Jaclyn Lanthier

Secretary of the Board at Lichen Sclerosus Support Network

Based in Canada

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Seniority

Manager

Department

General Business & Management

Location

Canada

Industry

Non-profit Organizations

Company size

3

Contact information

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Email

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j•••••••@lssupportnetwork.org

Phone

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Background

About Jaclyn Lanthier

As a dedicated Patient Advocate specializing in lichen sclerosus, vulvovaginal, and genitopelvic diseases, I bring a unique combination of medical insight and personal passion to my work. With extensive experience in research and collaboration with stakeholders in the fields of medicine and science, I strive to elevate patient voices and ensure their rights are prioritized. I am active in several ongoing LS research projects where I am either co-lead or patient representative and lead multiple knowledge translation and sharing efforts through The Lost Labia Chronicles and Lichen Sclerosus Support Network. My background in academia, knowledge translation, social media, and marketing allows me to effectively communicate complex medical information to diverse audiences, fostering awareness and understanding of these often misunderstood conditions. I excel in building relationships, presenting compelling narratives, and driving initiatives within non-profit organizations. Key strengths include: Strong Interpersonal Skills: I am adept at engaging with patients, healthcare professionals, and researchers to facilitate meaningful dialogue and collaboration to drive change. Project Management: With a keen eye for detail, I effectively manage multiple projects and timelines, ensuring that stakeholder needs are anticipated and met. Growth Mindset: I embrace challenges and continuously seek opportunities for personal and professional development, enhancing my ability to advocate effectively. Creative Resourcefulness: I thrive in dynamic environments, utilizing innovative approaches to problem-solving and content delivery. I am passionate about empowering patients and enhancing their quality of life through advocacy, education, and research, and support. Let’s connect to discuss how we can work together to advance patient rights and improve healthcare outcomes.

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