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    <title>In Sickness</title>
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    <description>In Sickness. Men and the Culture of Caregiving is a monthly podcast that will focus mostly on stories of male caregivers who have supported individuals with various diseases and medical conditions across all therapeutic areas including select cancers, ALS, Alzheimer’s, and numerous rare diseases. The podcast will highlight the growing population of male caregivers who are caring for their spouse, life partners, children family members, and friends, and joining the ranks of the throngs of women caregivers who have historically been central to this effort. The podcast is co-hosted and produced by Bob Coughlin and Paul Kidwell, with technical supervision provided by Dan Thibeault of Fast Twitch Media. 
For more information, please contact Paul Kidwell at paulkidwellbos@gmail.com.</description>
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    <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
    <itunes:summary>In Sickness. Men and the Culture of Caregiving is a monthly podcast that will focus mostly on stories of male caregivers who have supported individuals with various diseases and medical conditions across all therapeutic areas including select cancers, ALS, Alzheimer’s, and numerous rare diseases. The podcast will highlight the growing population of male caregivers who are caring for their spouse, life partners, children family members, and friends, and joining the ranks of the throngs of women caregivers who have historically been central to this effort. The podcast is co-hosted and produced by Bob Coughlin and Paul Kidwell, with technical supervision provided by Dan Thibeault of Fast Twitch Media. 
For more information, please contact Paul Kidwell at paulkidwellbos@gmail.com.</itunes:summary>
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      <itunes:name>Bob Coughlin &amp; Paul Kidwell</itunes:name>
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      <title>In Sickness</title>
      <description>In Sickness. Men and the Culture of Caregiving Launches as Podcast Sharing Powerful Stories of Male Caregivers</description>
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    <podcast:person role="Host">Bob Coughlin &amp; Paul Kidwell</podcast:person>
    <podcast:location>Boston, MA</podcast:location>
    <podcast:trailer url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_Trailer_Dan_mixdown.mp3" pubdate="Sun, 04 Feb 2024 15:31:01 -0500" length="941112" type="audio/mpeg">In Sickness Trailer Episode</podcast:trailer>
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      <title>The Elevator Ride: Talking About Prostate Cancer, Care, and Courage</title>
      <podcast:episode>21</podcast:episode>
      <link>https://blubrry.com/3713794/149970361/the-elevator-ride-talking-about-prostate-cancer-care-and-courage/</link>
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      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Mon, 17 Nov 2025 14:21:48 -0500</pubDate>
      <description><![CDATA[<p>Guests: </p><p>•	Dr. Benjamin Lowentritt – Medical Director, Prostate Cancer Program at Chesapeake Urology, Vice President, Physician Services for United Urology Group.</p><p>•	Bob Lane – Prostate cancer survivor and advocate (“Elevator Bob”)</p><p>Show Notes: </p><p>This episode of In Sickness. Men and the Culture of Caregiving explores prostate cancer from two sides — the clinical expertise of Dr. Benjamin Lowentritt and the lived experience of survivor Bob Lane. Together, they discuss early signs, diagnosis, treatment options, stigma, and the importance of support — including how one man’s “elevator story” became a symbol of connection for others facing the same journey.</p><p>Key Topics:</p><p>- Early detection and screening</p><p>- Navigating diagnosis and treatment</p><p>- Emotional toll and caregiving challenges</p><p>- Male stigma and health conversations</p><p>- Advocacy and community support</p>]]></description>
      <content:encoded><![CDATA[<p>Guests: </p><p>•	Dr. Benjamin Lowentritt – Medical Director, Prostate Cancer Program at Chesapeake Urology, Vice President, Physician Services for United Urology Group.</p><p>•	Bob Lane – Prostate cancer survivor and advocate (“Elevator Bob”)</p><p>Show Notes: </p><p>This episode of In Sickness. Men and the Culture of Caregiving explores prostate cancer from two sides — the clinical expertise of Dr. Benjamin Lowentritt and the lived experience of survivor Bob Lane. Together, they discuss early signs, diagnosis, treatment options, stigma, and the importance of support — including how one man’s “elevator story” became a symbol of connection for others facing the same journey.</p><p>Key Topics:</p><p>- Early detection and screening</p><p>- Navigating diagnosis and treatment</p><p>- Emotional toll and caregiving challenges</p><p>- Male stigma and health conversations</p><p>- Advocacy and community support</p>]]></content:encoded>
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      <itunes:duration>0:41:49</itunes:duration>
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      <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
      <itunes:summary>Guests: •	Dr. Benjamin Lowentritt – Medical Director, Prostate Cancer Program at Chesapeake Urology, Vice President, Physician Services for United Urology Group.•	Bob Lane – Prostate cancer survivor and advocate (“Elevator Bob”)Show Notes: This episode of In Sickness. Men and the Culture of Caregiving explores prostate cancer from two sides — the clinical expertise of Dr. Benjamin Lowentritt and the lived experience of survivor Bob Lane. Together, they discuss early signs, diagnosis, treatment options, stigma, and the importance of support — including how one man’s “elevator story” became a symbol of connection for others facing the same journey.Key Topics:- Early detection and screening- Navigating diagnosis and treatment- Emotional toll and caregiving challenges- Male stigma and health conversations- Advocacy and community support</itunes:summary>
      <itunes:title>Title: The Elevator Ride: Talking About Prostate Cancer, Care, and Courage</itunes:title>
      <itunes:episode>21</itunes:episode>
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      <title>Sharing the Journey of Early-Onset Colorectal Cancer Together</title>
      <podcast:episode>20</podcast:episode>
      <link>https://blubrry.com/3713794/148762548/sharing-the-journey-of-early-onset-colorectal-cancer-together/</link>
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      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Thu, 25 Sep 2025 12:59:13 -0400</pubDate>
      <podcast:license>©Openlytallproductions 2025</podcast:license>
      <description><![CDATA[<p>In this episode of In Sickness. Men and the Culture of Caregiviong, we dive deep into the emotional, physical, and logistical challenges faced by caregivers supporting loved ones with early-onset colorectal cancer (EOCRC). With more adults under 50 being diagnosed with this disease, caregivers are often caught off guard — juggling careers, families, and a sudden, life-altering diagnosis.</p><p>Joining the conversation are an oncologist who is recognized as the foremost authority on this condition, a husband who cared for his wife, and two patients. A woman who was diagnosed in her early 40’s and a much younger woman who received the diagnosis at 24. This group offers their unique experiences as well as compassionate guidance, community, and insight.</p><p>What You'll Learn in This Episode:</p><p>•	The unique challenges of caregiving for EOCRC patients</p><p>•	How early-onset symptoms differ and often lead to delayed diagnosis</p><p>•	Strategies for managing emotional burnout and caregiver fatigue</p><p>•	Navigating medical appointments, treatment plans, and advocating for your loved one</p><p>•	Balancing caregiving with work, parenting, and self-care</p><p>•	Building a support network </p><p>Featured Guests:</p><p>•	Dr. Kimmie Ng, Associate Chief, Division of Gastrointestinal Oncology, Dana-Farber Cancer Institute</p><p>•	Josh Trow, EOCRC Caregiver</p><p>•	Monica Dean, EOCRC Patient</p><p>•	Meagan Meadow, EOCRC Patient</p><p></p><p>To learn more, go to insickness.org</p>]]></description>
      <content:encoded><![CDATA[<p>In this episode of In Sickness. Men and the Culture of Caregiviong, we dive deep into the emotional, physical, and logistical challenges faced by caregivers supporting loved ones with early-onset colorectal cancer (EOCRC). With more adults under 50 being diagnosed with this disease, caregivers are often caught off guard — juggling careers, families, and a sudden, life-altering diagnosis.</p><p>Joining the conversation are an oncologist who is recognized as the foremost authority on this condition, a husband who cared for his wife, and two patients. A woman who was diagnosed in her early 40’s and a much younger woman who received the diagnosis at 24. This group offers their unique experiences as well as compassionate guidance, community, and insight.</p><p>What You'll Learn in This Episode:</p><p>•	The unique challenges of caregiving for EOCRC patients</p><p>•	How early-onset symptoms differ and often lead to delayed diagnosis</p><p>•	Strategies for managing emotional burnout and caregiver fatigue</p><p>•	Navigating medical appointments, treatment plans, and advocating for your loved one</p><p>•	Balancing caregiving with work, parenting, and self-care</p><p>•	Building a support network </p><p>Featured Guests:</p><p>•	Dr. Kimmie Ng, Associate Chief, Division of Gastrointestinal Oncology, Dana-Farber Cancer Institute</p><p>•	Josh Trow, EOCRC Caregiver</p><p>•	Monica Dean, EOCRC Patient</p><p>•	Meagan Meadow, EOCRC Patient</p><p><br /></p><p>To learn more, go to insickness.org</p>]]></content:encoded>
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      <itunes:duration>0:44:17</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
