Last Chapter Augusta

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Last Chapter Augusta End of life planning and compassionate support for individuals and families navigating advanced illness or a terminal diagnosis.

Blending hospice experience with holistic care to create meaningful, peaceful, and deeply personal end of life experiences.

Just checking… because nobody should have to learn all of this the hard way 🫶🏼There are SO many things families aren’t t...
29/08/2026

Just checking… because nobody should have to learn all of this the hard way 🫶🏼

There are SO many things families aren’t told until they’re already in the thick of it and then comes the guilt, the panic, and the “Wait… was I supposed to know this?!”

I’m here to make death and dying a lot less scary, confusing, and awkward.

Save it. Share it. And follow along because we’re talking about the stuff people REALLY want to know but are sometimes too afraid to ask.

Most families think hospice means losing control. The opposite is true. Hospice is not the boss of you, you still have a...
01/08/2026

Most families think hospice means losing control. The opposite is true. Hospice is not the boss of you, you still have all the power!

Hospice is about supporting your goals and honoring your choices. Whether it’s requesting more visits, changing hospice companies, refusing a medication, or even revoking hospice if circumstances change, you have rights every step of the way!

The more you understand those rights, the more confident you’ll feel advocating for yourself or a loved one.

I dedicated an entire section of my Hospice Guidebook to explaining your rights on hospice in plain, easy-to-understand language, because every family deserves to know all their rights.

If this post taught you something new, save it for later and share it with someone navigating hospice. And if you want to feel more prepared, my Hospice Guidebook covers your rights, comfort medications, signs to expect, caregiver tips, and so much more. The link is in my bio!

26/07/2026

People expect my biggest “ick” about morphine to be… giving it.

It’s not.

My actual morphine icks as a hospice nurse:
💊 When the morphine is clear instead of pink or blue. It can be much harder for families to see in the syringe, which can make measuring it feel more intimidating.
🙃 When the bottle doesn’t come with a bottle adapter. It helps prevent spills and makes drawing up medication so much easier.
📏 When the syringe has tiny markings instead of the larger one with four bold lines. Bigger, clearer markings give caregivers more confidence that they’re measuring the right dose.

Notice a pattern?

None of my “icks” are about morphine itself. They’re about making it easier for families to safely and confidently give a medication that can provide incredible comfort.

Morphine doesn’t have to be scary. Good education and the right equipment make all the difference. 💜

Have you ever felt nervous about giving comfort medications? You’re not alone! I’m breaking down what families need to know about hospice comfort meds in my Hospice Guidebook coming soon!

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