10.15.17 Some Things I Learned About Dementia – Vascular Dementia and Frontotemporal Dementia from November 2014

October 15, 2017 – This one is very basic information about Alzheimer’s.  I do not have Alzheimer’s, I have Vascular Dementia and Frontotemperal Dementia. Since I want ya’ll to know as much as you can about what you might see happening here’s what I found on the progression of both.

From the Alzheimer’s website about Vascular Dementia this is what they say about its progression:

Vascular dementia develops when brain cells are deprived of oxygen and die. This happens either because of diseases of the very small blood vessels deep in the brain (known as subcortical vascular dementia), or after a major stroke or a series of smaller strokes (both known as stroke-related dementia).  The series of smaller strokes is what I’ve had.

It is sometimes difficult to tell whether a person has Alzheimer’s disease or vascular dementia. It is also not unusual to have a mixed form of dementia, meaning the person has both vascular dementia and Alzheimer’s disease together.

Subcortical and stroke-related vascular dementia share some symptoms but have others that differ. They also tend to progress in different ways. Subcortical vascular dementia usually develops gradually and progresses slowly, like Alzheimer’s disease. In contrast, when vascular dementia follows a large stroke, symptoms usually develop suddenly. Stroke-related dementia often then follows a ‘stepped’ progression, with long periods when symptoms remain the same and short periods when they suddenly worsen (this pattern is seen because each stroke further damages the brain).

The symptoms of vascular dementia are overall broadly similar to those of Alzheimer’s disease – and become more similar as the dementia progresses – but with some important differences. The main early symptoms of vascular dementia are often not forgetfulness but rather:

  • difficulties with planning or organizing, following steps (eg cooking a meal) or making decisions
  • slower speed of thought
  • problems concentrating, including short periods of confusion.

You can help someone with vascular dementia by breaking tasks down into smaller steps and giving them plenty of time to think and speak.

A person with early stage vascular dementia is prone to apathy, mood swings and being unusually emotional. They are also particularly likely to have anxiety and depression, partly because they are more aware of the problems their dementia is causing.

Vascular dementia after a major stroke is often accompanied by physical symptoms, such as weakness of a limb, or problems with vision or speech. These early symptoms arise when the stroke has damaged a particular part of the brain. With rehabilitation the symptoms might get a little better or stabilise for a time.

As vascular dementia progresses, the symptoms become closer to those of middle and eventually later stage Alzheimer’s disease. Problems with memory loss, confusion, disorientation, reasoning and communication all become worse. The behavioral changes seen as vascular dementia progresses, such as irritability and agitation, are also similar to those of Alzheimer’s disease. Delusions, and less often hallucinations, are also seen. The late stage of vascular dementia is largely as described above for Alzheimer’s disease.

Each person will experience dementia differently. On average, people with vascular dementia live for around five years after symptoms begin, less than the average for Alzheimer’s disease. In many cases, the person’s death will be caused by a stroke or heart attack. For more information about Vascular Dementia, see our page on vascular dementia.

Symptoms of Frontotemporal Dementia

Each case of FTD is different, but the illness generally becomes more distinguishable from other brain conditions as it progresses. Symptoms may occur in clusters, and some may be more prevalent in early or later stages. Here is a list of ten signs of FTD:

  1. Poor judgment
  2. Loss of empathy
  3. Socially inappropriate behavior
  4. Lack of inhibition
  5. Repetitive compulsive behavior
  6. Inability to concentrate or plan
  7. Frequent, abrupt mood changes
  8. Speech difficulties
  9. Problems with balance or movement
  10. Memory loss

From the Alzheimer’s website about progression of Frontotemporal Dementia (including Pick’s disease)

This type of dementia is caused by damage to the frontal and/or temporal lobes at the front and sides of the brain by the ears. My frontal and temporal lobes have significantly shrunk (they call it atrophy).  These are the areas responsible for our behavior, our emotional responses and our language skills. There are three different types of frontotemporal dementia – one type that affects behaviour first, and two that affect language first.

During the early stages of frontotemporal dementia, memory of recent events may be unaffected. However, there will be other changes.

A person with behavioural variant frontotemporal dementia may appear uncharacteristically selfish and unfeeling. They may behave rudely, or may seem more easily distracted. Other early symptoms may include loss of inhibition, ritualised behaviour (eg tapping or repeatedly walking the same route) or compulsions and a liking for sweet foods. It is much more likely for those around the person to be aware of these changes than the person is themselves.

In a small number of people with frontotemporal dementia, the first symptoms are problems with recalling the names of objects and understanding words (semantic dementia) or with producing fluent speech (progressive non-fluent aphasia).

As frontotemporal dementia progresses, differences between these types lessen: people with the behavioural variant develop language problems and those with language problems develop behaviour changes. In the later stages, the symptoms of frontotemporal dementia become more similar to those of Alzheimer’s disease. There are some differences – for example, day-to-day memory loss and problems judging distance or seeing objects in three dimensions develop later in frontotemporal dementia, whereas changes in behaviour, such as agitation or aggression, develop earlier. Supporting a person with frontotemporal dementia can be a challenge as they may be younger and will have changes in behaviour and communication.

Each person’s experience of frontotemporal dementia will be different, but on average people live for six to eight years after symptoms begin. For more information on Frontotemporal Dementia, see our page on frontotemporal dementia.

This is the original blog from November 2014:

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Two things I’d like to share today are information from the alz.org site.

  • 10 Early Signs of Alzheimer’s
  • 7 Stages of Alzheimer’s.

autum branch with falling leaves divider
know the 10 signs
Could you spot the early signs of Alzheimer’s before the disease became severe? Often, Alzheimer’s symptoms are overlooked or misdiagnosed as other illnesses. Many times it is easily written off as being forgetful, or misdiagnosed as depression. The info graphic below (from dailyinfographic.com) lays out 10 early symptoms found in Alzheimer’s. While the disease will ultimately progress over time, early detection will delay the process. That means early diagnosis and early treatment will keep you or your loved ones with you that much longer.

There is also a comparison shown below between what is “typical” in an elderly person without Alzheimer’s compared to the actual Alzheimer’s warning signs.


autum branch with falling leaves divider

7 stages

It became obvious to my sister and I that Mama had Alzheimer’s when she was around the 4th to 5th stage. We realized soon that she had been going through the first four stages for maybe a couple of years without us realizing it. After that it was a little over a year that she went from stage 4/5 to stage 7.  I haven’t started putting empty boxes of food back in the freezer like she did, which is what first alerted us to a problem.  I have done smaller things that makes Roy shake his head because he knows they are not normal.

Below are three different ways to learn about the 7 stages of Alzheimer’s. First is a written explanation, second is a link to an Interactive tour of the brain showing the progression, and third is a graceful, poignant dance representation of the stages. I recommend watching all three. This is important information and it will stick with you better if you do.

Not everyone will experience the same symptoms or progress at the same rate. This seven-stage framework is based on a system developed by Barry Reisberg, M.D., clinical director of the New York University School of Medicine’s Silberstein Aging and Dementia Research Center.

curley dividersAlzheimer’s symptoms vary. The stages below provide a general idea of how abilities change during the course of the disease.

Stage 1: No impairment
Stage 2: Very mild decline
Stage 3: Mild decline
Stage 4: Moderate decline The stage I am in is between Stage 4 and Stage 5
Stage 5: Moderately severe decline
Stage 6: Severe decline
Stage 7: Very severe decline

STAGE 1: No impairment (normal function)
The person does not experience any memory problems. An interview with a medical professional does not show any evidence of symptoms of dementia.

STAGE 2: Very mild cognitive decline (may be normal age-related changes or earliest signs of Alzheimer’s disease)
The person may feel as if he or she is having memory lapses — forgetting familiar words or the location of everyday objects. But no symptoms of dementia can be detected during a medical examination or by friends, family or co-workers.

STAGE 3: Mild cognitive decline (early-stage Alzheimer’s can be diagnosed in some, but not all, individuals with these symptoms)
Friends, family or co-workers begin to notice difficulties. During a detailed medical interview,doctorsmay be able to detect problems in memory or concentration. Common stage 3 difficulties include:

  • Noticeable problems coming up with the right word or name
  • Trouble remembering names when introduced to new people
  • Having noticeably greater difficulty performing tasks in social or work settings
  • Forgetting material that one has just read
  • Losing or misplacing a valuable object
  • Increasing trouble with planning or organizing

STAGE 4: Moderate cognitive decline (Mild or early-stage Alzheimer’s disease)
At this point,acarefulmedicalinterviewshould be able to detect clear-cut symptoms in several areas:

  • Forgetfulness of recent events
  • Impaired ability to perform challenging mental arithmetic — for example, counting backward from 100 by 7s
  • Greater difficulty performing complex tasks, such as planning dinner for guests, paying bills or managing finances
  • Forgetfulness about one’s own personal history
  • Becoming moody or withdrawn, especially in socially or mentally challenging situations

STAGE 5: Moderately severe cognitive decline (Moderate or mid-stage Alzheimer’s disease)
Gaps in memory and thinking are noticeable,and individuals begin to need help with day-to-day activities. At this stage, those with Alzheimer’s may:

  • Be unable to recall their own address or telephone number or the high school or college from which they graduated
  • Become confused about where they are or what day it is
  • Have trouble with less challenging mental arithmetic; such as counting backward from 40 by subtracting 4s or from 20 by 2s
  • Need help choosing proper clothing for the season or the occasion
  • Still remember significant details about themselves and their family
  • Still require no assistance with eating or using the toilet

STAGE 6: Severe cognitive decline (Moderately severe or mid-stage Alzheimer’s disease)
Memory continues to worsen, personality changes may take place and individuals need extensive help with daily activities. At this stage, individuals may:

  • Lose awareness of recent experiences as well as of their surroundings
  • Remember their own name but have difficulty with their personal history
  • Distinguish familiar and unfamiliar faces but have trouble remembering the name of a spouse or caregiver
  • Need help dressing properly and may, without supervision, make mistakes such as putting pajamas over daytime clothes or shoes on the wrong feet
  • Experience major changes in sleep patterns — sleeping during the day and becoming restless at night
  • Need help handling details of toileting (for example, flushing the toilet, wiping or disposing of tissue properly)
  • Have increasingly frequent trouble controlling their bladder or bowels
  • Experience major personality and behavioral changes, including suspiciousness and delusions (such as believing that their caregiver is an impostor)or compulsive, repetitive behavior like hand-wringing or tissue shredding
  • Tend to wander or become lost

STAGE 7: Very severe cognitive decline (Severe or late-stage Alzheimer’s disease)

In the final stage of this disease, individuals lose the ability to respond to their environment, to carry on a conversation and, eventually, to control movement. They may still say words or phrases.

At this stage, individuals need help with much of their daily personal care, including eating or using the toilet. They may also lose the ability to smile, to sit without support and to hold their heads up. Reflexes become abnormal. Muscles grow rigid. Swallowing impaired.curley dividersTo learn more about the brain and specifically how Alzheimer’s changes it, CLICK HERE to go to Alz.org. If you find the brain steps 1-7 to be uninteresting, skip to step 8 where they start with the Alzheimer’s brain.

curley dividersSome of us learn things in different ways than others. I do better sometimes when I visually learn from seeing in action, rather than reading. I found this video which uses dance as a unique way of explaining the various stages.

As the three girls dance, the narrator explains the different stages of Alzheimer’s. Then, the purple dancer’s movements slowly begins to differ from the others, correlating to the mental and physical changes that mark each stage of the disease. Take a look.


dance you tube 7 stages autum branch with falling leaves divider

Please come back next time when I’ll share how Alzheimer’s drastically changes vision and about making a dementia friendly home. If you want to get an email whenever I post a blog (I write about other things, not just Alzheimer’s) find the “FOLLOW” box which is usually to the right hand side somewhere, enter your email and respond when the confirmation email is sent to you.

If you are in need of prayer for yourself, in your role as a caregiver, or if you have any specific questions please send me a comment with whatever information you want to share or ask about. I’ll say again that I’m not expert but I probably experienced with my mom a lot of things you’re going through and will try my best to help. If I don’t know the answer I will tell you I don’t know. I’ll never judge, I’ve been judged enough to last a life time and would never do that to someone else. My email address is rosalyn@selu.edu if that is an easier way to communicate.

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Philippians 4:6: “Don’t worry about anything; instead, pray about everything. Tell God what you need, and thank him for all he has done”.


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10.14.17 Some Things I Learned About Dementia – DO NO CORRECT THEM from November 2014

October 14, 2017 – Like I say below, the biggest thing I want to share to caregivers or people who know someone with Dementia is D O   N O T   C O R R E C T  T H E M.

Right now I don’t mind it too much for myself, but as time progresses in my dementia journey there will come a time when I want you to really pay attention to this blog post’s information. For now, just don’t make me feel foolish because I don’t remember. Something to remember is that  as soon as you or I say something a lot of the time I don’t remember what you or I just said. So you correcting me makes me even more confused.

