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        <title>HippraConnects</title>
        <link>https://redcircle.com/shows/supporting-physicians</link>
        <language>en-US</language>
        <copyright>All rights reserved.</copyright>
        <itunes:subtitle>Sharing Healthcare Knowledge</itunes:subtitle>
        <itunes:author>Hippra Podcast</itunes:author>
        <itunes:summary>HippraConnects helps to facilitate community awareness and medical knowledge-sharing to give a voice to those helping patients with rare diseases and challenging medical conditions.</itunes:summary>
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        <description><![CDATA[<p>Welcome to HippraConnects where we give a voice to those battling complex illnesses, challenging medical conditions or rare diseases and the healthcare providers who treat them as well as the support system that nurtures and sustains them.</p>]]></description>
        
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        <podcast:locked>no</podcast:locked>
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            <itunes:name>Hippra Podcast</itunes:name>
            <itunes:email>support@hippra.com</itunes:email>
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                <itunes:title>21. A Chat with Corben Parker, U.S. Army Veteran, Nurse, and Rare Disease Patient</itunes:title>
                <title>21. A Chat with Corben Parker, U.S. Army Veteran, Nurse, and Rare Disease Patient</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>This episode is a fascinating conversation with Corben Parker, US Army veteran, nurse, and patient. In 2021, Corben was diagnosed with a rare neurological disease called complex regional pain syndrome and has since become involved with the Everylife Foundation for Rare Diseases. In his story, Corben discusses his advocacy and commitment to treatment modalities that are outside conventional medicine for those with rare or difficult to treat illnesses. We thank him for his service, for his advocacy and for sharing his journey!</p>]]></description>
                <content:encoded>&lt;p&gt;This episode is a fascinating conversation with Corben Parker, US Army veteran, nurse, and patient. In 2021, Corben was diagnosed with a rare neurological disease called complex regional pain syndrome and has since become involved with the Everylife Foundation for Rare Diseases. In his story, Corben discusses his advocacy and commitment to treatment modalities that are outside conventional medicine for those with rare or difficult to treat illnesses. We thank him for his service, for his advocacy and for sharing his journey!&lt;/p&gt;</content:encoded>
                
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                <pubDate>Mon, 01 Jun 2026 15:57:56 &#43;0000</pubDate>
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                <itunes:duration>1736</itunes:duration>
                
                
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                <itunes:title>20. Stephanie Riordan and the Everylife Foundation for Rare Diseases</itunes:title>
                <title>20. Stephanie Riordan and the Everylife Foundation for Rare Diseases</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Join us for this fascinating look at the Everylife Foundation for Rare Diseases. In this episode, we are pleased to welcome Stephanie Riordan, Senior Director of Patient Programs at EveryLife Foundation as she shares information about how this program functions at the  intersection of art and health. Through creative expression, the community translates lived rare disease experience into advocacy, storytelling, and public impact. For more information, <a href="https://everylifefoundation.org/rare-artist/" rel="nofollow">please click here.</a></p>]]></description>
                <content:encoded>&lt;p&gt;Join us for this fascinating look at the Everylife Foundation for Rare Diseases. In this episode, we are pleased to welcome Stephanie Riordan, Senior Director of Patient Programs at EveryLife Foundation as she shares information about how this program functions at the  intersection of art and health. Through creative expression, the community translates lived rare disease experience into advocacy, storytelling, and public impact. For more information, &lt;a href=&#34;https://everylifefoundation.org/rare-artist/&#34; rel=&#34;nofollow&#34;&gt;please click here.&lt;/a&gt;&lt;/p&gt;</content:encoded>
                
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                <pubDate>Thu, 26 Feb 2026 16:36:02 &#43;0000</pubDate>
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                <itunes:duration>1672</itunes:duration>
                
                
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                <itunes:title>19. Laura Byer of the Alzheimer&#39;s Association of the National Capital Area - Part II Holiday Travel with Alzheimer&#39;s Patients</itunes:title>
                <title>19. Laura Byer of the Alzheimer&#39;s Association of the National Capital Area - Part II Holiday Travel with Alzheimer&#39;s Patients</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Join Laura Byer, Program Manager of the Alzheimer&#39;s Association of the National Capital Area for an informative discussion aimed at those supporting individuals with Alzheimer&#39;s with tips for helping dementia and Alzheimer&#39;s patients when traveling during the holiday season. Learn about the resources offered by the Alzheimer&#39;s Association of the National Capital Area and valuable tips for engaging with someone with this progressive disease that not only impacts the individual, but the family and friends who care for them. Contact the Alzheimer&#39;s Association: https://www.alz.org/ or call their helpline: <strong>800.272.3900.</strong></p>]]></description>
                <content:encoded>&lt;p&gt;Join Laura Byer, Program Manager of the Alzheimer&amp;#39;s Association of the National Capital Area for an informative discussion aimed at those supporting individuals with Alzheimer&amp;#39;s with tips for helping dementia and Alzheimer&amp;#39;s patients when traveling during the holiday season. Learn about the resources offered by the Alzheimer&amp;#39;s Association of the National Capital Area and valuable tips for engaging with someone with this progressive disease that not only impacts the individual, but the family and friends who care for them. Contact the Alzheimer&amp;#39;s Association: https://www.alz.org/ or call their helpline: &lt;strong&gt;800.272.3900.&lt;/strong&gt;&lt;/p&gt;</content:encoded>
                