      <itunes:summary>In this episode of In Sickness. Men and the Culture of Caregiviong, we dive deep into the emotional, physical, and logistical challenges faced by caregivers supporting loved ones with early-onset colorectal cancer (EOCRC). With more adults under 50 being diagnosed with this disease, caregivers are often caught off guard — juggling careers, families, and a sudden, life-altering diagnosis.Joining the conversation are an oncologist who is recognized as the foremost authority on this condition, a husband who cared for his wife, and two patients. A woman who was diagnosed in her early 40’s and a much younger woman who received the diagnosis at 24. This group offers their unique experiences as well as compassionate guidance, community, and insight.What You'll Learn in This Episode:•	The unique challenges of caregiving for EOCRC patients•	How early-onset symptoms differ and often lead to delayed diagnosis•	Strategies for managing emotional burnout and caregiver fatigue•	Navigating medical appointments, treatment plans, and advocating for your loved one•	Balancing caregiving with work, parenting, and self-care•	Building a support network Featured Guests:•	Dr. Kimmie Ng, Associate Chief, Division of Gastrointestinal Oncology, Dana-Farber Cancer Institute•	Josh Trow, EOCRC Caregiver•	Monica Dean, EOCRC Patient•	Meagan Meadow, EOCRC PatientTo learn more, go to insickness.org</itunes:summary>
      <itunes:title>Sharing the Journey of Early-Onset Colorectal Cancer Together</itunes:title>
      <itunes:episode>20</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
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    <item>
      <title>The Sandwiched Caregiver. In Between Love and Care.</title>
      <podcast:episode>19</podcast:episode>
      <link>https://blubrry.com/3713794/148206485/the-sandwiched-caregiver-in-between-love-and-care/</link>
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      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Tue, 02 Sep 2025 18:54:07 -0400</pubDate>
      <podcast:license>©Openlytallproductions 2025</podcast:license>
      <description><![CDATA[<p>If you're raising children while caring for aging parents at the same time, you're not alone. In this episode of In Sickness. Men and the Culture of Caregiving, co-hosts Bob Coughlin and Paul Kidwell explore the challenges of being a sandwich caregiver. The three podcast guests share their personal experiences as they explore the emotional, financial, and physical toll of being part of the "Sandwich Generation."</p>]]></description>
      <content:encoded><![CDATA[<p>If you're raising children while caring for aging parents at the same time, you're not alone. In this episode of In Sickness. Men and the Culture of Caregiving, co-hosts Bob Coughlin and Paul Kidwell explore the challenges of being a sandwich caregiver. The three podcast guests share their personal experiences as they explore the emotional, financial, and physical toll of being part of the "Sandwich Generation."</p>]]></content:encoded>
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      <itunes:duration>0:50:29</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin and Paul Kidwell</itunes:author>
      <itunes:summary>If you're raising children while caring for aging parents at the same time, you're not alone. In this episode of In Sickness. Men and the Culture of Caregiving, co-hosts Bob Coughlin and Paul Kidwell explore the challenges of being a sandwich caregiver. The three podcast guests share their personal experiences as they explore the emotional, financial, and physical toll of being part of the &quot;Sandwich Generation.&quot;</itunes:summary>
      <itunes:title>The Sandwiched Caregiver. In Between Love and Care.</itunes:title>
      <itunes:episode>19</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
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    <item>
      <title>Caregiving Writ Large</title>
      <podcast:episode>18</podcast:episode>
      <link>https://blubrry.com/3713794/147087053/caregiving-writ-large/</link>
      <guid>https://blubrry.com/3713794/147087053/caregiving-writ-large/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Wed, 16 Jul 2025 12:58:21 -0400</pubDate>
      <podcast:license>©Openlytallproductions 2025</podcast:license>
      <description><![CDATA[<p>The PBS “Caregiving” documentary has sparked a national conversation that will hopefully lead to change in the many issues facing caregivers. The film features intimate stories from a diverse group of caregivers that highlight the emotional, financial, and logistical tightrope that all of us caregivers walk each day. “Caregiving” shines a light on this essential yet mostly invisible work force and humanizes it by amplifying their emotional narratives and calling attention to burnout, isolation, and gaps in resources and recognition. If you are a caregiver, you will be heartened to know how this film stands on the precipice of action and change. Join the In Sickness team as we speak with Executive Producer, Tom Chiodo, Director, Christopher Durrance, and caregiver, Matt Cauli as they share stories that will help lift caregiving from a private burden to a public cause. To learn more, go to <a href="https://www.insickness.org">insickness.org</a>.</p>]]></description>
      <content:encoded><![CDATA[<p>The PBS “Caregiving” documentary has sparked a national conversation that will hopefully lead to change in the many issues facing caregivers. The film features intimate stories from a diverse group of caregivers that highlight the emotional, financial, and logistical tightrope that all of us caregivers walk each day. “Caregiving” shines a light on this essential yet mostly invisible work force and humanizes it by amplifying their emotional narratives and calling attention to burnout, isolation, and gaps in resources and recognition. If you are a caregiver, you will be heartened to know how this film stands on the precipice of action and change. Join the In Sickness team as we speak with Executive Producer, Tom Chiodo, Director, Christopher Durrance, and caregiver, Matt Cauli as they share stories that will help lift caregiving from a private burden to a public cause. To learn more, go to <a href="https://www.insickness.org">insickness.org</a>.</p>]]></content:encoded>
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      <itunes:duration>0:39:28</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
      <itunes:summary>The PBS “Caregiving” documentary has sparked a national conversation that will hopefully lead to change in the many issues facing caregivers. The film features intimate stories from a diverse group of caregivers that highlight the emotional, financial, and logistical tightrope that all of us caregivers walk each day. “Caregiving” shines a light on this essential yet mostly invisible work force and humanizes it by amplifying their emotional narratives and calling attention to burnout, isolation, and gaps in resources and recognition. If you are a caregiver, you will be heartened to know how this film stands on the precipice of action and change. Join the In Sickness team as we speak with Executive Producer, Tom Chiodo, Director, Christopher Durrance, and caregiver, Matt Cauli as they share stories that will help lift caregiving from a private burden to a public cause. To learn more, go to insickness.org (https://www.insickness.org).</itunes:summary>
      <itunes:title>Caregiving Writ Large</itunes:title>
      <itunes:episode>18</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
    </item>
    <item>
      <title>Rosalynn Carter and the National Caregiving Conversation</title>
      <podcast:episode>17</podcast:episode>
      <link>https://blubrry.com/3713794/146688275/rosalynn-carter-and-the-national-caregiving-conversation/</link>
      <guid>https://blubrry.com/3713794/146688275/rosalynn-carter-and-the-national-caregiving-conversation/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Mon, 30 Jun 2025 11:47:07 -0400</pubDate>
      <podcast:license>©Openlytallproductions 2025</podcast:license>
      <description><![CDATA[<p>Rosalynn Carter redefined the role of caregivers in American life, spotlighting their burdens and needs long before they became a national conversation. She founded the Rosalynn Carter Institute in 1987 which continues today as a guiding light for professional and family caregivers. This episode of In Sickness. Men and the Culture of Caregiving explores her deeply personal legacy and how that translated into a lifelong and very public commitment to caregivers and families through her work with The Carter Center and beyond. That work continues with an equally committed group of individuals who are ushering this legacy boldly into the future. Two of whom are featured on this podcast. To learn more, go to insickness.org.</p>]]></description>
      <content:encoded><![CDATA[<p>Rosalynn Carter redefined the role of caregivers in American life, spotlighting their burdens and needs long before they became a national conversation. She founded the Rosalynn Carter Institute in 1987 which continues today as a guiding light for professional and family caregivers. This episode of In Sickness. Men and the Culture of Caregiving explores her deeply personal legacy and how that translated into a lifelong and very public commitment to caregivers and families through her work with The Carter Center and beyond. That work continues with an equally committed group of individuals who are ushering this legacy boldly into the future. Two of whom are featured on this podcast. To learn more, go to insickness.org.</p>]]></content:encoded>
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      <itunes:duration>0:48:17</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Paul Kidwell</itunes:author>
      <itunes:summary>Rosalynn Carter redefined the role of caregivers in American life, spotlighting their burdens and needs long before they became a national conversation. She founded the Rosalynn Carter Institute in 1987 which continues today as a guiding light for professional and family caregivers. This episode of In Sickness. Men and the Culture of Caregiving explores her deeply personal legacy and how that translated into a lifelong and very public commitment to caregivers and families through her work with The Carter Center and beyond. That work continues with an equally committed group of individuals who are ushering this legacy boldly into the future. Two of whom are featured on this podcast. To learn more, go to insickness.org.</itunes:summary>
      <itunes:title>Rosalynn Carter and the National Caregiving Conversation</itunes:title>
      <itunes:episode>17</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
    </item>
    <item>
      <title>Henri Termeer, The Ultimate Caregiver</title>