It hurts the dementia patient when you make them feel foolish, or correct them like they should know better. I know my poor mama did not know better as time went on and unfortunately I won’t either.

Here’s the original 10.14.14 blog post:ALZ BLOG LOGOjpg

Thanks for coming back. I feel like Alzheimer’s caregivers and loved ones are connected with each other like a family because no one else really understands what it’s like. Reach out to others that you may know in this family of ours to ask questions and learn what to expect as time goes on. A dear senior gentleman at our church allowed my sister and I to visit him and his wife (who had Alzheimer’s and was just a few days from her death) and ask our questions. It is a very shocking thing to see someone with this disease near the end of their life. I truly believe we were better prepared to handle the end of our mother’s life because he allowed us to come talk and see his wife. We all need each other so if your loved one is near the end and you know of a caregiver near the beginning of the process. please open your heart and home to them so they can learn from you and be better prepared.

One of the important reasons for as many people as possible to be more aware of Alzheimer’s, is that:

By 2050, the number of people age 65 and older with Alzheimer’s disease is estimated to triple, from 5 million to as many as 16 million, unless medical breakthroughs prevent, slow or stop the disease. Alzheimer’s is the sixth leading cause of death in the United States. One in three seniors die who have Alzheimer’s or another dementia. Those with Alzheimer’s live an average of eight years after their symptoms become noticeable to others, but survival can range from 4-20 years, depending on age and other health conditions. (source: empowher.com)

autum branch with falling leaves dividerIf you learn only one thing from this and future blogs about dementia, it is what I am going to talk about today.

  • Your loved one will begin to tell you stories over and over and over, etc. etc. etc.
  • They may ask the same question over and over and over even after you’ve answered them.
  • You will tell them something one minute and the next thing you know it. they ask you about what you just told them in a way that you know means they didn’t remember you just told them.
  • Your loved one will call common objects by incorrect names or will call you the name of her brother or her other child.

This list can go on and on.



You may get aggravated by these actions of theirs but that is NOTHING compared to the hurt, depression, confusion and sadness you cause them by saying things like “I already told you that mama” or “How many times are you going to ask me that” or “Her name is not Susie it’s Donna, you know that daddy” or any other variation of correcting them.

Not correcting them is very difficult, especially early on when you don’t really know that the reason they are saying these things is something they can’t help. You don’t know they have dementia, you just think they’re forgetful and that you are helping them by reminding them what the correct thing is.

My strong recommendation is once something like that happens several times make every effort within your control to STOP CORRECTING THEM. One source I researched said to just smile and love them. They are not going to remember this information you just gave them very long but they will feel and maybe remember the hurt and sadness you caused. Don’t come back and tell them you are sorry, they won’t know what you are talking about and this will cause them more confusion.

Below is one of the most pleadingly direct, true poems from the perspective of a person with Alzheimer’s:

an alzheimers request by

That information is very basic. and I hope. to the point. A lot more information can be found on the internet. A look at communicating with your loved one that goes way beyond the scope of my simple “DO NOT CORRECT THEM” was found on the Lewy Body Dementia Association, Inc. (Lewy Body is a form of dementia) website and I’ve included it below.


As a person’s condition progresses, his or her ability to communicate diminishes. Understanding the effects of the disease will help you communicate as effectively as possible for as long as possible

Your loved one may:

  • Be unable to remember names, thoughts or memories
  • Use the wrong words or invent words
  • Mispronounce or repeat words
  • Have difficulty organizing thoughts
  • May be easily distracted
  • Use more nonverbal gesture
  • Lose ability to reason and understand
  • Use language that is more direct or accusatory
  • May become withdrawn and speak very little

Medications and other health problems also may affect communication. If you notice significant or abrupt changes in your loved one’s ability to communicate, talk to his or her physician.

