A free flowing movement class that brings out the dancer in you without needing any prior dance knowledge. Using music, we explore range of motion throughout the body and develop an awareness of movement in space. It is a full body workout.
Please keep a bottle of water nearby. Enjoy the session!
Instructors
Cecilia Fontanesi, PhD, BC-DMT
There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends, and the community.
Cardio, strength, balance and coordination exercises will be added in to the PWR Moves curriculum which explores exercises to improve range of motion, agility, and quality of movement in everyday living. We will review the PWR Moves positions and exercises. You may need a chair, water bottle, light weights (or canned goods). All levels welcome.
Instructors
Stacey Macaluso, Life Coach & Fitness Specialist, Founder of Mission PD
There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends, and the community.
Body mapping is diverse and can be used in different settings. This class will help you learn ways to use the eyes and body mapping in your ongoing exercise routine, rather that be boxing, large amplitude/big movements, strength, or balance.
We will use previous techniques to help integrate the whole body (left and right, lower and upper) during movements. For example, learn how to integrate the lower and upper half of your body while using the eyes to improve rotation during boxing.
Class will be a moderate to higher pace and level but seated variations will be given throughout class.
Equipment needed: Chair, exercise mat, hand towel, small hand weights, and a second chair/walker/foam roller/wall for support during chair to standing transitions
This class is live, so stay tuned towards the end of class and partake in a Q&A to discuss what worked for you or find what adjustments you could make!
Please keep a bottle of water nearby. Enjoy the session!
Instructors
Corey Emberton, Neuro and Movement Specialist, Level 3 Neurostudio Advanced Practitioner
There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends, and the community.
Maintain a step ahead with the PD-Connect BASIX™ program. A multi-FUNctional class focusing on Balance, Aerobics, Strength, Integration and eXcellence. Engage in our award winning live "Show" and enjoy aerobic activity, dance, strength and dynamic skills to stay ahead of your PD symptoms. The goal is for moderate to vigorous intensity, with modifications in standing and in the chair. Parkinson's-specific fitness couldn't be more fun!
Equipment needed: Chair, weights (or canned goods), and a tennis ball
Please keep a bottle of water nearby. Enjoy the session!
Instructor
Lisa Oei, PT, MSPT, DPT, Physical Therapist, Parkinson's Wellness Coach; PD-Connect, Corte Madera, California
SteF Farina, MCT
There is no charge to attend, but registration is required. This program is open to people with Parkinson's, their family, friends, and the community.
La enfermedad de Parkinson 101: lo que usted y su familia deben saber Regístrese Aquí
Acompañe a la Parkinson’s Foundation para aprender acerca de las causas, los síntomas y el manejo de la enfermedad de Parkinson, así como la participación en investigaciones.
Presentadora
Andrea Fuentes, MD
Profesora adjunta de clínica
Neurología y ciencia neurológica
Stanford Medicine
Explorando terapias complementarias para el Parkinson: los beneficios de la terapia física, del habla y ocupacional Regístrese Aquí
¡Acompáñenos en una charla en línea donde profundizamos en el mundo de las terapias complementarias y su papel fundamental en mejorar la calidad de vida de las personas que viven con la enfermedad de Parkinson!
Esta sesión interactiva se centrará en la importancia de la fisioterapia, la terapia del habla y la terapia ocupacional, brindando una comprensión integral de sus roles y los numerosos beneficios que ofrecen. No se pierda la oportunidad de participar en demostraciones en vivo de ejercicios terapéuticos diseñados específicamente para pacientes con Parkinson.
Presentadoras
Ana Sanchez Junkin, PT, DPT, NCS
Especialista clínica en neurología certificada
Profesora adjunta
MGH Institute of Health Professions
Dora Jasso, MA, CCC-SLP, CBIS
Patóloga del habla y el lenguaje
MountainView Regional Medical Center
Pamela Talero Cabrejo, OTD, BSOT(Col), OTR/L, CPAM, COT
Profesora adjunta
Programa post-profesional de terapia ocupacional
Departamento de terapia ocupacional
Jefferson College of Rehabilitation Sciences
Thomas Jefferson University
Avances en el tratamiento del Parkinson: ¿Qué hay de nuevo? Regístrese Aquí
Existen muchos medicamentos para mejorar la calidad de vida de las personas con la enfermedad de Parkinson (EP). Sin embargo, cada individuo responde de manera diferente a los medicamentos. Lo que funciona para uno no necesariamente funciona para otro.
