Showing posts with label lewy bodies with dementia. Show all posts
Showing posts with label lewy bodies with dementia. Show all posts

Wednesday, February 6, 2013

Many Friends and I cannot Remember Them!

I have met so many people since I started this blog, and i am lucky if I can tell you five of them. There is Carol, who for some reason thinks i know what I am talking about. Dr. Joe Sivak who has gone on to greater fame and forgotten us little folks, i know doc i am a pain in the ass. My friends Mary and Jim who live in canada. I know there are many ofthers my email list shows it. Hey you old Navy guy Dr. Gordon, I still know you.

The last week or more has been a real doosey for me. I have ussed the old brain cell way tooooo much and gotten exhausted, shaky, a bit lost in time. I helped a friend redo his computer after it was totallly infected and that took a couple of days to retreive everything for him and my head hurt and i felt like a zombie. Tax season, somebody shoot me. Then I put Windows 8 onn my machine, nice program. But I did a refresh without finding out what that really was, my thoughts and its thoughts just did not agree. It cleaned my machine and I had to re-install almost all of my programs, in the process I signed up for stuff that my wife had to get me out of, I have been a mess, I do not even understand the notes that I have made so I do not forget, toooo much fog and dust up in the old brain.

I guess I should keep it simple but I have that inner pit bull in me that does not want to let go even though I am not winning at fixing and doing things. This disease Alzheimer's and the FTD, they hit hard when they punch back, a lot harder than I can. Wanted to let you all know for better or worse I still am being a pain in the ass to those around me, just doing my job.

God Bless & Keep You & This Country of Ours!
joe














Wednesday, January 16, 2013

Hello

Yes I am still here you lucky people. Thought you might like to know that Yolanda from the documentary as of 15 minutes ago was still with us and fighting.

Things are getting screwery in my world. I know that the computer and calendar say it is 2013, but I am trying to figure out where 2011 & 2012 went. I do not remember them hardly.

We just got back from northern California visitig my daughter her hubby and 4 kids for a few days. My older daughter joined us with her 4, yess Lynn & I got a room for me to escape to. 8 grandkids and their parents is definetly more than I can handle. Extra drugs help but only to a point.

Physically things are still going the wrong way and that includes that brain cell that i have. If Lynn had not told me, I thought that I have been posting regularly, not so Mr. Brain.

I listen to all that they say is happening in research and trials as much as i can and actually i still not heard or remember if they have even come up with a definative cause for Alzheimer's.  Treatment does not seem to moved any further than a shot in the dark still. For me my world seems smaller and lonlier, my brain does not seem to really take in things around me anymore. Sleep and just stareing at the TV seem to be all that hold any interest no matter how hard I tried to pretend that I am with it. Oh well It Is What It Is.

take care until next time.

God Bless & Keep You & This Country of Ours!
joe

Monday, December 24, 2012

From the depths of the Ocean!

I read an article this day, the Scripps Oceanography team has been researching hte Mirianna Trench the deepest part of the world. They have found single cell life forms, get this the size of salad plates. Don't get one of these on your kisser. But even more fascinating I think is that they have fourn a crustascean with a chemeical inside it that may help get this Alzheimer sufferers. I hope to read or hear more on this . Go Scripps.

God Bless & Keep You & This Country of Ours!
joe

PS> From my family to yours a Very Merry Christmas and Happy Holidays To All.

Saturday, December 8, 2012

I find that it is easier to write here then to talk to others. I feel like things are becoming more confused and i am not sure wht the hell i am doing. I try to hide moset things and find it is getting harder. I try to remain happy on the outside, but inside is not so anymore. My days are just that days. they mean little, they hold no interest for me. I find being secluded much more frienndly. I feeel like everyone is watching me and not leaving me alone. The other day the shower door and I took a walk out of the shower. it is getting difficult to even take a shower. even worse harder to remember when and if i took one. this is the way life is for me now. I find it hard to enjoy my family and am beginning to drift from them, i wonder if this is the way it is for others, having some trouble finding the keys, fingers keep moombing around. Good thing for the drugs or I would looose it aroung everyone, the anger and distrust level in me is rising. i really am not in control too much anymore, i guess that is ok. the more i leave go of things the easier it seems to be, the less emotional i am and the less my head hurts.

take care until next time.

