&#34;Dizzy Directors&#34; is a refreshing take on the world of pots (Postural Orthostastic Tachycardia Syndrome), brought to you by two passionate college students who have POTS and also happen to be filmmakers. POTS is a condition causing a rapid increase in heart rate upon standing, leading to symptoms like dizziness, lightheadedness, and fatigue.  Join our dynamic hosts as they combine their love for storytelling with their curiosity about pots, delivering a podcast that is both informative and entertaining. Through their unique perspective, they explore the intricate world of pots, sharing their discoveries, insights, and even their filmmaking experiences along the way. Whether you&#39;re a fellow pots enthusiast or simply intrigued by their youthful energy and creativity, &#34;Dizzy Directors&#34; promises to be a delightful journey into the fascinating realm of pots.  Tune in and join our hosts as they bring pots to life through the lens of filmmaking!

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Summary In this episode of Dizzy Directors, hosts Tori Mosser and Lauren Clark reunite after a year to share significant life updates, including Lauren&#39;s transition to her senior year in college, her internship at Nickelodeon, and various film projects. Tori discusses her recent marriage and move to Dallas, along with her new role as a screenwriter. The conversation delves into their creative endeavors, emphasizing the importance of collaboration and authentic representation in film, particularly regarding chronic illness. In this conversation, Tori Mosser and Lauren Clark discuss the impact of online criticism on self-worth, the importance of creating safe spaces for individuals with disabilities, and share personal health updates related to chronic illnesses. They explore the challenges of navigating societal expectations, the emotional toll of negative comments, and the significance of community support. The discussion also delves into their individual health journeys, including diagnoses and treatments, emphasizing the need for understanding and validation in the face of chronic health issues. Chapters 00:00 Welcome Back and Life Updates04:40 Lauren&#39;s Film Projects and Achievements12:29 Tori&#39;s Marriage and New Beginnings18:23 Film Projects and Collaborations28:31 Writing and Representation in Film39:19 Navigating Online Criticism and Self-Worth45:34 Health Updates: Personal Struggles and Triumphs01:22:20 Finding Support and Moving Forward

Summary

In this episode of Dizzy Directors, hosts Tori Mosser and Lauren Clark reunite after a year to share significant life updates, including Lauren&#39;s transition to her senior year in college, her internship at Nickelodeon, and various film projects. Tori discusses her recent marriage and move to Dallas, along with her new role as a screenwriter. The conversation delves into their creative endeavors, emphasizing the importance of collaboration and authentic representation in film, particularly regarding chronic illness. In this conversation, Tori Mosser and Lauren Clark discuss the impact of online criticism on self-worth, the importance of creating safe spaces for individuals with disabilities, and share personal health updates related to chronic illnesses. They explore the challenges of navigating societal expectations, the emotional toll of negative comments, and the significance of community support. The discussion also delves into their individual health journeys, including diagnoses and treatments, emphasizing the need for understanding and validation in the face of chronic health issues.

Dizzy Directors Episode 8: WE'RE SO BACK!

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SummaryKatherine McCrackin shares her experience with POTS (Postural Orthostatic Tachycardia Syndrome) and the challenges she has faced in getting medical help. She discusses how her symptoms developed after surgery and the difficulty she had in finding doctors who believed her and could provide proper care. Lauren Clark and Tori Mosser also share their experiences with POTS and the lack of knowledge and understanding among doctors. They talk about the importance of finding supportive doctors and the role of the POTS community in providing information and support. They also discuss the challenges of being a student with POTS and the need for more accessibility on college campuses. The conversation revolves around the challenges and experiences of individuals with POTS (Postural Orthostatic Tachycardia Syndrome) and dysautonomia. They discuss the difficulties of getting a proper diagnosis, the lack of understanding and awareness of these conditions, and the impact on daily life and career choices. They also touch on the topic of medical gaslighting and the importance of trusting one&#39;s own experiences and advocating for oneself. The conversation highlights the need for more accessibility and accommodations in various settings, including the arts and corporate America.Takeaways<ul><li>POTS can be triggered by surgery and can cause debilitating symptoms</li><li>Many doctors are unfamiliar with POTS and may dismiss or misdiagnose patients</li><li>Finding supportive doctors who understand POTS is crucial for proper care</li><li>The POTS community provides valuable information and support for those with the condition</li><li>Accessibility and accommodations are important for students with POTS Getting a proper diagnosis for POTS and dysautonomia can be challenging due to a lack of understanding and awareness of these conditions.</li><li>Medical gaslighting is a common issue faced by individuals with POTS and dysautonomia, and it is important to trust one&#39;s own experiences and advocate for oneself.</li><li>Living with POTS and dysautonomia can have a significant impact on daily life and career choices, requiring accommodations and accessibility.</li><li>The arts industry may be more accommodating to individuals with chronic illnesses like POTS, while corporate America may present more challenges.</li><li>Connecting with others in the POTS and dysautonomia community can provide support, advice, and validation.</li></ul>Chapters00:00 Introduction and Personal Experience with POTS08:23 The Lack of Awareness and Knowledge Among Doctors14:24 The Lack of Accessibility on College Campuses40:45 Trusting Your Experiences and Instincts

