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What You Need to Know About Parkinson’s and In-Home Care

Comfort Home Care

In this article, we share vital information about Parkinson’s Disease, the role in-home care can have in managing its challenges, and the qualities to seek in an in-home care provider. Eating, bathing, dressing, grooming, mobility, and toileting are crucial for maintaining health and independence.

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Influencing Outcomes

Chicago Caregiving

Communication is critical First, exchange contact information with the primary medical team, which may include a passcode for patient privacy. As you provide information about the patient at home, the medical team should be giving you updates about the patient’s condition in the hospital. What is the plan for the next day?

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Caring for Someone with ALS

Traditions Health

Eventually, all the muscles that a person can control are affected, forcing the person to use a ventilator and/or feeding tube. When to Seek Help Caring for someone with ALS often presents many challenges for the patient’s primary caregiver. ALS can also impair the ability to think and cause significant changes to a person’s memory.

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The Secret is Out: Hospice Recertification Made Easy!

Hospice Nurse Hero

Please read full disclosure for more information. You’re like the detective gathering all the clues ( information ) from the past several months to support changes in the patient’s condition. You can also use the information from your admission and previous interdisciplinary group (IDG) meetings to help you document.

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Professional Boundaries in Nursing: Are You Crossing the Line?

Hospice Nurse Hero

Please read full disclosur e for more information. For instance, you may need to touch, feed, or even bathe a patient. As a nurse, it might be tempting to promise the family that you will be present when their loved one dies. This post may contain affiliate links. Now, let’s break that down in a little bit more.

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Ep.7: How to Navigate Social Media Marketing in Home-Based Care

Home Care Pulse

They’re looking for resources, they’re looking for more information, but they’re not ready to get care, right? Then, you know, maybe you’re sending them your newsletter or other information, which I won’t get into the newsletter. So there’s one that’s called bathing with dementia.

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Episode 26: How Do I Help The Caregiver?

Living With Hospice

And then of course, there's bathing in toilet and on and on and on and on and on, then collapsing from sheer exhaustion for a few hours of sleep when when you can get it. You know, we're just present. Because we're in the 11th hour fog when we're getting this information from hospice. So here's some things that you can do.