Sue Payne: From Sudden Voice Disorder Diagnosis to An Advocate Voice With Dysphonia International

In this episode of the Second Chance Queen podcast, Kristianna Mrjenovich interviews Sue Payne, a member of the board of directors for Dysphonia International. Sue shares her journey with spasmodic dysphonia, a neurological voice disorder that has significantly impacted her life. The conversation delves into the challenges of living with a voice disorder, the importance of mental health support, and the power of community and advocacy. Sue emphasizes the need for awareness and understanding of dysphonia, highlighting the emotional toll it can take and the resilience required to navigate such challenges. The episode concludes with a call to action for listeners to support Dysphonia International and to foster compassion and understanding in their communities.

• Sue Payne's journey with spasmodic dysphonia began unexpectedly in 2017.
• Mental health support is crucial for those dealing with voice disorders.
• Community and support systems play a vital role in coping with challenges.
• Finding purpose through advocacy can help redefine one's identity.
• Chronic conditions can lead to feelings of grief and loss.
• Awareness and education about dysphonia are essential for understanding.
• Patience and grace are needed in interactions with those with voice disorders.
• Dysphonia International provides valuable resources and support for individuals.
• Resilience can be cultivated through shared experiences and support.
• It's important to recognize the emotional impact of invisible disabilities.