LYME DISEASE RESOURCE CENTER, Inc.
Lyme Disease Resource Center, Inc. is an all-volunteer, community-based 501(c)(3) organization founded in 2013. Our mission is to be a peer guided, supportive and safe place for those living with Lyme Disease and their care partners, sharing strategies and resources for living well.
Lyme Disease Resource Center, Inc.
The Lyme Disease Resource Center, Inc. is a nonprofit organization dedicated to providing support and resources to individuals affected by Lyme disease and other tick-borne illnesses, as well as their caregivers.
History
Founded in 2013 by Maria Malaguti, who contracted Lyme disease and co-infections in 1997, the organization is an all-volunteer, community-based 501(c)(3) entity. Malaguti's experience with chronic illness motivated her to create a supportive environment for those facing similar challenges[1][2].
Mission
The Lyme Disease Resource Center aims to be a peer-guided, supportive, and safe space for individuals affected by Lyme disease. It shares strategies and resources to enhance well-being and quality of life for both patients and their caregivers[1][5]. The organization advocates for improved education, knowledge, treatment, and awareness of tick-borne diseases[1].
Services
- Support Groups: Peer-led groups offer a safe environment for individuals and their caregivers to share experiences and support each other[2].
- Holistic Therapies: These are provided free of charge to clients and their care partners, focusing on holistic approaches to wellness[2].
- Peer Counseling: One-on-one counseling is available for personalized support[2].
- Educational Resources: The center provides educational materials, forums, and workshops to educate the community about tick-borne diseases[1][2].
Governance
The organization has a diverse board of directors, which includes members such as Alison Wisher, Maria Malaguti, Dr. J. Patrick O'Grady, Nellie Wilson, and Krista Nugent. The board ensures an inclusive recruitment process and practices ethical governance[3].
Impact
By offering free services and support, the Lyme Disease Resource Center addresses the needs of an underserved population affected by tick-borne illnesses. It plays a crucial role in promoting awareness and education about Lyme disease, which is increasingly prevalent due to climate change and tick population increases[1][3].
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Web
lymedrc.org
Address
Northampton
Lyme Disease Resource Center, Inc. – a path to wellness a path to wellness a path to wellness Our mission is to be a peer guided supportive and safe place for those living with Lyme Disease and their care partners sharing strategies and resources to living well. Lyme Disease Resource Center Inc. is an allvolunteer communitybased 501c3 organization founded in 2013. All of our services are FREE.
Data & Similar organisations
Together, we can make a real impact in communities around the world. Help us bring hope and support.
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Discussions
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What are some effective strategies for raising awareness about Lyme Disease within local communities, and how can NGOs like the Lyme Disease Resource Center enhance their outreach efforts?
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Brooklyn Simmons
2 days ago
Odpovědí v diskuzi
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How can the Lyme Disease Resource Center strengthen its volunteer recruitment efforts to ensure that it has the diverse skills needed to support its mission effectively?
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Brooklyn Simmons
2 days ago
Latest reviews
Together, we can make a real impact in communities around the world. Help us bring hope and support.
💚 Thank you, Lyme Disease Resource Center, for being a beacon of hope and support for those affected by Lyme disease! Your all-volunteer efforts make such a difference in our community. Together, we can raise awareness and help each other on the path to wellness. 🌿
Brooklyn Simmons
Product Manager
🌟 Every little contribution counts! Whether it's volunteering your time or making a small donation, let's all come together to support the incredible work that LDRC is doing for those battling Lyme disease. ❤️ #SupportLocal #LymeDiseaseAwareness
Brooklyn Simmons
Product Manager
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