God Bless & Keep You & This Country of Ours!
joe

Tuesday, November 20, 2012

I have not posted recently on my own life. It seems to be getting more and more out of my control. Trying to remember to do things is nearing the statem of impossibility. Yet writing seems to still work for me. I was reading an article about a new gene they have found that works on the immune system and seems that it has some affects on Alzhiemers. What gene damned if I remember. But it only helps to confirm my non medical opinion that this disease is an auto imune disease. If i find the article in my notes i keep to help me i will post it. I know they are looking at stem cells as well and they hold some possible hope.

I  am finding it more difficult to post I do not know what to say anymore. I am tired of trying to really reach out and get our voices heard. I went back in my archives, I have been doing this blog for over six years and feel like i have gotten no where. Yes many of you have told me how it helps, i do read the comments that is how i know when you yell back at me.

The fuzzieness of this world is getting very hard to get throught. being quiet and not talking seems to becomming more the way I want to be. I prefer being left alone to drift off to other places that are kinder and more pleasant than this. Notes are starting to hang on my computer desk to help me remember things again and again i forget to look at them. enough for today.

Be kind to yourselves.

God Bless & Keep You & This Country of Ours!
joe

Monday, November 12, 2012

New Age of Caregiving Symposium 2012


I wanted to get in touch with you regarding the upcoming New Age of Caregiving Symposium 2012 which will be held on Friday, November 16 at the Hilton St. Petersburg Carillon Park.

Last year’s event was a huge success and we are excited to be bringing this opportunity to the Greater Tampa Bay again (if you are not in the Tampa Bay area or unavailable to attend on November 16, please share this with any connections that could benefit from it).

This entire day is devoted to supporting and nurturing the family and professional caregiver. Our intention is to provide new information, new resources and new guidance to help you create balance in your very busy and challenging lives.

Are you open to the idea of getting a massage, experiencing healing sound therapy, learning about nutrition that can prevent Alzheimer’s disease, laughing at yourself, meeting new people or finding out what resources are available to pay for home care? I hope so. Over 80 sponsors have come together to share their products and services to address your needs and wants because they care. You are encouraged to visit each vendor and spend time asking them questions. We live in an amazing community that embraces the art of collaboration and energetically this creates a sense of commitment that can only enhance the caregiving journey. There is no other healthcare-senior-caregiver event like this symposium. You are in for a grand day that has the ability to transform your daily life.

This year’s theme is healing and inspiration. When you review the line-up of speakers, breakout session leaders and honored guests you will see how much thought went into providing varied and numerous modalities that will encourage you to heal your mind, body & spirit. Our commitment to inspiring you will unfold as the day progresses. It could be a simple word, a piece of artwork, a healing touch that will ignite hope, excitement and purpose into your life. We thank you for joining us and send you love and light all year long.

Space is going quickly, so click and book your tickets today: http://newageofcaregivingsymposium.com/register/

For more information about the speakers, agenda, special services and more visit our official website: http://newageofcaregivingsymposium.com

Any questions?  Please let me know.  I would be happy to answer them for you.

Warmly,
Kim

The Caregiver Hour Radio Show: http://www.thecaregiverhour.com
Facebook: https://www.facebook.com/Thecaregiverhour
Twitter: http://www.twitter.com/kimlinder
LinkedIn: http://www.linkedin.com/company/2786843

this is an email i received so for those of you interested I am posting it.

God Bless,
joe

Monday, October 29, 2012

Home Safe!

