in FCS</itunes:title>
    <title>Episode 1 | In Their Shoes: Caregiver Voices in FCS</title>
    <itunes:summary><![CDATA[What does it really mean to support someone living with familial chylomicronemia syndrome (FCS)? In the debut episode of The Lipid Lens, host Dr. Marlys Koschinsky sits down with Dr. Albert Freedman, Nicole McCoy, and Phillip McCoy to explore the deeply personal side of an FCS diagnosis. Nicole shares her journey as a patient, while Phillip offers an honest look at what it means to show up as a partner and caregiver. Together, they reflect on what they wish they had known sooner and share the...]]></itunes:summary>
    <description><![CDATA[<p>What does it really mean to support someone living with familial chylomicronemia syndrome (FCS)? In the debut episode of <em>The Lipid Lens</em>, <b>host Dr. Marlys Koschinsky</b> sits down with <b>Dr. Albert Freedman</b>,<b> Nicole McCoy</b>, and<b> Phillip McCoy</b> to explore the deeply personal side of an FCS diagnosis. Nicole shares her journey as a patient, while Phillip offers an honest look at what it means to show up as a partner and caregiver. Together, they reflect on what they wish they had known sooner and share their advice for others navigating life with FCS. A powerful first episode for patients, caregivers, and the clinicians who care for them.</p><p><br/></p><p>For more FCS resources, visit learnyourlipids.com/lipid-disorders/familial-chylomicronemia-syndrome/. </p>]]></description>
    <content:encoded><![CDATA[<p>What does it really mean to support someone living with familial chylomicronemia syndrome (FCS)? In the debut episode of <em>The Lipid Lens</em>, <b>host Dr. Marlys Koschinsky</b> sits down with <b>Dr. Albert Freedman</b>,<b> Nicole McCoy</b>, and<b> Phillip McCoy</b> to explore the deeply personal side of an FCS diagnosis. Nicole shares her journey as a patient, while Phillip offers an honest look at what it means to show up as a partner and caregiver. Together, they reflect on what they wish they had known sooner and share their advice for others navigating life with FCS. A powerful first episode for patients, caregivers, and the clinicians who care for them.</p><p><br/></p><p>For more FCS resources, visit learnyourlipids.com/lipid-disorders/familial-chylomicronemia-syndrome/. </p>]]></content:encoded>
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    <pubDate>Fri, 15 May 2026 12:00:00 -0400</pubDate>
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    <itunes:duration>1834</itunes:duration>
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