Wescoe Foundation for Pulmonary Fibrosis

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Learn about IPF. Talk about IPF. Raise awareness for IPF. The Wescoe Foundation for Pulmonary Fibrosis is a 501(c)(3) non-profit organization that provides education, support, resources and advocacy for patients living with Idiopathic Pulmonary Fibrosis (IPF) and their care partners in order to sustain the highest possible quality of life.

Founded

2009

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0

X (Twitter)

156

Address

Coopersburg

Address: 229 N. Main St., CoopersburgWeb: Sign in to see organisation websiteX (Twitter): wescoeforpfEmployees: 4Volunteers: 25Revenue: 196214ICO: 274464618

Wescoe Foundation for Pulmonary Fibrosis Wescoe Foundation for Pulmonary Fibrosis Our Mission The Wescoe Foundation for Pulmonary Fibrosis provides support education advocacy and resources for patients living with Idiopathic Pulmonary Fibrosis IPF as well as their care partners and families in order to sustain the highest possible quality of life. Our Vision To Unite the Pulmonary Fibrosis Community. Our Story Support Resources Events What is Idiopathic Pulmonary Fibrosis IPF. Pulmonary Fibrosis is the progressive scarring of the lungs that occurs when air sacs known as alveoli gradually become replaced by fibrotic tissue or scar tissue.

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News about from their social media (Facebook and X).

Victoria

👏 Amazing updates on the ongoing research for IPF! It's so encouraging to see progress being made. For anyone looking to learn more or get involved, check out the resources provided by the Wescoe Foundation. Every little bit helps! 💪❤️

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Christine

💙 Thank you, Wescoe Foundation, for your tireless efforts in raising awareness about IPF! Together, we can make a difference and support those affected by this condition. Let's continue to spread the word and provide hope! 🌟

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Mark

2. How can caregivers and families of those living with IPF be better supported through educational resources and advocacy initiatives provided by organizations like the Wescoe Foundation?

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Mark

1. What are some effective strategies to raise awareness about Idiopathic Pulmonary Fibrosis (IPF) within local communities, and how can we engage more people in these efforts?

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