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      <video:title> Jen, Living with MMN </video:title>
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      <video:description> One of the key things for me with managing MMN is my support system. </video:description>
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    <loc>https://www.knowingpn.com/mmn-symptoms</loc>
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      <video:title> Jen, Living with MMN </video:title>
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      <video:description> Now that I look back, I think symptoms started before I even started recognizing them.</video:description>
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    <loc>https://www.knowingpn.com/mmn-diagnosis</loc>
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      <video:title>Jen, Living with MMN</video:title>
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      <video:description>After what felt like a revolving door of specialists and doctors, I finally found the right one to help me treat my MMN. </video:description>
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    <loc>https://www.knowingpn.com/mmn-management</loc>
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      <video:title>Jen, Living with MMN</video:title>
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      <video:description>It's very important to me to have a team that's patient and understands what I'm going through.</video:description>
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      <video:title>Jen, Living with MMN</video:title>
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      <video:description>MMN has taught me to not take life for granted. I truly appreciate what I can do. </video:description>
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    <loc>https://www.knowingpn.com/cidp/living-with-cidp</loc>
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      <video:title>Mark, Living with MMN</video:title>
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      <video:description>One day, Mark traveled from California to Spain. He noticed a tingling in his lower back but thought it was due to the long flight. Over the next few days, the tingling spread to his hands, legs, and feet, and by the end of his 10-day trip, he could barely walk. When he got home, Mark was misdiagnosed with Guillain-Barré syndrome (GBS) and then was diagnosed with CIDP 2 years later. A part-time casino party dealer and retired engineer, Mark gets treatment of his CIDP, including SCIg maintenance therapy.</video:description>
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      <video:title>Maddy, Living with MMN</video:title>
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      <video:description>Unlike many people living with CIDP, Maddy's condition started at an early age. She first began experiencing symptoms such as numbness and tingling in the sixth grade. It took several years and multiple doctors before she was finally diagnosed with CIDP. Today, Maddy lives in Louisiana and works in human resources at a local rehabilitation hospital. She gets treatment of her CIDP, including subcutaneous immunoglobulin (SCIg) maintenance therapy.</video:description>
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