If you have Parkinson’s disease, you may wonder whether there is a treatment that can do more than control symptoms—one that could actually slow or stop the disease from progressing. As of 2026, there are no approved disease-modifying therapies proven to slow, stop, or reverse Parkinson’s disease. However, researchers are actively studying treatments that target the underlying biology of Parkinson’s, and several promising approaches are being tested in clinical trials.

So what is happening behind the scenes—and could a disease-modifying treatment finally be getting closer? The Parkinson’s research pipeline has never been more active, and understanding what is being studied can help you make informed decisions about your care.

Exercise is one of the most important tools people with Parkinson’s disease can use to protect mobility, independence, and quality of life. Research shows that regular physical activity can improve walking, balance, strength, flexibility, mood, and other Parkinson’s symptoms. It may also have a protective effect on the brain and help slow aspects of Parkinson’s progression.

Could the right exercise routine actually help you stay stronger and more independent for longer? Research suggests that regular, intentional movement may do more than simply make you feel better today—it may help your body and brain better manage Parkinson’s over time.

When most people think about Parkinson’s disease, they think about tremors, stiffness, or slowed movement. But Parkinson’s can affect much more than movement. Depression, anxiety, apathy, and irritability are common non-motor symptoms of Parkinson’s and can significantly affect quality of life. 
The frustrating part? These symptoms can look very different from person to person—and sometimes the person experiencing them doesn't realize Parkinson’s may be contributing.

Knowing when someone with Parkinson’s disease needs additional help can be one of the hardest decisions a family faces. The goal isn't to take away independence—it is to provide enough support to keep the person safe, healthy, and living as independently as possible.
But how do you know when “a little help” is no longer enough? Recognizing the warning signs early can help families explore options before a crisis, fall, hospitalization, or caregiver burnout forces a decision.

Parkinson’s disease affects much more than movement. Depression and anxiety are common non-motor symptoms of Parkinson’s and can significantly affect quality of life, relationships, motivation, sleep, and the ability to manage everyday activities.
If you or someone you love with Parkinson’s has been feeling unusually sad, worried, withdrawn, or overwhelmed, there are reasons for these changes — and there are things you can do to feel better.

When most people think about Parkinson’s disease, they think about tremors, stiffness, or slowed movement. But Parkinson’s can also affect the senses. A reduced or lost sense of smell is a common non-motor symptom of Parkinson’s and may appear years — sometimes even decades — before a diagnosis.
Could losing your sense of smell be connected to Parkinson’s — and is there anything you can actually do about it? Understanding why it happens can help you recognize an important symptom and find ways to maintain nutrition, safety, and quality of life.

Memory problems, confusion, and changes in thinking can be some of the most difficult non-motor symptoms of Parkinson’s disease. While Parkinson’s is often associated with tremors and movement problems, it can also affect attention, memory, judgment, problem-solving, and the ability to process information.
The good news is that cognitive changes do not automatically mean dementia — and there are steps you can take to understand what is happening and get the right support.

Falls are one of the most common concerns for people living with Parkinson’s disease. Changes in balance, walking, posture, freezing, muscle stiffness, and blood pressure can increase fall risk—but small changes around the home can make a significant difference.
Your home should work with you, not against you. A few simple changes to floors, lighting, bathrooms, bedrooms, and everyday routines can help reduce hazards and make it easier to move around with confidence.

Parkinson’s Hallucinations & Delusions: What Caregivers Should Do
Watching someone you love experience hallucinations or delusions can be frightening and confusing. But these symptoms can occur in Parkinson’s disease and do not mean your loved one is “going crazy.” Hallucinations, delusions, and other changes in perception can have several causes, including Parkinson’s itself, medications, infections, or other medical problems. 

The most important thing you can do is not argue with what your loved one is experiencing—and not ignore it, either. Knowing how to respond can reduce fear, prevent conflict, and help the medical team find the right treatment.