Dizzy Directors: Interview with Katherine

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Summary In this episode, Lauren and Tori interview their moms about their experiences as parents of children with POTS. They discuss the challenges and emotions they faced when their children were first diagnosed and how POTS has affected their daily lives. They also talk about the importance of finding the right doctors and treatments, as well as the need for accommodations in school and work settings. The conversation highlights the impact of POTS on both the individuals with the condition and their families. The conversation revolves around the challenges faced by individuals with POTS (Postural Orthostatic Tachycardia Syndrome) and their parents. They discuss the difficulties in getting a proper diagnosis, the impact of POTS on daily life, and the frustration of being dismissed by doctors. They also touch on the potential genetic factors and triggers for POTS, such as concussions and COVID-19. The conversation highlights the need for more research and understanding of POTS, as well as the importance of finding knowledgeable doctors who can provide appropriate care. In this final part of the conversation, Lauren and Tori discuss the challenges of managing POTS in daily life and the difficulties of finding specialized doctors. They express their frustration with the lack of accessible treatment options and the impact of POTS on their education and career opportunities. They also discuss the importance of finding doctors who specialize in POTS and the need for more research and awareness. The conversation ends with a call for better support and resources for individuals with POTS and their families. Takeaways<ul><li>Parents of children with POTS face unique challenges and emotions when their child is diagnosed.</li><li>Finding the right doctors and treatments is crucial for managing POTS.</li><li>Accommodations in school and work settings are necessary to support individuals with POTS.</li><li>POTS not only affects the individual with the condition, but also their family members. Getting a proper diagnosis for POTS can be challenging, and individuals often face dismissal and medical gaslighting from doctors.</li><li>POTS may have genetic factors and can be triggered by events such as concussions and COVID-19.</li><li>There is a need for more research and understanding of POTS, as well as knowledgeable doctors who can provide appropriate care.</li><li>Parents play a crucial role in advocating for their children with POTS and navigating the healthcare system.</li></ul>Living with POTS can have a significant impact on daily life, including limitations on physical activities and the need for lifestyle adjustments.The conversation highlights the importance of support networks and finding ways to manage symptoms and improve quality of life. Managing POTS in daily life can be challenging and limiting, affecting education and career opportunitiesFinding specialized doctors who understand POTS is crucial for effective treatmentThere is a need for more accessible treatment options and resources for individuals with POTSIncreased research and awareness are necessary to improve understanding and support for POTS Chapters00:00 Introduction and Setting the Stage07:27 Navigating the Medical System: Finding the Right Doctors and Treatments14:31 The Impact of POTS on Families: Supporting Loved Ones32:08 Genetic Factors and Triggers for POTS40:51 The Impact of POTS on Daily Life48:19 Parental Advocacy and Navigating the Healthcare System

