“Lewy Body Dementia Caregiving – Insights & Experience” Seminar, April 19

Please join Brain Support Network, Stanford Parkinson’s Caregiver Support, and Avenidas for a seminar on Lewy Body Dementia caregiving:

Lewy Body Dementia Caregiving – Insights & Experience

Date:  Wednesday, April 19, 2017
Time:  2:30-4pm
Location:  Avenidas (avenidas.org), 450 Bryant St., Palo Alto – La Comida Dining Room

Speaker:  Christina Irving, LCSW, Family Caregiver Alliance

Panelists:  Three members of the Brain Support Network Lewy Body Dementia Caregiver Group including one woman whose husband is in middle stages, one woman whose father is in middle stages, and one gentleman whose wife died in December 2016 with presumed Lewy Body Dementia.

This event is free but please RSVP to Avenidas, phone 650-289-5400 so  that we have enough refreshments and materials for everyone.

 

“Reducing Personal Stress” – chapter 2 of “Caregiver Helpbook”

Organizations around the US, including Family Caregiver Alliance in the Bay Area (caregiver.org), teach a course called “Powerful Tools for Caregivers,” developed by an organization in Portland.  You can read general info about the self-care education program for family caregivers at powerfultoolsforcaregivers.org.

As part of the course, class participants receive a copy of a book titled “The Caregiver Helpbook.”  The book is available in both English and Spanish.  Brain Support Network volunteer Denise Dagan is reading the booklet and will be sharing the highlights, chapter by chapter.

The title of chapter two is “Reducing Personal Stress.”  Obviously this chapter explores the stress of caregiving.  As the book states:  “Studies show that a certain amount of stress is helpful.  It can challenge us to change and motivate us to do things we might not do otherwise.  However, when the amount of stress overwhelms our ability to cope with it, we feel ‘distress’ or ‘burnout.'”

“A basic premise of this chapter is that each of us has a reservoir of strength.  The challenge is to identify our strengths and build on them. … The philosophy of Virginia Satir, noted family therapist,…reminds us that how we perceive and respond to an event is a significant factor in how we adjust and cope with it.”

This chapter contains lots of useful worksheets.  You’ll need to purchase the book ($30) to obtain the worksheets.

Here’s Denise’s report on chapter two.

Robin


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Notes by Denise

The Caregiver Helpbook
Chapter Two – Reducing Personal Stress

Factors that Affect Stress:

* Whether your caregiving is voluntary or not.  “If you ‘inherited’ the job and feel you had no choice, the chances are greater for experiencing strain, distress, and resentment.”

* Your relationship with the care receiver.  “If the care receiver has always been demanding and controlling, you will probably feel more stress, anger, and resentment.  Sometimes people are caregiving with the hope of healing a relationship.  The healing may or may not happen.  If healing doesn’t happen, the caregiver may feel regret, depressed, and discouraged.  A professional counselor, spiritual advisor, or trusted friend can help deal with such feelings and emotions.”

* Your coping abilities.  “How you have coped with stress in the past predicts how you will cope now.  Identify your current coping strengths and build on them.  Learning new coping skills also will help make your caregiving situation less stressful.”

* Your caregiving situation.  “Does it require 24-hour-a-day availability, or just the occasional phone call?

* Whether support is available.  “Caregivers who feel isolated and without adequate support usually experience a higher level of stress.”

Steps to Maintain Health and Avoid Distress:

Step 1. Recognize your warning signs of stress.  “It’s important to recognize stress early and do something about it, before it causes you serious problems.”  The warning signs are different for each person.  They can be physical, like insomnia, or fatigue, or they may be “voiced in the words of others: ‘You look so tired,’…’Why are you snapping at me?’”

Step 2. Identify your sources of stress.  Examples are, demands on your time, energy, or money; conflicting responsibilities; difficulty meeting your caree’s needs; feeling trapped or isolated; family discord; unrealistic demands and expectations, etc.

Step 3. Identify what you can and cannot change.  “The only person you can change is yourself.  You may be able to change a situation, how you respond to it, or your perception of it, but you can’t change another person.”

Use these “guidelines to look at your situation and to determine what can and cannot be changed:”

– Accept the reality of your caregiving situation.  “…adapt to ongoing changes and losses caused by the care receiver’s illness.  These changes cause you to redefine your life.  What was normal has changed.  You are living with a new reality.”

– Educate yourself about the care receiver’s disease.  “You will be better able to identify what you can and cannot change when you understand the disease.”