      <podcast:episode>16</podcast:episode>
      <link>https://blubrry.com/3713794/146324913/henri-termeer-the-ultimate-caregiver/</link>
      <guid>https://blubrry.com/3713794/146324913/henri-termeer-the-ultimate-caregiver/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Mon, 16 Jun 2025 08:19:47 -0400</pubDate>
      <podcast:license>©Openlytallproductions2025</podcast:license>
      <description><![CDATA[<p>The latest episode of In Sickness. Men and the Culture of Caregiving honors Henri Termeer’s legacy as the ultimate patient advocate and caregiver. What better way to offer this tribute than with a group of people who knew him best and considered him a friend and mentor. Deborah Dunsire, John Crowley, David Meeker, John Maraganore, Bob Coughlin and Tamar Thompson reflected on Henri’s legacy and his personal influence on each and our industry. The conversation was rich, lively and filled with anecdotes, lessons learned and how Henri’s legacy continues to define the life science industry. To learn more go to <a href="https://www.insickness.org">insickness.org</a>.</p>]]></description>
      <content:encoded><![CDATA[<p>The latest episode of In Sickness. Men and the Culture of Caregiving honors Henri Termeer’s legacy as the ultimate patient advocate and caregiver. What better way to offer this tribute than with a group of people who knew him best and considered him a friend and mentor. Deborah Dunsire, John Crowley, David Meeker, John Maraganore, Bob Coughlin and Tamar Thompson reflected on Henri’s legacy and his personal influence on each and our industry. The conversation was rich, lively and filled with anecdotes, lessons learned and how Henri’s legacy continues to define the life science industry. To learn more go to <a href="https://www.insickness.org">insickness.org</a>.</p>]]></content:encoded>
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      <itunes:duration>0:50:48</itunes:duration>
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      <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
      <itunes:summary>The latest episode of In Sickness. Men and the Culture of Caregiving honors Henri Termeer’s legacy as the ultimate patient advocate and caregiver. What better way to offer this tribute than with a group of people who knew him best and considered him a friend and mentor. Deborah Dunsire, John Crowley, David Meeker, John Maraganore, Bob Coughlin and Tamar Thompson reflected on Henri’s legacy and his personal influence on each and our industry. The conversation was rich, lively and filled with anecdotes, lessons learned and how Henri’s legacy continues to define the life science industry. To learn more go to insickness.org (https://www.insickness.org).</itunes:summary>
      <itunes:title>Henri Termeer, The Ultimate Caregiver</itunes:title>
      <itunes:episode>16</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
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      <title>Fighting the Disease and Social Stigma of Male Breast Cancer.</title>
      <link>https://blubrry.com/3713794/145813158/fighting-the-disease-and-social-stigma-of-male-breast-cancer/</link>
      <guid>https://blubrry.com/3713794/145813158/fighting-the-disease-and-social-stigma-of-male-breast-cancer/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Tue, 27 May 2025 13:35:06 -0400</pubDate>
      <podcast:license>©Openlytallproductions 2025</podcast:license>
      <description><![CDATA[<p>Living with male breast cancer presents unique physical, emotional, and social challenges, many of which stem from the rarity of the condition and the societal stigma surrounding it. There are many misconceptions about this rare form of cancer, but in this episode of In Sickness. Men and the Culture of Caregiving, our two cancer patients – Arvind Natarajan and Steve Del Gardo - share their graphic stories and dispel much of the erroneous information about this condition. One patient even served double duty as his caregiver as well. We also were fortunate to have a clinician and male breast cancer specialist, Dr. Jose Pablo Leone, from Dana Farber Cancer Institute join the discussion and relate that although it might be rare, this disease is not uncommon. </p><p></p><p>This episode also represents a departure from our norm as we invited fellow podcaster and cancer caregiver, Charlotte Bayala, to join us. She was wonderful and after you listen to her on our podcast you can check her out on, <a href="https://podcasts.apple.com/us/podcast/the-cancer-caregiver/id1504166813">The Cancer Caregiver</a>. </p>]]></description>
      <content:encoded><![CDATA[<p>Living with male breast cancer presents unique physical, emotional, and social challenges, many of which stem from the rarity of the condition and the societal stigma surrounding it. There are many misconceptions about this rare form of cancer, but in this episode of In Sickness. Men and the Culture of Caregiving, our two cancer patients – Arvind Natarajan and Steve Del Gardo - share their graphic stories and dispel much of the erroneous information about this condition. One patient even served double duty as his caregiver as well. We also were fortunate to have a clinician and male breast cancer specialist, Dr. Jose Pablo Leone, from Dana Farber Cancer Institute join the discussion and relate that although it might be rare, this disease is not uncommon. </p><p><br /></p><p>This episode also represents a departure from our norm as we invited fellow podcaster and cancer caregiver, Charlotte Bayala, to join us. She was wonderful and after you listen to her on our podcast you can check her out on, <a href="https://podcasts.apple.com/us/podcast/the-cancer-caregiver/id1504166813">The Cancer Caregiver</a>. </p>]]></content:encoded>
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      <itunes:duration>0:49:58</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Paul Kidwell &amp; Bob Coughlin</itunes:author>
      <itunes:summary>Living with male breast cancer presents unique physical, emotional, and social challenges, many of which stem from the rarity of the condition and the societal stigma surrounding it. There are many misconceptions about this rare form of cancer, but in this episode of In Sickness. Men and the Culture of Caregiving, our two cancer patients – Arvind Natarajan and Steve Del Gardo - share their graphic stories and dispel much of the erroneous information about this condition. One patient even served double duty as his caregiver as well. We also were fortunate to have a clinician and male breast cancer specialist, Dr. Jose Pablo Leone, from Dana Farber Cancer Institute join the discussion and relate that although it might be rare, this disease is not uncommon. This episode also represents a departure from our norm as we invited fellow podcaster and cancer caregiver, Charlotte Bayala, to join us. She was wonderful and after you listen to her on our podcast you can check her out on, The Cancer Caregiver (https://podcasts.apple.com/us/podcast/the-cancer-caregiver/id1504166813). </itunes:summary>
      <itunes:title>Fighting the Disease and Social Stigma of Male Breast Cancer.</itunes:title>
    </item>
    <item>
      <title>The Flame of Caregiving Burning Brightly</title>
      <podcast:episode>14</podcast:episode>
      <link>https://blubrry.com/3713794/144871362/the-flame-of-caregiving-burning-brightly/</link>
      <guid>https://blubrry.com/3713794/144871362/the-flame-of-caregiving-burning-brightly/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Wed, 23 Apr 2025 18:01:12 -0400</pubDate>
      <podcast:license>©Openlytallproductions 2025</podcast:license>
      <description><![CDATA[<p>Compassion fatigue is quite literally, the emotional cost of caring. The physical and emotional exhaustion experienced by caregivers is a common thread in the caregiving experience. It’s a serious condition that affects anyone finding themselves in a helping or caregiving role. This episode of In Sickness had the privilege of speaking with three of the authors – Peter Dudley, Antoinette LeCouteur, Tammy Hurst - of the extraordinary book, <a href="https://www.amazon.com/Relit-Rekindle-Yourself-Darkness-Compassion/dp/B0DFY1F22Q?crid=9VJ36FQ76A3G&amp;dib=eyJ2IjoiMSJ9.dfGeTtA8jSx6_RYUqzAYUIWwfUBR_O8BvywlSNXNV1uloWy-DATXFq5Bhwc6817BEJ0NOxXehMGjekl11XstknceZnZZGmdNAkJ9lifAak9LHQgo2XVnDbr3BDo5YCvP8BMuPOS8nYuCZtQvETzkXlY3csCUy90fq9h75U9A4E7lXfevs04MA0iTplUQgzYU7jgDjBBk22SWMhO5LCgAbac6aStEuHN9NBDRWLI4iqw.KJ1_AnVWrrDQv8LRycNQi1tmO8ATUBINxJQQ_dww-tY&amp;dib_tag=se&amp;keywords=relit&amp;qid=1744286343&amp;sprefix=relit%2Caps%2C161&amp;sr=8-6">Relit</a>. It’s a collection of essays by individuals engaged in a “heart-based role” who succumbed to the eventual care inertia. Think the heart writ large. To learn more, go to <a href="https://www.insickness.org">insickness.org</a>.</p>]]></description>
      <content:encoded><![CDATA[<p>Compassion fatigue is quite literally, the emotional cost of caring. The physical and emotional exhaustion experienced by caregivers is a common thread in the caregiving experience. It’s a serious condition that affects anyone finding themselves in a helping or caregiving role. This episode of In Sickness had the privilege of speaking with three of the authors – Peter Dudley, Antoinette LeCouteur, Tammy Hurst - of the extraordinary book, <a href="https://www.amazon.com/Relit-Rekindle-Yourself-Darkness-Compassion/dp/B0DFY1F22Q?crid=9VJ36FQ76A3G&amp;dib=eyJ2IjoiMSJ9.dfGeTtA8jSx6_RYUqzAYUIWwfUBR_O8BvywlSNXNV1uloWy-DATXFq5Bhwc6817BEJ0NOxXehMGjekl11XstknceZnZZGmdNAkJ9lifAak9LHQgo2XVnDbr3BDo5YCvP8BMuPOS8nYuCZtQvETzkXlY3csCUy90fq9h75U9A4E7lXfevs04MA0iTplUQgzYU7jgDjBBk22SWMhO5LCgAbac6aStEuHN9NBDRWLI4iqw.KJ1_AnVWrrDQv8LRycNQi1tmO8ATUBINxJQQ_dww-tY&amp;dib_tag=se&amp;keywords=relit&amp;qid=1744286343&amp;sprefix=relit%2Caps%2C161&amp;sr=8-6">Relit</a>. It’s a collection of essays by individuals engaged in a “heart-based role” who succumbed to the eventual care inertia. Think the heart writ large. To learn more, go to <a href="https://www.insickness.org">insickness.org</a>.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_14.mp3" length="122113044" type="audio/mpeg" />
      <itunes:duration>0:50:53</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Paul Kidwell and Bob Coughlin</itunes:author>
