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The Long and Winding Road…

~ An Alzheimer's Journey and Beyond

The Long and Winding Road…

Category Archives: Tips

Guide to Evaluating Residential Dementia Care

22 Thursday Aug 2013

Posted by Ann Napoletan in A Place for Mom, Caregivers, Caregivers.com, Emeritus, Finding a Facility, Helpful Resources, Mom, Pat Summitt, The Early Years, Tips

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Tags

alzheimers, assisted living, dementia, long term care

Pat Summitt Foundation Guide

Kudos to the Pat Summitt Foundation for putting together this free 50+ page publication on evaluating long-term care options. 

Extracting my head from the sand

Long-term care decisions are among the most difficult you will ever face, and unfortunately it’s often a “baptism by fire” situation. That was certainly the case for us; my mom had been in the hospital and I’ll never forget standing in the hallway, numb, as the OT, PT, and social worker told me she couldn’t go home. Living independently was no longer an option. 

I shouldn’t have been caught off guard, but I was. Oh yes, I knew in my heart the day was coming, but I had buried my head deeply in the sand on the vast beach of denial. I didn’t know a darn thing about long-term care. Nothing.

So, with one week to find a facility and get Mom moved in, I dove in head first armed with — not much of anything. I had enlisted assistance from A Place For Mom, which helped immensely, but oh how I wish I’d had the Pat Summitt Foundation guide. This was all uncharted territory for me, and I learned as I went.

Business is business

While it would be lovely if everyone had their heart in the right place, the bottom line is – well, the bottom line. It comes down to dollars and cents, sales, and monthly numbers. All too often, the focus is on keeping the building full regardless of whether or not the facility can provide adequate care to meet the needs of potential residents.

In fact, a recent Frontline exposé on Emeritus Senior Living points out that facilities sometimes even seek out advanced dementia cases. Why? Well, those residents require a higher level of care, which equates to a higher monthly payment. And after all, it IS all about the bottom line, isn’t it? The facility may not be equipped or staffed to handle the care, but somehow that becomes secondary to filling the building. 

Asking the right questions

This is why it’s so very important to know exactly what to look for – and what to ask – when you’re evaluating options. The Summitt Foundation guide is divided into five chapters:

  • Dementia care options and services
  • Publicly available information about quality of care
  • Who to interview and what to ask
  • The value of observation
  • Strategies for being the best advocate you can be + list of additional resources

In addition, the e-booklet provides valuable interview guides specific to staffing, satisfaction surveys, chronic pain screening, and food service, as well as a worksheet for documenting observations. These comprehensive tools also include scoring guides and rationale to help you quantify your findings.

Eyes wide open

My nuggets of advice for families embarking on this journey:

  • Don’t wait until the last minute; start early so you’re somewhat prepared when the time comes.
  • Ask tons of questions and observe, observe, observe while you’re in the building.
  • Make unannounced visits at various times of the day/evening.
  • Talk to current residents and family members.
  • Listen to your gut – it will rarely lead you astray. If your instincts tell you something doesn’t feel right, trust yourself.
  • Download How to Evaluate the Quality of Residential Care for Persons With Dementia, by Sandra F. Simmons, Ph.D., John F. Schnelle, Ph.D., and Anna N. Rahman, Ph.D., and put it to good use!

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Week in Review…

10 Saturday Aug 2013

Posted by Ann Napoletan in Alzheimers.net, Blogging, Care Options, Caregivers, Caregivers.com, Emeritus, Helpful Resources, Mom, Neglect and Abuse, The Early Years, Tips

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Tags

alzheimers, assisted living, dementia

week-in-reviewHaving spent the last two days in bed slathered with Vicks and sleeping in a Nyquil-induced haze, I’m starting to feel human again. What a miserable couple of days it’s been.

I guess I feel like I’ve been a little out of sorts since the Frontline piece on Emeritus aired; it brought back memories I’d rather forget. And yes, years later, I’m still so angry at myself for trusting the staff at Outlook Manor the way I did. How I hope Mom knows I did the best I could at the time with the knowledge I had. There are no second chances in matters like this, but the opportunity remains to educate people so they won’t make the same mistakes… at least that’s something.