Conozca los avances en los tratamientos para la enfermedad de Parkinson, tanto para los síntomas motores como no motores y dónde nos encontramos en el camino hacia la medicina personalizada.
Presentador
Ramon Rodriguez, MD, FAAN
Especialista en neurología
Neurology One
EP Salud En Casa es presentado por Light of Day Foundation, cuya generosidad ha hecho posible esta programación.
Raise Awareness
11 Goals You Helped Us Accomplish in 2023
In a word, momentum was the theme for the Parkinson’s Foundation in 2023. Thanks to the Parkinson’s community, especially our donors, we worked hard to make life better for people with Parkinson’s disease (PD) through advancing research and prioritizing access to care.
Here are 11 ways you helped us keep the momentum in 2023:
In July 2023, we published a study that found that only 50% of people with Parkinson’s saw a general neurologist. As a result of these findings, we are expanding disease-specific training to neurologists and other healthcare providers, and pursuing ways to improve access to care across all demographic and population groups.
2. Provided Genetic Testing and Counseling to 11,000 people with PD
In 2023, our international genetics study PD GENEration: Mapping The Future of Parkinson’s Disease reached the milestone of providing genetic testing and counseling to 11,000 people with Parkinson’s. PD GENEration test results empower people, help them work alongside their doctor to tailor PD treatment, and can match them to gene-specific clinical trials. Thus far, PD GENEration data shows that 12.7% of people with Parkinson’s have a genetic link to the disease — much higher than the originally believed 5-10%.
To bring specialized Parkinson’s care to more people, we designate medical centers that know how to treat this complicated disease. In 2023, we designated eight new centers as part of our Global Care Network, with the first-ever designations in Wisconsin and Washington, and the country of Japan.
The Parkinson’s Virtual Biotech, a partnership with the Parkinson’s UK, is currently funding 13 potential medications in development that either address PD symptoms or aim to slow, stop, or prevent the disease altogether. This initiative gets us closer to delivering life-changing treatments in years, not decades.
A Parkinson’s breakthrough can happen at any time, in any lab, which is why we directly fund scientists who are conducting innovative studies attacking Parkinson’s from every angle. In 2023, we awarded $2.8 million across 30 promising research grants.
Dr. Wang is exploring a new way to target the cause of PD by using RNA-degrading technology. His lab is working to prevent over-accumulation of alpha-synuclein (a protein) in the brain, hopefully paving the way to halt the development of the disease.
Ensuring diversity and inclusivity in Parkinson’s research is critical to accelerating breakthroughs toward a cure. In 2023, we partnered with Morehouse Healthcare to expand genetic research in the Black community, making Morehouse the first historically Black institution of medicine to become a PD GENEration research site.
We awarded nearly $1 million in community grants to PD programs across 35 states. From non-contact boxing classes to educational events and wellness programs, we have invested more than $10.4 million in 787 community-based programs since 2011.
Even though 90,000 Americans are diagnosed with Parkinson’s every year, most healthcare professionals — including nurses, pharmacists and general practitioners — do not receive in-depth PD care training. We added new accredited online courses to our Education Series for Community Providers, which are designed to improve treatment and outcomes for people with Parkinson’s.
We launched 50 new Spanish pages on Parkinson.org. From symptoms to managing PD, these pages are designed to reach the Spanish-speaking Parkinson’s community and connect them to key information and tools.
10. Raised $3.5 million through Parkinson’s Champions
Parkinson’s Champions are a dedicated group of people in the PD community who fundraise to help us fight Parkinson’s. Parkinson’s Champions do it all, they run in prestigious races, cycle for Parkinson’s Revolution, host Facebook fundraisers, and more. In 2023, Parkinson’s Champions raised $3.5 million to propel us towards a cure.
Photo credit: Tricia Baron
On April 11, the producing team behind the Broadway hit, A Beautiful Noise: The Neil Diamond Musical presented $500,000 to the Parkinson’s Foundation in honor of legendary singer, songwriter and performer Neil Diamond, who is living with Parkinson’s.