Last we were heading to Omaha or had reached there, at any rate we spent the night in Omaha. I provided comic relief for my daughter bac, in Colorado, the wind was a bitch. We stopped for gas and to get something to eat. Watching me trying to get out of the car was like an Abbott & Costello skit. The wind was so hard it kept pushing me back into the car and shutting the door on me. Well I finally managed to get out and to food.
In the morning in Omaha we took off and went to the zoo, the wind had followed us. Got a scooter there did not want to take a chance with possible rain and mine. Well as the morning rolled on so did the wind and then the rain, what a day, but hte zoo is very nice.  We ledft for the car and it was down hill, now when you get this person moving down hill he can not stop, i pick up speed, my daughter was latched on to me like an anchor but no good, had to use the care parked next to us as a stopping post. We ledt for Iowa, well 5 minutes later we were in Iowa. We were going to stop in DesMoines, but it was still early so we went on to Lake Bluff, Illinois got in about 12:30 am, Thursday morning. Spent Thursday resting I think. Not sure what we did Friday, I forget. I think we went to lunch with my brother in law and family. my days are a bit messed up. On sunday we went to downtown Chicago and met up with John and his family, met a young black fellow and family from Philadelphia who were there, like us for the Monday night Bears game.  We went out for dinner and headed home.  On Monday Kathryn and I went to the one mueseum near Soldiers Field where the game was to be. We after staying at the museum went back to Soldiers Field and back to the car which we could not find, turns out we were on the wrong level. After finding said vehicle and downing our attire and face paint for the game we went into the stadium. What a great time we had, our seats were the best almost the entire game was played directly in front of us, just like watching on TV, and of course is was a great game Dah Bears won.
HOme ward bound to Lake Bluff in the rain, but we were happy., until Kathryn noticed her wallet was gone, this is 12:30 in the morning, so we searched the car nope, no where to be found. Started immediately contacting credit cards and such to report them lost. Tuesday Kathryn call the DMV in Calif. and reported here license lost and they sent a temp Fed-X to her, which she got wednesday. Well she went out to the car to start packing it to leave and things of all things, there is her wallet under the front tire of the car. Happiness showers the day again and off we went. We left Wednesday about noon and got home about 1am Saturday morning, we stopped in Arizona but both said no lets go home. So here we are.
It was fun, but very emotional for me, Chicago holds some real bad and heart wrenching memories for me. But this trip was for Kathryn she always wanted to see a Chicago Bears game in Chicago, so time getting shorter off we went.She has her memories and I have a very tired body and sore ass. But still had fun.
No more travels to hard on me and the old body. So there you have it. Thanks for listening.

God Bless & Keep You & This Country of Ours!
joe

Friday, October 19, 2012

Where in the world is joe?

Well he is in Lake Bluff, Illinois. After a much heroing journey through California to the Nevada border and the City of Sin, Las Vegas (actually loss wages), my daughter subjected me to the towering hieghts of Colorado, not only did she try to dump me off the mountains, she had the nerve to even drive through tunnels in them. She tried to get rid of me at 10,361 feet, buy i am a tuff bugger. I hang on for dear life, terrified of hieghts. We visited a wildlife refuge in Ritchfield, Co. Had to rid my sscooter on a 35 ft high ramp to view the animals. What a neat experience that was. Only bad part it was cold and windy as all get out.
We left Colorado and went on into Utah, what a beautiful State and the color of the mountains is just outstanding. from there we went onto Nebraska, got off the freeway to find the zoo we were goinhg to see in the morning, but aliens had removed it from existence, so onto Omaha to spend the night and see the Omaha zoo.
well i will leave it there for now. I and my daughter are both extremely wornen out, but we will survive. I know i left out alot of things but the brain does not want to give them to me to write. Really gets me upset and I miss my home and wife and feel very uncomfortable at this point.

