News and Blogs
For Lyme patients, effective rest is necessary and can take many forms; supporters play a critical role in helping us get it.
People living with Lyme need strong communication with supporters, which means being able to give and receive information in healthy and helpful ways.
Everyone living with Lyme or another tick-borne disease has a unique experience and a story that matters.
Blog for Supporters of People Living with Lyme and Other Tick-Borne Diseases
Generation Lyme's Supporters Blog helps parents, partners, caregivers, and other loved ones navigate their experiences supporting someone affected by Lyme and other tick-borne diseases.
Love Languages & Lyme Blog
Illness can change the ways we give, receive, and experience support. Love Languages & Lyme explored practical ways patients and supporters can navigate communication, connection, boundaries, and care when Lyme and other chronic illnesses affect everyday life.
If someone is trying to give you words of affirmation, is it okay to set a boundary around it? Absolutely!
Setting boundaries around quality time is essential when dealing with chronic illnesses like Lyme, whether you're the patient or someone supporting them.
Depending on health circumstances, it may not always be the ideal time to ask questions directly.
As a love language, physical touch may shift while living with an illness like Lyme disease.
Gen Lyme News & Blogs
Updates, announcements, events, and other news from Generation Lyme and our community.
Generation Lyme joins the LivLyme Foundation at the 6th annual LivLyme Summit for a talk about the importance of community.
Generation Lyme Co-Founders Jennifer, Brooke and Jesse recently sat down with Fred Diamond, host of the “Love, Hope, Lyme” podcast, for an emotional conversation about the power of community.
Presley Taylor is a passionate advocate for Lyme disease and Generation Lyme contributor sharing insights with patients, families, researchers, and anyone affected by this difficult condition.
Generation Lyme and Center for Lyme Action announce a new Community Partnership to leverage each nonprofit organization’s distinct resources to support current and future Lyme and tick-borne disease advocates.
We are thrilled to announce a milestone in our mission to empower Lyme disease patients and supporters everywhere: Generation Lyme has officially earned 501(c)3 nonprofit status.
For years, the CDC has been the backbone of a medical establishment that has denied the chronic symptoms of Lyme disease. This week, the CDC publicly changed that stance.
There was no holiday to celebrate the people of the Lyme disease community. So we created one.
Setting boundaries around gift-giving is a great way to avoid awkward moments and understand each other better.