Every year, the top neurologists and Parkinson’s experts in the world attend renowned conferences to share new information about PD treatments and research. In 2023, the Parkinson’s Foundation shared numerous research and care findings at two premier conferences.
As much as we accomplished in 2023, we are committed to doing more for the PD community in 2024. Your continued support is the only way we can make that happen. Thank you.
The Hospital Safety Guide is a resource for people with Parkinson's disease (PD) and their care partners filled with useful tools and information to prepare for and navigate a hospital stay.
Why is hospital safety important for people with Parkinson’s? People with PD are at a higher risk of hospitalization and face many challenges while in the hospital. Hospital staff may not be familiar enough with PD to understand symptoms or realize they can worsen when PD medication is not delivered on time. Careful preparation and clear communication can help minimize complications and recovery time.
The Hospital Safety Guide provides useful information and tools to help you advocate for your best care, including:
The Five Parkinson’s Care Needs
Forms to fill out with personal care details and medication schedules
Tips for care partners
Parkinson’s care information to share with the hospital care team
The Importance of Openly Talking About Hallucinations & Delusions in Parkinson’s
Psychosis can be a frightening word. Understanding what it means in Parkinson’s disease (PD) and how a person may experience symptoms can ease the fear and stigma surrounding this medical term. Hallucinations and delusions can be common in PD. Openly discussing these symptoms can help your healthcare team discover the best management strategies. Learn the different ways people experience these symptoms and how to address them.
If you live with Parkinson’s, some of your most challenging symptoms might be seemingly invisible to others. Known as non-movement symptoms, these can impact mood, sleep, thinking and more. Some are easier to talk about than others.
Not everyone with PD will have hallucinations or delusions, but up to 50% of people with Parkinson's can experience symptoms over the course of the disease. Studies show up to 90% of people do not proactively talk to their doctor about it, meaning the actual number may be higher.
It’s important to know that you are not alone. If you feel, hear or sense things that aren’t there, you may feel self-conscious, embarrassed or even scared to share your experiences. These feelings may lead to isolation and avoidance of care. While it can take courage to talk about your experience, rely on your doctor, neurologist or movement disorders specialist to be familiar with these symptoms.
In Parkinson’s, your doctor might use the term psychosis to describe anything from visual hallucinations caused by slight misperceptions to complex, detailed delusions: seeing things that aren't there or believing things that are not true. These tricks of the brain can seem like minor inconveniences, but often have a big impact on you and your loved ones. These symptoms can stem from Parkinson’s brain changes, medication, dementia or delirium — sudden hallucinations or delusions that can signal a medication or health issue.
Unaddressed, hallucinations and delusions can reduce quality of life for people with Parkinson's and their care partners. These can cause lack of sleep, increase stress and create fall risks or other safety issues. Symptoms can also increase hospitalization risk, care costs and need for long-term care.
Other medical conditions that can cause psychosis include:
Bipolar disorder
Brain tumor
Depression
Dementia
Lupus
Malignant lung neoplasm
Multiple sclerosis
Schizophrenia
Steroid treatment in autoimmune disorders
Stroke
Gradual Changes in Perception
Symptoms of Parkinson’s disease psychosis vary in severity. In early PD stages, you may be aware that what you are experiencing is not really there. You might lose that insight as Parkinson’s progresses. This happens slowly and gradually over time.
Psychosis symptoms can include:
Illusions or misperceptions: Misperceiving what is there — for example, a coat and hat on a rack might appear to be a person or a shadow may appear to be a mouse.
False sense of presence: The sense that someone is looking over your shoulder, in the room or lying next to you in bed, but when you look, no one is there.
False sense of something moving past: The awareness of something fleeting past or moving in the periphery, or sense something darting across the floor or someone walking through the hallway.
Hallucinations and delusions: Seeing or believing things that are not true, which can cause a range of feelings from undisturbed or anxious to agitated or frightened.
Types of Hallucinations
Some hallucinations recur with frequency, while others happen just once. Hallucinations are more common in people with sleep or cognitive problems or depression. While increasing medications can sometimes put people at risk for the onset of hallucinations, most people with Parkinson's will experience hallucinations after 10 years of diagnosis.
Hallucinations are less likely to occur when someone is engaged in an activity. They are more likely to happen when a person has vision problems, is alone or at night. Understanding how people with Parkinson's might experience these can help reduce the stigma.
