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Tips for Personal Care
Posted on September 15th, 2009 No commentsGuidelines for Helping with Daily Self-care Tasks
- *Simplify and clarify the task. Clothing garments with simple fasteners or a permed hairstyle any go far in enabling the person to complete a task independently. Clarify the task with environmental cues such as a comb and brush set out by the makeup mirror.
- *Reduce distractions such as background noise to confusing cues (such as clutter or similarly colored toilet and dressing stool covers.)
- *Keep a regular routine. A regular routine makes life more predictable and easier to cope with. This reduces confusion and improves the individual’s cooperation and ability to perform self-care.
- *Be flexible and patient. It is important to remain flexible and patient because the first attempt at getting a task done often will not work. Also, remember to not take refusals personally, the person with Alzheimer’s disease cannot help his/her behavior.
- *Use good communication techniques.
Techniques for Helping
- *Break the task into steps that are small enough to match the person’s abilities. For example, a person may need to have tasks broken into smaller steps such as: put toothpaste on the toothbrush, brush your teeth, rinse your mouth, and dry off your mouth.
- *Demonstrate the step. For example, when you say “wipe your mouth” you can wipe your own mouth.
- *Help begin the action. Even when you demonstrate a step, the person may still not be sure what to do. You can help by beginning the action until he/she remembers what to do.
- *Give the person time to finish the step. Rushing a person with Alzheimer’s dieses usually will increase confusion, embarrassment, and resistance.
For more information contact 317-218-5111 or www.behomelivelife.com
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Tips for Meaningful Days
Posted on August 4th, 2009 No commentsMeaningful activities are those events or tasks that are failure free opportunities for success. Here are some strategies for creating meaningful days for your loved one who has Alzheimer’s or another related dementia.
- *Look for activities that will be failure free. A craft project with a pre-set outcome or appearance may be too difficult, whereas arranging silk flowers in a vase is a failure free task.
- *Reduce distractions so the person can focus on the task, eliminating things such as background noise from the television.
- *Keep exercise and physical activity part of everyday, as it helps keep sleep and nighttime habits normal.
- *Familiar activities such as setting the table and folding laundry should be part of the daily routine that the person with Alzheimer’s disease helps with. The tasks are meaningful, familiar activities and assist to remain skills as long as possible.
- *If music, exercise, or spiritual activities were part of your family member’s routine each week, those type of activities should occur frequently during the week now as well.
For more information contact 317-218-5111.
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Elder Abuse
Posted on July 17th, 2009 No commentsProviding care for someone with Alzheimer’s or another related dementia can be one of the most stressful events in a person’s life. Often, caregivers are the children of elderly parents requiring 24 hour care. These adult children are not medical professionals nor do they have prior experience providing medical care. The typical caregiver often has a job during the day and is “sandwiched” between raising a family and caring for their parents.
According to the National Center on Elder Abuse, “between 1 and 2 million people have been injured, exploited or mistreated by someone on whom they depended for care or protection.” It is also estimated that only 1 in 14 cases of abuse are reported for investigation. Nearly everyone would assume that caregivers described in the previous statistics are paid caregivers. This is not always the case. It is estimated that nearly 50% of all abuse reported is perpetrated by an unpaid caregiver, typically a family member.
There are a variety of reasons caregivers become abusive to the aging senior for whom they are caring, especially if the individual has a diagnosis of dementia. Often people with dementia experience personality changes. A common statement professionals hear when interviewing a family caregiver is, “My dad was never like this before.” The person with dementia may refuse to bathe, eat, sleep, or even participate in activities he once enjoyed. Another common complaint is, “My mom asks me the same questions over and over.” Those repetitive statements and questions can be overwhelming to caregivers already burdened with tremendous responsibilities.
Many times caregivers will say, “I don’t know who I am anymore. All I do, day in and day out, is take care of someone else.” Caregivers forget to take time out to care for themselves. Often they don’t know where to turn for help, or refuse to ask for help from anyone.
