PARTNERSHIP FOR TICK-BORNE DISEASES EDUCATION

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Partnership for Tick-Borne Diseases Education's (PTDE) mission is to provide online and in-person educational content and materials on tick-borne diseases that can be acquired in the United States. PTDE develops resources that discuss the scientific and clinical evidence for a variety of learners, with content specific to the needs of individual medical professional groups and the general public. PTDE believes that a common understanding of the evidence will encourage the development and use of effective disease prevention programs and foster communication between patients and healthcare professionals that will lead to innovative approaches for diagnosing and managing tick-borne illnesses.

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Address: 25611 W Comfort Dr, WyomingWeb: Sign in to see organisation websiteICO: 474549381

Partnership for Tick-borne Diseases Education Welcome PTDE is renovating this site to better meet our mission. Please check back in late fall to see what weve accomplished. Partnership for Tickborne Diseases Education is a nonprofit 501c3 corporation dedicated to providing educational learning and materials about tickborne diseases based on scientific research. Our mission is to prevent Lyme and other tickborne diseases and to diminish the longterm consequences patients with these infections often face.

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Benjamin

- What strategies can we implement to effectively reach underserved communities with educational materials on tick-borne diseases?

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Helen

So excited to see the updates on your site! The work you’re doing is so important for raising awareness about tick-borne diseases. Can’t wait to share your materials with my friends! 🌱💚

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Ivy

- How can we leverage social media to raise awareness about tick-borne diseases and promote preventive measures among the general public?

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Lily

Kudos to PTDE for committing to such a crucial mission! Your efforts to educate the public on Lyme and other tick-borne diseases will make a huge difference. Looking forward to the new resources! 🎉📚

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Wyoming

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The aim of the Karl McManus Foundation is to erode the barriers to the recognition and treatment of Borreliosis, especially neuroborreliosis, in Australia and to contribute to knowledge in the world about borreliosis and other tick-borne infections.

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The aim of the Karl McManus Foundation is to erode the barriers to the recognition and treatment of Borreliosis, especially neuroborreliosis, in Australia and to contribute to knowledge in the world about borreliosis and other tick-borne infections.

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