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                <pubDate>Wed, 26 Nov 2025 18:04:51 &#43;0000</pubDate>
                <itunes:duration>1072</itunes:duration>
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                <itunes:title>18. Laura Byer of the Alzheimer&#39;s Association of the National Capital Area</itunes:title>
                <title>18. Laura Byer of the Alzheimer&#39;s Association of the National Capital Area</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Join Laura Byer, Program Manager of the Alzheimer&#39;s Association of the National Capital Area for an informative discussion aimed at those supporting individuals with Alzheimer&#39;s. Learn about the resources offered by the Alzheimer&#39;s Association of the National Capital Area and valuable tips for engaging with someone with this progressive disease that not only impacts the individual, but the family and friends who care for them. Contact the Alzheimer&#39;s Association: https://www.alz.org/ or call their helpline: <strong>800.272.3900.</strong></p>]]></description>
                <content:encoded>&lt;p&gt;Join Laura Byer, Program Manager of the Alzheimer&amp;#39;s Association of the National Capital Area for an informative discussion aimed at those supporting individuals with Alzheimer&amp;#39;s. Learn about the resources offered by the Alzheimer&amp;#39;s Association of the National Capital Area and valuable tips for engaging with someone with this progressive disease that not only impacts the individual, but the family and friends who care for them. Contact the Alzheimer&amp;#39;s Association: https://www.alz.org/ or call their helpline: &lt;strong&gt;800.272.3900.&lt;/strong&gt;&lt;/p&gt;</content:encoded>
                
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                <pubDate>Sun, 03 Aug 2025 14:42:04 &#43;0000</pubDate>
                <itunes:duration>1614</itunes:duration>
                
                
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                <itunes:title>17. A Chat with Epidemiologist, Dr. Tammy Smith</itunes:title>
                <title>17. A Chat with Epidemiologist, Dr. Tammy Smith</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Dr. Tammy Smith serves as the Regional Epidemiologist with the Communicable Disease Branch at the Department of Public Health in Raleigh, NC. Dr. Smith is also the CEO and President of Inspired Now Networks, Inc., a nonprofit organization focused on health awareness, education, and research.</p><p>Dr. Smith has a Doctorate of Public Health and an extensive background in research and public health. She has worked at Duke University Medical Center, where she co-authored multiple publications. She brings to HippraConnects important information and awareness of infectious diseases, prevention and important public health intitiatives.</p>]]></description>
                <content:encoded>&lt;p&gt;Dr. Tammy Smith serves as the Regional Epidemiologist with the Communicable Disease Branch at the Department of Public Health in Raleigh, NC. Dr. Smith is also the CEO and President of Inspired Now Networks, Inc., a nonprofit organization focused on health awareness, education, and research.&lt;/p&gt;&lt;p&gt;Dr. Smith has a Doctorate of Public Health and an extensive background in research and public health. She has worked at Duke University Medical Center, where she co-authored multiple publications. She brings to HippraConnects important information and awareness of infectious diseases, prevention and important public health intitiatives.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Fri, 27 Dec 2024 15:53:10 &#43;0000</pubDate>
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                <itunes:duration>2408</itunes:duration>
                
                
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                <itunes:title>16. An Informative Conversation on Orthopedics, Healthcare Disparities and Treatment Challenges in Underserved Communities.</itunes:title>
                <title>16. An Informative Conversation on Orthopedics, Healthcare Disparities and Treatment Challenges in Underserved Communities.</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>In this episode, we chat with two individuals committed to the study and practice of Orthopedic Medicine, Dr. Oluwadamilola Kolade an Ortho resident at Howard University and Ms. Moriah Martindale, a medical student at the University of Buffalo. Their focus is on sharing important information about orthopedics and addressing healthcare disparities/barriers to treatment in underserved communities. </p>]]></description>
                <content:encoded>&lt;p&gt;In this episode, we chat with two individuals committed to the study and practice of Orthopedic Medicine, Dr. Oluwadamilola Kolade an Ortho resident at Howard University and Ms. Moriah Martindale, a medical student at the University of Buffalo. Their focus is on sharing important information about orthopedics and addressing healthcare disparities/barriers to treatment in underserved communities. &lt;/p&gt;</content:encoded>
                
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                <pubDate>Mon, 01 Apr 2024 18:25:11 &#43;0000</pubDate>
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                <itunes:duration>1793</itunes:duration>
                
