Everyone’s focused on Parkinson’s.

Who’s focused on you?

Introducing:
Parkinson's Caregiving 101: Patience, Peace, and Practicality

Parkinson’s Caregiving 101: Patience, Peace & Practicality is a self-paced course that finally puts the caregiver at the center — with real tools, honest insights, and practical guidance for the life you’re actually living.


What if I am not  a born caregiver? 

Can our relationship survive this? 

We don't communicate the way we used to.

I'm afraid he is going to get hurt, or I will.

Is this what my whole life will be about?  

What do I do first? Find a better doctor? Write a will? Buy a better chair?

Imagine This

It’s another morning as your PWP’s caregiver. But today you started with a sense of love and confidence. 


From the moment your loved one was diagnosed, you said: “I want to be the best caregiver possible.” While the doctors and books focused on symptoms and medications, you wanted to know how to actually live this life. 


You know things can change quickly as Parkinson’s progresses. 

You want to be loving. 

You want to be patient. 


And you start each day knowing you have a head start — because you have prepared yourself. If something new comes up, if your loved one needs something you haven’t faced before, you have resources now. You took this course. You know where to find answers. You feel ready.

Hi. I’m Terri Pease, Ph.D

I’m an author and coach for Parkinson’s caregivers. For nearly ten years, I cared for my husband, who had Parkinson’s Disease.
 
My background in Human Development gave me tools I never expected to need — until Parkinson’s entered my marriage. 

I’d spent years traveling the country helping people and organizations navigate the hardest moments of their lives. 

That experience became the foundation for everything I now share with caregivers like you. 

My husband and I had nearly ten years together with Parkinson’s in our lives. After he died — peacefully, in my arms — I started writing down what I’d learned. That writing became my life’s work. 

Today more than 6,000 PD caregivers read my weekly Q&A column, turn to my book Love, Dignity and Parkinson’s: from Care Partner to Caregiver, and support each other in my private online community. Now I’ve built on all of that to create what so many of you have asked for: “I know what I’m supposed to do — but how do I actually do it?”



Because caregivers have feelings too.

And no one seems to notice.



You may feel like you don’t have the time — or the money — to choose something for yourself. 


You’ve got your PWP’s doctors for prescriptions. You can ask for a physical therapist. But the things PD caregivers need most won’t come from the neurologist’s office: 


• How to build a loving connection while caregiving. 

• How to be patient — day after day after day. 

• How to balance your own needs with your commitment to your PWP. 


These things matter deeply — and you won’t learn them from your PWP’s doctors, your spiritual advisors, or even a couple’s therapist. 


You need support from someone who has actually walked this path. Sure, you can find a support group. But too often those meetings focus on Parkinson’s itself. You still feel like you’re just “painted on the wall.”


Finally, someone who understands what your life is like.

Don't just take my word for it. 
Past students say it, this made all the difference. 

"I thought joy was impossible in caregiving, but this course showed me how to find it in the small moments. Terri reminded me that even now, joy is accessible if I look for it."

Alfonso

Solo caregiver for 3 years

“The Tools and Resources Module was eye-opening. I feel so much more prepared with practical strategies to manage safety and risks while still respecting my partner’s independence."

Keshina

Caregiver for 11 months

"I learned to see caregiving, not as something that’s been done to me, but as a choice I'm making with love. That shift changed everything.""

Ursula

Husband diagnosed 4 months ago

"This course felt like a lifeline. It helped me see that I’m not alone and that it’s okay to care for myself, too."

Jin-Yo

Caring for her mom who has Parkinson's

Six Modules Covering What
No One Else Talks About

Important topics that are crucial both to your wellbeing as a caregiver and to your ability to give your loved one, your PWP, the care you know they deserve.

01

Your Mindset

02

Looking at Your Relationship

03

Communication Strategies

04

Tools and Resources

05

Risks and Safety

06

Meaning and Mission

What kind of caregiver does your loved one need? 

