Lung Cancer Patients/Survivors: Free Attendance to the World Conference 2015 in Denver, CO, Sept 6-9
WCLC 2015: Patient Advocacy Travel Awards
Application is now closed. Stay tuned for announcement of award winners in July 2015. The International Association for the Study of Lung Cancer (IASLC) has opened the application process for lung cancer patient advocates to apply for Advocacy Travel Awards. Awardees receive a travel stipend, free conference registration, up to four nights’ accommodations, and a free IASLC Membership for 2016. “For the World Conference on Lung Cancer in 2015, we hope to engage and receive more applications from other regions of the world, including Europe, Asia, the Middle East and Latin America. We know that the cost of travel can be a deterrent, and we hope these travel awards will encourage more survivors and patient advocates from around the world to apply” says Glenda Colburn, chair of the IASLC Patient Advocacy Committee and a Director at Lung Foundation Australia. Read More
Patient Resource Lung Cancer Guide
IASLC partnered with Patient Resource Publishing to produce the 2013 Patient Resource Lung Cancer Guide. This publication provides lung cancer patients and their loved ones with the details they need upon diagnosis. The guide is published in partnership with the International Association for the Study of Lung Cancer and all content has been thoroughly reviewed by medical experts who treat lung cancer patients. The information includes details regarding treatment options, staging & pathology, symptom & side effect management and the many advocacy and financial resources available. Information presented in Patient Resource Cancer Guide: Lung Cancer is not intended as a substitute for the advice given by your health care provider.
National Comprehensive Cancer Network® Resources for Patients
The National Comprehensive Cancer Network® (NCCN®) aims to provide people with cancer and the general public with state-of-the-art cancer treatment information in easy-to-understand language. The NCCN Guidelines for Patients®, translations of the NCCN clinical guidelines, are meant to help patients with cancer talk with their physicians about the best treatment options for their disease. They offer resources for non-small cell lung cancer, malignant pleural mesothelioma, and lung cancer screening. NCCN Guidelines for Patients® do not replace the expertise and clinical judgment of the physician.
Mesothelioma Applied® Research Foundation
The Mesothelioma Applied Research Foundation is the only 501(c)3 non-profit organization dedicated to eradicating mesothelioma and easing the suffering caused by this cancer. The Meso Foundation funds peer-reviewed mesothelioma research; provides patient support services and education; and advocates Congress for increased federal funding for mesothelioma research.
Some of the resources available through its patient support and education services include: one-on-one medical consultations; financial support for patients in need; support groups; conferences for patients and their families; brochures about mesothelioma; a clinical trials booklet; a peer support system.