SomnusNooze e-newsletter
News, stories and updates from the world of sleep
News, stories and updates from the world of sleep
The 2021 Sleep/Wake Cyclers was the first grassroots fundraising campaign sponsored by the Hypersomnia Foundation designed specifically to raise money for research. Interest in conducting research into the causes of idiopathic hypersomnia and narcolepsy... read >
Are you a parent who has IH or narcolepsy, or are you thinking of becoming one? Do your hypersomnia medications interact with your hormonal birth control or hormone replacement therapy? Are you a healthcare provider caring for people with hypersomnias? If... read >
Insurance coverage is a major concern for people with chronic disease. Will health insurance appropriately cover doctor appointments, tests and treatments? If insurance doesn’t cover certain prescription medications, how can they be accessed for the... read >
The Hypersomnia Foundation announced its Diversity, Equity and Inclusion (DEI) Task Force last week on social media. This group of volunteers and HF Board Members are working to understand and identify the challenges people of diverse backgrounds may... read >
Having idiopathic hypersomnia (IH) or a related sleep disorder can be incredibly stressful for both person(s) who have a hypersomnia (PWH) and their supporters. We’ve just launched a new web page providing Tips for Supporters, which were developed by... read >
Start talking to someone with a hypersomnia about how hard it can be to stay awake all day, and soon enough we’ll be telling stories about napping in our cars. Many of us have our favorite napping spots and strategies. We also have concerns—are we... read >
The Hypersomnia Foundation community is forming a bike team, the Sleep/Wake Cyclers, to raise money for research on idiopathic hypersomnia and related sleep disorders. Our inaugural ride will be Saturday, June 12, 2021! We need riders! All ages... read >
In the spring of 2020, as the Covid-19 lockdowns began, we at the HF counted ourselves very fortunate that the Foundation has always minimized operating costs by working remotely and relying on a volunteer Board. Still, we lamented cancelling our... read >
The work of any rare disease organization naturally relies on community support, and this year—more than ever—you can help determine what the Hypersomnia Foundation can accomplish in 2021 by making a donation to HF today. Tony and Bertha Rye have... read >
The Hypersomnia Foundation has long felt that welcoming everyone, regardless of ethnicity, gender, religion, or any other demographic, is essential to who we are, and must be incorporated into our efforts to raise awareness and reach undiagnosed patients.... read >