Pudendal Neuralgia Patient Association

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The Pudendal Neuralgia Association, Inc. was established in 2013 as a non-profit organization. We provide educational services to pudendal neuralgia patients. Our mission is to provide educational services to medical personnel and those affected by pudendal neuralgia and their families through conferences, meetings, workshops, pamphlets, and online information. www.pudendalassociation.org

ICO

461285242

Facebook

1800

X (Twitter)

250

Address

Brockton

Address: 22 Bernard Cir, BrocktonWeb: Sign in to see organisation websiteFacebook: Pudendal-Neuralgia-Association-Inc-504820026251424X (Twitter): PNAssociationICO: 461285242

Pudendal Neuralgia Association, Inc. Upcoming events Registration link httpsus06web. zoom. usmeetingregisterMMa1u6QsTmu8bb5sGbIQ Complete meeting invitation You are invited to a Zoom meeting. When Mar 26 2025 0700 PM Eastern Time US and Canada Register in advance for this meeting httpsus06web.

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Pudendal Neuralgia Patient Association

Please come join us.

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Lucy

Looking forward to the upcoming support group! It's so important to connect with others who understand what we're going through. Let’s keep spreading the word! 🌟✨

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Eva

So grateful for organizations like the Pudendal Neuralgia Patient Association that are spreading awareness and providing support for those in need! 💙🙏

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Michelle

What strategies can be implemented to improve the outreach and accessibility of educational resources for pudendal neuralgia patients and their families?

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Hannah

How can collaboration with healthcare providers enhance the understanding and treatment of pudendal neuralgia within the medical community?

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