event

Chairs
Ali Moresco is the founder of Moresco Public Relations + Communications. Once focusing on entertainment PR and talent relations, Moresco made a pivot to healthcare PR four years ago when her world was turned upside down by an undiagnosed illness. It took her two years and eight specialists to find a doctor that would eventually crack the case- multiple complex chronic diseases and tick-borne diseases. Fortunately, Moresco pulls her experience living with chronic disease and “professional patient” skills to provide clients with experience-backed communications strategies in building loyal, long-lasting relationships with both media and patient communities.

Olivia Abrams is the CEO and Co-Founder of TiCK MiTT, a non-toxic tick removal product for people and pets. Diagnosed with Lyme disease at 8 years old, Olivia is still discovering how the complexities of the disease relate to her own health. The experience has led her on a mission to reduce cases of tick-borne illnesses by teaching individuals the importance of safe tick protection.

Connect with Lyme

January 28, 2025

HHS Presents – The Role of Mold Toxicity in Patients With Lyme Disease with Neil Nathan, MD

The purpose of this meeting is to engage the public-patients, caregivers, and healthcare providers, in particular-in an educational and informative session on the challenges of tick-borne disease diagnosis, particularly in people of color, outdoor workers, members of the military, children, older adults, and during pregnancy. Presentations by clinicians and researchers will provide insights into these complex and multi-faceted topics. The session will also feature updates on promising new diagnostic technologies.

January 29, 2025

Meditation for Lyme Patients

This event will provide restorative mindfulness workshop designed specifically for Lyme disease patients. Through guided meditation, gentle breathing exercises, and grounding techniques, this event will provide tools to manage stress, improve focus, and enhance emotional well-being. Whether you're newly diagnosed or managing long-term symptoms, this supportive space encourages healing and connection. The event will be adapted to those with varying physical needs.

November 20, 2024

The Quiet Epidemic Film Presentation at the U.S. Capitol

The goal of this webinar is to teach patients how to effectively advocate for change on the Federal, State, and local levels of government. Our presenters will discuss multiple topics including but not limited to: ways to engage with political representatives through letter writing, proclamation requests, how to participate in the upcoming Center for Lyme Action Fly-In and how to advocate for change hyper-locally, such as planning 5k's, social media fundraisers.