How does a caregiver avoid becoming abusive? First, the caregiver must have a good support system. Attending routine supports groups can provide opportunities to vent, ask questions, and receive advice. It’s important to realize that no one has to go through this alone.
Next, the caregiver cannot be afraid to ask for help. Relying on other family members, friends, members of their church, and community outreach programs may provide support to give the caregiver respite. Taking a break to care for one’s self is vital to being fresh and alert in order to provide for needs of their aging senior.
Caregivers should take every opportunity to learn as much as possible about the needs of their aging senior. For example, if a daughter is taking care of her father with Alzheimer’s, she should attend sessions and seminars which provide education, information and insight for the “just right” care he needs.
Caregivers also need to take credit for the care they are providing. Being “sandwiched” is not an easy task, but can be accomplished, and good quality of life can be maintained.
For more information contact Sollievo at 317-218-5111 or www.behomelivelife.com.
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Vascular Dementia
Posted on July 2nd, 2009 No commentsFollowing Alzheimer’s Disease, the second most common form of dementia is Vascular Dementia. This type of dementia is caused by blockages in the brain’s blood supply. Vascular dementia leads to a progressive decline in memory and cognitive function which in turn leads to poor quality of life. Generally, this form of dementia affects women more than men.
The most common form of vascular dementia is multi-infarct dementia caused by small strokes which often go unnoticed. Multi-infarct dementia damages those specific areas of the brain affected by the loss of blood. These strokes often affect the areas associated with learning, memory, and language and may cause temporary, partial blockages to the brain tissue. After time the damage caused to the brain interferes with basic cognitive functions and disrupts everyday functions, generally referred to as “activities of daily living.” Signs and symptoms of vascular dementia vary.
Signs/Symptoms of Vascular Dementia:
Behavioral Signs/Symptoms
- Slurred speech
- Language problems
- Abnormal behavior
- Wandering or getting lost
- Difficulty with procedural memory
- Difficulty drawing conclusions
Physical Signs/Symptoms
- Dizziness
- Extremity weakness
- Lack of concentration
- Unsteady gait
- Incontinence
For more information please contact us at 317-218-5111 or check out: www.mysollievo.com.
Uncategorized alzheimer's disease, Brain-derived neurotrophic factor, caregiver stress, educated families, elder abuse, memory loss, mild cognitive impairment, people with dementia are not children, symptoms of dementia, tips for people with alzheimer's, tips for people with dementia, Vascular Dementia -
Symptoms of Alzheimer’s Dementia
Posted on June 26th, 2009 No commentsAlzheimer’s disease has been in the news a lot these days. Recently there has been an increase in the number of commercials advertising medications that can help with the disease process. Even HBO had some success with its documentary, the “Alzheimer’s Project”. We’ve seen an increase in people inquiring about the symptoms of the disease process.
“When do I become concerned if I am forgetting things?
“How do I know if I have Alzheimer’s?”
Here are a few symptoms to look for:
- Loss of procedural memory. Forgetting how to do routine tasks that have been second nature .
- Misplacing items: Not recalling where you placed an item or finding it in a very strange place. For example, putting your keys in the freezer.
- Difficulty finding words: Having trouble finding the right words or understanding common words that you once understood.
- Difficulty with judgment or drawing conclusions.
- Changes in personality: You begin to experience mood changes or loss of initiative.
If you believe you are experiencing memory impairment, it is time to see a doctor. People over the age of 65 should consider annual memory exams, especially if there is a family history of Alzheimer’s or other related dementias. In some cases, dementia can be reversed.
For more information, please contact us at 317-218-5111 or www.behomelivelife.com
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Call to Action
Posted on April 13th, 2009 No commentsCALL TO ACTION
I received this information today in the Alzheimer’s Association’s ENewsletter. Please join all caregivers to make a difference in the lives of those who are battling this difficult disease.