A Parkinson’s diagnosis does not automatically mean it is time to stop driving. Many people with Parkinson’s disease continue to drive safely for years after diagnosis. The important question is whether Parkinson’s symptoms, medication side effects, or changes in vision, thinking, attention, or reaction time are beginning to affect driving ability.
The tricky part? Driving problems can develop gradually—and sometimes the person behind the wheel may not realize that anything has changed. Knowing the warning signs can help you protect independence while also protecting yourself and everyone else on the road.

If you or someone you love has Parkinson’s disease and has begun experiencing unusual, involuntary movements, you may wonder: “Is this Parkinson’s, or is something else happening?” Dyskinesia is a common concern for many people living with Parkinson’s, particularly those who have been taking levodopa for several years.
The good news? Dyskinesia does not mean you simply have to live with uncontrolled movements. Understanding why it happens is the first step toward finding a treatment approach that works for you.

“I have Parkinson’s. What do I do now?”
If you were recently diagnosed with Parkinson’s disease, you may be feeling frightened, overwhelmed, confused—or even relieved to finally have an explanation for symptoms you've been experiencing. There is no single “right” way to react. The important thing to remember is that you do not have to figure everything out at once.
Your diagnosis is the beginning of a new chapter—not the end of the life you know. Here are eight practical steps that can help you move forward with confidence.

Parkinson’s and Gut Health: Constipation, Digestion & How to Improve It
When people think about Parkinson’s disease, they often think about tremor, stiffness, and problems with movement. But Parkinson’s can affect much more than movement. Gut and digestive problems—including constipation—are common non-motor symptoms of Parkinson’s and can significantly affect comfort and quality of life.
Could your digestive system be telling you something about Parkinson’s? Understanding the connection between Parkinson’s and gut health may give you practical ways to feel better and support your overall well-being.

When most people hear “Parkinson’s treatment,” they immediately think about medication. Medication is an important part of managing Parkinson’s disease, but it is not the only tool available. Exercise, physical and occupational therapy, speech therapy, rehabilitation, lifestyle strategies, and advanced treatments such as deep brain stimulation (DBS) may all have a role in helping people manage Parkinson’s.
Could something beyond medication help you move better, communicate more easily, remain independent, or regain better control of your symptoms? Understanding your options is the first step.

A Parkinson’s diagnosis can bring a long list of questions: Is this definitely Parkinson’s? Are my medications working properly? Why are my symptoms changing? What can I do about walking, balance, tremor, pain, or other problems? While a general neurologist can provide Parkinson’s care, a movement disorder specialist has additional expertise in conditions such as Parkinson’s disease.
And you don't necessarily have to wait until Parkinson’s becomes difficult to manage. Knowing when specialized care could help may make a meaningful difference in diagnosis, treatment, and quality of life.

Pain is a surprisingly common symptom of Parkinson’s disease, yet it is sometimes overlooked because Parkinson’s is often associated primarily with tremor, stiffness, and slow movement. Parkinson’s-related pain can affect the muscles, joints, back, neck, feet, or other areas of the body and may significantly interfere with sleep, mobility, mood, and quality of life.
The important thing to know is that you don't simply have to “live with” Parkinson’s pain. Understanding what is causing it is the first step toward finding the right treatment.

Retirement planning can feel complicated for anyone, but a Parkinson’s diagnosis can add another layer of questions. How long will you be able to work? Will healthcare costs increase? What happens if you need help with daily activities someday? And how can you plan for the future without allowing Parkinson’s to take over your vision of retirement?
The good news is that planning early can give you more choices—not fewer. You don't have to predict exactly what the future will look like to make a thoughtful retirement plan today.

One of the first questions many people have after a Parkinson’s diagnosis is, “How quickly will this get worse?” It is a completely understandable question. Parkinson’s disease is progressive, but that does not mean everyone follows the same timeline or experiences the same symptoms in the same order.
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Here’s the part that may bring some reassurance: a Parkinson’s diagnosis does not come with a stopwatch. Understanding what can affect progression can help you focus on what you can do today to live as well as possible.

