Posts Tagged ‘memory loss’

Sollutions

Friday, September 25th, 2009

A recent research study from Great Britain suggests that the use of antipsychotic drugs to manage difficult behaviors associated with Alzheimer’s disease and other related dementias may double the patient’s risk for death.

                In 2005 the FDA issued a “black box” warning of all atypical antipsychotics used in those patients with dementia.  The FDA initiated the warning after studies in the United States discovered a higher risk of sudden death in patients with an Alzheimer’s diagnosis after 180 days use of these medications.  In 2008, this warning was extended to include first generation antipsychotics as well.

                Most eldercare experts who specialize in the care of those with dementia agree that the use of antipsychotic medications is not necessary to manage difficult behavioral challenges in those with dementia.  Many times these medications have a variety of side effects that cause additional concerns for caregivers.  These medications may cause the person with dementia to become dozy, lethargic, and apathetic.  When a person with dementia sleeps all day as a result of medication, caregivers may see him/her have difficulty sleeping at night.  Caregivers often also find that the person with dementia may develop an unsteady gait and an increase in saliva which can cause difficulty in swallowing.

                The key to managing difficult behaviors is in how the caregiver perceives the person with dementia.  The caregiver must be able to separate the person from the disease and remember that all care performed is for a “person” and not a “disease.”  All behaviors are a form of communication.  Often when a person with dementia is becoming frustrated the first step to resolving this frustration is to find out what unmet need he/she may have.  Ultimately all people yearn to be safe and to have their core psychological needs met.

                Caregivers must provide a means to ensure that the person with dementia has a personally meaningful day and night.  This means that throughout the course of the day he/she is engaged in activities or projects that are familiar, meaningful, and purposeful.  For example, Helen’s caregiver knows that Helen is a mother of three children. Helen is pacing her home waiting for her “kids” to get home from school.  Knowing that the children are now grown and will not be “walking through the door at 3:15pm” her caregiver has discovered that Helen’s afternoon routine was to make a snack for the children before they came home from school.  Her caregiver sets up a snack for Helen to make and begins to validate her feelings of motherhood and her desire to keep her children safe.  The caregiver also begins to reminisce during this time about her children and her routine as a mother.  Through this process her “unmet” need is resolved and she now is feeling safe and content.

                This is not a simple process that occurs quickly. To effectively communicate and reminisce with a person with dementia, a caregiver must have a good understanding of the life story of the person. 

                A stressed out caregiver may feel that antipsychotic medication is the best and only option; however, after weighing the side effects of this type of medication and researching other alternatives, they may find there are better, more effective, ways to help manage the stress of challenging behaviors.  As these studies have shown, the risk of sudden death is high, and the improvement in the quality of life is not a guaranty.

                For more information the alternative to antipsychotic medication to resolve challenging behaviors, please contact Alzheimer’s Care Group at 317-218-5111 or www.alzcaregroup.com or www.behomelivelife.com.

Sensory Kit: Spiritual

Wednesday, April 1st, 2009

Approach and Communication

 

            As Alzheimer’s disease progresses it can impact the way a person may communicate.  Communication is vital in the care giving process.  It is the way we express our ideas, feelings, and wants.  In order to maintain a quality life, this basic need must be met.   

 

            An individual with Alzheimer’s may have trouble finding the right words, may misunderstand statements that are made, may repeat the same words or statements, or may revert to speaking a native tongue.  As the disease progress, caregivers may also see the person relying more on gestures than words.  For example, it may be easier to point to an object such as a cup of water, than to ask for a drink.  She may pat the sides of her waist to indicate she needs to go to the bathroom.  Some people may have trouble speaking in coherent statements where the phrases sound more like “word salad.”  Word salad is an incomprehensible mixture of incoherent words or phrases.    Caregivers must rely on gestures and other forms of nonverbal communication in order to understand what the person is trying to communicate.

