Molly Harrigan Occupational Therapy

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Molly Harrigan Occupational Therapy Outpatient OT Services in the home: Specialties in Cognition and Aging in Place Accepting insurances for occupational therapy services

https://www.pressherald.com/caregiver/
10/13/2026

https://www.pressherald.com/caregiver/

Friday, October 23, 2026 7:45 a.m. – 5:00 p.m. Hannaford Hall, Abromson Centerat USM Portland Hosted by the Maine Trust for Local News with Age Maine (formerly the Southern Maine Agency on Aging) EMPLOYER LEADERSHIP FORUM 7:45 a.m. The business case for supporting employees who care for loved ones...

10/11/2026

What looks like “acting out” may actually be communication.

Yelling. Hitting. Pushing caregivers away. Refusing care. Throwing things. Pacing. Swearing. Becoming suddenly agitated.

These behaviors can be difficult and upsetting, but a person living with dementia may no longer be able to clearly explain what is wrong or what they need.

Instead of asking:

❌ “Why are they acting like this?”

Try asking:

💜 “What might this behavior be telling me?”

Look for possible reasons

Before assuming the behavior is simply part of dementia, consider:

🔹 Pain or discomfort — Could something hurt?
🔹 Hunger or thirst — When did they last eat or drink?
🔹 Toileting needs — Could they need the bathroom or be constipated?
🔹 Fear or confusion — Do they understand what is happening?
🔹 Overstimulation — Is the environment noisy, crowded, or overwhelming?
🔹 Fatigue — Are they tired or being asked to do too much?
🔹 Frustration — Are they struggling to communicate or complete a task?
🔹 Approach to care — Are they feeling rushed, corrected, restrained, or pressured?
🔹 Medical changes — Pain, infection, dehydration, medication effects, or delirium can sometimes contribute to sudden behavior changes.

What caregivers can try

💜 Approach slowly and calmly.
💜 Use short, reassuring sentences.
💜 Avoid arguing, correcting, or demanding an explanation.
💜 Give the person more time to respond.
💜 Reduce noise and stimulation.
💜 Step away briefly when safe if tension is escalating.
💜 Redirect toward something familiar or comforting.
💜 Look for patterns—what happened before, during, and after the behavior?

Remember

The behavior is what you see.
The reason is what you need to find.

A sudden or significant change in behavior deserves extra attention, especially when accompanied by changes in alertness, pain, fever, weakness, eating or drinking, urination, breathing, or other new symptoms. Contact the healthcare team for guidance; seek urgent help when there is an immediate safety or medical concern.

💜 Caregiver reminder: The goal isn't simply to “stop” a behavior. Understanding what may be driving it can help you respond to the person behind the behavior.

From the Dementia Care Behavior Guide
Created by a Registered Nurse & Certified Dementia Care Provider.

10/09/2026

Family caregivers often learn to hide their hardest moments because someone still depends on them. They cry where nobody can see, pull themselves together, and return to the medications, meals, appointments, decisions, and responsibilities waiting for them. The tears don't mean they cannot handle caregiving. Sometimes they are the only private release available to someone who's held too much together for too long.

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10/09/2026

On lunch break, I helped feed my mom.

And as I sat there, I remember thinking, Thank God I get to get some juice in her. Look how dry her lips are. She must be so thirsty.

And then I realized how much my thinking has changed.

There was a time when I worried constantly about hydration, nutrition, UTIs, falls, broken bones, emergency rooms. When Mom was still walking the halls at her last place, I lived in that constant fight-or-flight mode. I was always trying to keep her safe. Keep her healthy. Prevent the next crisis.

I don’t really worry about those things in the same way anymore.

And I think I needed to realize that.

Because now, when lunch comes, Mom sits at the table with the people who need the most help. On the other side of the little wall, there are people feeding themselves. Spouses helping spouses. Daughters helping their mothers.

And there I was, feeding mine.

Honestly, it was incredibly nourishing for me.

And incredibly sad.

I never in my life imagined that one of my parents would need help with absolutely everything. Getting dressed. Getting clean. Eating. Drinking. Every basic thing we once took completely for granted. Back to a child.

There. I said it.

Why is it devastating when someone dies suddenly, in an accident, because life ended too soon?

And why is it devastating in an entirely different way when someone spends almost a decade slowly declining right in front of everyone’s eyes?

I have no answers, friends.

I know only this:

I will keep showing up.

I will feed her. I will give her a drink. I will hold her hand. I will bring whatever little bit of life and comfort I can into her day.

And after lunch, Mom looked at me and gave me that smile.

That little glimmer.

And for a moment, I thought, Maybe I’m doing exactly what I’m supposed to be doing.

I hope.

Sending love to all of you walking this road.

Share your struggles and glimmers! 💜💜

10/09/2026

On today’s episode, we’re checking in on the U.S. POINTER study one year later. Study participant Linda Pietras shares her experience and reflects on the lifestyle changes she’s continued. We’re also joined by Dr. Molly Split, a neuropsychologist at Butler Hospital, who discusses her research exploring what helps people engage in and sustain healthy behaviors, including the role of self-confidence.

🎧 Listen now wherever you get your podcasts: alz.org/speakingofalz 💜

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