Who wrote this?
CallowayGuides is a publishing name, not a person. There is no author's name or biography on this guide. No nurse, doctor, or other healthcare professional wrote or reviewed it, and we don't want you to assume otherwise.
An independent guide for families, compiled from cited published sources. Not written or reviewed by a healthcare professional, and not a substitute for your hospice team.
How the guide was prepared is stated in the note on its last page, under "About this book." If anything you read there changes your mind, ask for your money back. If you would rather read a book by a hospice clinician, that is a sound choice, and your hospice team may be able to suggest one.
I watch free videos, and my hospice gave me booklets. Why would I need this?
You may not. The free videos are good, and so are the booklets your hospice hands out. Keep using them. The videos give you an overview. The booklets cover their part. This guide puts the steps in one place, in order, so you can look something up in the moment instead of searching for the right video at night.
Much of the information behind it is public, and we say so. What you are paying for is having it gathered, organized, and sourced.
Does this replace my hospice team?
No. Use it alongside your team, never instead of them. If anything in it differs from what your team has told you, follow your team and ask them about the difference. Each chapter ends with questions to take to them, and Appendix B gathers those questions in one place.
Does it tell me how much medicine to give?
No. The guide gives no medication doses. Your hospice team sets those. It tells you what to watch for, what to ask, and when to call before you do anything else.
Can it tell me how long is left, or how it will go?
No, and no one can promise that. The signs in Chapter 5 can help you understand what you are looking at and ask better questions, but they can't give you a date. Some deaths are hard even with good care. The guide says so, and tells you what to ask for if that happens.
Where does the information come from?
From published sources, listed at the end of each chapter and gathered under All Sources at the back. They include Medicare and the Centers for Medicare & Medicaid Services, the National Institute on Aging, the National Cancer Institute, the American Cancer Society, MedlinePlus, the FDA, the Hospice Foundation of America, and National POLST. Where the sources don't settle something, the guide tells you. Some practical suggestions, such as how to press for help when a call isn't returned, are not drawn from a published source.
The guide is not affiliated with or endorsed by any of these organizations. This edition's information was checked in November 2026.
The person I'm caring for isn't on hospice yet, or has an illness other than cancer or dementia. Is it still useful?
It can be. The symptom chapters are organized around what you are seeing, not around one diagnosis, and the guide says what changes when someone isn't on hospice. Cancer and dementia each have their own chapter. Other illnesses do not. It also covers nursing homes and caring from far away.
How do I get it, and can I read it on my phone?
It is a PDF. After you pay, you go straight to a download page, and the link also comes to you by email. It opens on a phone, tablet, or computer, and you can print any page you want near the bed.
Is it for people outside the United States?
No. The phone numbers, Medicare rules, and legal forms are for the United States. Elsewhere they are different, so please ask your local care team instead.
What if it isn't what I needed?
The 90-Day No-Questions Refund covers you. Any time in the 90 days after you buy, reply to your delivery email and ask for your money back. We don't ask why, and we won't ask anything about the person you are caring for. You don't have to send or delete anything.