      <itunes:summary>Compassion fatigue is quite literally, the emotional cost of caring. The physical and emotional exhaustion experienced by caregivers is a common thread in the caregiving experience. It’s a serious condition that affects anyone finding themselves in a helping or caregiving role. This episode of In Sickness had the privilege of speaking with three of the authors – Peter Dudley, Antoinette LeCouteur, Tammy Hurst - of the extraordinary book, Relit (https://www.amazon.com/Relit-Rekindle-Yourself-Darkness-Compassion/dp/B0DFY1F22Q?crid=9VJ36FQ76A3G&amp;dib=eyJ2IjoiMSJ9.dfGeTtA8jSx6_RYUqzAYUIWwfUBR_O8BvywlSNXNV1uloWy-DATXFq5Bhwc6817BEJ0NOxXehMGjekl11XstknceZnZZGmdNAkJ9lifAak9LHQgo2XVnDbr3BDo5YCvP8BMuPOS8nYuCZtQvETzkXlY3csCUy90fq9h75U9A4E7lXfevs04MA0iTplUQgzYU7jgDjBBk22SWMhO5LCgAbac6aStEuHN9NBDRWLI4iqw.KJ1_AnVWrrDQv8LRycNQi1tmO8ATUBINxJQQ_dww-tY&amp;dib_tag=se&amp;keywords=relit&amp;qid=1744286343&amp;sprefix=relit%2Caps%2C161&amp;sr=8-6). It’s a collection of essays by individuals engaged in a “heart-based role” who succumbed to the eventual care inertia. Think the heart writ large. To learn more, go to insickness.org (https://www.insickness.org).</itunes:summary>
      <itunes:title>The Flame of Caregiving Burning Brightly</itunes:title>
      <itunes:episode>14</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:location>Boston MA</podcast:location>
    </item>
    <item>
      <title>Takeda: Many Caregiver Voices, One Caregiver Mission</title>
      <podcast:episode>13</podcast:episode>
      <link>https://blubrry.com/3713794/144388674/takeda-many-caregiver-voices-one-caregiver-mission/</link>
      <guid>https://blubrry.com/3713794/144388674/takeda-many-caregiver-voices-one-caregiver-mission/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Wed, 09 Apr 2025 16:24:58 -0400</pubDate>
      <podcast:license>©Openlytallproductions 2025</podcast:license>
      <description><![CDATA[<p>In this episode of In Sickness, we were the fortunate guests of Takeda Pharmaceuticals as they asked us to take part in their annual celebration of Rare Disease Day by recording our podcast in front of an audience of over 50 energized employees. What a thrill for Bob and I to speak with three of their employees who are also caregivers. Equally delighted to field questions from the audience. Takeda is a company that clearly understands that by supporting caregivers, they can improve patient outcomes. After hearing from our hosts at Takeda, which included one of their executive leaders I believe they also do this because it is the right thing to do. To learn more, go to insickness.org.</p>]]></description>
      <content:encoded><![CDATA[<p>In this episode of In Sickness, we were the fortunate guests of Takeda Pharmaceuticals as they asked us to take part in their annual celebration of Rare Disease Day by recording our podcast in front of an audience of over 50 energized employees. What a thrill for Bob and I to speak with three of their employees who are also caregivers. Equally delighted to field questions from the audience. Takeda is a company that clearly understands that by supporting caregivers, they can improve patient outcomes. After hearing from our hosts at Takeda, which included one of their executive leaders I believe they also do this because it is the right thing to do. To learn more, go to insickness.org.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/Tadeka_R2.mp3" length="108944195" type="audio/mpeg" />
      <itunes:duration>0:45:24</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
      <itunes:summary>In this episode of In Sickness, we were the fortunate guests of Takeda Pharmaceuticals as they asked us to take part in their annual celebration of Rare Disease Day by recording our podcast in front of an audience of over 50 energized employees. What a thrill for Bob and I to speak with three of their employees who are also caregivers. Equally delighted to field questions from the audience. Takeda is a company that clearly understands that by supporting caregivers, they can improve patient outcomes. After hearing from our hosts at Takeda, which included one of their executive leaders I believe they also do this because it is the right thing to do. To learn more, go to insickness.org.</itunes:summary>
      <itunes:title>Takeda: Many Caregiver Voices, One Caregiver Mission</itunes:title>
      <itunes:episode>13</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:location>Boston, MA</podcast:location>
    </item>
    <item>
      <title>When Caregivers and Biopharma Companies Collaborate</title>
      <podcast:episode>12</podcast:episode>
      <link>https://blubrry.com/3713794/142713480/when-caregivers-and-biopharma-companies-collaborate/</link>
      <guid>https://blubrry.com/3713794/142713480/when-caregivers-and-biopharma-companies-collaborate/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Fri, 28 Feb 2025 11:06:41 -0500</pubDate>
      <podcast:license>©Openlytallproductions 2025</podcast:license>
      <description><![CDATA[<p>Collaboration between caregivers and biopharma companies can lead to innovations that benefit both the patient and their support systems, leading to better health outcomes, more effective therapies, and a higher quality of life for all involved. In this special Rare Disease Day 2025 podcast you will hear the story of Ron and Marla Chapleau and how they have cared for their Aiden who has an ultrarare neurodegenerative disease for over two decades. You will also hear how one company, Vigil Neuroscience, is developing a therapy to help treat Aiden’s condition and the strong bond that has developed between Vigil and the Chapleau family. to learn more, go to <a href="https://www.insickness.org">insickness.org.</a></p>]]></description>
      <content:encoded><![CDATA[<p>Collaboration between caregivers and biopharma companies can lead to innovations that benefit both the patient and their support systems, leading to better health outcomes, more effective therapies, and a higher quality of life for all involved. In this special Rare Disease Day 2025 podcast you will hear the story of Ron and Marla Chapleau and how they have cared for their Aiden who has an ultrarare neurodegenerative disease for over two decades. You will also hear how one company, Vigil Neuroscience, is developing a therapy to help treat Aiden’s condition and the strong bond that has developed between Vigil and the Chapleau family. to learn more, go to <a href="https://www.insickness.org">insickness.org.</a></p>]]></content:encoded>
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      <itunes:duration>0:55:09</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin and Paul Kidwell</itunes:author>
      <itunes:summary>Collaboration between caregivers and biopharma companies can lead to innovations that benefit both the patient and their support systems, leading to better health outcomes, more effective therapies, and a higher quality of life for all involved. In this special Rare Disease Day 2025 podcast you will hear the story of Ron and Marla Chapleau and how they have cared for their Aiden who has an ultrarare neurodegenerative disease for over two decades. You will also hear how one company, Vigil Neuroscience, is developing a therapy to help treat Aiden’s condition and the strong bond that has developed between Vigil and the Chapleau family. to learn more, go to insickness.org. (https://www.insickness.org)</itunes:summary>
      <itunes:title>When Caregivers and Biopharma Companies Collaborate</itunes:title>
      <itunes:episode>12</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:location>Boston</podcast:location>
    </item>
    <item>
      <title>PAWS That Care</title>
      <podcast:episode>12</podcast:episode>
      <link>https://blubrry.com/3713794/139654499/paws-that-care/</link>
      <guid>https://blubrry.com/3713794/139654499/paws-that-care/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Thu, 12 Dec 2024 12:38:00 -0500</pubDate>
      <podcast:license>©openlytallproductions 2024</podcast:license>
      <description><![CDATA[<p>At first glance Sawyer looks like most Golden Retrievers. Floppy ears, kind eyes and a never-stop-wagging tail. But then you step inside the home of Ron and Linda Baxter and see him in action helping Linda who has MS and is in a wheelchair. On any given day Sawyer can aid Linda in retrieving and carrying items, opening and closing doors, providing mobility assistance, and assisting with navigation. Plus, he provides emotional support to Linda as well as Ron who finds him invaluable in reducing the pressures and commitment of being a caregiver. This episode looks at caregiving through the eyes of Sawyer, the couple who embraces him and the organization who trains him. To learn more, go to insickness.org.</p>]]></description>
      <content:encoded><![CDATA[<p>At first glance Sawyer looks like most Golden Retrievers. Floppy ears, kind eyes and a never-stop-wagging tail. But then you step inside the home of Ron and Linda Baxter and see him in action helping Linda who has MS and is in a wheelchair. On any given day Sawyer can aid Linda in retrieving and carrying items, opening and closing doors, providing mobility assistance, and assisting with navigation. Plus, he provides emotional support to Linda as well as Ron who finds him invaluable in reducing the pressures and commitment of being a caregiver. This episode looks at caregiving through the eyes of Sawyer, the couple who embraces him and the organization who trains him. To learn more, go to insickness.org.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_Sawyer_mixdownR1.mp3" length="39249638" type="audio/mpeg" />
      <itunes:duration>0:27:15</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin and Paul Kidwell</itunes:author>
      <itunes:summary>At first glance Sawyer looks like most Golden Retrievers. Floppy ears, kind eyes and a never-stop-wagging tail. But then you step inside the home of Ron and Linda Baxter and see him in action helping Linda who has MS and is in a wheelchair. On any given day Sawyer can aid Linda in retrieving and carrying items, opening and closing doors, providing mobility assistance, and assisting with navigation. Plus, he provides emotional support to Linda as well as Ron who finds him invaluable in reducing the pressures and commitment of being a caregiver. This episode looks at caregiving through the eyes of Sawyer, the couple who embraces him and the organization who trains him. To learn more, go to insickness.org.</itunes:summary>
