LogoSteady
I didn't know I was allowed to ask for help until someone handed me this number.
Portrait of Margaret, a caregiver with warm eyes and grey hair

Margaret

Caregiver since 2019 Β Β·Β  Portland, OR

If you're managing someone else's Parkinson's, you already know what it costs. Steady was built for exactly this β€” the invisible labor, the interrupted sleep, and the questions you're too tired to Google at 2Β a.m.

This is a crisis. With solutions.

0M

caregivers in the U.S.

That's 10 million people who woke up this morning, checked a pill organizer before their own coffee, and started a shift with no clock-out time.

0%

report clinical depression

Not sadness. Clinical depression β€” the kind that makes Tuesday feel like the same Tuesday you've been living for three years, with no end visible.

0hrs

of unpaid care per week

That's a part-time job with no pay, no benefits, no performance review β€” just the quiet knowledge that if you stop, someone falls.

β€œCaregiver burnout isn't a character flaw. It's what happens when a person with finite energy is handed an infinite task without support.”

β€” Parkinson's Foundation, 2024 Caregiver Impact Report

Everything here is free. No strings.

We built these tools because they didn't exist in one place. Download, print, share β€” no account required.

Parkinson's Stage-by-Stage Symptom Guide

Free guide

A plain-language walkthrough of what to expect at each stage β€” what changes, what stays the same, and how to adapt your caregiving approach without losing yourself.

Printable Medication Tracker

Free tool

A daily log designed for complex medication windows β€” with space for on/off periods, dyskinesia notes, and columns for the symptoms your neurologist actually needs to hear about.

5-Minute Caregiver Burnout Self-Assessment

Free Β· 5 min

Twelve questions that take five minutes but might change the next five months. No diagnosis, no judgment β€” just a clear picture of where you are right now.

Download the Caregiver Starter Kit

The full kit includes all three guides above, plus a 30-day check-in calendar and a one-page emergency reference for freezing episodes.

No spam. Unsubscribe anytime. Your information stays private.

What to expect. What to do.

Parkinson's moves at its own pace. This guide doesn't tell you when β€” it tells you what to watch for, and what to hold on to.

1

Early β€” Mild Symptoms

Tremor usually affects one side. Handwriting may shrink. Balance is mostly intact. Your person may still be driving, working, and managing most daily tasks.

Caregiver focusThis is the window to build systems together β€” medication routines, exercise habits, advance directives. The hardest thing: grieving what might come while celebrating what still is.

β†’ Prepare together

2

Moderate β€” Both Sides Affected

Tremor, rigidity, and slowness affect both sides. Posture changes. Falls become a real risk. Daily tasks take longer and may need assistance.

Caregiver focusHome safety becomes urgent. Bathroom grab bars, non-slip mats, a raised toilet seat β€” small changes that prevent emergency-room Tuesdays. Medication timing windows narrow here.

β†’ Adapt the home

3

Mid-Stage β€” Balance & Speed

Balance is significantly impaired. Falls are frequent. Reflexes slow. Eating and dressing take meaningful effort. Independence requires more support.

Caregiver focusYou are likely now a full-time caregiver, even if you don't call it that. Respite care isn't a luxury at this stage β€” it's a medical necessity for both of you.

β†’ Build your team

4

Advanced β€” Significant Assistance Needed

Standing alone is possible but risky. Most daily activities require help. Freezing episodes are more common. Cognitive changes may begin.

Caregiver focusFreezing episodes: don't pull, don't rush. Try a visual cue β€” a line of tape on the floor, a rhythmic count, a hand placed calmly on their shoulder. This is the 2 a.m. call we're here for.

β†’ Manage freezing

5

Late Stage β€” Full Support

Wheelchair-bound or bed-bound. Swallowing difficulties. Significant cognitive and communication changes. Round-the-clock care is required.

Caregiver focusYour job now is presence, comfort, and advocacy. You don't have to do this alone. Palliative care teams, hospice support, and our 24/7 line exist precisely for this chapter.

β†’ You're not alone

Want the full printable version?

The downloadable stage guide includes medication timing charts, freezing episode protocols, and a one-page emergency summary for first responders.

Get the Full Guide

You're not the first. You won't be the last.

Three caregivers. Three different situations. One thing in common: they all found the support they needed β€” and they all said they wish they'd found it sooner.

β€œDad is in Phoenix. I'm in Boston. I manage his medication windows from my phone at 6 a.m. before my own kids wake up. Steady's coordinator called me back in twenty minutes. Twenty minutes.”

Portrait of Priya, a woman in her 40s with dark hair and a calm expression

Priya

Daughter, remote caregiver Β Β·Β  Caregiver since 2021

Boston, MA

β€œMy wife can't hold a fork anymore. I learned to cook everything one-handed so she wouldn't feel watched. The caregiver burnout assessment told me things about myself I'd been avoiding for two years.”

Portrait of Robert, a man in his 60s with silver hair and kind eyes

Robert

Spouse, full-time caregiver Β Β·Β  Caregiver since 2018

Asheville, NC

β€œI do twelve-hour nights at the hospital and come home to a second shift. Nobody tells you that's not sustainable. Steady's respite coordinator found me eight hours of relief in the first week.”

Portrait of Diane, a nurse in her 50s with a warm smile and tired but hopeful eyes

Diane

Nurse, night-shift caregiver Β Β·Β  Caregiver since 2022

Chicago, IL

Whenever you're ready. We're not going anywhere.

1-800-555-0199 Β Β·Β  Available 24 hours, 7 days a week