– Identify unrealistic expectations, especially your own.  “If you have unrealistic expectations of yourself (like, ‘I can do everything myself.’), your expectations of what can be changed probably will be unrealistic also.”

– Seek and accept support.  “Often you can make changes only with the help of others.  Seeking and accepting support may be the single most important factor in making constructive changes.”

– Identify what you still have, rather than focus on what is lost.  With some modifications you may still be able to achieve some  life goals, like travel (shorter trips or with a third person to help).  “Many caregivers, as they learn more about themselves, experience personal growth.  That is the ‘gift’ that can often be found in difficult times.”

– Let go of what cannot be changed.  “Accepting the situation as it is…releases new energy for…seeing new possibilities.”

Step 4. Take action to manage your stress.  “There are many different tools for managing stress.  But you must find what is most effective for you.”

Proven ways to manage stress include:

> Managing your thoughts, beliefs, and perceptions.  “As a caregiver there may be times when the only thing you can change is how you view a situation.  There are several tools for managing thoughts, beliefs, and perceptions.  Two that can be helpful are:”

* Reframing is learning to look at things in a different (more positive) way.  There’s a worksheet for this on page 35.  “For example, a caregiver who is angry at her brother for helping only once a month versus taking the view that ‘any help, no matter how little, will lighten my load.’”  Reframing can make you feel less burdened and more in control.
“Changing your perception from a caregiver to care manager is a way of reframing.  As a care manager you assume an active role and reach beyond giving hands-on care, to planning and coordinating care and using available resources.”

* Self-talk is what we say to ourselves.  “Negative self talk (I can’t, I should have, Nothing I cook is ever good enough for mother.) can lead to depression.”  Positive statements counteract the effects of negative thinking.  “This helps to change one’s attitude, promote relaxation, and reduce stress.”  Instead, tell yourself, “I am preparing nutritious food.  I am doing my best.  That is good enough.”

With determination, patience, and practice, you can change your self-talk from negative to positive.”  Follow these steps:
– Identify your negative thoughts.
– Write your negative thoughts to identify and clarify them.
– Challenge your negative thoughts.  Give them a good argument.  They probably won’t hold up as reasonable or logical.
– Write a simple, positive statement for each thought you want to change.
– Memorize and repeat the chosen statements to establish the habit of positive self talk.
– Put your written statements where you see them frequently, as a visual reminder.

> Practicing self-care means that you:
* Learn and use stress reduction techniques.
* Attend to your own health care needs,
* Get proper rest and nutrition.
* Exercise regularly.
* Take time off without feeling guilty.
* Participate in pleasant, nurturing activities
* Acknowledge and take satisfaction in the things you do well, and Reward yourself on a regular basis.
* Seek and accept the support of others.
* Seek supportive counseling when you need to, or talk with a trusted counselor, religious advisor, or friend.
* Identify and acknowledge your feelings.  Don’t rely on drugs, alcohol, cigarettes, or tranquilizers.
* Tell others what you need.  Don’t assume “they should know.”
* Change the negative ways you view situations.
* Set goals and prioritize.

> Getting social support.  “Support from family, friends, and others is an important stress buffer.”  Consider a support group.

> Using techniques that lower stress.  “It’s little help to identify your stressors if you don’t take action early to reduce them.  Recognize obstacles to your taking action.”  These quick and easy stress-busting techniques can fit into your busy life:

* Employ basic wellness practices; proper diet, adequate sleep, regular exercise.

* Breathing for relaxation;  Close your eyes.  Focus on your breathing.  Inhale to the count of seven, slowly and deeply. Exhale to the count of seven, as you let go of stress.  Repeat for one or two minutes (or longer).

* Meditation aids in relaxation and in achieving physical and mental well-being.  There is a meditation instruction on page 33. Many hospitals and clinics have mindfulness-based stress reduction classes.  Many are even free!

* Music is often used specifically for healing and decreasing stress and tension.  “Music can be healing for both you and your care receiver, either together or alone.  People with dementia, especially, respond to music when they may respond to little else.”  Use these steps as a guideline:
1. Choose soothing music you like.
2. Relax and close your eyes.
3. Breathe deeply and easily.
4. Lose yourself int he music, listening with your body, not your mind.
5. After the music is finished, open your eyes and notice how you feel.

* Humor.  “Tears and laughter are closely related.  They each offer a release of tension and are often intermingled.  Humor does not minimize the seriousness of a situation; rather, it helps you embrace it.”  Read the comics, watch a funny TV show.

> Developing plans of action.  Use those tools from chapter one!

