Regardless of where you are in your Parkinson’s journey there are many things you can do to live well. Managing daily life with Parkinson's disease involves learning and adjusting as symptoms and needs change. This program addresses some common challenges and will provide important information, resources, and strategies to help you every day. Attendees will gain information to help find the balance between a proactive approach and wondering what lies ahead.

This event is free and open to people with Parkinson's and their families. Registration is required as in-person seating is limited.

Speakers:
Alex Baumgartner, MD, UCHealth Anschutz
Emma Bjore, MD, Ivinson Medical Group

Thank you to our event partners, the Laramie Parkinson's Support Group, Ivinson Memorial Hospital and the University of Wyoming Center on Aging. 

Sleep issues are common in Parkinson's disease, from nighttime interruptions to daytime sleepiness. This program explores the causes, symptoms, and impact of common sleep issues on both individuals with Parkinson's and care partners. Attendees will learn practical ways to improve sleep and know when to seek professional support. 

This event is free and open to people with Parkinson's and their families. Registration is required as in-person seating is limited.

Acompañe a la Parkinson’s Foundation para un día de aprendizaje, baile, una feria de recursos, almuerzo, juegos, rifas, y mucho más. Nuestro evento educativo en español ayudará a los asistentes a explorar las opciones de tratamiento para el Parkinson, como por ejemplo, medicamentos y cirugía. Hablaremos acerca de cómo manejar los síntomas nuevos y los cambios y aprenderemos acerca de recursos locales juntos con la comunidad.

Este programa es gratuito y está disponible para las personas con Parkinson, sus familiares, amigos, personas de apoyo y Promotores de Salud (Community Health Workers).

Hay dos formas de asistir:

• En persona el sábado 4 de abril de 9:00 am – 2:00 pm hora del Pacífico en el Museum of Latin American Art, 628 Alamitos Ave, Long Beach, CA 90802. El estacionamiento y el almuerzo son gratuitos y hay una zona de actividades para niños disponible.
  Asistir en persona
• En línea via Zoom el sábado 4 de abril de 10:00 am – 2:00 pm hora del Pacífico. Una vez inscrito, recibirá un correo electrónico con el enlace para ver el programa en vivo. 
  Ver en línea en casa

Check-in, lunch and resource fair begin at Noon.

This program provides an overview of current Parkinson's research and its impact on treatment and care. Participants will learn  the difference between studies targeting symptoms and those aiming to slow disease progression, as well as explore recent advancements and how ongoing research may shape future therapies and personal care.

Expert Speakers

Rachel K. Spooner, PhD
Director, Translational Motor Imaging Laboratory
Institute for Human Neuroscience, Boys Town National Research Hospital
Assistant Clinical Professor, Department of Pharmacology and Neuroscience, Creighton University

Jamison Hofer, DO, AQH
Board Certified Neurologist
Neurology Consultants of Nebraska

Maggie Caulfield, PhD
Director of Research Programs
Parkinson's Foundation

This is an in-person program. Check-in, lunch, and resource fair begin at Noon.

Parking: Parking is complimentary for program attendees. For driving directions, please click here.

There is no charge to attend, but registration is required as lunch is provided. This program is open to people with Parkinson's, their families and friends, medical providers/practitioners, and the community. 

Join the Parkinson's Foundation and Up ENDing Parkinsons for a morning of exercise and community to kick off the spring events in Northern CA. We will be having a live rock-climbing demo, community resources, and more. 

No experience necessary and equipment will be provided. Free onsite parking and light snacks and refreshments will be provided.

Check-in & Resource Fair* begins at 11:00 a.m. and the program starts at 11:30 a.m. 

Join the Parkinson’s Foundation for the New York Chapter Parkinson’s Symposium. Attendees will learn about symptoms, treatment options and strategies to help navigate the challenges of living with PD. While each person’s experience is unique, the more you know, the more empowered you will be to play an active role in your care and manage your life with Parkinson’s.

*The Resource Fair will feature local Community Partners that provide services and support for the Parkinson’s Community.

We are excited to welcome amazing speakers from Parkinson’s Foundation Centers of Excellence at:

Columbia University Irving Medical Center
Julian Agin-Liebes, MD
Hiral Shah, MD

Mt Sinai Beth Israel
Joohi Jimenez-Shahed, MD
Joan Miravite, DNP

NYU Langone Medical Center
Giulietta Riboldi, MD, PhD
Betsy Thomas, MD

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.

Parkinson's Foundation: The PD Solo Network - Living Alone While Living with PD

There are two sessions available: You are welcome to choose one or attend both.
– 1 p.m. to 2:30 p.m. ET
– 7:30 p.m. to 9 p.m. ET

Please note: These meetings are intended for individuals diagnosed with Parkinson’s disease who live alone, by choice or circumstance – only. If this is not your situation, please contact the Parkinson’s Foundation Helpline to receive information about resources that best meet your needs. Call the Helpline at 1-800-473-4636 (1-800-4PD-INFO) or helpline@parkinson.org.

