This is our virtual bulletin board for Peggy Chun's Peg's Legs caregivers, family, friends, and fans. Peggy was an artist living with Amyotrophic Lateral Sclerosis (ALS). She lived for over six years with ALS and was ventilator dependent since 2003. She was cared for by the amazing "Peg's Legs" caregivers and the "Healthcare Alternatives" team in her home gallery and studio in Honolulu, Hawaii. Peggy passed away on November 19th, 2008, but her legacy lives on...
Monday, May 5, 2008
May is ALS Awareness Month!
National ALS Awareness Month is a month long series of activities geared to increase public awareness of ALS, raise funds for research and advocate for public policies that will benefit people with ALS. Fore more info, go to ALSA.org
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