Dizzy Directors: Interview with Lauren & Tori's Moms

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SummaryIn this episode of Dizzy Directors, Tori&#39;s boyfriend Jacob joins the conversation to share his firsthand experience of witnessing Tori&#39;s episodes of POTS flare-ups. They discuss how they met, the embarrassing moments, and the challenges of dealing with POTS in their relationship. They also talk about the difficulties of getting proper medical care and the need to advocate for themselves. They share stories of episodes happening on set during film productions and how they navigate those situations. Overall, the conversation highlights the importance of support and understanding in managing POTS. In this conversation, Lauren and Tori discuss various topics including their experiences with health issues, the challenges they face in daily life, and the unique aspects of living in different regions. They also touch on the presence of horses on their college campuses and share anecdotes about unusual incidents that have occurred at their schools.Takeaways<ul><li>Having a supportive partner who understands and witnesses your POTS episodes can make a big difference in managing the condition.</li><li>Medical gaslighting and the need to advocate for oneself are common challenges faced by individuals with POTS.</li><li>Episodes of POTS can happen at any time and in any setting, including on film sets.</li><li>Open communication and educating others about POTS can help create a supportive environment.</li><li>Proper medical care and access to IV fluids are essential in managing POTS flare-ups. Living with chronic health issues can be challenging and inconvenient</li><li>Having a support system of understanding friends and family is important</li><li>Regional differences can impact daily life experiences</li><li>Unusual incidents can occur at college campuses</li><li>Finding remote internships can be beneficial for individuals with health issues</li></ul>Chapters 00:00 Introduction and Background06:04 Experiencing POTS Episodes on Film Sets12:08 Dealing with Medical Gaslighting and Advocating for Care29:22 Experiences with Health Issues39:31 Unusual Incidents at College Campuses53:53 Regional Differences and Daily Life Experiences

Dizzy Directors: Interview with Jacob

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SummaryIn this episode of Dizzy Directors, Rey shares their experience living with POTS (Postural Orthostatic Tachycardia Syndrome) and how it has affected their life in college. They discuss their journey of self-discovery and the challenges they faced in getting diagnosed with various conditions. They also talk about the frustrations of navigating the medical system and the lack of understanding and support from some healthcare professionals. Rey emphasizes the importance of self-advocacy, self-care, and finding a supportive community of friends who understand their experiences. Takeaways <ul><li>Living with POTS can be challenging and often involves navigating a complex medical system.</li><li>Self-advocacy and self-care are crucial for managing chronic illnesses like POTS.</li><li>Finding a supportive community of friends who understand your experiences can provide valuable support.</li><li>The medical system can be frustrating and may involve medical gaslighting, but it&#39;s important to persist in seeking proper diagnosis and treatment.</li></ul> Chapters 00:00 Introduction and Disclaimer00:49 Ray&#39;s Experience with POTS and College05:23 Challenges in Getting Diagnosed and Internalized Ableism07:48 Frustrations with the Medical System09:42 Different Experiences with POTS Diagnosis11:35 Dealing with Medical Gaslighting16:07 Navigating College and Disability Services25:01 Managing Temperature Control and Accommodations28:45 Connecting with Others with POTS32:31 Sharing Experiences and Building Supportive Friendships38:09 Overcoming Internalized Ableism39:43 Balancing Treatment Options and Challenges43:57 Advice for Those with POTS or Chronic Illness45:30 Conclusion

