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The Long and Winding Road…

~ An Alzheimer's Journey and Beyond

The Long and Winding Road…

Tag Archives: caregiving

Caring for the Caregiver: Essential Oils

24 Sunday May 2015

Posted by Ann Napoletan in Caregiver Burnout, Caregivers

≈ 8 Comments

Tags

alzheimers, alzheimers caregiving, caregivers, caregiving, essential oils

I was recently introduced to essential oils, and have become very interested in their therapeutic properties. Up to this point, my experience had been limited. I knew they smelled good and that lavender was said to decrease stress and improve sleep, but it didn’t go much further than that. It was really conversations with a few friends that piqued my curiosity.

Why Essential Oils?

Essential oils are nothing new; in fact, they’ve been around for centuries. However, with increasing concerns over use of harmful chemicals in everything from household cleaners to shampoo, there is definitely a heightened interest in natural alternatives. Oils have many practical household applications, but I’m most interested in what they can do for our mind, body, and spirit. Continue reading →

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Long-Term Care: Extra Support When You Need It

08 Sunday Mar 2015

Posted by Ann Napoletan in Care Options, Caregivers, Guilt and Regrets, Helpful Resources, Hospice, Mom, Support system

≈ 9 Comments

Tags

alzheimers, caregiver support, caregiving, hospice, long-term care ombudsman

The decision to place a loved one in a care facility is heart wrenching no matter the circumstances. When the time comes, we are filled with uncertainty, apprehension, and an overwhelming sense of guilt. They took care of us; how can we not do the same? What will people think? Does this make me a bad daughter/son/husband/wife?

 

The Critical Role of Managing Care

I think it’s so important for caregivers to understand that placing a loved one is in no way synonymous with failure. Dementia is a long, agonizing road, and not everyone is equipped to care for a family member at home. Sometimes the decision to seek assistance makes you a better caregiver in the long run.

When you place a loved one your role will change, but you will remain the most essential member of the care team. Now you will oversee their care and act as their most staunch advocate. With daily care left to a team of experienced caregivers, you can be the daughter/son/husband/wife again. You can focus on their wellbeing, creating moments of joy, and just loving them. I can’t think of a more crucial role.

But with all of that said, what resources are available to provide help when needed?

The Long-Term Care Ombudsman Program

As a nurse, Jan Larsen-Fendt spent more than 20 years working with the elderly in various settings including rehab, long-term care, and hospice. When she retired, she wanted to continue her work with the elderly in some capacity, so she trained to become an Ombudsman.

What is the definition of a Long-Term Care Ombudsman? According to the Administration on Aging:

Long-Term Care Ombudsmen are advocates for residents of nursing homes, board and care homes, assisted living facilities and similar adult care facilities. They work to resolve problems of individual residents and to bring about changes at the local, state and national levels that will improve residents’ care and quality of life.

When she completed her training and became certified, Jan said, “I felt as though I should have a cape and a shirt with a big “O” on it!! I could finally DO something about people’s complaints/concerns.”

She wants caregivers to know there are places to turn for help when issues arise in care facilities. “The Ombudsman program is a government program and works side by side with the Department of Health,” Jan explains. “If you have concerns that are not being addressed by the facility your loved one is in, contact your local Ombudsman.”

Facilities are required by law to display posters bearing Long-Term Care Ombudsman contact information. You can also consult The National Consumer Voice for Quality Long-Term Care to find the Ombudsman in your area.

Thoughts on Hospice

Jan highly recommends engaging hospice sooner than later. Unmanageable staff-to-resident ratios can and often do lead to issues in long-term care facilities. While the staff may want to do more for a resident, the workload simply might not allow it.

As a hospice nurse, Jan explains, she was charged with overseeing care and serving as a patient advocate. Hospice typically does not operate under the same staffing constraints that impede LTC facilities so they are able to provide an extra sets of eyes and ears.”