What in the World is Dementiaville?

This week on Alzheimer.net, I did a piece about Hogewey Village (aka Dementiaville) in the Netherlands. How wonderful it would be to imagine that someday, care like this could be available all over the world. Right now, the biggest barrier to adoption is one we’re all too familiar with – cost. It took a cool $25 million-plus to build Hogewey, not to mention the astronomical cost of running it.

Still, it’s not something we should immediately dismiss as impossible. Perhaps there are aspects of this model that can be repeated on a less grand, but still effective, scale. The current model in the U.S. is in large part not working, and it’s our responsibility to figure out how best to take care of those who took care of us for so many years.

Dementia Dogs

Monday’s Caregivers post introduced readers to Kaspa and Oscar. These two dogs from Scotland have been specially trained to provide assistance to dementia patients, and the results have been overwhelmingly positive. In addition to helping with prompts,  reminders, companionship, and exercise, they also have a knack for sensing when a period of agitation is coming on, and they can often redirect their owner before things escalate.

Is It Time to Consider Assisted Living?

Also this week, I did a post on Caregivers calling out 8 signs that may indicate it’s time to start thinking about assisted living. Making that decision is one of the most gut wrenching things we’ll ever face, and when the time comes, it’s much easier to stick your head in the sand than face reality. Ask me how I know…

I hope that perhaps this list will allow you to step back and evaluate things a bit more objectively. The decision is extremely personal, and no two families or situations are the same.

Until You’ve Walked in Their Shoes….

Last but not least, this week I’ve seen several extremely harsh comments concerning placement in assisted living. I want to stress that, for a variety of reasons, not everyone is able to take care of loved ones at home. I find it terribly unfair to suggest that placing a spouse or parent in a care facility means they are loved any less. That is simply ludicrous. We must all do what’s best in our own situations.

Bottom line, never judge another until you’ve walked in their shoes. Although I do believe the system very much broken, there are without question some wonderful facilities that provide loving, compassionate care. Planning ahead is the best way to ensure adequate time for the due diligence necessary to find the right option for your family.

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Dementia Today: Dementia and Bereavement

30 Tuesday Jul 2013

Posted by Ann Napoletan in Caregivers, Expectations, Grieving, Helpful Resources, Life After Caregiving, Tips

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An excellent article I felt worthy of sharing. Whether you’re just beginning this journey, somewhere in the middle, or trying to adjust to that final loss, it touches on feelings you’ve likely had or will have at some point.

Source: Dementia Today, July 2013
http://www.dementiatoday.com/grief-and-bereavement/

Dementia and Bereavement

When a person develops dementia, the people closest to them are likely to experience feelings of grief and bereavement not only in the period after the person’s death, but also before they die, as the illness progresses. A carer may adapt and come to terms with one stage of the person’s illness only to find that their behaviour alters or their abilities decline further and the grieving starts all over again. This factsheet is for carers, friends and relatives of people with dementia. It looks at some of the feelings that people close to someone with dementia might experience and suggests some ways to cope with them.

Loss

A sense of loss is one of the most powerful feelings that people experience when someone close to them develops dementia. Depending on your relationship with the person and your individual circumstances you may grieve for the loss of:

  • the person you once knew
  • the future you had planned together
  • the relationship you once shared
  • their companionship, support or special understanding
  • your own freedom to work or to pursue other activities
  • finances or a lifestyle that you once took for granted.

The Ups and Downs

Grieving is an up and down process. In the earlier stages of the person’s dementia, you may swing between despair and wild optimism that a cure will soon be found. You may even deny that anything is wrong with the person and try to suppress your feelings.

Later, if you have accepted the situation, you may find that there are periods when you can cope well and make the best of things. At other times, you may feel overwhelmed by sadness or anger, or you may simply feel numb. People who care for someone with dementia often feel resentful at times for the restrictions placed on their own life, and may feel unhappy that things have not turned out as they would have hoped. Some people are shocked to find that they sometimes wish that the person they are caring for were dead.