 

            Despite the fact that communication may become more challenging as Alzheimer’s disease progresses, sensitive ongoing communication is important.  Although the person with Alzheimer’s may not respond to each statement, she still benefits from continued communication.

 

Tips to enhance communication:

 

·         Identify yourself by name and what you are going to do for/with the person. Even if you have known the person for years, it is still important to identify yourself and the task.

·         Call the person by his/her familiar name.

·         Use short, simple, one step instructions

·         Give the person plenty of time to respond to questions and statements

·         Limit available choices to two (2) for the person to decide from ( i.e. the blue dress or the red dress, a brownie or ice cream)

·         Don’t ask questions that rely on memory (remember when you ate eggs for breakfast last week?).

·         Speak in a strong clear voice; don’t yell unless the person has a hearing impairment.

·         Don’t talk down or childlike.

·         Turn negatives into positives. Say “Let’s go here” instead of “Don’t go in there.”

·         Turn questions into statement.  Say “Let’s go eat” instead of “Are you ready for lunch?”

·         Be aware of your tone of voice.  Convey an easy going attitude.

·         Approach from the front and never from behind.

·         Use positive, friendly facial expressions.

·         Be aware of your stance – avoid standing with hands on the hip or crossed arms.

·         Focus on feelings not on facts.

·         Validate feelings and help put those feelings into words.

·         Be patient, flexible and understanding.

 

 

            Good communication will bolster self worth, validate feelings, stimulate memories, and calm and reassure.

Alzheimer’s in the News

Monday, March 30th, 2009

This week in the news, the Alzheimer’s Association released its Facts and Figures 2009.  According to the Alzheimer’s Association 5.3 Million Americans have Alzheimer’s disease and the direct and indirect cost to the nation is $148 billion dollars annually.  Additionally, Newt Gingrich presented The National Alzheimer’s Strategic Plan for improving the care of those with Alzheimer’s disease and other related dementia to Congress.

What are you going to do to make a difference in the lives of those with Alzheimer’s and their caregivers? 

So often we become stuck in the mindset that people with dementia have no hope.  The media often reports the stories of heart ache and despair, but we never hear the heroic stories of people making a difference for others being afflicted with this devastating disease.

Who are those heroes?

·         Families who continue to make life the life of the loved one valuable even when that means adapting past interests to current abilities

·         Families who continue to visit their loved one even when it appears she doesn’t remember them any longer

·         Family members who regularly rotate care and responsibility to ensure the primary caregiver receives some respite

·         Caregivers in long term care who engage their residents in dementia with personally meaningful activities

·         Caregivers who provide care despite  Congress cutting Medicare/Medicaid benefits

·         Owners of nursing homes who put Person Centered Care before the dollar

·         Innovators who continue to find new ways to bring quality of life to some who can no longer remember

Are you making a difference?  Do you know where to begin? 

For more information:  Call 317-218-5111 or www.alzcaregroup.com

Aging in America – Aging in Indiana

Wednesday, February 11th, 2009

Aging in America – Aging in Indiana

In 1999, Ken Dychtwald, Ph.D, published in Age Power the following:  “Currently, 47 percent of people over age 85 – the world’s fastest growing demographic segment – suffer from some form of dementia”.  As a nation, we are not prepared for the boomers who start turning 65 in 2011.  We’re in a crisis and very few states have a commissioned task force to prepare for aging and dementia.  Young or old, insured or not, republican or democrat, we should all be concerned.  If I’m preaching to the choir, help me take this to our mayors and governors.

Brain Protein Could Halt Alzheimer’s

Wednesday, February 11th, 2009

I read this interesting article in McKnight’s Long Term Care and Assisted Living Newsletter yesterday.  It will be interesting to see how this research continues to develop.

 

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.

The Better Alternative to Antipsychotic Medications

Friday, January 16th, 2009

A recent research study from Great Britain suggests that the use of antipsychotic drugs to manage difficult behaviors associated with Alzheimer’s disease and other related dementias may double the patient’s risk for death.