Types of hallucinations include:
Visual: Seeing people or animals that are living or deceased.
Auditory: Hearing things like voices or music.
Olfactory: Smelling things that aren’t there, such as chemicals burning or gasoline.
Tactile: Feeling as if something is on or underneath the skin, which might cause scratching.
Visual hallucinations can seem as if you are having a vivid dream, despite knowing you are awake — seeing distorted, cartoon-like strangely colored animals and people, bugs, figures hovering on the ground. People have reported seeing fairies or colonies of tiny people. Some people find these entertaining to watch, while others find it frightening.
Common visual hallucinations for people with PD can include:
Seeing someone sitting in your home, possibly in your living room or at your dining table. It can range from a friendly presence like a visitor or to the distressing sense of an intruder.
Some veterans with PD have reported seeing elaborate, detailed military bootcamps outside, with a drill sergeant and service members.
People in cities and urban areas may see out-of-place wildlife, such as deer or skunks.
Auditory hallucinations can cause distraction or poor sleep. People may think neighbors are doing yard work or having a party in the middle of the night. Sounds may seem to come from the attic, basement or walls.
Understanding Delusions
Delusions can distress the person with Parkinson's and their loved ones, sometimes causing isolation, embarrassment, fear, suspicion or jealousy, or resulting in anger or violence toward a care partner. Delusions can create safety or legal problems. Care partners, who may recognize psychosis symptoms before the person with PD, should share these with their loved one’s doctor.
Though delusions are not reality based, they often seem real to the person experiencing them. These often have common themes, including:
Persecution: Believing someone is trying to deceive or bring harm. You may suspect a trusted person wants to steal from you or family is plotting against you. Some people suspect their caregiver is trying to poison them and become suspicious of medication or food.
Jealousy: Believing a spouse or partner is being unfaithful. Othello syndrome is the false certainty of and preoccupation with a partner’s imagined infidelity.
Reference: Feeling like a song or a TV show is speaking directly to you. This may feel like something you want to act on.
Other forms can include:
Fregoli delusion: Believing different people are actually a single person changing their appearance or in disguise.
Cotard’s syndrome: Thinking you are dead, decaying, do not really exist or your blood or internal organs are missing.
Capgras syndrome: Believing an identical imposter has replaced a friend, spouse, family member or pet.
Delirium
Seek medical attention if you experience a sudden change as they are not typical of Parkinson’s. When hallucinations or delusions begin within hours or days, it can be due to changing, stopping, increasing or decreasing a medication, or can signal another medical issue, such as:
urinary tract infection or pneumonia
dehydration
substance withdrawal
high or low blood sugar
low blood pressure
surgery or hospitalization
organ failure
Managing the Impact
There are several ways to help a loved one experiencing PD psychosis. Find the best methods that work for you. These techniques can help manage the impact:
A stable, calm, familiar environment is essential for someone experiencing psychosis.
Keep a routine.
Try to keep a well-lit, clutter-free home — this can minimize visual misperception, hallucinations and injuries.
Use a nightlight in the bedroom. Unfamiliar environments might worsen symptoms.
Offer reassurance that the person with PD is safe, loved and symptoms are not their fault. This can the reduce fear and shame around hallucinations and delusions.
During an episode, do not argue or rationalize. Leave the room if necessary.
Orient your loved one with calendars, photos or messages on post-its.
Remove items that may cause a safety issue, such as area rugs. Explore our home safety page for more.
Focusing on good sleep habits, getting enough exercise and seeking out stress management strategies are vital for people experiencing hallucinations and delusions and those who care for them. Care partners also need adequate rest and breaks from care to burnout risk.
Your doctor can recommend safe management strategies or adjust your medications. Many antipsychotic medications used to treat psychosis should not be used in PD — they can act on dopamine receptors and worsen Parkinson’s symptoms.
While not for everyone, Pimavanserin (Nuplazid®) is a newer antipsychotic that does not block dopamine. It is approved by the U.S. Food and Drug Administration (FDA) specifically for the treatment of Parkinson's disease psychosis. Other medications considered safe options to treat psychosis in PD include Quetiapine (Seroquel®) and Clozapine (Clozaril®). Learn more about medications used to treat psychosis.
Learn More
Explore our resources about hallucinations and delusions in Parkinson’s: