Guest blogger Lisa Peabody is a volunteer advocate with the National Brain Tumor Society. Recently, she joined National Brain Tumor Society staff participating in the annual Alliance for Childhood Cancer Action Day.
The first Sunday of each month brain tumor survivors, patients, family, and caregivers use Twitter to share experiences, ideas, and information. The Brain Tumor Social Media chat (#btsm) was started a little over a year ago by Liz Salmi. The chats are moderated by Liz and Catherine Blotner and is promoted as a “patient-run Twitter [...]
National Brain Tumor Society is one of many disease-based organizations to join the chorus of supporters of stronger funding for the National Institutes of Health (NIH). The agency – through the National Cancer Institute (NCI) and other institutes – is the largest funder of brain tumor research in the country. Dwindling investment in this agency [...]