> Finding hope and meaning.  “It is a way to make sense of our circumstances. … A search for meaning can be a conscious choice.  There are many ways to stimulate your search.”
– Ask yourself questions like, “What am I to learn from this?”
– Reflect on your experience, especially after a difficult time.
– Talk with a trusted person to help clarify your thoughts and feelings.  As you tell your story, it often takes on meaning.
– Writing is another way to clarify your thoughts and feelings, like talking to yourself.  Reread your journal periodically.
– Seek spiritual renewal

– Denise

Creating a care plan in 10 steps (from caring.com)

Although the article described below is titled “10 Steps to Creating a Dementia Care Plan,” I think nine of the steps apply to all caregivers, whether dementia is part of the picture or not.

The ten steps are:

* Step 1: Know the type of dementia.
(Robin’s note:  to make this more generic, I’d change this to “Know the diagnosis.”)

* Step 2: Connect with the Alzheimer’s Association.
(Robin’s note:  not necessary if you aren’t dealing with dementia.  And many caregivers for those with non-Alzheimer’s dementia would argue that the Alzheimer’s Association doesn’t know much about non-AD dementias.)

* Step 3: Start early.

* Step 4: Address current concerns.

* Step 5: Find out how much money and coverage is available for care.

* Step 6: Figure out where your loved one will live now.

* Step 7: Identify situations that will force change.

* Step 8: Talk to a lawyer.

* Step 9: Ask for help if you need it.

* Step 10: Take care of the caregiver.

If developing a care plan sounds daunting, note that there are some good resources available to help you.  You can:

* hire a geriatric care manager (caremanager.org).  These are often social workers or RNs.

* hire a social worker from a home care agency, from Family Caregiver Alliance (caregiver.org) if you are in the San Francisco Bay Area, or from one of the other California caregiver resource centers if you are in CA (caregiver.org/californias-caregiver-resource-centers)

* hire a law firm with a care planner on staff.

The full article is copied below.

Robin

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10 Steps to Creating a Dementia Care Plan
January 24, 2017
Caring.com
By Madeline Vann, MPH

Creating a care plan for your loved one with dementia can give you and your family a way to anticipate and deal with the changes the illness brings. But you’ll also need time, a willingness to learn and an open mind to ensure that your loved one’s plan is well suited to him or her.

Dementia care planning breaks down into broad categories such as learning about your loved one’s type of dementia, facing logistics such as daily living and safety, medical care, and the emotional needs of all involved. There is no standard dementia care plan, however, because each person with dementia and their families are unique.

“The first thing I want to tell families is that nothing in your life has prepared you to be a caregiver,” says Nancy Alterman, LCSW, a geriatric social worker and a clinical instructor at the New Jersey Institute for Successful Aging (NJISA), part of the Rowan University School of Osteopathic Medicine.

This guide can help you get started with your loved one’s dementia care plan.

Step 1: Know the type of dementia.

“What we mostly talk about is Alzheimer’s disease because it is the most common [type of dementia],” says Alterman. But, she points out, there are many other types of dementia. Each form of dementia follows a different course over time. And each type, in combination with other health conditions your loved one may have, could require different approaches to management, either at home or in a memory care community. Getting a correct diagnosis and learning about the type of dementia your loved one has will help you plan.

At this stage, you might want to create a binder that will contain contact information for everyone involved in your loved one’s health care, including medical personnel, as well as information about the dementia and working documents related to the steps you’re taking to create a dementia care plan.

Step 2: Connect with the Alzheimer’s Association.

The Alzheimer’s Association provides a lot of information online, offers a free, 24-hour helpline, and hosts support groups throughout the country. Even if your loved one has a dementia other than Alzheimer’s disease, you can find information and local support for your whole family through the association.

Step 3: Start early.

It’s easy to put off planning, either because your loved one has days when everything is close to normal, or perhaps because you don’t want to grapple with difficult questions.

“We know that when people do plan early, as hard as it is, it’s like giving themselves and their families a gift. They’ve had those complicated conversations, they’ve made decisions, and so when they get into the more challenging stages of the disease, they’ve already talked it through and made a plan,” says Ruth Drew, Director of Family and Information Services with the Alzheimer’s Association. Perhaps the most important reason to start early with creating a dementia plan is that the person with dementia may still be able to express their preferences for care in the future.

Step 4: Address current concerns.

