Lyme Disease Resource Center, Inc. of Northampton, MA

Lyme Disease Resource Center, Inc. of Northampton, MA Lyme Disease Resource Center, Inc. is an all-volunteer, community-based 501(c)(3) organization founded in 2013.

The Lyme Disease Resource Center’s Vision is:

“…to provide clients and care partners with tick-borne disease a place to find guidance and emotional support on a path to wellness”

“…to educate the community by providing: material, forums and workshops on the issues surrounding tick-borne disease.”

“…to advocate for better education, knowledge, treatment and awareness of tick-borne diseases.”

“…to connect tick-borne disease support and educational groups across Massachusetts and beyond.”

06/24/2026
06/21/2026

Recently, several news outlets have reported on the case of John Reagan, a 66‑year‑old retired New Hampshire man who developed severe Powassan virus

06/19/2026

By Joel Zelkowitz, Esq. The spring 2026 tick season has been alarming across New York, New Jersey, Connecticut, and the surrounding northeast region. For

06/16/2026

If you’ve been living with a chronic condition for months or even years, you may find yourself asking a frustrating question: How am I still struggling with this? You’ve seen doctors, followed treatment plans, tried medications, and made lifestyle changes, yet symptoms persist, progress feels slow, and daily life can still feel overwhelming.

Chronic illness can be physically and emotionally exhausting, but you don’t have to navigate it by yourself. Pathway Patient Advocates is here to help you make sense of your care, ask the right questions, and move forward with greater clarity and confidence. If you’re wondering why you’re still struggling, it may be time for extra support because your healthcare journey deserves guidance, compassion, and a clear path forward.

Learn more about how we can help at https://gnanow.org/blogs/how-am-i-still-struggling-with-my-chronic-condition.html

📞 Need help? Call us at (947) 517-8395
🌐 www.PathwayPA.com

06/15/2026

✨ ADVOCACY WIN FOR THE LYME COMMUNITY ✨

There’s encouraging news from Washington, D.C., this week: Thanks to the tireless efforts of our advocacy partner, the Center for Lyme Action, our fellow Lyme organizations, and patient advocates like you, the House Appropriations Committee has approved significant funding increases for Lyme disease, alpha-gal syndrome, and other tick-borne disease programs.

Highlights include:

✔️ +$10M for NIH Lyme and tick-borne disease research
✔️ +$1M for CDC Lyme disease programs
✔️ +$1M for CDC vector-borne disease programs
✔️ $5M for LymeX innovation initiatives

The bill also includes important report language that helps ensure federal agencies continue prioritizing Lyme and tick-borne disease research, surveillance, and patient needs.

While there is still work ahead before these investments become law, this is a significant step forward—and a powerful reminder that advocacy works.

Thank you to every patient, caregiver, clinician, researcher, advocate, and supporter who has helped make progress like this possible. Together, our voices are being heard.

We’ll continue to keep you updated as the appropriations process moves forward.

For more information on how Project Lyme is making an impact, check out our website: https://projectlyme.org/our-impact/

Center for Lyme Action

Our friends at A Place To Go are hosting an in person support group this Friday:💚💚💚
06/10/2026

Our friends at A Place To Go are hosting an in person support group this Friday:

💚💚💚

06/07/2026

Address

37 Bridge Street #171
Northampton, MA
01061

Telephone

+14135887388

Website

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