Advocate Impact: Forum 2009
Last month, over 600 advocates from around the country marched on Capitol Hill to demand that our lawmakers make Alzheimer’s a national priority.
During meetings with advocates, members of Congress made the following commitments:
188 indicated support to end the two-year waiting period for Medicare;
181 indicated support for a $250 million increase in Alzheimer research funding; and
83 indicated support the creation of an Alzheimer’s Solutions Project Office.
65 members indicated support for all 3 issues!
You can catch a glimpse of the action at: http://www.alz.org/forum
We have great momentum and now is the time to “seal the deal”. Read on…
What Can I Do Now?
Ask your members to co-sponsor the End the Medicare Two-year Wait Bill!
People under age 65 with dementia who lose their jobs are likely to lose job-related health insurance. Many become uninsured and uninsurable. Just when they need coverage the most, federal law requires them to wait two years to become eligible for Medicare. Because of this wait, families face soaring out-of-pocket costs for health care or completely forego care.Email your members of Congress now. Ask them to co-sponsor the Ending the Medicare Disability Waiting Period Act of 2009 (S.700 / H.R.1708).
Go to: http://alz.kintera.org/endthewait
For more information on how you can make a difference in the lives of those with Alzheimer’s contact us at 317-218-5113 or www.behomelivelife.com.
Uncategorized alzheimer's dementia, alzheimer's disease, be home live life, Brain-derived neurotrophic factor, British Medical Journal, call to action, call to action: aging in indiana, caregiver stress, dementia, dementia care, Economic stimulus legislation, educated families, elder abuse, Ending the Medicare Disability Waiting Period Act of 2009, katrina degraff, memory loss, mild cognitive impairment, opportunities to say yes, people with dementia are not children, tips for people with alzheimer's, tips for people with dementia -
My dad sleeps all the time. He won’t get involved in any of the activities at the nursing home.
Posted on March 13th, 2009 No commentsBegin by assessing the current activity calendar with the Activity Director at the nursing home. Discussing your dad’s interests prior to the onset of dementia with the Activity Director will determine the best schedule of personally meaningful activities for your dad. You may need to adapt an activity to your dad’s level of ability today, but that doesn’t mean he still couldn’t enjoy some of his favorite hobbies.
Take, for example, fishing. I use a fishing kit with my grandfather when I visit him in the nursing home. We straighten the tackle box, practice tying knots, casting the line, and looking at photos of his past fishing trips. He never actually goes fishing, but he is able to reminisce about the hobby and spend time mentoring me on the best way to catch a bluegill!
For more tips: check out our website at www.behomelivelife.com or call 317-218-5111
Uncategorized Age Power, alzheimer's dementia, alzheimer's disease, be home live life, Brain-derived neurotrophic factor, British Medical Journal, call to action: aging in indiana, caregiver stress, dementia, dementia care, Economic stimulus legislation, educated families, elder abuse, katrina degraff, ken dychtwald, memory loss, mild cognitive impairment, opportunities to say yes, people with dementia are not children, sollievo, stimulus checks, stimulus package, tips for people with alzheimer's, tips for people with dementia -
My dad keeps asking the same questions over and over again.
Posted on March 12th, 2009 3 comments“My dad keeps asking the same questions over and over again.”
Short term memory loss is typical with someone who has Alzheimer’s. Caregivers may feel themselves becoming very frustrated with repetitive questions and may not know how to help the person with Alzheimer’s.
Tip:
Caregivers should answer the question. Provide multiple cues to help the person with Alzheimer’s try to remember the answer.
For example, when asked “When are we going to eat?” try these responses:
Answer #1: “We will eat at noon.” Point to a clock and ask if the person if they remember what noon looks like on the clock. Then say: “When you smell the bacon cooking you will know that the BLT’s are ready to eat.”
Answer #2: “Are you hungry now? We could have a snack.”