Tips for better communication Although you may find these changes frustrating and even alarming, you can counter them. Consider using these tips to improve communication with your loved one:

  • Make the effort. When communicating becomes difficult, your first response may be to stop. Recognize that communicating effectively may take more time and energy. Making the effort will help you sustain this vital aspect of your relationship with your loved one as well as preserve your loved one’s dignity.
  • Try to understand. Rather than correcting mispronunciations or inaccurate statements, recognize that your loved one may no longer be able to consistently come up with the right words, or may have trouble comprehending what you’re saying. Be patient and use phrases such as “I’m sorry, could you repeat that?” or keep the flow of conversation going by providing the elusive word.
  • Speak slowly, calmly and quietly. This will allow the person time to process what you are saying. People with dementia often watch our non-verbal cues (facial expression, body language, tone of voice) to interpret what we are saying and may mirror our mood.
  • Avoid quizzing, testing or trying to teach the person to remember. These techniques won’t work and will only serve to embarrass and humiliate. Imagine the feelings associated with not being able to recall a child’s name during such a test. Instead of saying, “Do you know who this is?”, try “Here is your granddaughter Susan who has come to visit.”
  • Reassure and comfort. Do not reality orient. The person may be worried about the children, parents, going “home” even if living at home or going to work even if long retired. Trying to convince them of the truth is generally fruitless and can be frustrating or even frightening. Jump into their world and help to make it less frightening by providing lots of reassurance. For example, if your loved one is worried because the children are not home from school yet, provide an explanation that might be acceptable and reassuring such as, “the children are staying at a friends house tonight, they are having a nice time”. If your loved one does not recognize you, go along with it or try stepping out of the room and announce your identity upon your return.
  • Be aware of your nonverbal communication. Speak slowly, calmly and in a normal volume. People with dementia can be sensitive to changes in mood, voice, posture or facial expression. You can do wonders to ease tension by smiling at a frustrating moment. If you have difficulty understanding what your loved one is saying, listen for the feelings behind what he or she is trying to communicate and validate those feelings. For example, say, “I know that you’re frustrated right now” or “I’m glad you’re so happy today.”
  • Forgive yourself when you don’t always respond appropriately. You may find it difficult to communicate with as much understanding and patience as you’d like to. Keep in mind that because of the memory loss, your loved one is unlikely to remember everything you say.
  • Simplify your communication. Stand directly in front of your loved one and make eye contact. Communicate one idea at a time and use simple instructions. Try breaking even simple tasks into one-step commands. If you’re helping with a task, let your loved one know what you’re going to do next. If possible, demonstrate what you want your loved one to do — such as brushing teeth or putting on a jacket. If you must repeat things, try to use the same words. If your loved one doesn’t understand a second time, then try rewording. Avoid abstract concepts, which your loved one may find difficult to grasp. For example, phrases such as “jump into bed” can be confusing. Instead, use direct statements such as “it’s time to get into bed.”
  • Validate the feeling behind the words. Even if you are unable to understand what is being communicated, look at the non-verbal signs of emotion. Is she upset? Joyful? Afraid? Respond accordingly providing lots of affection and comfort.
  • Reminiscence can be very useful and validating. Persons with dementia usually retain their memories from long ago. Discussing these memories and prior accomplishments often provide a sense of security.
  • Do not try to argue or reason with the person. Their ability to reason is no longer there, and the person will not be able to remember your reasoning or rationally weigh your points. Do not argue with the person over what they see, hear or feel. If the person is seeing things you don’t see, reassure him and respond to his or her feelings about it. Remember that these ideas or hallucinations are very real to the person who is experiencing them. Rather, offer reassurance and validation (e.g., “I know this is troubling for you, let me see if I can help”).
  • Reduce clutter, extraneous noises or confusing aspects in the environment. Check out any real basis to the person’s fear. For example, the person may “hear people” in the next room because the TV is on.
  • If the person misplaced something and thinks you or someone else “stole it,” offer to help look for the item. Keep track of frequent hiding places, and if possible keep duplicates of the item.
  • Accept changes. Keep in mind that the changes you see and hear in your loved one are a result of the disease, not of your loved one trying to be difficult or hurtful. When your loved one says inappropriate things, remember it’s the disease talking. Try not to take it personally.

Even when your loved one no longer responds in the way he or she once did, your efforts to communicate will help to keep him or her engaged in life for as long as possible.

autum branch with falling leaves dividerLAST NOTE FROM ME: This is related to the orange colored sentences underlined above. Remember that they are not going to come back into your world, the real world, so learn early on to live with them in whatever little bizarre world their deteriorating brain is creating for them. Even though they may have periodic lucid moments or even hours they eventually go back to their little bizarre world so when they do, go with them. Living in their world (when you are with them) is the kindest, more loving thing you can do for them and it will eliminate a lot of frustration on your part.