God Bless & Keep You & This Country of Ours!
joe













Wednesday, October 3, 2012

International Stem Cell Awareness Day - 10/3/2012


I was approached by the following to post something on Stem Cell Research and how it can possibly help brain disorders and others. Normally I do not do this but I found this interesting and thought you might also. I did not write this as you will see, the company is acknowledged and the end and I was given written permisssion to post it.

Five Factoids on Stem Cells
International Stem Cell Awareness Day - October 3, 2012

Stem cells have the potential to revolutionize the treatment of human disease. Scientists and researchers have been working diligently to unlock the potential of stem cells and significant strides have been made in the less than 15 years since the discovery of a method to grow and replicate human stem cells. Stem cells allow scientists to study human development (and how it could go wrong), develop better and safer drugs and offer potential treatments for devastating diseases and injuries.

#1: Stem cells are “master” cells that have the ability to grow into any one of the body’s more than 200 cell types, including brain, blood, pancreas and heart cells.

#2: Stem cells can reproduce into red cells that carry oxygen throughout the body, white cells for fighting infections and platelets that create clots and prevent excessive bleeding.

#3: Stem cell research is predicted to improve treatment options for incurable conditions such as Alzheimer’s disease, Huntington’s disease, Parkinson’s disease, spinal cord injuries and traumatic brain injuries, among many others.

#4: Scientists are conducting stem cell studies to develop cures for the more than 1.3 million Americans that suffer from spinal cord injuries. This is highly significant because no other form of treatment or drugs have been able to restore function for patients with paralysis.

#5: Stem cells can self-renew. They are capable of replenishing themselves for long periods of time. Through natural division, one Petri dish can hold up to 5 million pluripotent stem cells meaning scientists can create normal human cells in large scale for the first time in human history.

“This is a critical and historic time for stem cell research,” said Peter Donovan, director, Sue & Bill Gross Stem Cell Research Center, UC Irvine. “We’re literally on the brink of developing new treatments for countless life-threatening illnesses and debilitating injuries, and raising awareness about this research is one of the best things people can do to help accelerate the process.”

There are several research programs taking place at the Sue & Bill Gross Stem Cell Research Center at UC Irvine that continue to break down barriers and open doors to new treatments for major diseases and injuries including Alzheimer’s Disease. An estimated 35 million people worldwide suffer from Alzheimer’s disease, five million of whom live in the U.S.  Frank LaFerla, Ph.D., director of UC Irvine’s Institute for Memory Impairments and Neurological Disorders, andMatthew Blurton-Jones, Ph.D. of the Sue & Bill Gross Stem Cell Research Center, UC Irvine, have shown potential treatment in humans. Their work with stem cells is expected to move to clinical trials within five years.

Support stem cell research. To learn more, visit www.StemCellsOfferHope.com

Sabrina Suarez
Vice President
12711 Newport Ave., Suite H
Tustin, CA 92780
P 714.573.0899 x227
C 714.606.6934

 
God Bless & Keep You & This Country of Ours!
joe

Wednesday, September 26, 2012

My Friends.

today has been a rather calm day for me. after the last few weeks it is much welcomed. i still do not sort things out well, but i am a bit more aware i think this day. i think i have acquired sleep life away syndrome. I get up about 8 am do my morning stuff sit down and it is noon or one oclock already.  Next I know it is 4 or 5 diner time. Yes i sleep about 7 hours at night, but tht does not seem to matter. I have sat down a number of times this week to post, but as usual i just go dormant and cannot remember what i want to say or why i am at th computer. Lynn handles the check book now. I have to contact the DMV license renewal time. Although i do not drive anylonger, they will probably not renew my license, test and i will not get along. Just another part of one's life taken away by this fricken pain in the ass disease.  it is getting harder to keep some sense of humor and my mouth shut. It is what it is.

till next time take care of yourselves.

God Bless & Keep You & This Country of Ours!
joe

Sunday, September 16, 2012

There is a new community some of you may or may not know of now on the web. I have joined it,  it consists of people involved with Alzheimer's, sufferers, caregivers, etc. It is called The Alzheimer's Community   , you can register and join, of course it is free. Come take a look and help spread the word.