      <itunes:title>PAWS That Care</itunes:title>
      <itunes:episode>12</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:location>Boston, MA</podcast:location>
    </item>
    <item>
      <title>A Caregiver’s Slow Burn</title>
      <podcast:episode>11</podcast:episode>
      <link>https://blubrry.com/3713794/138849298/a-caregivers-slow-burn/</link>
      <guid>https://blubrry.com/3713794/138849298/a-caregivers-slow-burn/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Sat, 23 Nov 2024 09:29:00 -0500</pubDate>
      <podcast:license>©Openlytallproductions 2024</podcast:license>
      <description><![CDATA[<p>All caregivers reach a point where the responsibilities of caregiving bumps heads with the demands of life. It’s usually a combination of physical, emotional and/or mental exhaustion brought on by caring for a loved one over a prolonged period. That’s what happened to podcast guest Kate Washington, who cared for her husband as he endured a series of serious health setbacks. She tried to keep up with the increasing demands of his many illnesses, without adequate support or self-care. Until she couldn’t. It’s an experience she chronicled in her excellent book, <a href="https://www.amazon.com/Already-Toast-Caregiving-Burnout-America/dp/0807011509">Already Toast: Caregiving and Burnout in America</a>. Joining Kate on the podcast to offer a clinical perspective is Michelle Feng, a licensed psychologist and healthcare executive with a specialization in geriatrics, behavioral medicine, and caregiving. To learn more, visit insickness.org.</p>]]></description>
      <content:encoded><![CDATA[<p>All caregivers reach a point where the responsibilities of caregiving bumps heads with the demands of life. It’s usually a combination of physical, emotional and/or mental exhaustion brought on by caring for a loved one over a prolonged period. That’s what happened to podcast guest Kate Washington, who cared for her husband as he endured a series of serious health setbacks. She tried to keep up with the increasing demands of his many illnesses, without adequate support or self-care. Until she couldn’t. It’s an experience she chronicled in her excellent book, <a href="https://www.amazon.com/Already-Toast-Caregiving-Burnout-America/dp/0807011509">Already Toast: Caregiving and Burnout in America</a>. Joining Kate on the podcast to offer a clinical perspective is Michelle Feng, a licensed psychologist and healthcare executive with a specialization in geriatrics, behavioral medicine, and caregiving. To learn more, visit insickness.org.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_Burnout_mixdownF.mp3" length="60497654" type="audio/mpeg" />
      <itunes:duration>0:42:00</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin and Paul Kidwell</itunes:author>
      <itunes:summary>All caregivers reach a point where the responsibilities of caregiving bumps heads with the demands of life. It’s usually a combination of physical, emotional and/or mental exhaustion brought on by caring for a loved one over a prolonged period. That’s what happened to podcast guest Kate Washington, who cared for her husband as he endured a series of serious health setbacks. She tried to keep up with the increasing demands of his many illnesses, without adequate support or self-care. Until she couldn’t. It’s an experience she chronicled in her excellent book, Already Toast: Caregiving and Burnout in America (https://www.amazon.com/Already-Toast-Caregiving-Burnout-America/dp/0807011509). Joining Kate on the podcast to offer a clinical perspective is Michelle Feng, a licensed psychologist and healthcare executive with a specialization in geriatrics, behavioral medicine, and caregiving. To learn more, visit insickness.org.</itunes:summary>
      <itunes:title>A Caregiver’s Slow Burn</itunes:title>
      <itunes:episode>11</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:location>Boston, MA</podcast:location>
    </item>
    <item>
      <title>Patients and Caregivers in Focus</title>
      <podcast:episode>10</podcast:episode>
      <link>https://blubrry.com/3713794/138478967/patients-and-caregivers-in-focus/</link>
      <guid>https://blubrry.com/3713794/138478967/patients-and-caregivers-in-focus/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Wed, 13 Nov 2024 17:00:44 -0500</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>For this episode of In Sickness. Men and the Culture of Caregiving we took the podcast on the road. At the invitation of Pfizer, Inc. we recorded our podcast at the company’s New York City headquarters as part of their annual “Patients in Focus” week. Host, Paul Kidwell, had the pleasure of speaking with Pfizer’s VP, Global Patient Advocacy, Emma Andrews and Jason Resendez who is the CEO of the National Alliance for Caregiving. Among the topics discussed were the evolving role of caregivers, the need for more interaction between caregivers and the biopharmaceutical industry, and some of the needs that both groups are filling. </p>]]></description>
      <content:encoded><![CDATA[<p>For this episode of In Sickness. Men and the Culture of Caregiving we took the podcast on the road. At the invitation of Pfizer, Inc. we recorded our podcast at the company’s New York City headquarters as part of their annual “Patients in Focus” week. Host, Paul Kidwell, had the pleasure of speaking with Pfizer’s VP, Global Patient Advocacy, Emma Andrews and Jason Resendez who is the CEO of the National Alliance for Caregiving. Among the topics discussed were the evolving role of caregivers, the need for more interaction between caregivers and the biopharmaceutical industry, and some of the needs that both groups are filling. </p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_Pfiser_mixdownR2.mp3" length="53468047" type="audio/mpeg" />
      <itunes:duration>0:37:07</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bod Coughlin and Paul Kidwell</itunes:author>
      <itunes:summary>For this episode of In Sickness. Men and the Culture of Caregiving we took the podcast on the road. At the invitation of Pfizer, Inc. we recorded our podcast at the company’s New York City headquarters as part of their annual “Patients in Focus” week. Host, Paul Kidwell, had the pleasure of speaking with Pfizer’s VP, Global Patient Advocacy, Emma Andrews and Jason Resendez who is the CEO of the National Alliance for Caregiving. Among the topics discussed were the evolving role of caregivers, the need for more interaction between caregivers and the biopharmaceutical industry, and some of the needs that both groups are filling. </itunes:summary>
      <itunes:title>Patients and Caregivers in Focus</itunes:title>
      <itunes:episode>10</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:location>Boston, MA</podcast:location>
    </item>
    <item>
      <title>The Never-ending Ripples of Care</title>
      <podcast:episode>8</podcast:episode>
      <link>https://blubrry.com/3713794/137801566/the-never-ending-ripples-of-care/</link>
      <guid>https://blubrry.com/3713794/137801566/the-never-ending-ripples-of-care/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Wed, 23 Oct 2024 14:38:01 -0400</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>Stories of individuals living with and enduring the challenges of any disease never fail to move and inspire others. This is especially true when the illness becomes fatal, and life is shortened. Maria Middleton was an exceptional young girl when she was diagnosed with a rare brain cancer and only 15 when she passed away. I use the word exceptional because during her final months when she was experiencing the brunt of her illness, Maria took the time to touch and move others. She wanted to strengthen their own personal resolve and encourage them to never lose hope. She cared that much. Maria’s message continues to ripple around the world even after her death. Maria’s parents Susan and Brian share the profound story of their daughter on this episode of In Sickness. Men and the Culture of Caregiving. To learn more, go to insickness.org.</p>]]></description>
      <content:encoded><![CDATA[<p>Stories of individuals living with and enduring the challenges of any disease never fail to move and inspire others. This is especially true when the illness becomes fatal, and life is shortened. Maria Middleton was an exceptional young girl when she was diagnosed with a rare brain cancer and only 15 when she passed away. I use the word exceptional because during her final months when she was experiencing the brunt of her illness, Maria took the time to touch and move others. She wanted to strengthen their own personal resolve and encourage them to never lose hope. She cared that much. Maria’s message continues to ripple around the world even after her death. Maria’s parents Susan and Brian share the profound story of their daughter on this episode of In Sickness. Men and the Culture of Caregiving. To learn more, go to insickness.org.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_Middleton_mixdownR2.mp3" length="63636546" type="audio/mpeg" />
      <itunes:duration>0:44:11</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
      <itunes:summary>Stories of individuals living with and enduring the challenges of any disease never fail to move and inspire others. This is especially true when the illness becomes fatal, and life is shortened. Maria Middleton was an exceptional young girl when she was diagnosed with a rare brain cancer and only 15 when she passed away. I use the word exceptional because during her final months when she was experiencing the brunt of her illness, Maria took the time to touch and move others. She wanted to strengthen their own personal resolve and encourage them to never lose hope. She cared that much. Maria’s message continues to ripple around the world even after her death. Maria’s parents Susan and Brian share the profound story of their daughter on this episode of In Sickness. Men and the Culture of Caregiving. To learn more, go to insickness.org.</itunes:summary>
      <itunes:title>The Never-ending Ripples of Care</itunes:title>
      <itunes:episode>8</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:location>Boston, MA</podcast:location>
    </item>
    <item>
      <title>Cancering and Caring</title>
      <podcast:episode>7</podcast:episode>
      <link>https://blubrry.com/3713794/136041127/cancering-and-caring/</link>
