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.
It’s not easy to go through tick-borne diseases. Everyone’s experience is different, and it’s important to understand that each experience is real and meaningful.
Feeling, expressing, or showing gratitude can be both healing and challenging for people living with tick-borne diseases.
As a supporter of a Lyme or tick-borne disease patient, you may not be able to cure a condition or make symptoms disappear, but you can help them cope.
Showing respect is a meaningful and essential way for supporters to help people living with tick-borne diseases.
You may find yourself encouraging your loved one with Lyme to prioritize their self-care. It's important to remember your own, too.
Supporters of tick-borne disease patients often want to appear strong, capable, and unwavering in their commitment to help.
If you can genuinely listen to your loved one, you will show the compassion Lyme patients deeply need and appreciate.
The topic of pride gives all of us at Generation Lyme an opportunity to celebrate members of the LGBTQIA+ community.
When someone you care about is living with Lyme disease, community becomes more important than ever.
As a supporter of someone living with Lyme, it may seem like you're constantly adapting to new boundaries.
Even if you're not the one physically fighting Lyme, it can still directly affect your life story.
When someone you care about changes their behavior, it can feel like you need to make a big adjustment, too.
Your support and willingness to reflect are valuable as the person in your life processes the changes that can occur while living with Lyme disease.
Change can be a loaded word, interpreted as positive or negative. Lyme disease inevitably brings some of both kinds of change for the one living with it and those who support them.
It isn't just the person healing from Lyme who has to figure out which things can and cannot be controlled with this disease.
We know caregiving can be challenging. It's okay to make mistakes, and it's okay to be compassionate with yourself when you do.
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.
When someone needs help (and you want to help them), asking questions may not necessarily seem like the most efficient thing to do in the moment.
When supporting someone dealing with an illness, it can be challenging to find the right words.
Gen Lyme News & Blogs
Updates, announcements, events, and other news from Generation Lyme and our community.
Signed into law on September 30, 2026, this legislation builds on the original 2019 law named after the late Senator Kay Hagan of North Carolina.
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.
Progress moves slowly—but during Lyme Disease Awareness Month 2021, we took a leap forward.
Project Lyme and Generation Lyme are spreading the word about Lyme disease to express the urgency patients experience in their pursuit of help.
Setting boundaries around gift-giving is a great way to avoid awkward moments and understand each other better.