Do you struggle with explaining your invisible illness to others? Do you wish there was a quick way to get the point across to family, friends and acquaintances? Or are you ready to become an advocate for myositis and want to enhance your elevator speech?
Join award-winning journalist, writer, and advocate Lindsay Guentzel for a powerful empowerment clinic that will help you harness the transformative power of storytelling. Diagnosed in 2023 with dermatomyositis associated with antisynthetase syndrome, Lindsay is now an active voice in the myositis community, using her expertise to raise awareness and inspire others.
In this session, Lindsay will teach you how to craft and deliver your personal story in 60 seconds or less—empowering you to connect, inspire, and make an impact. Learn how to channel your experiences and voice to advocate for yourself and others, and leave with the confidence to share your journey with purpose.
Whether the impact you want to make will be during Rare Disease Week advocacy on Capitol Hill with EveryLife Foundation at the end of February or simply being understand by those who know you in your every day life, this webinar is the perfect presentation.