      <guid>https://blubrry.com/3713794/136041127/cancering-and-caring/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Tue, 10 Sep 2024 14:37:39 -0400</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>It takes courage and compassion to be a police officer. The same is true for a caregiver. Just ask Clifton Huffmaster whose day job finds him working as a detective in the Special Victims Unit with the Concord Police Department in Concord, California. This takes courage. He’s also a graduate from the Theological Union at Berkeley College from which he holds a PhD. Maybe that’s where compassion comes from. When Clifton’s wife Lauren was diagnosed with metastatic breast cancer his world turned upside down as he assumed the unfamiliar territory as her caregiver. This is where he found the need to be both courageous and compassionate. </p><p>On this episode of In Sickness. Men and the Culture of Caregiving, Clifton and Lauren dive deep into the emotions of living with breast cancer in the shadows of uncertainty. They have gone from the depths of fear to the top of Joy’s Mountain. To learn more go to insickness.org.</p>]]></description>
      <content:encoded><![CDATA[<p>It takes courage and compassion to be a police officer. The same is true for a caregiver. Just ask Clifton Huffmaster whose day job finds him working as a detective in the Special Victims Unit with the Concord Police Department in Concord, California. This takes courage. He’s also a graduate from the Theological Union at Berkeley College from which he holds a PhD. Maybe that’s where compassion comes from. When Clifton’s wife Lauren was diagnosed with metastatic breast cancer his world turned upside down as he assumed the unfamiliar territory as her caregiver. This is where he found the need to be both courageous and compassionate. </p><p>On this episode of In Sickness. Men and the Culture of Caregiving, Clifton and Lauren dive deep into the emotions of living with breast cancer in the shadows of uncertainty. They have gone from the depths of fear to the top of Joy’s Mountain. To learn more go to insickness.org.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_007_mixdownR2.mp3" length="78646846" type="audio/mpeg" />
      <itunes:duration>0:54:36</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Paul Kidwell and Bob Coughlin</itunes:author>
      <itunes:summary>It takes courage and compassion to be a police officer. The same is true for a caregiver. Just ask Clifton Huffmaster whose day job finds him working as a detective in the Special Victims Unit with the Concord Police Department in Concord, California. This takes courage. He’s also a graduate from the Theological Union at Berkeley College from which he holds a PhD. Maybe that’s where compassion comes from. When Clifton’s wife Lauren was diagnosed with metastatic breast cancer his world turned upside down as he assumed the unfamiliar territory as her caregiver. This is where he found the need to be both courageous and compassionate. On this episode of In Sickness. Men and the Culture of Caregiving, Clifton and Lauren dive deep into the emotions of living with breast cancer in the shadows of uncertainty. They have gone from the depths of fear to the top of Joy’s Mountain. To learn more go to insickness.org.</itunes:summary>
      <itunes:title>Cancering and Caring</itunes:title>
      <itunes:season>1</itunes:season>
      <itunes:episode>7</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:season>1</podcast:season>
      <podcast:location>Boston, MA</podcast:location>
    </item>
    <item>
      <title>Changed Lives. A Constant Heart</title>
      <podcast:episode>6</podcast:episode>
      <link>https://blubrry.com/3713794/133008546/changed-lives-a-constant-heart/</link>
      <guid>https://blubrry.com/3713794/133008546/changed-lives-a-constant-heart/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Mon, 15 Jul 2024 11:22:28 -0400</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>For all caregivers, their lives are divided into two parts. Before diagnosis and After Diagnosis. This is particularly true for those who must manage one of the more insidious illnesses, Alzheimer’s Disease, where the changes taking place before the diagnosis and once the disease has become fully onset, are significant for the patient and care partner alike. Marty Schreiber is the former Governor of Wisconsin, author of, My Two Elaines. Learning, Coping and Surviving as an Alzheimer’s Caregiver. The book chronicles Marty’s experience as primary support and caregiver for his wife of 60 years who was diagnosed with Alzheimer’s. The book and this podcast provides a transparent look into the heart of the disease and its personal, physical and emotional impact on the patient and those courageous souls, like Marty, who provide unrelenting support for their loved ones. To learn more and find resources related to this episode, go to insickness.org. </p>]]></description>
      <content:encoded><![CDATA[<p>For all caregivers, their lives are divided into two parts. Before diagnosis and After Diagnosis. This is particularly true for those who must manage one of the more insidious illnesses, Alzheimer’s Disease, where the changes taking place before the diagnosis and once the disease has become fully onset, are significant for the patient and care partner alike. Marty Schreiber is the former Governor of Wisconsin, author of, My Two Elaines. Learning, Coping and Surviving as an Alzheimer’s Caregiver. The book chronicles Marty’s experience as primary support and caregiver for his wife of 60 years who was diagnosed with Alzheimer’s. The book and this podcast provides a transparent look into the heart of the disease and its personal, physical and emotional impact on the patient and those courageous souls, like Marty, who provide unrelenting support for their loved ones. To learn more and find resources related to this episode, go to insickness.org. </p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_MartyR4_mixdownR4.mp3" length="56246597" type="audio/mpeg" />
      <itunes:duration>0:39:03</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin and Paul Kidwell</itunes:author>
      <itunes:summary>For all caregivers, their lives are divided into two parts. Before diagnosis and After Diagnosis. This is particularly true for those who must manage one of the more insidious illnesses, Alzheimer’s Disease, where the changes taking place before the diagnosis and once the disease has become fully onset, are significant for the patient and care partner alike. Marty Schreiber is the former Governor of Wisconsin, author of, My Two Elaines. Learning, Coping and Surviving as an Alzheimer’s Caregiver. The book chronicles Marty’s experience as primary support and caregiver for his wife of 60 years who was diagnosed with Alzheimer’s. The book and this podcast provides a transparent look into the heart of the disease and its personal, physical and emotional impact on the patient and those courageous souls, like Marty, who provide unrelenting support for their loved ones. To learn more and find resources related to this episode, go to insickness.org. </itunes:summary>
      <itunes:title>Changed Lives. A Constant Heart</itunes:title>
      <itunes:season>1</itunes:season>
      <itunes:episode>6</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:season>1</podcast:season>
      <podcast:location>Boston, MA</podcast:location>
    </item>
    <item>
      <title>A Father Rises in Support of his Son</title>
      <podcast:episode>5</podcast:episode>
      <link>https://blubrry.com/3713794/132889045/a-father-rises-in-support-of-his-son/</link>
      <guid>https://blubrry.com/3713794/132889045/a-father-rises-in-support-of-his-son/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Wed, 26 Jun 2024 11:15:00 -0400</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>For Josh Argall, life couldn’t get much better. He was a 25-year-old first-time father of, Devin, who quickly became the center of Josh’s universe. Josh’s world was rocked when he and Devin’s mother noticed that their three-year-old son was somewhat slow in reaching some of the physical milestones like crawling and walking that are typically associated with children his age. In the months following, Josh’s world changed dramatically as Devin went through numerous doctor visits and misdiagnoses. Finally, a specialist at Children’s Hospital in Milwaukee diagnosed Devin as having Duchenne Muscular Dystrophy, a rare and progressive neuromuscular disease that, at the time, had few treatment options and little hope for a cure or long-term survival. The diagnosis shattered Josh’s world and sent him spiraling into a world of sadness, depression and despair. </p><p>On this episode of In Sickness. Men and the Culture of Caregiving, Josh shares how he went from the lowest of the lows to the realization that if his son was going to get better, he needed to face this adversity and join in the effort. Debra Miller, CEO and Founder of CureDuchenne, joins Josh in the discussion and provides valuable insight into the disease, and the patient and caregiver journey. To learn more and find resources related to this episode, go to insickness.org.</p>]]></description>
      <content:encoded><![CDATA[<p>For Josh Argall, life couldn’t get much better. He was a 25-year-old first-time father of, Devin, who quickly became the center of Josh’s universe. Josh’s world was rocked when he and Devin’s mother noticed that their three-year-old son was somewhat slow in reaching some of the physical milestones like crawling and walking that are typically associated with children his age. In the months following, Josh’s world changed dramatically as Devin went through numerous doctor visits and misdiagnoses. Finally, a specialist at Children’s Hospital in Milwaukee diagnosed Devin as having Duchenne Muscular Dystrophy, a rare and progressive neuromuscular disease that, at the time, had few treatment options and little hope for a cure or long-term survival. The diagnosis shattered Josh’s world and sent him spiraling into a world of sadness, depression and despair. </p><p>On this episode of In Sickness. Men and the Culture of Caregiving, Josh shares how he went from the lowest of the lows to the realization that if his son was going to get better, he needed to face this adversity and join in the effort. Debra Miller, CEO and Founder of CureDuchenne, joins Josh in the discussion and provides valuable insight into the disease, and the patient and caregiver journey. To learn more and find resources related to this episode, go to insickness.org.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_005_mixdownR3.mp3" length="55258655" type="audio/mpeg" />
