A patient advocate realizes that perfect can become the enemy of good care for OSA patients who fail or refuse CPAP.| Sleep Review
For Immediate Release WASHINGTON, D.C. – March 12, 2025 – On March 18th, over 250 advocates... Read More The post Headache on the Hill 2025 to Bring Over 250 Advocates to Capitol Hill to Demand Action for Headache Disorders appeared first on AHDA.| AHDA
The stories of our advocates are the driving force behind what we do. We know that... Read More The post Headache on the Hill Patient Advocate Spotlights: New Daily Persistent Headache appeared first on AHDA.| AHDA
Narcolepsy Network is delighted to announce its 38th Annual Conference, taking place Friday, October 24 through Sunday, October 26, 2025, at the Royal Sonesta Minneapolis Downtown. For nearly 40 years, Narcolepsy Network’s Annual Conference has been the premier event for people living with narcolepsy or idiopathic hypersomnia (IH) and their supporters. The program is thoughtfully [...] The post Narcolepsy Network Announces its 38th Annual Conference appeared first on Sleep Education.| Sleep Education
Join Wake Up Narcolepsy for an insightful event that will foster collaboration and share professional and lived experiences.| Sleep Education
If you’re not managing your stress, your stress is managing you. Learn how to stop the stress cycle and feel like yourself again.| Emily Roach Health Coach
A holistic patient advocate looks at the root causes of illnesses. They support adjustments to nutrition, movement, and mindset. Independent health advocate| Emily Roach Health Coach
How Project Sleep is leading the charge for better sleep health - Patient Advocacy - Sleep Education has reliable information about sleep, sleep disorders, and treatment options with accurate medical and scientific insights.| Sleep Education
Breast cancer treatment isn’t one-size-fits-all. Personalized care is tailored to you. Learn more about tailored plans and treatment.| Susan G. Komen®
The outlook for the Huntington's community has never been brighter, Louise Vetter, president and CEO of the HDSA, said at the organization's annual convention.| Huntington's Disease News