My world has been very mixed up lately. I really do not know what is going on in it much anymore. Lynn has to do the check book now, even the calculator does not do what i wnat it to do. Talking is becmoing one of those one time I knew how to do that and make sense.But that is the way it goes.

I sit here and have all these things to say and when I go to they go somewhere other than on this page, it pisses me off. Making a decisssion for me takes alot of time. So much that I forget what it is that I am trying to answer or do.

God Bless & Keep You & This Country of Ours!
joe

I just remembered something, I have noticed that most of my so called friends have disappeared from my life, just as they did when I stopped drinking. Quit being a drunk and loose your friends, have your brain eaten away loose your friends, seems interesting.

Sunday, September 9, 2012

Where the HELL is my brain?

The last couple of days have been really a fricken mess. Right now I can think kind of stratight. Over the last days I have forgotten what i was doin, how i got where I did and from where i got there. Talking has been utterly confussing even to me. I have needed help in getting around physically, legs did not want to work, when they did they wanted to go somewhere other than I was headed. Good things for walls and hand rails or I would have surelly met the floor. That damned thing kept moving on me. I feel like a plane, i have to make a wide circle to get to where i am goinging. Things seem to be happening quickly now, with more and more bad days and days i cannot remember. I can no longer tell you by the evening what I did in the morning , let alone yesterday and the past is fading as well. I am starting to feeel best just sitting in quiet and not talking or being talked to or having the boob tube on. It has become dangerous for me in the shower. Good thing it is not real wide or I would definitely get swaying from side to side and go through the doors. Even sitting on the seats we have in it has become an experience as my wet ass slides off and old shaking legs can barely keep me up there.

Till next time, be good to yourselves.

God Bless & Keep You & This Country of Ours!!!!!
joe

Friday, August 31, 2012

I am back.

A couople of weeks ago i posted that i was taking coconut oil becaues i promised a friend. Well still am and have nothing to report. It goes in and comes out. I remain the same and am getting a little bit worse each and evry day. So will continue and report. So far as i am concerned it is a ll HYPE, btu just because no hlep here so far does not mean that it might not help some people for a time.

We had the radio show on Alzheimer's Speaks Radio. I had a good time talking with Lori and feel good that someone agrees that our voices need to be heard and listened to. We may do it again some day. Will try to get link to the actual broadcast so you can hear it.  I have to say taht after the hour I was shot the rest of the day. I cannot concentrate that long and stay foccused without my head and body letting me know about it. If any of you listened I hope you enjoyed and would appreceiate hearing from you.

Now i need to fight another battle my body chringes at temps over 75, I just become worthless, more so.

For now take care of yourselves.

God Bless & Keep You & This Country of Ours!!!!
joe

Friday, August 24, 2012

Hello To All

I have added new resource sites again, soon will need a website for them alone.

I went fishing behind my pond the other night. A hose ame loose on the filtering system and Mr. Fix It, went out after midnight to meet the challenge. Well all went well, connected the hose back up got the system running again, stood up turned and immediately found myself tangled up on the ground in the plants, a plant stand in the dark.  Just a badly bruised ego, some bruses scratches and aches but I am use to that, I am not stable a foot.

One thing I do to try and keep my well let us say graying matter working, is to do towels for the week on Friday, yes that is today. I got up did normal cleansing stuff, changed all the towels, put the dirty ones in the washer and behold it cleaned them. I put them in the dryer, mind you this was about 9am, it is now 7pm. My wife came home about 11am I aksed her where she had been, she gave me that look and said I told you I was going shopping. OK. I just now asked what day it was and was told Friday, immediately my wife said the towels, well you got it they were stilll in the drlyer. So I just finished folding them and putting them away, a bit behind my time.

Don't forget Tuesday to listen to the radio web show, well i guess better said i do not forget to get on it.