                
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                <itunes:title>15. Reproductive Health Impact with Rev. Deneen Robinson</itunes:title>
                <title>15. Reproductive Health Impact with Rev. Deneen Robinson</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p><strong>Rev. Deneen Robinson discusses Reproductive Health (RH) Impact and the Collaborative for Equity &amp; Justice,</strong> a fiscally sponsored program of The Praxis Project, a 501(c)(3) public charity. RH Impact is one of the nation’s leading experts and an advocate for change in the Black maternal health and infant mortality crises.  RH Impact works to create transnational solutions that optimize Black maternal, infant, sexual, and reproductive wellbeing. RH shifts systems and culture through training, research, technical assistance, policy, advocacy, and community-centered collaboration. To learn more visit <a href="http://www.rhimpact.org/" rel="nofollow"><u>www.rhimpact.org</u></a> for more information. </p><ul><li>Follow them on these social media channels:</li><li>FB/Meta: <a href="https://www.facebook.com/ReproductiveHealthImpact?mibextid=9R9pXO" rel="nofollow">rhimpact_</a></li><li>YouTube:  <a href="https://www.youtube.com/@rhimpact_" rel="nofollow">rhimpact_</a></li><li>IG:  <a href="https://www.instagram.com/rhimpact_/" rel="nofollow">rhimpact_</a></li><li>TikTok:  <a href="https://www.tiktok.com/@rhimpact_?_r=1&_t=8fnqkcbRfgY" rel="nofollow">rhimpact_</a></li><li>LinkedIn: <a href="https://www.linkedin.com/company/reproductivehealthimpact/mycompany/" rel="nofollow">Reproductive Health Impact</a></li><li>Subscribe to their Newsletter: <a href="http://www.rhimpact.org/" rel="nofollow">www.rhimpact.org</a></li></ul>]]></description>
                <content:encoded>&lt;p&gt;&lt;strong&gt;Rev. Deneen Robinson discusses Reproductive Health (RH) Impact and the Collaborative for Equity &amp;amp; Justice,&lt;/strong&gt; a fiscally sponsored program of The Praxis Project, a 501(c)(3) public charity. RH Impact is one of the nation’s leading experts and an advocate for change in the Black maternal health and infant mortality crises.  RH Impact works to create transnational solutions that optimize Black maternal, infant, sexual, and reproductive wellbeing. RH shifts systems and culture through training, research, technical assistance, policy, advocacy, and community-centered collaboration. To learn more visit &lt;a href=&#34;http://www.rhimpact.org/&#34; rel=&#34;nofollow&#34;&gt;&lt;u&gt;www.rhimpact.org&lt;/u&gt;&lt;/a&gt; for more information. &lt;/p&gt;&lt;ul&gt;&lt;li&gt;Follow them on these social media channels:&lt;/li&gt;&lt;li&gt;FB/Meta: &lt;a href=&#34;https://www.facebook.com/ReproductiveHealthImpact?mibextid=9R9pXO&#34; rel=&#34;nofollow&#34;&gt;rhimpact_&lt;/a&gt;&lt;/li&gt;&lt;li&gt;YouTube:  &lt;a href=&#34;https://www.youtube.com/@rhimpact_&#34; rel=&#34;nofollow&#34;&gt;rhimpact_&lt;/a&gt;&lt;/li&gt;&lt;li&gt;IG:  &lt;a href=&#34;https://www.instagram.com/rhimpact_/&#34; rel=&#34;nofollow&#34;&gt;rhimpact_&lt;/a&gt;&lt;/li&gt;&lt;li&gt;TikTok:  &lt;a href=&#34;https://www.tiktok.com/@rhimpact_?_r=1&amp;_t=8fnqkcbRfgY&#34; rel=&#34;nofollow&#34;&gt;rhimpact_&lt;/a&gt;&lt;/li&gt;&lt;li&gt;LinkedIn: &lt;a href=&#34;https://www.linkedin.com/company/reproductivehealthimpact/mycompany/&#34; rel=&#34;nofollow&#34;&gt;Reproductive Health Impact&lt;/a&gt;&lt;/li&gt;&lt;li&gt;Subscribe to their Newsletter: &lt;a href=&#34;http://www.rhimpact.org/&#34; rel=&#34;nofollow&#34;&gt;www.rhimpact.org&lt;/a&gt;&lt;/li&gt;&lt;/ul&gt;</content:encoded>
                
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                <pubDate>Mon, 05 Feb 2024 20:09:40 &#43;0000</pubDate>
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                <itunes:duration>1075</itunes:duration>
                
                
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                <itunes:title>14. Amniotic Fluid Embolism Foundation with Executive Director, Miranda Klassen.</itunes:title>
                <title>14. Amniotic Fluid Embolism Foundation with Executive Director, Miranda Klassen.</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>In this podcast, we welcome Miranda Klassen, Executive Director of the Amniotic Fluid Embolism Foundation (AFE), for an enlightening and valuable discussion of a condition that may severely impact the health of pregnant women. Amniotic Fluid Embolisms occur when a mother has an allergic-like immune response to amniotic fluid or fetal material that enters her bloodstream during labor or after. This birth complication can be life-threatening to both mother and baby. The Amniotic Fluid Embolism Foundation (AFE) works to spread awareness, provide resources, support impacted families, and educate medical professionals. You can learn more about the AFE Foundation at <a href="http://afesupport.org/" rel="nofollow">afesupport.org</a>.</p>]]></description>
                <content:encoded>&lt;p&gt;In this podcast, we welcome Miranda Klassen, Executive Director of the Amniotic Fluid Embolism Foundation (AFE), for an enlightening and valuable discussion of a condition that may severely impact the health of pregnant women. Amniotic Fluid Embolisms occur when a mother has an allergic-like immune response to amniotic fluid or fetal material that enters her bloodstream during labor or after. This birth complication can be life-threatening to both mother and baby. The Amniotic Fluid Embolism Foundation (AFE) works to spread awareness, provide resources, support impacted families, and educate medical professionals. You can learn more about the AFE Foundation at &lt;a href=&#34;http://afesupport.org/&#34; rel=&#34;nofollow&#34;&gt;afesupport.org&lt;/a&gt;.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Mon, 25 Sep 2023 17:09:44 &#43;0000</pubDate>
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                <itunes:duration>1460</itunes:duration>
                
