NEWS RELEASE: Kleine-Levin Syndrome Foundation Urges Lawmakers to Bring National Awareness to KLS research Foundation Honors KLS community on Rare Disease Day by lobbying for inclusion in NIH Sleep Research Plan Feb. 28, 2022 – WASHINGTON: The Kleine-Levin Syndrome Foundation today honors Rare Disease Day by calling for the inclusion of Kleine-Levin Syndrome (KLS) in […]
