Last month PCLA President Patrick LoSasso and Board Member Mark Siegel traveled to Washington, DC, for the 2019 Parkinson’s Advocacy Forum. They and 150 other advocates from across the country in [...]
Since retiring from her 30-year career in social work, Gail Buckley pursues her passions of mentoring young women, traveling the world, and making art. In addition to serving on PCLA’s Board of Directors, she has served for many years on the Board of her family’s charitable foundation, which supports educational and health related causes. Gail has been living with Parkinson’s disease for seven years.
Sandy Yaras is the leader of PCLA’s "Let Talk About Parkinson’s" support group and our "PCLA Online" virtual support group. He was diagnosed in 2004 at the age of 63. Sandy taught middle school students for over 20 years and is also an artist, writer, and stand-up comic.
Judy Yaras is Vice-President of PCLA and Director of Museum Shop Operations at Fashion Institute of Design & Merchandising. Her professional background spans the healthcare and retail industries, teaching, and includes boardroom experience for a number of nonprofits.
The risks of being a caregiver is that we are HUMAN BEINGS and sometimes we get sick. Almost every caregiver I know puts their loved one’s health above their own. I care for my husband who has had Parkinson’s for 19 years, he was diagnosed when he was 36. He’s had deep brain stimulation surgery, two seizures, a number of falls that have sent us to the ER and his colon burst and he became septic and gravely ill. All this and we are only 55.
In 2000, at the age of 36, Mike Weinman was diagnosed with PD. An experienced finance and operations executive, Mike has served as Treasurer of PCLA since its founding. He also runs a support group for those living with Young Onset Parkinson’s disease. We spoke to Mike about his experience as a support group leader, his role in the formation of PCLA, and how Parkinson’s has impacted his family.
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Our mission is to improve the quality of life for those living with Parkinson’s disease, their families and care partners. Our goal is to connect people to the information, support services, programs and activities they need to enhance wellness and live an active, engaged life moving forward. We are a 501(c)3 non-profit organization.