                
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                <itunes:title>13. Fetal Health Foundation with Co-Founder, Lonnie Somers</itunes:title>
                <title>13. Fetal Health Foundation with Co-Founder, Lonnie Somers</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>We are so pleased to have with us, Lonnie Somers, Co-Founder of The Fetal Health Foundation. The Fetal Health (or Hope) Foundation’s mission is to support families receiving a fetal syndrome diagnosis. <a href="http://fetalhealthfoundation.org/" rel="nofollow">fetalhealthfoundation.org</a>. The foundation provides life-saving research, increases the awareness of fetal syndrome and shares leading medical information on this disorder. Learn more about the fascinating story of Lonnie and his wife, Michelle’s journey and discovery as parents of twin girls diagnosed with a fetal syndrome disorder. The parents went on to become founders of the Fetal Health Foundation to help other parents experiencing similar circumstances. https://www.fetalhealthfoundation.org/story/our-founder-s-story/.</p>]]></description>
                <content:encoded>&lt;p&gt;We are so pleased to have with us, Lonnie Somers, Co-Founder of The Fetal Health Foundation. The Fetal Health (or Hope) Foundation’s mission is to support families receiving a fetal syndrome diagnosis. &lt;a href=&#34;http://fetalhealthfoundation.org/&#34; rel=&#34;nofollow&#34;&gt;fetalhealthfoundation.org&lt;/a&gt;. The foundation provides life-saving research, increases the awareness of fetal syndrome and shares leading medical information on this disorder. Learn more about the fascinating story of Lonnie and his wife, Michelle’s journey and discovery as parents of twin girls diagnosed with a fetal syndrome disorder. The parents went on to become founders of the Fetal Health Foundation to help other parents experiencing similar circumstances. https://www.fetalhealthfoundation.org/story/our-founder-s-story/.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Mon, 07 Aug 2023 16:39:26 &#43;0000</pubDate>
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                <itunes:duration>2198</itunes:duration>
                
                
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                <itunes:title>12. 5 P Minus Society Interview with Executive Director, Laura Castillo</itunes:title>
                <title>12. 5 P Minus Society Interview with Executive Director, Laura Castillo</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p><span>We are quite pleased to present Laura Castillo, Executive Director of the 5 P Minus Society. The 5 P Minus Syndrome is a disorder of chromosome deletion that impacts a small number of children in this country (50-60). Also known as Cri du Chat Syndrome, it is typically accompanied by physical and developmental delays often requiring life-time support for those impacted. The 5 P Minus Society provides crucial education, information and support for these families. Please support their efforts: </span><a href="https://fivepminus.org/" rel="nofollow">https://fivepminus.org/</a><span>.</span></p>]]></description>
                <content:encoded>&lt;p&gt;&lt;span&gt;We are quite pleased to present Laura Castillo, Executive Director of the 5 P Minus Society. The 5 P Minus Syndrome is a disorder of chromosome deletion that impacts a small number of children in this country (50-60). Also known as Cri du Chat Syndrome, it is typically accompanied by physical and developmental delays often requiring life-time support for those impacted. The 5 P Minus Society provides crucial education, information and support for these families. Please support their efforts: &lt;/span&gt;&lt;a href=&#34;https://fivepminus.org/&#34; rel=&#34;nofollow&#34;&gt;https://fivepminus.org/&lt;/a&gt;&lt;span&gt;.&lt;/span&gt;&lt;/p&gt;</content:encoded>
                
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                <pubDate>Thu, 01 Jun 2023 17:21:00 &#43;0000</pubDate>
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                <itunes:duration>1455</itunes:duration>
                
                
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                <itunes:title>11. DNPs of Color - Founder, Dr. Danielle McCamey</itunes:title>
                <title>11. DNPs of Color - Founder, Dr. Danielle McCamey</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Join this enlightening conversation with Dr. McCamey, the Founder and President of Doctors of Nursing Practice of Color (DNPs of Color) and her journey to enhance the medical profession by supporting and encouraging those working in advanced nursing or seeking degrees in advanced nursing. DNPs of Color is a non-profit organization and their mission is to serve DNPs of Color through networking, mentorship and advocacy to increase diversity in doctoral studies, clinical practice and leadership: <a href="https://www.dnpsofcolor.org/" rel="nofollow">https://www.dnpsofcolor.org/</a>.</p>]]></description>
                <content:encoded>&lt;p&gt;Join this enlightening conversation with Dr. McCamey, the Founder and President of Doctors of Nursing Practice of Color (DNPs of Color) and her journey to enhance the medical profession by supporting and encouraging those working in advanced nursing or seeking degrees in advanced nursing. DNPs of Color is a non-profit organization and their mission is to serve DNPs of Color through networking, mentorship and advocacy to increase diversity in doctoral studies, clinical practice and leadership: &lt;a href=&#34;https://www.dnpsofcolor.org/&#34; rel=&#34;nofollow&#34;&gt;https://www.dnpsofcolor.org/&lt;/a&gt;.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Wed, 31 May 2023 19:04:16 &#43;0000</pubDate>
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                <itunes:duration>1400</itunes:duration>
                
