Tag Archives: caregivers

AlzAuthors marks 4th anniversary with a book sale

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I am so proud to be part of the AlzAuthors group. I can’t believe the group of Alzheimer’s and dementia writers is marking its 4th anniversary! It has been so rewarding to see this group expand over the years and I applaud the hard work of the core founders who have shared our books to caregivers around the world.

If you haven’t visited the website in awhile, check out the redesign. I love it!

To mark the occasion, AlzAuthors is hosting a book sale and raffle. Choose from 19 free and discounted books. My award-winning collection of personal essays, The Reluctant Caregiver, is just 99 cents during the promotion, which runs through June 27th. (Note: Amazon is still processing the discounted rate as of Friday morning, but you can use this link to buy the book for 99 cents at other major digital book retailers right now.)

You can also enter a raffle to win free books from select AlzAuthors contributors.

Please spread the word to fellow dementia caregivers and thank you for your support!

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Medicare and Respite Care – What Does it Cover? — The Imperfect Caregiver

Respite care is an issue I care about passionately, prompting me to launch Respite Care Share a few years ago. This guide offers an excellent overview about what respite care benefits Medicare covers. 

When it comes to our loved ones that may be living with health conditions that hinder their ability to perform everyday functions, we want to provide them with the best care. Statistics show that often, it is a family member that takes on this role as a full-time caregiver. Being a caregiver is one of […]

via Medicare and Respite Care – What Does it Cover? — The Imperfect Caregiver

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May 2, 2019 · 5:05 pm

CBD for Caregivers book available now

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I’m excited to share my latest book, CBD for Caregivers. This brief but informative e-book will shed light on what is one of the top health trends of 2019: CBD (cannabidiol.) Hemp-derived CBD is being soil in oil-based tinctures, edibles, topicals and infused into tea and coffee. How can this potentially beneficial supplement help caregivers?

I look beyond the hype and take you on the journey of an average middle-aged woman with no marijuana experience who explores CBD with an open mind and a healthy dose of skepticism. What I found is that CBD holds promise as a healthier way to deal with stress and pain. There are no miracle drugs and some of the more fantastical claims are indeed bunk. But I would also challenge those who argue that positive CBD claims are all just a giant placebo effect.

In addition to an overview of what CBD is and how it may help caregivers, the e-book contains a roundup of my CBD product reviews that are a popular feature on my website, CBDforCaregivers.com.

For my loyal blog followers, you can download CBD for Caregivers for free for a limited time. I would kindly ask that you leave a review at your favorite digital retailer if you grab a free copy. The book is available at the following digital book retailers.  There was a hiccup with Amazon but hopefully it will be available via Kindle soon as well.

I look forward to hearing your feedback on the book and CBD in general. If you’ve tried it, I’d love to hear your opinion.

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Dementia is a thief, but should caregivers be stripped of all joy?

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The complex emotional toll of Alzheimer’s has been in the news the past week. The Washington Post wrote an article about B. Smith, the model, restaurateur and lifestyle guru who has early-onset Alzheimer’s and how her husband has formed a relationship with another woman. B. Smith’s loyal fans were not happy about this development.

Dan Gasby tried to defend himself amidst withering criticism, saying in interviews that B. Smith told him to “go on” after her diagnosis in 2014. He says he’s a better caregiver to his wife now that he’s happier.

Gasby has at least one high-profile supporter: Patti Davis, daughter of Ronald Reagan. In her essay, titled, Alzheimer’s is a cruel thief. Don’t blame caregivers for still finding joy, she reflects upon the emotional devastation an Alzheimer’s diagnosis can bring and what that can do to a couple. She encourages the public to be more sympathetic to those in Gasby’s position.

The issue is at its heart an emotional gut-punch so the fact that it inspires heated opinions is not surprising. What I’ve learned over the years as a  family caregiver for someone with dementia is that I wouldn’t want someone to judge my choices and so I try to refrain from judging others, as long as no harm is being done. While I may not make the same choice as Gasby has made, I cannot rule it out completely either. Those who are outraged on social media would better use their energy volunteering at a memory care center or arranging respite care for a caregiver in their life.

As Patti Davis says, Alzheimer’s is a cruel thief. How much should we allow the disease to steal from caregivers?

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4 Disturbing Dementia Behaviors and How You Can Go From Frustration to Connection — The Imperfect Caregiver

This blog post by Bobbi Carducci is a good reminder on how dementia caregivers must learn a new way to connect and communicate with their loved one, as verbal skills begin to decline. She offers good tips on how you can manage some of the most difficult dementia behaviors.

