Erythromelalgia-Erythermalgia Association

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The Erythromelalgia Association is a non-profit organization dedicated to increasing awareness of the symptoms and treatments for this rare disease among health care practitioners and the general public; providing emotional support and educational services for people with erythromelalgia, and raising money to help fund research to find a cure.

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911950872

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The Erythromelalgia Association | Information, Research, Support Live Empowered. About Learn More Resources Learn More Support Learn More TEAs mission is to empower all those affected by EM to improve their quality of life. Take TEAs A Patients Guide to Erythromelalgia with you to your next doctor visit. The Patient Guide is a booklet covering all aspects of EM symptoms diagnosis treatment daily coping tips and more.

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Robin

💖 Thank you for the incredible work you do to raise awareness for Erythromelalgia! It's inspiring to see a community come together to support those affected by this rare condition. Every little bit helps in empowering patients and their families! 🌟

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Paul

1. What strategies can individuals with Erythromelalgia use to effectively communicate their symptoms and needs to healthcare providers during appointments?

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Deborah

2. How can community support groups for Erythromelalgia patients create a safe space for sharing coping strategies and emotional experiences?

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Patricia

🌈 I'm so grateful for the resources provided by the Erythromelalgia Association! The Patient Guide is essential for anyone dealing with EM, and it’s a fantastic tool for navigating this challenging journey. Keep spreading the word! 🙌

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