      <itunes:duration>0:38:21</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
      <itunes:summary>For Josh Argall, life couldn’t get much better. He was a 25-year-old first-time father of, Devin, who quickly became the center of Josh’s universe. Josh’s world was rocked when he and Devin’s mother noticed that their three-year-old son was somewhat slow in reaching some of the physical milestones like crawling and walking that are typically associated with children his age. In the months following, Josh’s world changed dramatically as Devin went through numerous doctor visits and misdiagnoses. Finally, a specialist at Children’s Hospital in Milwaukee diagnosed Devin as having Duchenne Muscular Dystrophy, a rare and progressive neuromuscular disease that, at the time, had few treatment options and little hope for a cure or long-term survival. The diagnosis shattered Josh’s world and sent him spiraling into a world of sadness, depression and despair. On this episode of In Sickness. Men and the Culture of Caregiving, Josh shares how he went from the lowest of the lows to the realization that if his son was going to get better, he needed to face this adversity and join in the effort. Debra Miller, CEO and Founder of CureDuchenne, joins Josh in the discussion and provides valuable insight into the disease, and the patient and caregiver journey. To learn more and find resources related to this episode, go to insickness.org.</itunes:summary>
      <itunes:title>A Father Rises in Support of his Son</itunes:title>
      <itunes:season>1</itunes:season>
      <itunes:episode>5</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:season>1</podcast:season>
      <podcast:location>Boston, MA</podcast:location>
    </item>
    <item>
      <title>A Life-time Commitment of Care</title>
      <podcast:episode>4</podcast:episode>
      <link>https://blubrry.com/3713794/132636408/a-life-time-commitment-of-care/</link>
      <guid>https://blubrry.com/3713794/132636408/a-life-time-commitment-of-care/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Mon, 20 May 2024 11:44:10 -0400</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>When you have a child diagnosed with any illness, you can only hope your efforts don’t require a lifetime commitment. The hope is for a short-lived illness that comes with a diagnosis followed by a cure. For former MassBio President, Bob Coughlin, he has lived through the in utero cystic fibrosis diagnosis of his son, Bobby, the physical challenges of caring for a young CF patient, and the constant involvement as a CF patient advocate raising awareness and all-important research money. Also, a time where CF treatments improved allowing Bobby to enjoy his teen years, finish high school, graduate college and begin his professional career. Despite this progress Bob has not remained stagnant and continues to advocate for patients with CF and other unmet medical needs. He also never stopped plying his most important role as his son’s caregiver where he remains committed, passionate, and always involved. Bob is joined on the podcast, Charlotte McKee, M.D., Chief Medical Officer of <a href="https://www.sionnatx.com">Sionna Therapeutics</a>, a clinical stage biopharmaceutical company, developing therapeutics to treat cystic fibrosis. </p><p>To learn more, visit <a href="https://www.insickness.org">insickness.org</a>.</p>]]></description>
      <content:encoded><![CDATA[<p>When you have a child diagnosed with any illness, you can only hope your efforts don’t require a lifetime commitment. The hope is for a short-lived illness that comes with a diagnosis followed by a cure. For former MassBio President, Bob Coughlin, he has lived through the in utero cystic fibrosis diagnosis of his son, Bobby, the physical challenges of caring for a young CF patient, and the constant involvement as a CF patient advocate raising awareness and all-important research money. Also, a time where CF treatments improved allowing Bobby to enjoy his teen years, finish high school, graduate college and begin his professional career. Despite this progress Bob has not remained stagnant and continues to advocate for patients with CF and other unmet medical needs. He also never stopped plying his most important role as his son’s caregiver where he remains committed, passionate, and always involved. Bob is joined on the podcast, Charlotte McKee, M.D., Chief Medical Officer of <a href="https://www.sionnatx.com">Sionna Therapeutics</a>, a clinical stage biopharmaceutical company, developing therapeutics to treat cystic fibrosis. </p><p>To learn more, visit <a href="https://www.insickness.org">insickness.org</a>.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_EP4_mixdownR4.mp3" length="53034934" type="audio/mpeg" />
      <itunes:duration>0:36:49</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
      <itunes:summary>When you have a child diagnosed with any illness, you can only hope your efforts don’t require a lifetime commitment. The hope is for a short-lived illness that comes with a diagnosis followed by a cure. For former MassBio President, Bob Coughlin, he has lived through the in utero cystic fibrosis diagnosis of his son, Bobby, the physical challenges of caring for a young CF patient, and the constant involvement as a CF patient advocate raising awareness and all-important research money. Also, a time where CF treatments improved allowing Bobby to enjoy his teen years, finish high school, graduate college and begin his professional career. Despite this progress Bob has not remained stagnant and continues to advocate for patients with CF and other unmet medical needs. He also never stopped plying his most important role as his son’s caregiver where he remains committed, passionate, and always involved. Bob is joined on the podcast, Charlotte McKee, M.D., Chief Medical Officer of Sionna Therapeutics (https://www.sionnatx.com), a clinical stage biopharmaceutical company, developing therapeutics to treat cystic fibrosis. To learn more, visit insickness.org (https://www.insickness.org).</itunes:summary>
      <itunes:title>A Life-time Commitment of Care</itunes:title>
      <itunes:season>1</itunes:season>
      <itunes:episode>4</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:season>1</podcast:season>
    </item>
    <item>
      <title>A Rare, Caring Family </title>
      <podcast:episode>3</podcast:episode>
      <link>https://blubrry.com/3713794/132446228/a-rare-caring-family/</link>
      <guid>https://blubrry.com/3713794/132446228/a-rare-caring-family/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Tue, 30 Apr 2024 09:25:00 -0400</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>At 17, Mason Smith was your typical teenager and living a life filled with school, sports, lots of hanging out with friends and more growing up. That all came to an abrupt stop when his mother was diagnosed with a fatal and ultra-rare neurodegenerative disease, adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP). This young man who was just sprouting his wings took a harsh turn into adulthood as part of his Mom’s primary care team when she began to exhibit behaviors that were noticeable to Mason’s Aunt Heidi. Together, they both felt the need for further medical testing given that ALSP had already taken the lives of other family members. Mason knew that an ALSP diagnosis would change his mother’s life and usher him into adulthood and caregiving. To learn more visit <a href="https://www.insickness.org">insickness.org</a>.</p>]]></description>
      <content:encoded><![CDATA[<p>At 17, Mason Smith was your typical teenager and living a life filled with school, sports, lots of hanging out with friends and more growing up. That all came to an abrupt stop when his mother was diagnosed with a fatal and ultra-rare neurodegenerative disease, adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP). This young man who was just sprouting his wings took a harsh turn into adulthood as part of his Mom’s primary care team when she began to exhibit behaviors that were noticeable to Mason’s Aunt Heidi. Together, they both felt the need for further medical testing given that ALSP had already taken the lives of other family members. Mason knew that an ALSP diagnosis would change his mother’s life and usher him into adulthood and caregiving. To learn more visit <a href="https://www.insickness.org">insickness.org</a>.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_EP3_mixdownR3.mp3" length="57342980" type="audio/mpeg" />
      <itunes:duration>0:39:49</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin and Paul Kidwell</itunes:author>
      <itunes:summary>At 17, Mason Smith was your typical teenager and living a life filled with school, sports, lots of hanging out with friends and more growing up. That all came to an abrupt stop when his mother was diagnosed with a fatal and ultra-rare neurodegenerative disease, adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP). This young man who was just sprouting his wings took a harsh turn into adulthood as part of his Mom’s primary care team when she began to exhibit behaviors that were noticeable to Mason’s Aunt Heidi. Together, they both felt the need for further medical testing given that ALSP had already taken the lives of other family members. Mason knew that an ALSP diagnosis would change his mother’s life and usher him into adulthood and caregiving. To learn more visit insickness.org (https://www.insickness.org).</itunes:summary>
      <itunes:title>A Rare, Caring Family </itunes:title>
      <itunes:season>1</itunes:season>
      <itunes:episode>3</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <podcast:season>1</podcast:season>
    </item>
    <item>
      <title>The Unfairest of Fights</title>
      <podcast:episode>2</podcast:episode>
      <link>https://blubrry.com/3713794/131731000/the-unfairest-of-fights/</link>