Please come back next time when I’ll share the a video I recently saw for the first time about how their vision changes as the disease progresses. It’s one of the things I truly wish I had known when mama was suffering with Alzheimer’s. I’ll also share with you the seven stages of Alzheimer’s and a video I found that depicts the stages using dance.

Please let me know if you are in need of prayer for yourself in your role as a caregiver or if you have any specific questions. Send me a comment with whatever information you want to share or ask about. I’ll say again that I’m not an expert, but I probably experienced with my mom a lot of things you’re going through and will try my best to help. If I don’t know the answer I won’t improve but will tell you I don’t know. I’ll never judge, I’ve been judged enough to last a life time and would never do that to someone else. My email address is rosalyn@selu.edu if that is an easier way to communicate.

autum branch with falling leaves dividerIsaiah 41:10: “Don’t be afraid, for I am with you. Don’t be discouraged, for I am your God. I will strengthen you and help you. I will hold you up with my victorious right hand” (NLT).


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Some Things I Learned About Dementia 11.14.14 First Post Dementia Overview

10367601_541945785942421_1370303081116848230_n Where do I start when sharing about Alzheimer’s? When I speak of Alzheimer’s here, it may also pertain to one of the other forms of dementia. Alzheimer’s is the most common form of dementia. Here is a link to the different forms of dementia so you can learn a bit more about them.

My mama, Josie Mae Cochran Blum Traylor died at age 87. On her death certificate a contributing cause of death was dementia. I plan to write more in future posts about her and our family’s experience as she suffered and died. I hope that what I will share will be helpful to those early on in this experience. I will share how life was for us while she lived with us and how I came to love that beautiful little Christian lady more every day until she left us on December 18, 2007.

I am by far NO expert on dementia. I can just share with you my own experience, and what I have learned online bringing it all into one place to help you. It’s important that you understand that if what I share about my experience is different than what your loved one’s doctor tells you: Listen to the Doctor.

My inspiration for writing this was all the things I learned AFTER my mother passed away that I deeply wish I knew when she was still with us enduring this horrible disease. When we first started noticing that something was not right, I searched for any information I could find, which back then wasn’t much. I found the most helpful information came from personal blog posts of real life experiences by caretakers of their family member or friend who had dementia.

I hope to become a resource like that to share what we learned during her life, and since then, about Alzheimer’s. I’ve invited friends and family to contribute since my experience is with my mother and others experiences were with their father, sister, brother, grandfather, grandmother, etc. We all experienced things from different perspectives.

While I’m writing this to help the caregiver understand more, you might not be the caregiver. Instead you’re a grandchild, child, other family member, friend or church family. 10689816_537425689727764_867424369629248004_nSome of what I have to share is for everyone who has anyone in their life with Alzheimer’s.

The individual who says “Why even go visit, they won’t know I was there as soon as I walk out the door”. I urge you to read and learn what you really CAN do.

I collected videos, stories, songs, graphics, blog posts and more that I will shared each week. These are not only about the person with Alzheimer’s but things that will help the caregiver survive the overwhelming struggles you will face. I’ve been the caregiver and learned a lot that helped me cope. I want to share that with you

These blog posts will come out weekly, probably on Fridays. The next post will have a general VERY IMPORTANT point I’d like to start with. It is the main thing that I’ve wanted to share for so long that may sound simple, but will make such a difference in a person life who is living with dementia. Someone, probably either God or my mama, have laid on my heart that others can be helped by the experience we had and I hope that turns out to be the case.

Please come back next time when I’ll share the number one thing you can do for your loved one from the very beginning of dementia. If you want to get an email whenever I post a blog (I write about other things, not just Alzheimer’s) find the “FOLLOW” box which is usually to the right hand side somewhere, enter your email and respond when the confirmation email is sent to you.

If you are in need of prayer for yourself, in your role as a caregiver, or if you have any specific questions please send me a comment with whatever information you want to share or ask about. I’ll say again that I’m not expert but I probably experienced with my mom a lot of things you’re going through and will try my best to help. If I don’t know the answer I will tell you I don’t know. I’ll never judge, I’ve been judged enough to last a life time and would never do that to someone else. My email address is rosalyn@selu.edu if that is an easier way to communicate.

I’ll close with a video I just found that gives a short summary of what Alzheimer’s disease is, how it progresses and why awareness is so important. The medical terms may go right over your head. Some went right over my head and I majored in Psychology. I think the video itself is extremely helpful in seeing how their brains are changing forever throughout this process.

tangle placque


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