Lupus Has No Face: Uniting and Empowering the Lupus Community
Welcome to the Lupus Has No Face Podcast, hosted by Savannah Burks! We're more than just a podcast; we're also a 501(c)(3) non-profit organization committed to building a supportive community for everyone affected by Lupus.
This is your space, whether you're living with a Lupus diagnosis and seeking support, a friend or family member trying to understand the condition better, or a healthcare professional looking for patient insights. We also welcome chronic illness support groups, autoimmune disease advocates, and mental health professionals who help patients navigate the emotional impacts of chronic conditions.
Our mission is clear: we don't just help Lupus patients; we also raise public awareness and provide vital education about this autoimmune disease. We're here to give you the tools you need to cope with the emotional and mental challenges of Lupus, emphasizing self-care and health education. Through powerful stories and building a strong community, we aim to empower individuals, especially women, to live fulfilling lives while managing their condition.
Join us as we put a face to Lupus, one story at a time. To keep up with all our latest content, subscribe to the podcast. If you've enjoyed this episode, please leave a review.
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Lupus Has No Face: Uniting and Empowering the Lupus Community
Welcome to the Lupus Has No Face Podcast, hosted by Savannah Burks! We're more than just a podcast; we're also a 501(c)(3) non-profit organization committed to building a supportive community for everyone affected by Lupus.
This is your space, whether you're living with a Lupus diagnosis and seeking support, a friend or family member trying to understand the condition better, or a healthcare professional looking for patient insights. We also welcome chronic illness support groups, autoimmune disease advocates, and mental health professionals who help patients navigate the emotional impacts of chronic conditions.
Our mission is clear: we don't just help Lupus patients; we also raise public awareness and provide vital education about this autoimmune disease. We're here to give you the tools you need to cope with the emotional and mental challenges of Lupus, emphasizing self-care and health education. Through powerful stories and building a strong community, we aim to empower individuals, especially women, to live fulfilling lives while managing their condition.
Join us as we put a face to Lupus, one story at a time. To keep up with all our latest content, subscribe to the podcast. If you've enjoyed this episode, please leave a review.
From warrior to Instructor: Training the Next Generation of Caregivers
Lupus has No face Podcast
1 hour 33 minutes
1 month ago
From warrior to Instructor: Training the Next Generation of Caregivers
Join us for a powerful conversation with special guest Deaconess Lisa Jones, a true embodiment of strength and dedication. Born and raised in Milwaukee, Lisa is a loving mother of four and grandmother who is fiercely battling Lupus. Beyond her personal fight, she is deeply committed to the community as a state-certified caregiver and an instructor for CBRF homes (Community-Based Residential Facilities). Lisa also brings her entrepreneurial spirit to the table as the owner of Harper’s Training Academy. Tune in as Lisa shares her journey of living with Lupus while balancing family, professional caregiving, and running a business, proving that a chronic illness is not a barrier to service and success.
Thank you for tuning in to "Lupus Has No Face," a podcast dedicated to sharing real stories and insights on living with Lupus and other invisible illnesses. Join your host, Savannah Burks, as she explores the struggles and triumphs of individuals navigating their health journeys, all while juggling life's many challenges. Don't miss an episode! Subscribe, listen, and share on all major podcast platforms. For more content and updates, follow us on social media and join the conversation.
Lupus has No face Podcast
Lupus Has No Face: Uniting and Empowering the Lupus Community
Welcome to the Lupus Has No Face Podcast, hosted by Savannah Burks! We're more than just a podcast; we're also a 501(c)(3) non-profit organization committed to building a supportive community for everyone affected by Lupus.
This is your space, whether you're living with a Lupus diagnosis and seeking support, a friend or family member trying to understand the condition better, or a healthcare professional looking for patient insights. We also welcome chronic illness support groups, autoimmune disease advocates, and mental health professionals who help patients navigate the emotional impacts of chronic conditions.
Our mission is clear: we don't just help Lupus patients; we also raise public awareness and provide vital education about this autoimmune disease. We're here to give you the tools you need to cope with the emotional and mental challenges of Lupus, emphasizing self-care and health education. Through powerful stories and building a strong community, we aim to empower individuals, especially women, to live fulfilling lives while managing their condition.
Join us as we put a face to Lupus, one story at a time. To keep up with all our latest content, subscribe to the podcast. If you've enjoyed this episode, please leave a review.