                
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                <itunes:title>10. Interview with Louise Vetter of the Huntington&#39;s Disease Society of America</itunes:title>
                <title>10. Interview with Louise Vetter of the Huntington&#39;s Disease Society of America</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>An informative discussion with Louise Vetter, President and CEO of the Huntington&#39;s Disease Society of American. Learn more about this rare disease and how this non-profit organization offers support through community service, advocacy, research and education. https://hdsa.org/</p><p><br></p>]]></description>
                <content:encoded>&lt;p&gt;An informative discussion with Louise Vetter, President and CEO of the Huntington&amp;#39;s Disease Society of American. Learn more about this rare disease and how this non-profit organization offers support through community service, advocacy, research and education. https://hdsa.org/&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;</content:encoded>
                
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                <pubDate>Wed, 29 Mar 2023 17:42:37 &#43;0000</pubDate>
                <itunes:duration>1851</itunes:duration>
                
                
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                <itunes:title>9. Interview with Ana Rath, Director of Orphanet</itunes:title>
                <title>9. Interview with Ana Rath, Director of Orphanet</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Ana Rath, Director of Orphanet shares how this valuable resource gathers information on rare diseases to improve the diagnosis, care and treatment of patients who are diagnosed with these challenging medical conditions. The goal of Orphanet, with a global outreach, is to provide high-quality information on rare diseases and ensure equal access to knowledge for all stakeholders. For more information contact Orphanet: https://www.orpha.net/consor/cgi-bin/index.php.</p>]]></description>
                <content:encoded>&lt;p&gt;Ana Rath, Director of Orphanet shares how this valuable resource gathers information on rare diseases to improve the diagnosis, care and treatment of patients who are diagnosed with these challenging medical conditions. The goal of Orphanet, with a global outreach, is to provide high-quality information on rare diseases and ensure equal access to knowledge for all stakeholders. For more information contact Orphanet: https://www.orpha.net/consor/cgi-bin/index.php.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Fri, 24 Mar 2023 15:05:25 &#43;0000</pubDate>
                <itunes:duration>1001</itunes:duration>
                
                
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                <itunes:title>8. Interview with Melissa Bryce, Executive Director, The Global Foundation for Peroxisomal Disorders</itunes:title>
                <title>8. Interview with Melissa Bryce, Executive Director, The Global Foundation for Peroxisomal Disorders</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>We welcome Melissa Bryce, Executive Director, The Global Foundation for Peroxisomal Disorders. Join us to hear about these rare genetic disorders and how they impact the lives of many children and families. The Foundation&#39;s mission is to improve the lives of individuals with Peroxisomal Disorders by funding research, championing scientific collaboration and empowering families and professionals through educational support services.</p>]]></description>
                <content:encoded>&lt;p&gt;We welcome Melissa Bryce, Executive Director, The Global Foundation for Peroxisomal Disorders. Join us to hear about these rare genetic disorders and how they impact the lives of many children and families. The Foundation&amp;#39;s mission is to improve the lives of individuals with Peroxisomal Disorders by funding research, championing scientific collaboration and empowering families and professionals through educational support services.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Tue, 28 Feb 2023 16:41:33 &#43;0000</pubDate>
                <itunes:duration>1408</itunes:duration>
                
                
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                <itunes:title>7. Interview with Diana Gray, President and CEO, the Hydrocephalus Association</itunes:title>
                <title>7. Interview with Diana Gray, President and CEO, the Hydrocephalus Association</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Join us for this fascinating interview with Diana Gray, the President and CEO of an amazing organization, the Hydrocephalus Association whose mission is to find a cure for hydrocephalus and support those living with this rare disease. Ms. Gray provides and informative overview of hydrocephalus and how it impacts patients and families. We urge you to support their efforts: https://www.hydroassoc.org/about-us/.</p>]]></description>
                <content:encoded>&lt;p&gt;Join us for this fascinating interview with Diana Gray, the President and CEO of an amazing organization, the Hydrocephalus Association whose mission is to find a cure for hydrocephalus and support those living with this rare disease. Ms. Gray provides and informative overview of hydrocephalus and how it impacts patients and families. We urge you to support their efforts: https://www.hydroassoc.org/about-us/.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Wed, 25 Jan 2023 19:47:05 &#43;0000</pubDate>
                <itunes:duration>1456</itunes:duration>
                