Think about how much you have spent in time, money, in struggle, trying to get it right. Trying to fulfill your promise to be the best caregiver. You’ve bought books, you’ve tried therapists who didn’t understand what you needed, you’ve bought one more gizmo, all trying to put the pieces in place for giving your loved one with PD, your PWP the care you want to give. 


 Bu have you asked what kind of caregiver your loved one needs?
 Here’s my answer. 


 People with Parkinson’s need a caregiver who has thought through their own emotions and made an affirmative choice to take on this role. 


 People with Parkinson’s need a care partner or caregiver who has set up the team of professionals and community supports to help over the long haul. 


 People with Parkinson’s need a caregiver who knows that their own well-being is the most important thing to maintain a caring commitment even as Parkinson’s is constantly challenging them. 


 Your person with Parkinson’s needs you to get the real tools and information, and strategies to do what you wanted to do. To be the best caregiver you can be. 


 If you’re asking yourself “How can I spend money on myself?” the answer is clear. A session or two with a therapist can cost up to $500. A spa-day will cost more than that and at the end you’ll come back to the same struggles, just with better skin and a new haircut. And if you’re like many of us, you’ve bought lift chairs he can't use and buckets of cleaning supplies, and all sorts of things, hoping to find that one right thing.


 I don’t know if those things were a waste or not. 


But you can be sure. If you’ve decided after Module 1 that this course is not right for you, just ask for a refund, no questions asked. There’s no risk, really. And the possibility of a newfound sense of clarity and confidence about your personal approach to caregiving.


So you've been thinking about it. You've asked yourself, "Why won't anyone help me understand what's happening?"  


Well here I am, and this is your chance to get real-world answers, and the help you need.


It takes more than good intentions. It takes action.



Frequently Asked Questions

The course Introduction session is available to you as soon as you have enrolled. Then future modules become available every week.

Parkinson's Caregiving 101 is an on-demand self study course. Later this year I will be offering options for group-based in-person support.

I do also offer one-to-one coaching packages as they become available. You can email terri@terripease.com to learn about this option.

I designed this course to support PD caregivers. But if you are a caregiver for someone with a different diagnosis you can enroll with confidence. If you decide after Module 1 that this course is not for you, you can get a full refund, no questions asked.

Definitely not. You are reading this on your phone or computer, and that's all you need.

You will get reminder emails to make sure you know when each session is coming, and how to find what you're looking for.

I know that caregiving keeps you busy. So each Module is designed for you to watch and listen at your convenience and view the recordings in smaller sections.

I'm fully aware that I could easily ask much more for a course of this depth. But I've created this program to be accessible for almost any caregiver.

  • Access to 24 video lessons in six on-demand video modules — available for as long as the course is online
  • Downloadable templates and resource pages
  • A separate workbook for each module, along with an audio file and written transcript
  • Your personalized Caregiver Log Book
  • Additional bonus support downloads

While this course is designed for people who are in the earlier months or years of caregiving, those who have more experience have still found useful information and support here. And with my no questions asked guarantee, you can feel confident in starting the program.

Praise for my approach to supporting caregivers.

All my reading I never found anything like her. She was using the exact words I was saying. Wow! Terri is so helpful

Bess
Caregiving for 6 months

"She definitely speaks from experience and from the heart. She is practical while being compassionate.

Henry 
New Caregiver

Since connecting with Terri, I find that my days have become more peaceful and my relationship with my husband has improved because of my “new” attitude. Thank you, Terri, for helping me to find that peace and understanding!

Giuliana
8 years of caregivng

"Aut dicta commodi nostrum quidem delectus molestiae ad et ex odit."

Samantha
CEO / Founder

You show up for your PWP every single day. It’s time someone showed up for you. 

This course gives you the confidence, clarity, and practical tools to be the caregiver you already want to be — without losing yourself in the process. You don’t have to figure this out alone. You don’t have to keep searching for answers that no one around you seems to have. And even without working with me directly, you’ll have what you need to move forward — at your own pace, in your own way. Enroll today. Work at your own pace. Feel prepared.

Risk-Free GuaranteeComplete Module 1 and request a full refund if it's not right for you — no questions asked.

Questions? Reach out at support@seaburyhouse.com

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