Feelings like these are a normal part of grieving but if you experience them, it is important to realise that you may be under a great deal of stress, and you may need to seek emotional support for yourself.

Tips:

  • Talk about your feelings to an understanding professional, to other people coping with a similar situation, to a trusted friend or to supportive members of your family. Don’t bottle up your feelings.
  • Relieve tension through crying, shouting or punching a cushion. However, make sure that the person you are caring for is safe and out of earshot first, or you may distress them.
  • Invite friends to drop in for a chat or to phone you regularly.
  • Make sure that you see your GP if you are feeling low or anxious, or if you are very tired and unable to sleep. It is important to try to prevent normal feelings of sadness from slipping into depression, which is much harder to deal with.
  • Consider your own needs. If you spend a lot of time with the person with dementia, taking regular breaks can keep you in touch with the outside world and raise your morale.
  • Make time for yourself each day. Just relaxing with a cup of tea or having a good chat on the phone will help you recharge your batteries and cope with your emotions.

Long-term Care

If the person goes into long-term care you may grieve at another change in your relationship. The relief which you might feel initially may be replaced by feelings of loss and grief, mixed up with guilt, which can last for a surprisingly long time. You may miss the person’s presence. You may experience feelings of emptiness. You may feel very tired, both physically and emotionally.

Tips:

  • Try to take it easy until you feel your energy levels rise again.
  • If your daily routine previously revolved around caring for the person, giving a structure to your day may help you get through the difficult early months.
  • If you still want to be involved in caring for your relative while they are in care, speak to the staff and explain exactly what you would like to continue to do for them.
  • Don’t fall into the trap of building your life around visiting the person in their new home. You need to build a new life for yourself that includes these visits.
  • Remember that there is no ‘right’ or ‘wrong’ way to feel. You experience your own feelings in your own way, and no one has the right to tell you how you should feel.

Final Stages of Dementia

In the final stages of dementia the person may be unable to recognize you or communicate with you. This can be very painful. Although the relationship seems very nearly over, you are unable to mourn fully because the person is still alive.

Tips:

  • Holding the person’s hand or sitting with your arm around them may be comforting for both of you.
  • There is no right or wrong way through the caring role, take comfort from the knowledge that you have done the best that you could.

(See also Factsheet 417, Later stages of dementia.)

When the Person Dies

Some people who have loved ones with dementia find that they grieve so much during the course of the illness that they have no strong feelings left when the person dies. Others experience a range of overwhelming reactions at different times. These may include:

  • numbness, as though their feelings are frozen
  • inability to accept the situation
  • shock and pain, even if the death has been expected for a long time
  • relief, both for the person with dementia and themselves
  • anger and resentment about what has happened
  • guilt over an incident that happened in the past
  • sadness
  • feelings of isolation
  • a feeling of lack of purpose.

It can take a long time to come to terms with the person’s death. Those who have been full-time carers for a long time will be left with a huge void when this role ends.

Tips:

  • Try to avoid making any major decisions in the early months if you are still feeling shocked or vulnerable.
  • Accept that, even though you may generally be coping, there may be times when you feel particularly sad or upset.
  • If you find events such as anniversaries or birthdays distressing, ask friends and family for support.
  • Stay in touch with your GP. You are likely to be more vulnerable to physical illness, as well as to anxiety or depression, following bereavement.

Getting Back on Your Feet

Although you may feel very tired after someone close to you dies or goes into long-term care, the time will come when you are ready to re-establish your own life and move forward. Remember that it takes time to adjust, and the length of time will vary from person to person.

You may feel very unconfident at first and find it difficult to take decisions, make polite conversation or cope with social gatherings. Don’t give up – your confidence will gradually return. Take things slowly, and make sure that you have plenty of support from family and friends, professionals and other people in a similar situation to yourself. If people offer to help, try allowing them to do so – don’t refuse straight away.

When you feel ready to do so, talk about the person you have lost. Reminisce with friends and family who can also benefit from the opportunity to share feelings and memories.

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Marilyn, BA (before Alzheimer's)

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