Plan around the problems that you and your loved ones are currently facing with dementia. The Alzheimer’s Association offers an online navigator tool to help you plan around your current situation. Consider whether you need solutions to problems with:

• Communication. Is it time for family members and caregivers to get some pointers from a dementia care expert about how to communicate well with someone who has dementia? Rebecca Axline, a licensed clinical social worker (LCSW) with Houston Methodist Hospital’s Nantz National Alzheimer Center, explains that communication strategies will depend on the type of dementia your loved one has. “Someone who has vascular dementia can be triggered to remember things while someone with Alzheimer’s disease can not,” says Axline. In some cases, family members will have to learn how to avoid unnecessary arguments with the person who has dementia.

• Emotional health. “Is the person with dementia dealing with anxiety and frustration, feeling like they are not at home when they are, or are they forgetful and confused but overall very content?” asks Drew. You might need to talk to a doctor or therapist about emotions that make everyday living difficult for your loved one.

• Medication management. Is your loved one able to take their prescribed medications at the right time, and not repeat doses?

• Money management. Is your loved one still able to handle money and balance their checkbook? Who will help or take over their finances when he or she can no longer manage? Be aware that financial scammers may target older adults with cognitive problems , so it’s wise to monitor your loved one’s finances.

• Safety. Is your loved one wandering, unsafe around appliances such as gas stoves, or losing their balance and vision? Can your loved one drive safely alone? Each safety challenge has its own solution.

• Sleep. Is your loved one’s sleep pattern changing? How is that affecting family life? Significant sleep changes can accompany some dementias.

Step 5: Find out how much money and coverage is available for care.

Take a look at any insurance plans, long-term care plans and other dementia care financing options so you know how much money your loved one has available. If this step is overwhelming, find a professional, such as a social worker experienced in dementia care, with the expertise to guide you. In some cases, the details of coverage for dementia care could determine where your loved one will live.

Step 6: Figure out where your loved one will live now.

Alterman is an advocate for moving to an assisted living community that offers memory care soon after a dementia diagnosis.

“If you go soon enough, you can almost guarantee you will never need a nursing home,” she says. The additional benefit to moving in sooner rather than later is that you will learn your way around the facility before too much damage is done to learning and memory. But, she says, make sure you choose a facility with a memory care wing. “At some point, you will need specialized care.”

However, some families prefer for their loved one to stay home for as long as possible if the family is large enough and close enough, geographically, to support them. This is a part of the dementia care plan that will likely change over time.

Consider issues such as:

• Who is available to help care for your loved one over time? Are they available to provide care at home, or will they be helping to oversee care at a facility?

• Is it better for your loved one to stay in their current community or move closer to a friend or family member who can help? Are there memory care facilities in the new community?

• What other forms of support are nearby? If your loved one wants to stay home as long as possible, learn about day care programs, respite care, and home health care options in their community.

Step 7: Identify situations that will force change.

“Home becomes unsafe when someone is big on wandering or is fecal incontinent,” says Alterman. These are two reasons families decide to move a loved one with dementia into a facility, but they’re only two possible problems you might encounter as dementia progresses. Once you know what to expect from your loved one’s type of dementia, everyone involved, including the person with dementia, should talk about what kinds of dementia symptoms would require significant changes in plan, says Alterman. You may need to include your loved one’s doctor in this conversation.

Step 8: Talk to a lawyer.

If your loved one does not already have legal documents sich as a will, living will, healthcare power of attorney and financial power of attorney, make an appointment as soon as possible with a lawyer whose practice includes eldercare law. This process should allow your loved one to choose a friend or family member to make decisions on their behalf if they are no longer able to do so.

Step 9: Ask for help if you need it.

By the time you tackle the first eight steps, you’ll likely know if you or your family need someone to guide you. Axline points out that for many families, dementia care planning can be very emotional. “It’s fine to say that maybe this is just too emotionally connected and you need to get outside help,” she says.

The center where Axline works facilitates family meetings to try to help everyone involved share their concerns and preferences. You can ask a therapist, social worker, or clergy member to help organize and run these family meetings. She points out that family members may also need individual therapy if the process of dementia care planning is triggering strong emotions and conflicts.

Step 10: Take care of the caregiver.

Axline recommends taking time to grieve over changing plans and relationships, and to practice good self-care throughout the dementia care planning. This means staying on top of your own health and fitness, and maintaining your relationships and interests. Taking care of the caregiver will make it more likely that the person who has dementia will be well cared for as well.

Finally, be flexible.

“You want to start early and make a plan, but then things are going to change over time, so you might need to tweak your plan,” says Drew.

It’s a good idea to revisit the dementia care plan at least annually to make sure it’s working well. If the disease is progressing rapidly, you may need to change the plan more often.