Life in the world of Alzheimer's never a remembering moment.

God Bless & Keep You & This Country of Ours!
joe

Sunday, August 19, 2012

August 28, 2012 - Alzheimer's Speaks Radio

Yes you lucky buggers at 9am PST on Tuesday, August 28, 2012, yours truly will be babbling on Alzheimer's Speaks Radio on the Web. Click on title of show below. There is a phone number that you can call in on and ask questions. Suggest 10 minutes before show time, not sure if you can during the show. But you get one hour of me if I last. Lori La Bay is the host and runner of the site.
Making Choices For Those Who Can't & Living with Dementia

A side note of sorts, I promised a friend that I would try the Coconut Oil and I have been. To this point I cannot say anything except I have not died from it. No changes to my inabilities at all, in fact my balance is even worse and moving this battleship from spot to spot is getting harder. I am sure that has nothing to do with the coconut oil. My brain cells are still scrambled and bouncing alll over eahc other more so.

Those of you that may remember The HBO Alzheimer's Project and the PBS The Forgetting, with joy for those who passed there are only 5 of us still in this miserable state, Yolanda Sanmartino, Chuck Jackson, Isabel McKenna, Nacho Sanchez and myslef, that is all out of about 11+ or so of us.

Till Next Time Take Care of Yourselves.

God Bless & Keep You & This Country of Ours!
joe

Thursday, June 14, 2012

Dear Carolyn,

Thank you for your comment regargding your mother. You are probably right she has no idea she is repeating herself, I don't. Just smile and listen and let her know you love her. DO NOT ARGUE WITH A PERSON WITH DEMENTIA, you loose everytime. We are always right, we know we are right and you are squirelly get use to it, and let it roll off your back. In past posts if you care to read I believe we have covered somethings not to do with us.

Before I forget welcome to our family. You are not alone, this family is World wide so plenty of help and resources listed on the side. Come back and let us know, just how crazy mom has driven you. I am not making light just the facts and know here you have support.

God Bless & Keep You & This Country of Ours!!!
joe

Friday, June 1, 2012

Faces and Names don't always match.

The other day i do not remember when it was my younest daughter and i were siting on the couch talking and I looked at her and could not remember her name. Which is Kathryn. I tried to say it but i just was not able to. Finally it came out and she just looked at me and said you forgot my name, tried to cover it up, but she had me dead to rites. We did laugh about it, but it bothers me. Living with us she understands more about what is happening then the other kids and she just  I think the word is placates me, and says don't worry dad it is ok.

God Bless & Keep You & This Country of Ours!
joe

Thursday, May 31, 2012

Alan Arnette Completes 7 Summits Climb.


Climb4AD (The 7 Summits Climb for Alzheimer's)
Alan Arnette climbed the 7 Summits of the world in memory of his mother, Ida Arnette, who passed away from Alzheimer’s disease. Help Alan raise awareness of the growing prevalence of the disease and share your memories of caring for a loved one with Alzheimer’s. Email C4ADFBWall@biosector2.com with your story.

Support Alan as he has us.

God Bless & Keep You & This Country of Ours!
joe

Wednesday, May 9, 2012

Ghost Writer For My Blog!


