Based at Sanford Research, a nonprofit research institution, CoRDS is a centralized international patient registry for all rare diseases.
Join PWN4PWN and CoRDS to help generate awareness and more information on your Narcolepsy.
Ready to enjoy life?
Dive into our resources to find treatments, doctors, and others with Narcolepsy to know you’re not alone!
Our team host monthly and weekly events to bring you into our family.
Members
Patients/Parents/Partners welcome to not being alone! On the search for ways to stay awake or get better rest? We'll provide all information for free but please consider to support us for just $10 dollars a year and become a member! This includes your very own Patient Medical Information Card for those sudden cataplexy moments we’ve all experienced!
Doctors
Welcome! We honor all PCP, sleep specialists, psychiatrists, pulmonologists, or anyone just curious about how sleep affects their patients. We will provide live and recorded video sessions and the latest documents to keep you up to date on symptoms, treatments, and diagnostics that help your continuing education and allow you to be one of our NARCOLEPSY SUPERSTARS! Let's lower the average time for a narcolepsy diagnostic!
Sponsors
Where would we be without you? You keep us all up to date with the newest treatments, clinical trials, and patient assistance programs! Hosting events for newly diagnosed, and our doctors to help them know when the new treatments are coming out. Providing a platform for patient voices.
One thing we would like to share with all of our visitors is that hundreds if not thousands of patients per year are misdiagnosed for depression, sleep apnea (which can coincide), insomnia, and many other comorbidities that coincide with Narcolepsy. At PWN4PWN we give you a platform to learn from each other about your treatment, clinical trials, holistic option, and payment assistant programs.
Meet Our Sponsors
