Project Lyme is a leading Lyme and tick-borne disease nonprofit dedicated to conquering Lyme through research and education. Project Lyme has awarded over $1.7 million for Lyme and tick-borne disease research to date. Their funded projects have led to unprecedented advances in prevention, diagnosis and treatment of tick-borne illness.
We are thrilled to present Sweat for a Cause, benefiting Project Lyme on Sunday, February 4th in Manhattan.
Kim Strother will join us to lead one of her signature workouts (you may know her from Instagram, and the Melissa Wood Health app!) Amanda Tiberi of Amanda Nova will lead a Kundalini meditation and Cindy Luffred of Revealing Soul will use aura photography to capture your energy field and through her intuitive senses, help you understand the meaning behind the photograph.
This workout is accessible to all levels of fitness. If you are unable to join us for the workout portion, please join us for meditation, aura photography and socializing!
Guests will have the chance to mingle and connect over their shared journey post workout and meditation. Light bites and refreshments will be provided by Kitchen Remedy.
Tickets are limited and first come, first serve. The first 25 ticket holders will receive a gift bag. Please bring your own yoga mat for the workout portion of the event!
If you are interested in sponsoring Sweat for a Cause , please send a note to info@amorescopr.com.
Connect with Kim Strother: https://www.instagram.com/kimstrother/
Connect with Amanda Tiberi: https://www.instagram.com/amandanovawellness/
Connect with Cindy Luffred: https://www.instagram.com/revealingsoul/
This event is sponsored by TiCK MiTT and Moresco Public Relations and Communications.
December 23, 2024
MAL meet-ups occur a couple of times a month and are geared towards mothers raising children with Lyme, or mothers with Lyme themselves. It serves as a support group where you will discuss a common theme each meeting, share stories of your own struggle caused by Lyme, as well as hear advice from other mothers going through the same things as you. Join us by registering through the webpage!
November 20, 2024
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.
November 19, 2024
Illness invalidation, by medical professionals or others, is a common experience for patients with Lyme disease. This talk will discuss recent scientific articles in Lyme and other illnesses about the patient effects of invalidation. It will also discuss the gendered history of invalidation and how it influences the medical encounter today.
