News & Resources
Publications
Numerous studies supported by Three Lakes Foundation have been spotlighted in industry leading journals, publications, and at medical conferences. We invite you to dive into our work by exploring this collection of publications, scholarship, and features.
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PRESS RELEASES
The Latest News and Research
The Latest
News and Research
RECENT
Navigating a diagnosis of pulmonary fibrosis can be challenging, but it's not a journey you have to travel alone. There are many organizations that can help you find the resources and support you need. While we don't create these resources ourselves, we are here to connect you to partners and opportunities that can assist. We will continue to add to these resources as more become available.
Resources for Patients and Caregivers
Resources
for Patients
and Caregivers
The Erin Popovich Endowment is a charitable organization within the CHEST Foundation. Its vision is to provide patients with ILD the resources they need to face their diagnosis with courage and strength. The endowment was created by the family of Erin Popovich, who suffered from ILD. Seeing Erin live with ILD for 10 years taught the Popovich family exactly what other patients need to face this devastating diagnosis with dignity and strength. The endowment focuses on three principle goals: access to resources and information; empowerment to improve patient independence and support; and research to enhance physician understanding of the disease and therapies.
To speak to someone at the foundation, email: chestfoundation@chestnet.org
The Erin Popovich Endowment
PF Warriors is an all-volunteer organization that serves a global community of PF/ILD patients and their families. PF Warriors believes in the power of peer-to-peer support. Members know what it’s like to wake up every day with lung disease and struggle to live with the “new normal” life. For patients diagnosed with PF/ILD, members of PF Warriors are available to answer questions, lend an ear to listen and a shoulder to lean on. PF Warriors hold monthly presentations from physicians and other medical professionals, which cover topics as diverse as boosting the immune system and infection control to current clinical research trials, lung transplantation and pulmonary rehabilitation.
To reach PF Warriors, call 214-444-8425 or email support@pfwarrior.com
PF Warriors
The Pulmonary Fibrosis Foundation (PFF) mobilizes people and resources to provide access to high quality care and leads research for a cure so people with PF can live longer, healthier lives .For those living with PF, obtaining the most accurate and current information can be a challenging and frustrating task. That’s why PFF launched the PFF Help Center, which provides patients, caregivers, and healthcare providers with the most up-to-date medical information, support services, and information about other essential resources.
To speak with the PFF Help Center Staff, call 844-825-5733 or email help@pulmonaryfibrosis.org.
Pulmonary Fibrosis Foundation
Information for
Patients & Caregivers
Navigating a diagnosis of pulmonary fibrosis can be challenging, but it's not a journey you have to travel alone. There are many organizations that can help you find the resources and support you need. While we don't create these resources ourselves, we are here to connect you to partners and opportunities that can assist. We will continue to add to these resources as more become available.
RESOURCES