by vcc | Mar 2, 2022 | KLS in the Media
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...
by vcc | Jan 12, 2015 | Uncategorized, Videos
Great video from our friend Mat Sherman, what a great attitude and a powerful reminder for all of us! For more videos from Mat and his experiences with KLS, check out his YouTube page, and don’t forget to subscribe. Thanks for letting us share the video Mat!...
