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

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.

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.

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.

Join the Parkinson’s Foundation and PD Active to hear from keynote speaker Ray Dorsey, MD, co-author of “The Parkinson’s Plan.” The presentation will overview key points of the book including how prevention, better care, smarter policy and advocacy can change the future of Parkinson’s. 

Doors open at 1 pm and presentations start at 1:30 pm on Thursday, Jan. 29. Come together with your community for an interactive presentation and “The Parkinson’s Plan” book signing (while supplies last).

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

In partnership with PD Active. Registration information will be shared among the Parkinson's Foundation and PD Active, and attendees can opt out of email updates from either group at any time. 

Changes in memory, attention, and problem-solving are common non-motor symptoms of Parkinson’s that can affect daily life, relationships, and independence. In this webinar, we’ll explore how Parkinson’s impacts cognitive function and what veterans and care partners can do to recognize, manage, and adapt to these changes. We'll also discuss when to seek additional support, how the VA addresses cognitive health, and which tools and therapies may help maintain brain function and quality of life. 

Speakers

Anita Sim, PhD 
Neuropsychologist, Minneapolis VA Health Care System  

Christy Becker, MA, CCC-SLP 
Speech-Language Pathologist, Minneapolis VA Health Care System

Konner Kielman, OTD, OTR/L, LSVT BIG Certified 
PD/MD Staff Occupational Therapist, Minneapolis VA Health Care System

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.

The Parkinson's Foundation is proud to partner with U.S. Department of Veterans Affairs to improve the health, well-being and quality of life for veterans with PD.