“Don’t ever hesitate to ask for a referral to hospice. Don’t let a nurse just say, ‘No, he’s not ready for that.’ It’s up to the doctor. There are many ways to get a person on hospice,” says Jan. “Hospice does not always mean imminent death. We have even had people ‘graduate’ from the program.”

Don’t Go It Alone

The bottom line is this. Even if a loved one is not under your direct, 24×7 care, your role as his or her care manager is vital. But remember, you aren’t alone. There are agencies and services you can call on for assistance. Your local Office on Aging is a great place to start; don’t hesitate to reach out to them for guidance.

During my mom’s illness, I enlisted the help of the LTC Ombudsman. The office could not have been more supportive. I was immediately struck by their passion and dedication to ensuring our loved ones are being properly cared for.

We also utilized hospice services and found the extra support to be a godsend. Mom was on hospice for a relatively short period, but during that time, the caring compassion shown to us as a family was incredible.

Please don’t wait to reach out for support; this is a journey that doesn’t have to be traveled alone.

 

 

 

 

 

 

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Banner Alzheimer’s Institute: 2015 Dementia Dialogues Webinar Series

18 Sunday Jan 2015

Posted by Ann Napoletan in Caregivers, Coursework & Learning Opportunities, Events, Helpful Resources, Tips

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Tags

alzheimers, alzheimers education, banner alzheimers institute, caregiving, dementia, dementia webinar

Here are some amazing 2015 online education opportunities, straight from The Banner Institute.

Scheduled each third Wednesday, Dementia Dialogues offers a different, pertinent webinar topic each month. For those who are not comfortable with the Internet or who don’t have access, an exclusively audio version is offered as well.

The January webinar will take place this coming Wednesday, Jan 21. Click here to learn more and register!

January 21 – Everything You Always Wanted to Know about Dementia but were Afraid to Ask:  There is a lot of conflicting information, misinformation and unanswered questions surrounding Alzheimer’s and dementia. Join us to gain some clarity with dementia as our experts discuss some questions commonly posed to them. Come prepared to ask your unanswered questions.

February 18 –  Lack of Insight into Dementia:  “My person is in denial about their illness” is a phrase heard all too often in the dementia world. However, some people with this disease are simply unable to see changes within themselves – they have lack of insight. During this Dialogue, you will learn the difference between denial and lack of insight, and will receive strategies to avoid confrontation with a person who cannot accept cognitive losses.

March 18 – Planning for Care across the Stages of Dementia:  Dementia is a disease that requires planning – constantly. Each stage brings unique challenges and needs and by being pro-active rather than reactive, caregivers can help lighten their load and have the confidence they are making decisions as their person would wish. Learn about specific plans that should be made during the various stages of dementia.

April 15 – Alzheimer’s Medications:  Observing benefit of the approved medications for the treatment Alzheimer’s disease can be difficult to see as they don’t modify the course of the disease but can assist in managing symptoms.  Join this Dialogue to learn about medications, reasonable expectations for use, potential side effects and tips for common issues.

May 20 – Planning Successful Travel:  Travel is a joy that many people share throughout their lives. When someone develops dementia, many strategies for daily life can be disrupted by leaving home. While it may require extra thought, travel can still be enjoyable for someone with dementia. Just in time for summer travel, learn tactics to make your trips as successful as possible.

June 17 – Men as Caregivers:  Many men are finding themselves caring for their wife or mother with dementia. It turns out that some stereotypical male qualities can come in quite handy for caregivers of someone with dementia. Join this frank discussion to learn strategies from some successful male caregivers.

And coming during the second half of 2015: 

July 15 – Understanding Psychosis

August 19 – Maintaining Realistic Expectations as Dementia Progresses

September 16 – Best Lessons from Powerful Tools for Caregiving

October 21 – How and When to Execute Powers of Attorney

November 18 – Preparing for the Holidays

December 16 – The Gift of Presence

 

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Marilyn, BA (before Alzheimer's)

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