Dizzy Directors: Interview with Rey

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SummaryDr. Bianca Miret, a chiropractic neurologist and functional medicine practitioner, discusses her approach to treating POTS and dysautonomia. She explains the role of the vagus nerve and the interconnectedness of various systems in the body. Dr. Miret emphasizes the importance of a personalized treatment approach and addresses common symptoms of dysautonomia. She also discusses the prevalence of POTS in men and women and the challenges of getting a proper diagnosis. Additionally, she highlights the significance of lifestyle changes in managing POTS and dysautonomia. In this conversation, Dr.Bianca Miret discusses individualized treatment for dysautonomia, emphasizing the importance of personalized recommendations. She explains the connection between blood sugar fluctuations and the stress response in dysautonomia patients. Dr. Miret also highlights the significance of balancing blood sugar and meal frequency, as well as maintaining a healthy circadian rhythm. She addresses the misconception that POTS is solely a cardiac condition and emphasizes its neurological nature. Dr. Miret advocates for increased awareness of dysautonomia and the need for collaboration between the functional and medical communities in healthcare. She also discusses the potential future advancements in understanding the genetic component of dysautonomia and preventive measures.Takeaways<ul><li>Chiropractic neurology and functional medicine can be effective in treating POTS and dysautonomia.</li><li>The vagus nerve plays a crucial role in dysautonomia and can be targeted for treatment.</li><li>Symptoms of dysautonomia can vary and may include dizziness, unexplained anxiety, gut dysfunction, and sleep disturbances.</li><li>POTS is more prevalent in women, but men can also be affected.</li><li>A personalized approach to treatment is necessary, considering the individual&#39;s specific symptoms and underlying dysfunctions.</li><li>Lifestyle changes, such as adjusting water and electrolyte intake, can be beneficial in managing POTS and dysautonomia. Dysautonomia treatment should be individualized and tailored to each patient&#39;s specific needs.</li><li>Balancing blood sugar and meal frequency is crucial for dysautonomia patients.</li><li>Maintaining a healthy circadian rhythm can help stabilize cortisol levels and improve energy throughout the day.</li><li>Dysautonomia is a neurological condition that involves dysfunction in the brain&#39;s communication with the heart and other systems.</li><li>Increased awareness and collaboration between the functional and medical communities are needed to improve dysautonomia diagnosis and treatment.</li></ul>Chapters 00:00 Introduction and Explanation of Chiropractic Neurology02:15 Overview of Carolina Functional Neurology Center03:15 Treatment Approach for POTS and Dysautonomia05:56 Prevalence of POTS in Men and Women09:50 Common Symptoms of Dysautonomia15:35 The Role of the Vagus Nerve in Dysautonomia25:17 Key Lifestyle Changes for POTS and Dysautonomia26:21 Individualized Treatment for Dysautonomia27:38 The Importance of Personalized Recommendations28:07 Blood Sugar Fluctuations and Stress Response29:28 Balancing Blood Sugar and Meal Frequency30:45 Circadian Rhythm and Cortisol31:17 Treating the Whole Person33:01 POTS as a Neurological Issue36:32 Increasing Awareness of Dysautonomia39:35 Medical Gaslighting and Misdiagnosis42:16 Recognizing Early Signs of Illness45:52 The Future of Medicine

Interview with Dr. Bianca Miret

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SummaryIn this episode, Lauren Clark discusses the impact of POTS (Postural Orthostatic Tachycardia Syndrome) on women during their menstrual cycles. She shares advice and research findings on managing POTS symptoms during menstruation, including the importance of salt intake, hydration, and self-care. Lauren also explores the connection between lightheadedness and POTS, as well as the potential for abnormal menstrual cycles in individuals with POTS. She emphasizes the need to track symptoms and seek medical advice. The episode concludes with a discussion on preventing POTS flares and the importance of understanding and managing POTS symptoms.Takeaways<ul><li>Managing POTS symptoms during menstruation requires attention to salt intake, hydration, and self-care.</li></ul> <ul><li>Lightheadedness is a common symptom of POTS, and it can be more pronounced during menstruation.</li></ul> <ul><li>Individuals with POTS may experience abnormal menstrual cycles, and tracking symptoms is important for understanding the condition.</li></ul> <ul><li>Preventing POTS flares involves getting rest, staying hydrated, and following medical advice.</li></ul>Chapters 00:00 Introduction to the Topic00:56 Managing POTS Symptoms during Menstruation05:47 Abnormal Cycles and POTS07:42 Symptoms of POTS and Menstruation09:41 Preventing POTS Flares10:40 Research on POTS and Menstruation13:06 Characteristic Symptoms of POTS14:35 Living with POTS and Menstruation15:33 Upcoming Episodes and Conclusion

Dizzy Directors: Talking about Menstruation Cycles!

