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Celebrating Inaugural World Narcolepsy Day
Hanes Women's 100% Cotton T-shirt
- Sizes S - XXXL
- View Sizing Guide
About this campaign
By supporting this fundraiser, you will help Project Sleep to advance our advocacy and awareness efforts year-round.
Learn more about our BOLD GOALS to raise awareness of narcolepsy, reduce delays to diagnosis, and reduce stigma for people living with narcolepsy. Thank you for your support!
IMPORTANT: Orders within the U.S. should arrive by Friday, Sept. 20, but are not 100% guaranteed. Orders outside of the U.S. will take longer and will NOT arrive in time for World Narcolepsy Day on Sept. 22, 2019. We apologize about this, and hope to do better next year. Thanks for your patience and understanding. <3
World Narcolepsy Day (Sept. 22, 2019) is a day dedicated to raising awareness of narcolepsy on a global scale. Established by 24 patient advocacy organizations across 6 continents, #WorldNarcolepsyDay unites the international narcolepsy community to inspire action, increase public knowledge, and elevate the voices of the 3 million people living with narcolepsy worldwide. Learn more: https://project-sleep.com/worldnarcolepsyday/
Project Sleep is a a 501(c)(3) non-profit dedicated to improving lives by raising awareness about sleep health and sleep disorders. Project Sleep proudly collaborated with 23 additional patient advocacy organizations around the world to establish the inaugural World Narcolepsy Day for Sept 22, 2019! Learn more: https://project-sleep.com/
Break down stigma. Wear your shirt with pride. We are not alone!
Comments
Share Why You Support "Celebrating Inaugural World Narcolepsy Day"
Supporters
16 years into my diagnosis, and this condition is still a mystery in many ways. But the ongoing research into genetic factors and autoimmune effects have helped in the journey.
Because I know what it's like to have Narcolepsy!
To support Julie’s hard work. I am forever grateful to know you and be involved with narcolepsy awareness/advocacy!
❤️
I have narcolepsy and understand the need for awareness, advocacy and research. We need to speak up and tell the world what we’ve lost to this disease. Scientific research/findings give us new treatment options and hope of a normal life.
For Kari Wright