                
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                <itunes:title>6. Interview with Rebecca Aune - National Organization for Rare Disorders</itunes:title>
                <title>6. Interview with Rebecca Aune - National Organization for Rare Disorders</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>This is an informative discussion with Rebecca Aune, Director of Education Programs for the National Organization for Rare Disorders (NORD). Ms. Aune shares how NORD supports the rare disease community, those struggling with orphan or rare disorders, their families and healthcare providers.</p>]]></description>
                <content:encoded>&lt;p&gt;This is an informative discussion with Rebecca Aune, Director of Education Programs for the National Organization for Rare Disorders (NORD). Ms. Aune shares how NORD supports the rare disease community, those struggling with orphan or rare disorders, their families and healthcare providers.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Mon, 28 Nov 2022 18:17:54 &#43;0000</pubDate>
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                <itunes:duration>1726</itunes:duration>
                
                
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                <itunes:title>5. Interview with Renee Moten, Founder of Functional Fitness</itunes:title>
                <title>5. Interview with Renee Moten, Founder of Functional Fitness</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Learn how Renee Moten helps individuals minimize knee pain and increase activity levels to maximize quality of life for those bothered by ongoing knee discomfort.</p>]]></description>
                <content:encoded>&lt;p&gt;Learn how Renee Moten helps individuals minimize knee pain and increase activity levels to maximize quality of life for those bothered by ongoing knee discomfort.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Thu, 17 Nov 2022 15:50:38 &#43;0000</pubDate>
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                <itunes:duration>1240</itunes:duration>
                
                
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                <itunes:title>4 - Interview with Dr. Gisele Youmbi, Pharmacist and Entrepreneur</itunes:title>
                <title>4 - Interview with Dr. Gisele Youmbi, Pharmacist and Entrepreneur</title>

                <itunes:episode>4</itunes:episode>
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Join us in learning about the world of pharmacy, its impact on our lives and ways in which this profession has become frontline in healthcare to help us overcome challenges from personal medical needs to community disease prevention.</p>]]></description>
                <content:encoded>&lt;p&gt;Join us in learning about the world of pharmacy, its impact on our lives and ways in which this profession has become frontline in healthcare to help us overcome challenges from personal medical needs to community disease prevention.&lt;/p&gt;</content:encoded>
                
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                <pubDate>Sat, 17 Sep 2022 11:55:00 &#43;0000</pubDate>
                <itunes:duration>1757</itunes:duration>
                
                
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                <itunes:title>3 - Interview with Mehreen – The Journey of Living with Microphthalmia</itunes:title>
                <title>3 - Interview with Mehreen – The Journey of Living with Microphthalmia</title>

                <itunes:episode>3</itunes:episode>
                <itunes:season>1</itunes:season>
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>In this episode of HippraConnects, Eesha Imam interviews her cousin Mehreen about her journey of living and growing up with Microphthalmia. Mehreen talks about some small challenges living with the condition, overcoming mental barriers, not letting Microphthalmia hold her back, doing what makes you happy, finding a support group and much more!</p><p><br></p><p>Thank you to Mehreen for coming on the show and take care!</p><p><br></p><p>For more information on Hippra Check us out on:</p><p><a href="https://linktr.ee/hippra" rel="nofollow">https://linktr.ee/hippra</a></p><p><a href="https://www.facebook.com/hippraapp/" rel="nofollow">https://www.facebook.com/hippraapp/</a></p><p><a href="https://twitter.com/hippra1" rel="nofollow">https://twitter.com/hippra1</a></p><p><a href="https://www.linkedin.com/company/hippra" rel="nofollow">https://www.linkedin.com/company/hippra</a></p><p> </p>]]></description>
                <content:encoded>&lt;p&gt;In this episode of HippraConnects, Eesha Imam interviews her cousin Mehreen about her journey of living and growing up with Microphthalmia. Mehreen talks about some small challenges living with the condition, overcoming mental barriers, not letting Microphthalmia hold her back, doing what makes you happy, finding a support group and much more!&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;&lt;p&gt;Thank you to Mehreen for coming on the show and take care!&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;&lt;p&gt;For more information on Hippra Check us out on:&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://linktr.ee/hippra&#34; rel=&#34;nofollow&#34;&gt;https://linktr.ee/hippra&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://www.facebook.com/hippraapp/&#34; rel=&#34;nofollow&#34;&gt;https://www.facebook.com/hippraapp/&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://twitter.com/hippra1&#34; rel=&#34;nofollow&#34;&gt;https://twitter.com/hippra1&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://www.linkedin.com/company/hippra&#34; rel=&#34;nofollow&#34;&gt;https://www.linkedin.com/company/hippra&lt;/a&gt;&lt;/p&gt;&lt;p&gt; &lt;/p&gt;</content:encoded>
                
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                <pubDate>Fri, 18 Mar 2022 17:16:13 &#43;0000</pubDate>
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                <itunes:duration>2427</itunes:duration>
                
                
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                <itunes:title>2 - The Future of Healthcare</itunes:title>
                <title>2 - The Future of Healthcare</title>