                In 2005 the FDA issued a “black box” warning of all atypical antipsychotics used in those patients with dementia.  The FDA initiated the warning after studies in the United States discovered a higher risk of sudden death in patients with an Alzheimer’s diagnosis after 180 days use of these medications.  In 2008, this warning was extended to include first generation antipsychotics as well.

                Most eldercare experts who specialize in the care of those with dementia agree that the use of antipsychotic medications is not necessary to manage difficult behavioral challenges in those with dementia.  Many times these medications have a variety of side effects that cause additional concerns for caregivers.  These medications may cause the person with dementia to become dozy, lethargic, and apathetic.  When a person with dementia sleeps all day as a result of medication, caregivers may see him/her have difficulty sleeping at night.  Caregivers often also find that the person with dementia may develop an unsteady gait and an increase in saliva which can cause difficulty in swallowing.

                The key to managing difficult behaviors is in how the caregiver perceives the person with dementia.  The caregiver must be able to separate the person from the disease and remember that all care performed is for a “person” and not a “disease.”  All behaviors are a form of communication.  Often when a person with dementia is becoming frustrated the first step to resolving this frustration is to find out what unmet need he/she may have.  Ultimately all people yearn to be safe and to have their core psychological needs met.

                Caregivers must provide a means to ensure that the person with dementia has a personally meaningful day and night.  This means that throughout the course of the day he/she is engaged in activities or projects that are familiar, meaningful, and purposeful.  For example, Helen’s caregiver knows that Helen is a mother of three children. Helen is pacing her home waiting for her “kids” to get home from school.  Knowing that the children are now grown and will not be “walking through the door at 3:15pm” her caregiver has discovered that Helen’s afternoon routine was to make a snack for the children before they came home from school.  Her caregiver sets up a snack for Helen to make and begins to validate her feelings of motherhood and her desire to keep her children safe.  The caregiver also begins to reminisce during this time about her children and her routine as a mother.  Through this process her “unmet” need is resolved and she now is feeling safe and content.

                This is not a simple process that occurs quickly. To effectively communicate and reminisce with a person with dementia, a caregiver must have a good understanding of the life story of the person. 

                A stressed out caregiver may feel that antipsychotic medication is the best and only option; however, after weighing the side effects of this type of medication and researching other alternatives, they may find there are better, more effective, ways to help manage the stress of challenging behaviors.  As these studies have shown, the risk of sudden death is high, and the improvement in the quality of life is not a guaranty.

                For more information the alternative to antipsychotic medication to resolve challenging behaviors, please contact Alzheimer’s Care Group at 317-218-5111 or www.alzcaregroup.com or www.behomelivelife.com.

Katrina’s Korner

Tuesday, August 5th, 2008

I recently had the pleasure of spending sometime at a delightful facility in Indianapolis.  I was there in the evening time for a meeting and to my surprise many of the residents were participating in a fantastic music program.  A few women were singing out enthusiastically while the rest of the group were clapping hands and smiling broadly.  The reason I was so impressed was the fact that it was after 7:00 pm and there was a group of more than twenty residents in the activity room.  Everyone was dressed and looked great.  I couldn’t help but stop the two CNAs that were helping with the group to pay them a compliment.  It is so rare to see residents up and engaged in activity programming later than six o’clock.  I know that many residents get up early to start the day with the assistance of CNAs and are tired by the time supper is served.  Often caregivers must start getting residents up early just to make sure that everyone is up by breakfast.  It would be reasonable to assume that many residents would be tired by the time breakfast is served.  The good news is that many facilities are changing the way they look at a daily routine.  In many cases facilities have moved breakfast to a later time to allow residents to sleep in.  There are a few facilities that even allow their residents to sleep in and once they wake up naturally, they are offered the opportunity to have a continental breakfast.  In Colorado I work with buildings that actually serve a continental breakfast as residents get up, a brunch at 10:00am, a large lunch at 2:00pm, dinner at 5:30 pm, and finally a late snack at 7:00 pm.  This five meal approach ensures many more choices throughout the day for the residents and has done a great deal towards decreasing weight loss.