      <guid>https://blubrry.com/3713794/131731000/the-unfairest-of-fights/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Tue, 26 Mar 2024 09:33:00 -0400</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>If you’re looking for a fair fight, don’t pick one with cancer. Odds are that cancer rarely loses and its adversary won’t have a puncher’s chance of bringing on defeat. Anyone confronted with caring for someone with a cancer diagnosis typically has no shortage of personal will, but not necessarily successful in finding a way to beat cancer. Just ask Miguel Barron who supported his wife in her two-year ordeal living with metastatic breast cancer, providing constant love, compassion, and dedication. Miguel also endured the emotional pressures of caring for someone with a progressive and punishing illness like cancer as he lived with loneliness and an overwhelming sadness during this time. Miguel captured his experience in a no holds-barred book, <a href="https://www.theboxerscorner.com">The Boxer’s Corner</a>, that peers deep into his soul and shines a questioning light on the industry that creates medicines and supports patients. To learn more visit <a href="https://www.insickness.org">insickness.org</a>.</p>]]></description>
      <content:encoded><![CDATA[<p>If you’re looking for a fair fight, don’t pick one with cancer. Odds are that cancer rarely loses and its adversary won’t have a puncher’s chance of bringing on defeat. Anyone confronted with caring for someone with a cancer diagnosis typically has no shortage of personal will, but not necessarily successful in finding a way to beat cancer. Just ask Miguel Barron who supported his wife in her two-year ordeal living with metastatic breast cancer, providing constant love, compassion, and dedication. Miguel also endured the emotional pressures of caring for someone with a progressive and punishing illness like cancer as he lived with loneliness and an overwhelming sadness during this time. Miguel captured his experience in a no holds-barred book, <a href="https://www.theboxerscorner.com">The Boxer’s Corner</a>, that peers deep into his soul and shines a questioning light on the industry that creates medicines and supports patients. To learn more visit <a href="https://www.insickness.org">insickness.org</a>.</p>]]></content:encoded>
      <enclosure url="https://media.blubrry.com/3713794/ins.blubrry.com/3713794/In_Sickness_Miguel_Barron_mixdownR2.mp3" length="50506212" type="audio/mpeg" />
      <itunes:duration>0:35:03</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin and Paul Kidwell</itunes:author>
      <itunes:summary>If you’re looking for a fair fight, don’t pick one with cancer. Odds are that cancer rarely loses and its adversary won’t have a puncher’s chance of bringing on defeat. Anyone confronted with caring for someone with a cancer diagnosis typically has no shortage of personal will, but not necessarily successful in finding a way to beat cancer. Just ask Miguel Barron who supported his wife in her two-year ordeal living with metastatic breast cancer, providing constant love, compassion, and dedication. Miguel also endured the emotional pressures of caring for someone with a progressive and punishing illness like cancer as he lived with loneliness and an overwhelming sadness during this time. Miguel captured his experience in a no holds-barred book, The Boxer’s Corner (https://www.theboxerscorner.com), that peers deep into his soul and shines a questioning light on the industry that creates medicines and supports patients. To learn more visit insickness.org (https://www.insickness.org).</itunes:summary>
      <itunes:title>The Unfairest of Fights</itunes:title>
      <itunes:season>1</itunes:season>
      <itunes:episode>2</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
      <itunes:image href="https://assets.blubrry.com/coverart/episode/3713794/orig/131731000-1711460014.jpg" />
      <image>https://assets.blubrry.com/coverart/episode/3713794/orig/131731000-1711460014.jpg</image>
      <podcast:season>1</podcast:season>
      <podcast:person role="Guest" href="https://www.theboxerscorner.com/the-author">Miguel Barron</podcast:person>
      <podcast:location>Boston, MA</podcast:location>
    </item>
    <item>
      <title>A Father Chooses</title>
      <podcast:episode>1</podcast:episode>
      <link>https://blubrry.com/3713794/131209866/a-father-chooses/</link>
      <guid>https://blubrry.com/3713794/131209866/a-father-chooses/</guid>
      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Wed, 28 Feb 2024 13:07:00 -0500</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>John Crowley’s life was on the upswing after completing his MBA studies at Harvard Business School and beginning a new position as an investment banker. Without any warning his seemingly good fortune changed dramatically with the diagnosis of two of his children who contracted a rare, inherited disorder for which there were few treatments. His new path directed him towards creating a start-up biotech company that would research this once fatal disease and discover new treatments for his kids. John’s story is heroic and what he accomplishes against unimaginable odds is riveting. To learn more about this podcast, go to <a href="https://www.insickness.org">insickness.org</a>. There, you can hear other episodes, see the producer's bios and connect with them!</p>]]></description>
      <content:encoded><![CDATA[<p>John Crowley’s life was on the upswing after completing his MBA studies at Harvard Business School and beginning a new position as an investment banker. Without any warning his seemingly good fortune changed dramatically with the diagnosis of two of his children who contracted a rare, inherited disorder for which there were few treatments. His new path directed him towards creating a start-up biotech company that would research this once fatal disease and discover new treatments for his kids. John’s story is heroic and what he accomplishes against unimaginable odds is riveting. To learn more about this podcast, go to <a href="https://www.insickness.org">insickness.org</a>. There, you can hear other episodes, see the producer's bios and connect with them!</p>]]></content:encoded>
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      <itunes:duration>0:38:02</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin and Paul Kidwell</itunes:author>
      <itunes:summary>John Crowley’s life was on the upswing after completing his MBA studies at Harvard Business School and beginning a new position as an investment banker. Without any warning his seemingly good fortune changed dramatically with the diagnosis of two of his children who contracted a rare, inherited disorder for which there were few treatments. His new path directed him towards creating a start-up biotech company that would research this once fatal disease and discover new treatments for his kids. John’s story is heroic and what he accomplishes against unimaginable odds is riveting. To learn more about this podcast, go to insickness.org (https://www.insickness.org). There, you can hear other episodes, see the producer's bios and connect with them!</itunes:summary>
      <itunes:title>A Father Chooses</itunes:title>
      <itunes:season>1</itunes:season>
      <itunes:episode>1</itunes:episode>
      <itunes:episodeType>full</itunes:episodeType>
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      <podcast:season>1</podcast:season>
      <podcast:location>Boston, MA</podcast:location>
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      <link>https://blubrry.com/3713794/130733844/in-sickness-trailer-episode/</link>
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      <dc:creator>Bob Coughlin &amp; Paul Kidwell</dc:creator>
      <pubDate>Sun, 04 Feb 2024 15:31:01 -0500</pubDate>
      <podcast:license>©openly tall productions</podcast:license>
      <description><![CDATA[<p>Coming Soon: In Sickness. Men and the Culture of Caregiving is a monthly podcast that will focus on stories of male caregivers who have supported individuals with various diseases and medical conditions across all therapeutic areas including select cancers, ALS, Alzheimer’s, and numerous rare diseases. The podcast will highlight the growing population of male caregivers who are caring for their spouse, life partners, children family members, and friends, and joining the ranks of the throngs of women caregivers who have historically been central to this effort. The podcast is co-hosted and produced by Bob Coughlin and Paul Kidwell, with technical supervision provided by Dan Thibeault of Fast Twitch Media. </p>]]></description>
      <content:encoded><![CDATA[<p>Coming Soon: In Sickness. Men and the Culture of Caregiving is a monthly podcast that will focus on stories of male caregivers who have supported individuals with various diseases and medical conditions across all therapeutic areas including select cancers, ALS, Alzheimer’s, and numerous rare diseases. The podcast will highlight the growing population of male caregivers who are caring for their spouse, life partners, children family members, and friends, and joining the ranks of the throngs of women caregivers who have historically been central to this effort. The podcast is co-hosted and produced by Bob Coughlin and Paul Kidwell, with technical supervision provided by Dan Thibeault of Fast Twitch Media. </p>]]></content:encoded>
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      <itunes:duration>0:00:58</itunes:duration>
      <itunes:explicit>false</itunes:explicit>
      <itunes:author>Bob Coughlin &amp; Paul Kidwell</itunes:author>
      <itunes:summary>Coming Soon: In Sickness. Men and the Culture of Caregiving is a monthly podcast that will focus on stories of male caregivers who have supported individuals with various diseases and medical conditions across all therapeutic areas including select cancers, ALS, Alzheimer’s, and numerous rare diseases. The podcast will highlight the growing population of male caregivers who are caring for their spouse, life partners, children family members, and friends, and joining the ranks of the throngs of women caregivers who have historically been central to this effort. The podcast is co-hosted and produced by Bob Coughlin and Paul Kidwell, with technical supervision provided by Dan Thibeault of Fast Twitch Media. </itunes:summary>
      <itunes:title>In Sickness Trailer Episode</itunes:title>
      <itunes:episodeType>trailer</itunes:episodeType>
      <podcast:location>Boston, MA</podcast:location>
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