The Problem:

Researchers Ask the Wrong Questions

About Us

We are people with Parkinson’s dedicated to elevating the voices of those with lived experience of Parkinson’s to inform the way Parkinson’s is understood, treated, and ultimately cured.

What We Offer

Resolve Parkinson’s offers opportunities for you to contribute to a changed future. You can help us transform the future of Parkinson’s.

Despite decades of studies and billions of dollars invested, the scientific community has yet to uncover what Parkinson’s truly is, what causes it, and how to stop or prevent its progression. This persistent failure to make meaningful progress in Parkinson’s research stems, in part, from researchers asking the wrong questions. 

There is an Alarming Volume of Unproductive Research

Simon Stott of the Cure Parkinson’s Trust highlights a staggering reality: as of December 31, 2023, over 171,000 studies on Parkinson’s had been published — 82% of them since the year 2000. In 2023 alone, researchers produced 11,605 reports. Yet, the core mysteries of Parkinson’s remain unsolved.

Many studies focus on animal models, inducing Parkinson’s-like symptoms in species that cannot naturally contract the disease. These experiments often produce “promising results,” yet their findings rarely translate into human treatments. Despite this, such studies dominate research efforts, leaving patients and caregivers grasping at fleeting hopes fueled by headlines rather than breakthroughs.

A Billion-Dollar Question

The lack of progress is not due to insufficient funding. The Michael J. Fox Foundation has raised nearly $1 billion for Parkinson’s research. Combined with investments from the National Institutes of Health and other organizations like the Cure Parkinson’s Trust and the American Parkinson’s Foundation, funding over the past 25 years exceeds $3 billion. However, this significant financial commitment has yet to yield transformative results.

Breaking the Cycle of Failure

The scientific community appears trapped in an endless cycle of unproductive research. It is time to explore a new path — one that prioritizes asking the right questions and incorporating insights from those who live with Parkinson’s every day.

The scientific community appears trapped in an endless cycle of unproductive research. It is time to explore a new path — one that prioritizes asking the right questions and incorporating insights from those who live with Parkinson’s every day.

Steps Towards a Solution

Resolve Parkinson’s is dedicated to challenging the status quo in Parkinson’s research by focusing on patient-driven priorities and fostering collaboration. Our solutions include:

By shifting focus to these strategies, we aim to disrupt stagnation and drive research toward outcomes that truly matter to those living with Parkinson’s. Learn more about our vision for the future and how we’ll get there.

The Problems We See

The System of Care is Poorly Designed

The current system to assist people with Parkinson’s appears to have evolved without rational planning. Systemic issues include lack of patient access to Parkinson’s specific care, ineffective drug therapies, and a poorly socialized standard of care in health settings. This has led many patients to try to manage their care on their own.

The Definition of Parkinson’s is Too Narrow

Parkinson’s is a multisystemic syndrome rather than solely a movement disorder limited to brain neurology. A focus on non-motor symptoms is critical to understanding how Parkinson’s evolves and how early intervention may slow or halt the disease.

Alternative Therapies are Excluded from Research

Led by desperation and ineffective drug therapies, patients with Parkinson’s have found relief through lifestyle changes and treatments that aren’t patentable or otherwise able to be monetized. These approaches have been eschewed by the mainstream medical community.

There is a Lack of Access to Quality Care

Most patients with Parkinson’s lack access to multidisciplinary teams of specialists including neurologists trained in Parkinson’s, movement disorder specialists, physical and occupational therapists, and mental health professionals. This team approach has proven to be the most effective model of care for Parkinson’s patients.

The Patient Voice is Being Ignored

Parkinson’s patients need to have a seat at the table throughout the clinical research process. Patient input into how resources are used is a critical missing element that will bring about change if broadly applied. Positioning the patient voice more powerfully will disrupt stagnation and drive change.

Research Targets Are Profit-Driven

The pharmaceutical industry ecosystem dictates where research funding is allocated. Patients with Parkinson’s need to be positioned as leaders in the fight to improve care and find a cure. Their voice needs to be a critical component of legislation and research targets.
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