What’s the SOCIAL experience of living with narcolepsy?
Your social life experiences with narcolepsy matter!
I’m excited to share a new survey that Project Sleep is conducting to better understand the social experiences and unmet needs of people living with narcolepsy and idiopathic hypersomnia.
This survey is for individuals diagnosed with narcolepsy or idiopathic hypersomnia (18+ years old). It should take about 10-15 minutes, and your responses are anonymous. International respondents are welcome! Take the survey by the deadline of Sunday, April 11, 2021.
Can supporters or family members of people with narcolepsy take the survey?
While we highly value the perspectives of the amazing supporters and family members in our community, this particular survey is for those diagnosed themselves. Thank you for understanding and please help us spread the word.
Improving social support for narcolepsy!
This survey is being conducted by Project Sleep, a 501(c)(3) non-profit organization dedicated to raising awareness about sleep health and sleep disorders. Your responses will help Project Sleep to better address unmet community needs in the future. Tell us what matters to YOU by taking the survey today.
The social aspects of life with narcolepsy may be invisible, but are still real! Share your input.
To collect a wide variety of perspectives, please share this opportunity with your contacts and communities. Deadline to participate is quickly approaching: Sunday, April 11, 2021.
Thank you for your invaluable support and input!
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