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.
Overworking Ourselves: Juggling Motherhood Entrepreneurship and Invisible Illness
Lupus has No face Podcast
1 hour 14 minutes
3 months ago
Overworking Ourselves: Juggling Motherhood Entrepreneurship and Invisible Illness
On this episode of "Lupus Has No Face," host Savannah Burks and special guest Vee Taylor dive into the raw, truth about juggling it all. From the tear-jerking emotions of a child's first day of school to the physical toll of overworking, they're not holding back. They get real about how to find balance as a "serial entrepreneur," the importance of self-care, and why you need to listen to your body before it forces you to sit down. This episode is a must-listen for any mother, entrepreneur, or anyone fighting an invisible illness.
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.
