Free APDA conference for patients, caregivers slated for February
Third annual program to be hosted by American Parkinson Disease Association
The American Parkinson Disease Association (APDA) has announced that it will host its third annual, free, virtual conference for people with Parkinson’s disease and their caregivers on Feb. 19-20. The program is scheduled to run from 12 p.m. to 4 p.m. ET each day.
Tailored to “educate, empower and engage the PD [Parkinson’s disease] community,” the two-day event aims to provide support and information — as well as updates on Parkinson’s research and treatments — to help those affected by the disease live better. In the first two years, more than 6,000 individuals attended the virtual conference.
Those interested in attending can register on the APDA website.
“With the APDA Virtual Parkinson’s Conference, we are offering a unique platform for participants from across the country and beyond to gain insights, share experiences, and build a stronger, more informed Parkinson’s community,” Leslie A. Chambers, the APDA’s president and CEO, said in a press release from the nonprofit.
The event will feature more than 20 speakers, including medical professionals who will discuss the latest advancements in treatment and symptom management for Parkinson’s, and individuals living with the disease who will share their personal experiences. Attendees will have opportunities to connect with others and participate in various activities throughout the event.
‘Educate, empower and engage’ is theme of APDA conference this year
Topics at this third annual conference will include strategies for pain and falls management, and information on how palliative care may help people living with the disease. Palliative care aims to improve quality of life for people with serious illnesses — focusing on addressing the physical, emotional, and social needs of patients and their families. Several sessions will provide opportunities for live Q&A with the speakers.
New Parkinson’s treatments will be another area of focus, with “leading medical experts” on hand to discuss therapies in development, according to the APDA.
We are excited to bring the APDA Virtual Conference back for the third year in a row. … By offering virtual programs like this one, we’re reaching more people who need us, including those who face obstacles like mobility challenges, geographic isolation, or busy schedules that make attending in-person events difficult.
Also available will be interactive activities, including creating music, improvisation, journaling, or fitness to improve balance and strength. With concurrent breakout sessions, participants may choose the topics that are most interesting to them and best related to their journey.
“We are excited to bring the APDA Virtual Conference back for the third year in a row,” said Rebecca Gilbert, MD, PhD, the APDA’s chief mission officer. “We understand the importance of making credible information and resources available to everyone impacted by Parkinson’s, no matter where they live.”
Gilbert added that “by offering virtual programs like this one, we’re reaching more people who need us, including those who face obstacles like mobility challenges, geographic isolation, or busy schedules that make attending in-person events difficult.”
Registration is free and includes an option for donating to the APDA. Since its founding in 1961, the APDA has raised and invested more than $280 million to provide patient services and educational programs, raise awareness about the disease, and support research. The nonprofit bills itself as “a nationwide grassroots network.”
According to Chambers, “APDA is steadfastly committed to improving the lives of all those affected by Parkinson’s disease by providing a wide range of programs, resources, education, and support.”
About the Author