Often the behavior of someone with dementia is so changeable and unpredictable it’s almost impossible to figure out what is going on, leaving the caregiver confused and frustrated. Why is your spouse confused with you and so alert when someone comes to visit? Why does your mother, who is usually calm and agreeable, suddenly become […]

via 4 Disturbing Dementia Behaviors and How You Can Go From Frustration to Connection — The Imperfect Caregiver

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January 31, 2019 · 9:19 pm

Happy holidays

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Mom and Dad at Christmas, circa mid-1980s.

The holidays can be stressful for caregivers, but they also offer moments of magic and the potential to create memories that you will cherish for the rest of your life.

I hope that you enjoy the time spent with family and other loved ones over the holidays. For those of us remembering those who have departed, it can be a comfort to reflect upon happy moments and favorite memories.

And if you feel yourself being overworked or stressed out, don’t be shy about asking for help!

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When You Should Say “No” in Caregiving — The Purple Jacket

Caregivers, try practicing the art of saying “no” during the increased demands of the holiday season. Not only is it acceptable to say no, it is healthy and necessary so that you don’t get burned out. Saying “no” can be the beginning of an equally important conversation: “I need help with caregiving.”

We welcome back guest writer, Kayla Matthews to The Purple Jacket! Caregiving for an elderly relative is a role that falls on different family members and professional caregivers depending on the family and expectations. And many families often fail to discuss how much responsibility a caregiver should take on and for how long. When the […]

via When You Should Say “No” in Caregiving — The Purple Jacket

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December 18, 2018 · 6:21 pm

Exploring natural stress relief for caregivers with CBD hemp oil

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Caregiving is stressful. Even the most well-adjusted individual can find themselves struggling with the mix of emotions that a caregiver can experience. On top of stress, being a caregiver can be isolating, leading to depression.

I know I was totally stressed out when I was a caregiver for my parents.  There was that “always on edge” feeling, waiting for that phone call that someone had fallen or someone was headed to the ER. As a long-distance caregiver, there was a sense of helplessness and lack of control. When I moved in with my mother to help in her recovery from a colostomy, I experienced a different kind of stress. My mother and I were complete opposites personality-wise, and we often butted heads.

As I look for ways to help caregivers deal with stress, I’ve explored many options. While yoga and meditation can be beneficial, it can be difficult for caregivers to find time for such activities.  Pharmaceuticals work for some people, but come with a host of side effects. The key is to find something that could help relieve stress, anxiety and depression, but without making one loopy or sleepy. Caregivers have to remain alert in order to perform medical tasks.

Lately, I’ve been hearing a lot about Cannabidiol (CBD) hemp oil, and its potential in naturally relieving anxiety and depression, without the psychoactive side effects of marijuana.  My curiosity was piqued. There is  a lot of misinformation about CBD and hemp oil, so I began to investigate its potential for caregivers. Hemp comes from the cannabis plant but it is not marijuana and contains very little THC, which is what causes marijuana’s “high.”

Recently I launched a website, CBDforCaregivers.com. It’s an informational site that includes reviews of CBD hemp oil products that I’ve personally tried. My focus is on how these products can help ease anxiety and depression, along with offering pain relief. (The physical labor involved in caregiving can cause chronic pain.)

I’m excited about the potential of CBD hemp oil products, but the products remain in a murky legal state for now. The hemp provisions in the Farm Bill of 2018, if it passes, could remove the cloud of uncertainty at the federal level, though some states are targeting stores that sell CBD products.

It’s important to check your local laws and consult your doctor before using any natural supplement.

If you’ve tried CBD hemp oil, I’d love to hear about your experience.

 

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Food And Alzheimer’s: How To Maximize Nutrition And Make Mealtimes Easier — The Diary of An Alzheimer’s Caregiver

Good tips here! While my dad retained a remarkable appetite when he was in the memory care center, when he landed in the hospital, his appetite dissipated. Caregivers should be prepared to “bend the rules” and let dessert be eaten first, etc. In the end, it doesn’t matter about the order of consumption, as long as your loved one is happy and eating.

Sign up to get these posts and a whole lot more delivered right to your inbox! The Diary of An Alzheimer’s Caregiver – Appreciate the good, laugh at the crazy, and deal with the rest! 97 more words

via Food And Alzheimer’s: How To Maximize Nutrition And Make Mealtimes Easier — The Diary of An Alzheimer’s Caregiver

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August 21, 2018 · 8:35 pm

Win a FREE trip to the National Caregiving Conference in Chicago

Please share this with any current family caregivers in your life. It is so inspiring to be in a room with fellow caregivers, sharing the ups and downs of the caregiving experience.

The Imperfect Caregiver is honored to be among those who will be presenting at the Third Annual Caregiving Conference in Chicago, November 9th and 10th. For a sneak preview of the presenters Caregiving.com is having a virtual summit May 14 – May 24. Virtual Caregiving Summit Our virtual summit, featuring conversations with our National Caregiving […]

via Win a FREE trip to the National Caregiving Conference in Chicago — The Imperfect Caregiver

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