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SummaryIn this episode, hosts Lauren and Tori introduce themselves and their podcast, Dizzy Directors, where they discuss POTS (Postural Orthostatic Tachycardia Syndrome) and dysautonomia. They share their personal experiences with POTS and how it has impacted their lives as filmmakers. The conversation covers topics such as misdiagnosis, symptoms, medications, challenges in daily life, and the support they receive from professors and accommodations. They also discuss the importance of raising awareness about POTS and using filmmaking as a platform to share their stories and help others. This conversation explores the topic of POTS (Postural Orthostatic Tachycardia Syndrome) and its impact on the lives of individuals. The conversation covers various aspects of POTS, including symptoms, heart rate fluctuations, blood pressure, managing episodes, and the challenges faced by individuals with POTS. The conversation also delves into the effects of temperature on POTS symptoms and the importance of support from friends and family. The hosts discuss the origin of the name &#39;Dizzy Directors&#39; and how POTS can affect creativity as a director. They also touch on the challenges of student filmmaking and the need for understanding and flexibility in the industry. TakeawaysPOTS is a medical condition that affects the autonomic nervous system and can cause a range of symptoms such as dizziness, fatigue, and heart palpitations.Misdiagnosis and delayed diagnosis are common with POTS, and it can take time to find the right treatment and management strategies.Living with POTS can present challenges in daily life, including difficulties with physical exertion, social interactions, and managing symptoms.Supportive professors and accommodations can make a significant difference for individuals with POTS who are pursuing careers in filmmaking or other demanding fields.Raising awareness about POTS and sharing personal experiences through platforms like filmmaking can help educate others and provide support to those living with the condition. POTS is a condition characterized by symptoms such as dizziness, high heart rate, and blood pressure fluctuations.Individuals with POTS may experience different variations of the condition, including seizures and fainting.Managing POTS episodes involves staying hydrated, consuming salt, and taking prescribed medications.Supportive reactions from friends and family during POTS episodes can be helpful, while panicking or overreacting can worsen the situation.Temperature fluctuations can significantly impact POTS symptoms, with individuals experiencing both heat intolerance and cold sensitivity.Directing with POTS can be challenging due to the physical and mental demands of the role, as well as the unpredictable nature of the condition.Student filmmaking presents additional challenges, such as unreliable crew members and limited resources.Balancing work and health as a director with POTS requires understanding and flexibility from both the individual and their team. Chapters 00:00 Introduction to Dizzy Directors01:13 Understanding POTS and Dysautonomia03:20 Personal Experiences with POTS06:27 Misdiagnosis and Medical Journey08:19 Challenges and Symptoms of POTS10:05 Medications and Treatment Options12:34 Impact on Daily Life and Social Interactions21:13 Supportive Professors and Accommodations25:10 Using Filmmaking to Raise Awareness27:36 Q&amp;A: Explaining POTS and Personal Experiences28:15 Understanding POTS29:07 Symptoms and Variations of POTS30:03 Heart Rate and POTS31:12 Effects of POTS on Daily Life32:15 Chronic Nature of POTS33:05 Genetic Testing for POTS34:13 Diagnosing POTS35:13 Blood Pressure and POTS36:21 Managing POTS Episodes37:32 Supportive Reactions to POTS Episodes38:46 What Others Should Know About POTS39:21 Managing POTS with Salt and Water40:06 Safety Precautions During POTS Episodes42:35 Temperature and POTS47:42 Origin of the Name &#39;Dizzy Directors&#39;48:56 Impact of POTS on Creativity as a Director52:39 Challenges of Directing with POTS58:31 Challenges of Student Filmmaking01:00:48 Balancing Work and Health as a Director01:01:04 Conclusion

Dizzy Directors Intro Episode

"Dizzy Directors" is a refreshing take on the world of pots (Postural Orthostastic Tachycardia Syndrome), brought to you by two passionate college students who have POTS and also happen to be filmmakers. POTS is a condition causing a rapid increase in heart rate upon standing, leading to symptoms like dizziness, lightheadedness, and fatigue.

Join our dynamic hosts as they combine their love for storytelling with their curiosity about pots, delivering a podcast that is both informative and entertaining. Through their unique perspective, they explore the intricate world of pots, sharing their discoveries, insights, and even their filmmaking experiences along the way. Whether you're a fellow pots enthusiast or simply intrigued by their youthful energy and creativity, "Dizzy Directors" promises to be a delightful journey into the fascinating realm of pots.

Tune in and join our hosts as they bring pots to life through the lens of filmmaking!