APDA, Author at American Parkinson Disease Association

Parkinson’s Perspectives: Musicians with Parkinson’s

Posted on September 15, 2026September 15, 2026 by APDA

Perspectives from People with Parkinson’s At the American Parkinson Disease Association (APDA), we know that some of the most...see more powerful insights about Parkinson’s disease (PD) come from the people affected by it. Their perspectives – the challenges, victories, and hard-won wisdom – can be incredibly valuable to those on a similar path and others who […]

The Different Medications of Parkinson’s Explained

Posted on September 3, 2026September 3, 2026 by APDA

Smart Patients Blog Series 2 of 5: Dr. Gilbert Discusses Parkinson’s Disease Medications This article is part 2 in...see more our Smart Patients Blog Series Parkinson’s disease (PD) medications continue to expand, which is giving patients more options than ever before. However, choosing between different formulations, delivery systems, and add-on therapies can be confusing. This post […]

Special Edition: “Ask the Physical Therapist” with Teresa Baker

Posted on September 2, 2026September 9, 2026 by APDA

Special guest expert! October is National Physical Therapy Month and...see more to commemorate the month and to spotlight the important role physical therapy (PT) can play in a life with Parkinson’s, we invited Teresa Baker, PT, DPT, a board-certified clinical specialist in neurologic physical therapy from Boston […]

One Person’s Story. Thousands of Reasons For Hope.

Posted on August 27, 2026September 21, 2026 by APDA

APDA Northwest Chapter Board Member Jake Miller joined the APDA Optimism...see more Walk with one goal: to share his Parkinson’s journey and invite others to support an organization and cause that has become deeply meaningful to him. The response has been extraordinary. Currently, Jake has raised more than […]

Helping People with PD Thrive Through Signature Programs

Posted on August 27, 2026August 27, 2026 by APDA

At APDA, every Signature Program is thoughtfully designed in collaboration with...see more people living with PD, care partners, healthcare professionals, and community leaders. That way, we can make sure they address real needs at every stage of the PD journey. Each program is carefully developed and refined before […]

Research You Can Understand. Progress You Can Celebrate

Posted on August 27, 2026September 9, 2026 by APDA

Parkinson’s disease research is advancing at an exciting pace, but let’s...see more be honest: it can also feel overwhelming. Scientific terms and complex studies can make it seem like researchers are speaking an entirely different language. The good news? You don’t need a PhD to appreciate why these […]

“Ask the Doctor” with Dr. Rebecca Gilbert

Posted on August 27, 2026August 27, 2026 by APDA

Q. Do the medications for PD cause nightmares? I sometimes wake up...see more screaming as if I just had a nightmare. I don’t remember the dreams, so this symptom doesn’t bother me too much, although it bothers my wife! A. There are two potential explanations for what you are […]

APDA Advances Parkinson’s Priorities

Posted on August 24, 2026August 24, 2026 by APDA

The second Advisory Council on Parkinson’s Research, Care, and Services (ACPRCS) took place on August...see more 24, 2026. Below are key takeaways and next steps, along with ways for you to inform the Council’s efforts to develop a national strategy to prevent, diagnose, treat, and ultimately cure Parkinson’s disease (PD). August 24 […]

American Parkinson Disease Association Launches Spanish-Language Microsite, Expanding Support for Underserved Parkinson’s Community

Posted on August 24, 2026August 24, 2026 by APDA

NEW YORK, NY, AUGUST 24, 2026 – The American Parkinson Disease Association (APDA) today announced the launch of a...see more new Spanish-language microsite, expanding access to critical information and resources for Spanish-speaking people living with Parkinson’s disease (PD) and their care partners and families. With a mission to provide the support, education, research, and community that […]

The Impact of APDA Community Initiatives

Posted on August 18, 2026August 18, 2026 by APDA

The World Parkinson Congress (WPC) is an international conference that takes place every three years and brings together researchers,...see more clinicians, people with Parkinson’s disease (PD), care partners, and PD advocates to share information on the science of PD as well as the best clinical, wellness, and exercise practices to better the lives of people with […]

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