At first, Parkinson’s medication may seem to provide reliable relief. But over time, you may notice that a dose doesn't last as long, symptoms return before your next dose, or movement becomes less predictable. These changes can be frustrating and sometimes frightening—but they do not necessarily mean that treatment has stopped working.
If your medication seems to be “wearing off,” there are several things your healthcare team can do. Keep reading to learn what may be happening, what information to track, and what treatment options may be available.

​A Parkinson's diagnosis can feel like it rewrites your whole story overnight. But according to Dr. Neil Koppel, DC, a chiropractor and acupuncturist with more than 25 years of experience, your diagnosis is only one chapter — not the whole book. In a recent PD Talk hosted by the Parkinson's Association of Southwest Florida, Dr. Koppel broke down what Parkinson's disease actually changes in the brain and body, and what you can still influence starting today.

Curious what the research really shows about posture, exercise, and Parkinson's disease — and where the evidence still has limits? Keep reading, because the answers may change how you think about your next walk, your next appointment, and your next conversation with your care team.

For some people living with Parkinson’s disease, medications eventually become less predictable. Tremors may return between doses, stiffness and slowness may fluctuate, or involuntary movements called dyskinesias may become difficult to control. When medication adjustments are no longer providing consistent symptom control, deep brain stimulation (DBS) may be an option worth discussing with a Parkinson’s specialist.
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Could DBS help you or someone you love regain more predictable “on” time and better control over troublesome movement symptoms? Here’s what you should know before considering this advanced Parkinson’s treatment.

You're at dinner, at church, or running errands, and suddenly there's no warning at all — just an urgent, undeniable need to find a bathroom, right now. If that sounds familiar, you're not imagining it, and you're not alone.
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Here's the part most people never hear from their neurologist: bladder trouble in Parkinson's disease isn't a plumbing problem — it's a wiring problem. And once you understand the wiring, you can actually do something about it. Keep reading to find out what's really going on, and the treatments urologists use to help patients regain control.

Why Speech Exercise Is a Game-Changer for Parkinson's Disease
If you or someone you love has Parkinson's disease, you already know it can affect movement — tremors, stiffness, slower steps. But did you know it very often affects your voice, too? A soft voice, slurred words, or trouble swallowing aren't just “getting older.” They're common, treatable symptoms of Parkinson's disease (PD) that up to 90% of people with PD will experience — and most neurologists never bring it up.
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That's exactly why the Parkinson's Association of Southwest Florida (PASWFL) invited speech-language pathologist Judy Jenner, MS, CCC, to lead a recent PD Talk, “Speech Exercise and PD: Learn the Benefits and Process.” We've turned that full session into an easy-to-read transcript, and below we're breaking down the highlights — what these symptoms look like, why they happen, and, most importantly, what you can do about it starting today. Keep reading to learn more.

Navigating Memory Changes in Parkinson's Disease: What's Normal vs. What's Not
You forgot why you walked into the kitchen. Again. And now you're wondering: is this just getting older, or is this Parkinson's disease talking?

That question sits quietly behind a lot of Parkinson's diagnoses, and it deserves a real answer — not a scary one. Here's what's actually happening in your brain, what's normal, what's worth flagging to your doctor, and the strategies that genuinely help.
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In Parkinson's disease, memory itself is often less affected than attention, mental processing speed, problem-solving, and word-finding. The brain changes behind PD's motor symptoms can also slow thinking, and stress, medication, and depression compound the effect — but this is different from dementia, and there's a lot you can do about it.

A Parkinson’s diagnosis often brings an immediate question: “What happens next?” One of the biggest concerns for individuals and families is how quickly Parkinson’s disease will progress and how much it will eventually affect daily life. The truth is that Parkinson’s progression is highly individual, and there is no reliable timetable that applies to everyone.

​Wondering what the next five, 10, or even 20 years could look like? Understanding how Parkinson’s progresses—and what can influence that progression—can replace some of the uncertainty with knowledge and a plan.