Katrina’s Korner

Monday, June 9th, 2008

Worst storms in Indiana since 1913

 

Many people in southern Indiana have been experiencing horrible living conditions since severe storms hit two weeks ago.  Tornadoes and rain destroyed trees, farm land, and homes causing many people to find shelter at churches and with other family members.

 

Storms can be a source of fear and stress for those living in nursing homes.  From alarms sounding to alert caregivers to a loss of power making the environment dark and uncomfortable, there are many factors that can cause people with dementia to become even more confused and disoriented. 

 

Things to remember if you have a loved one living in a care center:

·       Each facility has an evacuation plan that must be followed when emergencies are declared.  Ask your social service department to give you details so you can know where your loved one will be if a natural disaster occurs.

·         Any change in routine is disruptive to a person with dementia.  Your support will help relieve some of the stress that occurs.

·       Caregivers have many things to do and remember during severe storms.  Often the phone lines can be overwhelmed with many families calling to check in on residents.  Caregivers need to be able to ensure the safety of everyone and this is never an easy task.  Remember:  If there is a severe problem you WILL be notified.

 

Water and wind damage can be challenging to repair.  Patience and understanding can go a long way in helping to make the goals of task achievable.

Katrina’s Korner

Wednesday, May 14th, 2008

Important things to remember when visiting…

My mom is a never-ending song in my heart of comfort, happiness, and being.  I may sometimes forget the words but I always remember the tune.  ~Graycie Harmon

 

“Mom doesn’t know me anymore.  It’s too hard to see her walk away with the other residents.  She doesn’t even remember I visited.”

 

Ever feel like that?  Like the one person who is your touch stone to safety has no clue who you are?  It can be a devastating feeling to experience.  One day Mary’s daughter, Sue, came in to visit.  Mary kept referring to her as Joyce.  Sue was becoming more and more upset by the minute.  When I asked if she was okay she replied, “She is calling me by her sister’s name.  And she HATED her sister.”

 

Sue was very upset and ended up leaving.  A while later Mary walked up to me and said, “My daughter was here but I think she got mad and left.” 

 

The best piece of advice to remember when you are visiting a loved one with dementia is that the person with dementia may not remember you by name, but he/she will remember that you are someone important in his/her life. 

 

My grandpa often calls me Becky which is my mom’s name.  He may get his facts mixed up about my life and her life, but when he tells me that he loves me I know it’s real.  Those are the important moments for me.  And he feels better to have spent time with someone he loves.  Try to focus on the abilities your loved one with dementia has rather than those that he/she might have lost.

 

For more information contact Katrina@alzcaregroup.com.

 

Katrina’s Korner

Friday, February 1st, 2008

“Mom was never like this before….”
I was talking to a woman the other day whose mother has Alzheimer’s.  Her mom has begun to walk up to men who live in the same Alzheimer’s center as she does and kiss them on the mouth.  She also becomes combative during showers and has started to use curse words.  As I was talking with the daughter, she began to cry and said, “Mom was never like this before…..”   Watching mom or dad acting in different ways can be very hard.  Caregivers often feel the need to justify the actions of their loved ones.  They want professionals to understand that mom wasn’t like this and not to be angry with her when she curses at them during care. Here are a few things to remember when coping with a loved one whose behavior is different from past behaviors: 

  • All behavior has meaning.  When mom becomes upset during a shower, she is trying to communicate something.  She isn’t trying to be difficult.
  • Don’t take it personal.  The conflicts that are occurring are caused by the disease process. 
  • It’s all about safety.  When caring for a loved one with Alzheimer’s, caregivers need to remember to make the loved one feel safe.  This will go a long way towards reducing conflicts.

If you are feeling overwhelmed, then find a support group.  Ask for help.  You don’t have to walk through this alone.