                <itunes:episode>2</itunes:episode>
                <itunes:season>1</itunes:season>
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Hippra&#39;s vision on the future of healthcare.</p><p><br></p><p>For more information on Hippra Check us out on:</p><p>https://linktr.ee/hippra</p><p>https://www.facebook.com/hippraapp/</p><p>https://twitter.com/hippra1</p><p>https://www.linkedin.com/company/hippra</p>]]></description>
                <content:encoded>&lt;p&gt;Hippra&amp;#39;s vision on the future of healthcare.&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;&lt;p&gt;For more information on Hippra Check us out on:&lt;/p&gt;&lt;p&gt;https://linktr.ee/hippra&lt;/p&gt;&lt;p&gt;https://www.facebook.com/hippraapp/&lt;/p&gt;&lt;p&gt;https://twitter.com/hippra1&lt;/p&gt;&lt;p&gt;https://www.linkedin.com/company/hippra&lt;/p&gt;</content:encoded>
                
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                <pubDate>Sat, 26 Feb 2022 16:19:53 &#43;0000</pubDate>
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                <itunes:duration>323</itunes:duration>
                
                
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                <itunes:title>1 - Interview with Heather Ferguson, Founder and Executive Director at Lymphedema Advocacy Group</itunes:title>
                <title>1 - Interview with Heather Ferguson, Founder and Executive Director at Lymphedema Advocacy Group</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Janice McRae, Founder and CEO of Hippra, interviews Heather Ferguson, Founder and Executive Director at Lymphedema Advocacy Group.</p><p><br></p><p>Get in Contact with the Lymphedema Advocacy Group!</p><p>Website: <a href="https://lymphedematreatmentact.org/" rel="nofollow">https://lymphedematreatmentact.org/</a></p><p>Instagram: <a href="https://www.instagram.com/lymphedematreatmentact/" rel="nofollow">https://www.instagram.com/lymphedematreatmentact/</a></p><p>Twitter: <a href="https://twitter.com/LymphedemaAct" rel="nofollow">https://twitter.com/LymphedemaAct</a></p><p>LinkedIn: <a href="https://www.linkedin.com/company/lymphedema-advocacy-group" rel="nofollow">https://www.linkedin.com/company/lymphedema-advocacy-group</a></p><p>Facebook: <a href="https://www.facebook.com/lymphedematreatmentact/" rel="nofollow">https://www.facebook.com/lymphedematreatmentact/</a></p><p>YouTube: <a href="https://www.youtube.com/channel/UCkQTLwcaiNr4e-Xulw4ruag" rel="nofollow">https://www.youtube.com/channel/UCkQTLwcaiNr4e-Xulw4ruag</a></p><p><br></p><p>For more information on Hippra Check us out on:</p><p><a href="https://linktr.ee/hippra" rel="nofollow">https://linktr.ee/hippra</a></p><p><a href="https://www.facebook.com/hippraapp/" rel="nofollow">https://www.facebook.com/hippraapp/</a></p><p><a href="https://twitter.com/hippra1" rel="nofollow">https://twitter.com/hippra1</a></p><p><a href="https://www.linkedin.com/company/hippra" rel="nofollow">https://www.linkedin.com/company/hippra</a></p>]]></description>
                <content:encoded>&lt;p&gt;Janice McRae, Founder and CEO of Hippra, interviews Heather Ferguson, Founder and Executive Director at Lymphedema Advocacy Group.&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;&lt;p&gt;Get in Contact with the Lymphedema Advocacy Group!&lt;/p&gt;&lt;p&gt;Website: &lt;a href=&#34;https://lymphedematreatmentact.org/&#34; rel=&#34;nofollow&#34;&gt;https://lymphedematreatmentact.org/&lt;/a&gt;&lt;/p&gt;&lt;p&gt;Instagram: &lt;a href=&#34;https://www.instagram.com/lymphedematreatmentact/&#34; rel=&#34;nofollow&#34;&gt;https://www.instagram.com/lymphedematreatmentact/&lt;/a&gt;&lt;/p&gt;&lt;p&gt;Twitter: &lt;a href=&#34;https://twitter.com/LymphedemaAct&#34; rel=&#34;nofollow&#34;&gt;https://twitter.com/LymphedemaAct&lt;/a&gt;&lt;/p&gt;&lt;p&gt;LinkedIn: &lt;a href=&#34;https://www.linkedin.com/company/lymphedema-advocacy-group&#34; rel=&#34;nofollow&#34;&gt;https://www.linkedin.com/company/lymphedema-advocacy-group&lt;/a&gt;&lt;/p&gt;&lt;p&gt;Facebook: &lt;a href=&#34;https://www.facebook.com/lymphedematreatmentact/&#34; rel=&#34;nofollow&#34;&gt;https://www.facebook.com/lymphedematreatmentact/&lt;/a&gt;&lt;/p&gt;&lt;p&gt;YouTube: &lt;a href=&#34;https://www.youtube.com/channel/UCkQTLwcaiNr4e-Xulw4ruag&#34; rel=&#34;nofollow&#34;&gt;https://www.youtube.com/channel/UCkQTLwcaiNr4e-Xulw4ruag&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;&lt;p&gt;For more information on Hippra Check us out on:&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://linktr.ee/hippra&#34; rel=&#34;nofollow&#34;&gt;https://linktr.ee/hippra&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://www.facebook.com/hippraapp/&#34; rel=&#34;nofollow&#34;&gt;https://www.facebook.com/hippraapp/&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://twitter.com/hippra1&#34; rel=&#34;nofollow&#34;&gt;https://twitter.com/hippra1&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://www.linkedin.com/company/hippra&#34; rel=&#34;nofollow&#34;&gt;https://www.linkedin.com/company/hippra&lt;/a&gt;&lt;/p&gt;</content:encoded>
                