Or
Answer #3: “Would you like to help me prepare lunch?”
If this tip isn’t working, try to figure out what need is un-met. Is the person with Alzheimer’s feeling unsure of himself or the situation? Is he feeling scared? Does he need to eat now because he is hungry? Is he looking for something to do?
Fulfilling an un-met need or using redirection may be an effective tool in reducing repetitive questions and redirecting his thoughts to something different.
For more tips: check out our website at www.behomelivelife.com or call 317-218-5111
Uncategorized Age Power, alzheimer's dementia, alzheimer's disease, be home live life, Brain-derived neurotrophic factor, British Medical Journal, call to action: aging in indiana, caregiver stress, dementia, dementia care, Economic stimulus legislation, educated families, elder abuse, katrina degraff, ken dychtwald, memory loss, mild cognitive impairment, opportunities to say yes, people with dementia are not children, PHD, sollievo, stimulus checks, stimulus package, tips for people with alzheimer's, tips for people with dementia -
How Do I Get My Mom to Take a Shower?
Posted on March 11th, 2009 No comments“How can I get my mom to take a shower?”
Providing personal care is a very demanding job. Our goal as caregivers should always be do the task “with” the person who has dementia, never to do the task “for” someone with dementia. Most tasks can be completed successfully; however, many times these tasks will need to be adapted to the person’s abilities.
Base the bathing task on the routine your mom used prior to the onset of dementia. Did she take a bath or a shower? When did she bathe and how often? Did she wash her hair during her shower? Once you identify her past routine, you can structure the current routine around her personal preferences.
Remember these tips:
Ensure that the bathroom is comfortable for showering. Is the temperature comfortable and is the lighting appropriate?
Make sure all necessary items for the shower are waiting in the bathroom. You don’t want to leave in the middle of the shower to find a towel or soap.
Make the experience a relaxing pleasure, not a demanding chore.
Allow your mom the opportunity to complete as much of her shower herself, as possible. You may need to stay close by for safety, but remember that dignity is important.
If an argument begins, stop the shower. Try again later or you may even consider a sink bath.
Remember, keeping your mom relaxed and feeling safe the important part. There are many ways to keep a person clean without immersing her completely in the water.
For more tips: check out our website at www.behomelivelife.com or call 317-218-5111
Uncategorized alzheimer's dementia, alzheimer's disease, be home live life, Brain-derived neurotrophic factor, British Medical Journal, call to action: aging in indiana, caregiver stress, dementia, dementia care, Economic stimulus legislation, educated families, elder abuse, katrina degraff, ken dychtwald, memory loss, mild cognitive impairment, opportunities to say yes, people with dementia are not children, PHD, stimulus checks, stimulus package, tips for people with alzheimer's, tips for people with dementia -
Brain Protein Could Halt Alzheimer’s
Posted on February 11th, 2009 No commentsI read this interesting article in McKnight’s Long Term Care and Assisted Living Newsletter yesterday. As with all research, we must give the researchers time to see how this develops.
Brain Protein Could Halt Alzheimer’s
The key to slowing, or even stopping, the progression of Alzheimer’s disease may lie in a naturally occurring protein produced by the brain, according to recent research.
Brain-derived neurotrophic factor (BDNF) is produced by the brain’s entorhinal cortex, which helps support memory. In patients with Alzheimer’s disease, researchers found that production of BDNF is significantly decreased. By injecting the protein into aged animals and animals bred to exhibit Alzheimer’s-like symptoms, scientists at the University of California, San Diego, were able to stimulate the brain’s memory circuits and prevent cell death caused by disease or brain damage.
The effects of the protein were “potent,” researchers said. The animals that received the treatment soon began producing more BDNF on their own, and researchers noted improved memory function and other long-term benefits. The treatment was deemed safe and effective in animal models, leading researchers to believe the treatment work similarly in humans. Their research was published in the Feb 8 issue of the journal Nature Medicine.


