Webinar – Education and Advocacy in ALS

In February this year, Dr. Emily Plowman prepared and presented data from her research in Amyotrophic Lateral Sclerosis to the ALS Association. Unlike some venues that are only accessible to a few, this presentation was in the form of a webinar, available for anyone to view here. This unique format is one of the ways in which Dr. Plowman is transparent about early findings in her research to support people with ALS, or PALS. The ALS Association has been an outstanding partner for Dr. Plowman’s research interests as they are committed to providing information to PALS and caregivers that may make meaningful differences in quality and quantity of life.

Past webinars by Dr. Plowman for the ALSA can be viewed at the above link as well as other presentations by other researchers working with ALS populations.