What is the PD Solo Network: 

A virtual network for people living with Parkinson's disease (PD) who live alone, by choice or circumstance. The purpose of this group is to create a community of support for those living without a care partner. People living with PD are the experts about what challenges, changes and accommodations are needed on a daily basis. This network will provide a place to share ideas, concerns, brainstorm strategies, suggestions, resources & to build relationships.

The Parkinson's Foundation is providing the initial funding and support to kick start this network. It will most likely become a very strong network that will operate independently although the Parkinson's Foundation will always be an entity of support & information for the participants.

2026 Meeting Dates:

• January 13, 2026
• February 10, 2026
• March 10, 2026
• April 14, 2026
• May 12, 2026

• June 9, 2026

There is no charge to attend, but registration is required in order to receive the Zoom link.

Parkinson's Foundation: The PD Solo Network - Living Alone While Living with PD

There are two sessions available: You are welcome to choose one or attend both.
– 1 p.m. to 2:30 p.m. ET
– 7:30 p.m. to 9 p.m. ET

Please note: These meetings are intended for individuals diagnosed with Parkinson’s disease who live alone, by choice or circumstance – only. If this is not your situation, please contact the Parkinson’s Foundation Helpline to receive information about resources that best meet your needs. Call the Helpline at 1-800-473-4636 (1-800-4PD-INFO) or helpline@parkinson.org.

What is the PD Solo Network: 

A virtual network for people living with Parkinson's disease (PD) who live alone, by choice or circumstance. The purpose of this group is to create a community of support for those living without a care partner. People living with PD are the experts about what challenges, changes and accommodations are needed on a daily basis. This network will provide a place to share ideas, concerns, brainstorm strategies, suggestions, resources & to build relationships.

The Parkinson's Foundation is providing the initial funding and support to kick start this network. It will most likely become a very strong network that will operate independently although the Parkinson's Foundation will always be an entity of support & information for the participants.

2026 Meeting Dates:

• January 13, 2026
• February 10, 2026
• March 10, 2026
• April 14, 2026
• May 12, 2026

• June 9, 2026

There is no charge to attend, but registration is required in order to receive the Zoom link.

Parkinson's Foundation: The PD Solo Network - Living Alone While Living with PD

There are two sessions available: You are welcome to choose one or attend both.
– 1 p.m. to 2:30 p.m. ET
– 7:30 p.m. to 9 p.m. ET

Please note: These meetings are intended for individuals diagnosed with Parkinson’s disease who live alone, by choice or circumstance – only. If this is not your situation, please contact the Parkinson’s Foundation Helpline to receive information about resources that best meet your needs. Call the Helpline at 1-800-473-4636 (1-800-4PD-INFO) or helpline@parkinson.org.

What is the PD Solo Network: 

A virtual network for people living with Parkinson's disease (PD) who live alone, by choice or circumstance. The purpose of this group is to create a community of support for those living without a care partner. People living with PD are the experts about what challenges, changes and accommodations are needed on a daily basis. This network will provide a place to share ideas, concerns, brainstorm strategies, suggestions, resources & to build relationships.

The Parkinson's Foundation is providing the initial funding and support to kick start this network. It will most likely become a very strong network that will operate independently although the Parkinson's Foundation will always be an entity of support & information for the participants.

2026 Meeting Dates:

• January 13, 2026
• February 10, 2026
• March 10, 2026
• April 14, 2026
• May 12, 2026

• June 9, 2026

There is no charge to attend, but registration is required in order to receive the Zoom link.

Parkinson's Foundation: The PD Solo Network - Living Alone While Living with PD

There is one session available: 
– 7:30 p.m. to 9 p.m. ET

Please note: These meetings are intended for individuals diagnosed with Parkinson’s disease who live alone, by choice or circumstance – only. If this is not your situation, please contact the Parkinson’s Foundation Helpline to receive information about resources that best meet your needs. Call the Helpline at 1-800-473-4636 (1-800-4PD-INFO) or helpline@parkinson.org.

What is the PD Solo Network: 

A virtual network for people living with Parkinson's disease (PD) who live alone, by choice or circumstance. The purpose of this group is to create a community of support for those living without a care partner. People living with PD are the experts about what challenges, changes and accommodations are needed on a daily basis. This network will provide a place to share ideas, concerns, brainstorm strategies, suggestions, resources & to build relationships.

The Parkinson's Foundation is providing the initial funding and support to kick start this network. It will most likely become a very strong network that will operate independently although the Parkinson's Foundation will always be an entity of support & information for the participants.

2026 Meeting Dates:

• January 13, 2026
• February 10, 2026
• March 10, 2026
• April 14, 2026
• May 12, 2026

• June 9, 2026

There is no charge to attend, but registration is required in order to receive the Zoom link.