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                <pubDate>Fri, 04 Feb 2022 18:59:36 &#43;0000</pubDate>
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                <itunes:duration>1147</itunes:duration>
                
                
                <itunes:explicit>no</itunes:explicit>
                
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                <itunes:title>Introduction to HippraConnects</itunes:title>
                <title>Introduction to HippraConnects</title>

                
                
                <itunes:author>Hippra Podcast</itunes:author>
                
                <description><![CDATA[<p>Janice McRae, founder, introduces to the mission of Hippra and what to expect from the HippraConnects podcast!</p><p>Thank you and please share with your friends! </p><p><br></p><p>For more information on Hippra Check us out on:</p><p>https://linktr.ee/hippra</p><p>https://www.facebook.com/hippraapp/</p><p>https://twitter.com/hippra1</p><p>https://www.linkedin.com/company/hippra</p>]]></description>
                <content:encoded>&lt;p&gt;Janice McRae, founder, introduces to the mission of Hippra and what to expect from the HippraConnects podcast!&lt;/p&gt;&lt;p&gt;Thank you and please share with your friends! &lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;&lt;p&gt;For more information on Hippra Check us out on:&lt;/p&gt;&lt;p&gt;https://linktr.ee/hippra&lt;/p&gt;&lt;p&gt;https://www.facebook.com/hippraapp/&lt;/p&gt;&lt;p&gt;https://twitter.com/hippra1&lt;/p&gt;&lt;p&gt;https://www.linkedin.com/company/hippra&lt;/p&gt;</content:encoded>
                
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                <pubDate>Fri, 04 Feb 2022 18:42:58 &#43;0000</pubDate>
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                <itunes:duration>173</itunes:duration>
                
                
                <itunes:explicit>no</itunes:explicit>
                
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                <itunes:title>HippraConnects Trailer</itunes:title>
                <title>HippraConnects Trailer</title>

                <itunes:episode>1</itunes:episode>
                <itunes:season>1</itunes:season>
                <itunes:author>Hippra Podcast</itunes:author>
                <itunes:summary>Do you want to learn more about the latest updates in all things medicine and healthcare? Keep up with current medical events and news from an array of medical professionals with HippraConnects bi-weekly. If you’re interested in the healthcare or medicine please checkout the podcast.


For more information on Hippra Check us out on:
https://linktr.ee/hippra
https://www.facebook.com/hippraapp/
https://twitter.com/hippra1
https://www.linkedin.com/company/hippra 

</itunes:summary>
                <description><![CDATA[<p>Do you want to learn more about the latest updates in all things medicine and healthcare? Keep up with current medical events and news from an array of medical professionals with HippraConnects bi-weekly. If you’re interested in the healthcare or medicine please checkout the podcast.</p><p><br></p><p>For more information on Hippra check us out on:</p><p><a href="https://linktr.ee/hippra" rel="nofollow">https://linktr.ee/hippra</a></p><p><a href="https://www.facebook.com/hippraapp/" rel="nofollow">https://www.facebook.com/hippraapp/</a></p><p><a href="https://twitter.com/hippra1" rel="nofollow">https://twitter.com/hippra1</a></p><p><a href="https://www.linkedin.com/company/hippra" rel="nofollow">https://www.linkedin.com/company/hippra</a></p><p><br></p>]]></description>
                <content:encoded>&lt;p&gt;Do you want to learn more about the latest updates in all things medicine and healthcare? Keep up with current medical events and news from an array of medical professionals with HippraConnects bi-weekly. If you’re interested in the healthcare or medicine please checkout the podcast.&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;&lt;p&gt;For more information on Hippra check us out on:&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://linktr.ee/hippra&#34; rel=&#34;nofollow&#34;&gt;https://linktr.ee/hippra&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://www.facebook.com/hippraapp/&#34; rel=&#34;nofollow&#34;&gt;https://www.facebook.com/hippraapp/&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://twitter.com/hippra1&#34; rel=&#34;nofollow&#34;&gt;https://twitter.com/hippra1&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;a href=&#34;https://www.linkedin.com/company/hippra&#34; rel=&#34;nofollow&#34;&gt;https://www.linkedin.com/company/hippra&lt;/a&gt;&lt;/p&gt;&lt;p&gt;&lt;br&gt;&lt;/p&gt;</content:encoded>
                
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                <pubDate>Fri, 14 Jan 2022 20:02:08 &#43;0000</pubDate>
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                <itunes:duration>62</itunes:duration>
                
                
                <itunes:explicit>no</itunes:explicit>
                
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