Tips for Helping Someone With Alzheimer’s Disease Handle Daily Life
Caring for someone who has Alzheimer’s disease can be a frustrating experience. The person who takes on the role of their nurse, companion and protector must remain patient and flexible when planning and tackling the different practical aspects of the disease. At the same time, they must deal with their own heartbreak and strong emotions.
There are many ways of dealing with everyday routines in such a way that life can run as smoothly as possible for all concerned. Here are just a few suggestions that could help ensure safety and maintain dignity in five ‘typical’ situations.
Communication
The disease erodes communication skills, therefore the person’s words and behaviour may seem, at first, to make little or no sense - they may have trouble understanding what you want to say to them too. This can be extremely frustrating and distressing; however, there are ways to ease the situation. Speak clearly, maintaining eye contact and using simple language and sentence structure. Ask ‘yes or ‘no’ questions and keep your tone respectful and calm.
Never interrupt them when they are speaking, and avoid too many distractions – turn off the radio and try not to hold complicated conversations when you are out on a busy street. Use visual cues. For instance, you could point to the toilet if you want to ask the person if they need to use the bathroom. Try not take it personally. After all, the gentleman who used to be able to confidently arrange all his finances and insurance, including classic car insurance
 for his beautiful vintage mustang, himself every single year, or the lady who ran a busy household single-handedly must now battle this degenerative disease to make even the simplest of basic needs or preferences understood.
Mealtimes
In the earlier stages, the person will be better able to cope with preparing and eating food independently. However, as they grow more dependent on you, it will be up to you to make sure they maintain a healthy, regular diet. Good nutrition is crucial, to avoid physical weakness and infections. Make sure the person is comfortable when eating. Check that dentures fit well and that prescribed drugs are not interfering with certain foods or inhibiting the appetite.
You may need to help the person with the physical act of using a knife and fork – and remind them of table manners if appropriate. Reduce mealtime distractions to a minimum– turn off the phone and TV and clear the table of any unnecessary items, such as magazines or flowers. If you are not able to be with the person when they eat, make sure they know how to prepare the food or heat it up safely.
Medical visits
As with any disease of this seriousness, regular medical visits cannot be avoided. They can be a useful chance to connect with the person’s doctor and medical team and to ask any questions you may have. However, you can only get the most out of these appointments if you prepare the person who has Alzheimer’s disease for them as best as you can.
Try to fix the appointment at a time of day when you know that the person will be at their best and, if possible, when the medical waiting room will be quietest. Bring snacks, a drink, any required medication and an activity to keep the person happy while waiting. Make a list of all the points you want to raise with the doctor in advance – keeping your queries as specific as possible. When in the room, take notes of everything that is said and, if the person wants to answer the doctor themselves, sit yourself behind them so you can quietly nod or shake your head in support of their replies.
The Holidays
Preparing for the holidays can be a bitter-sweet occasion: you remember how the person used to celebrate or participate in holidays of yore. Yet you can still glean happy times from spending holidays with a loved one with Alzheimer’s if you do a little forward planning. Consider what the person used to enjoy about the season and try to include them in the same activities as much as possible. If they used to bake the cake, get them to measure or stir in the ingredients. Let them help you wrap gifts – concentrate on the process rather than the end result and rejoice in their efforts and involvement.
Tone down the decorations, as too much unfamiliar ‘razzle-dazzle’ can cause distress. Avoid lighting candles and other potential safety hazards and do not display replica fruit or berries, as this might prove confusing. Keep music and celebrations low key with plenty of chances for naps and breaks away from the party. Schedule visitors for the person’s best time of day and judge how long they should stay by how the person is coping. Try to have a few visitors on separate days instead of everyone at once if possible.
Sleep
Sleep disturbances can take their toll on both you and the person you are caring for. Often, Alzheimer’s disease can reverse a person’s former sleep patterns, causing drowsiness in the day and periods of wakefulness at night. This can progress until deep nightly sleep is replaced with less restorative round-the-clock naps.
Consider cutting down the person’s caffeine and alcohol intake, especially in the evenings. If they insist on a drink, serve them a soft drink or non-alcoholic wine or beer in their favourite glass. Sleeping pills are generally discouraged for people with Alzheimer’s disease, as they can cause confusion, which can then lead to falls. Instead, plan the day so that the person starts off at their most active, then winds down physically towards bedtime. Establish a bedtime routine and leave a night light on in their room for comfort.
Disclaimer: The avobe was not written by me but for this blog. I have full written permission from the writer to claim credit and post at my will. We will be working on other posts in the future.  When you see me end it with joe (ir) you will know that the post is a collaboration. I think I should name my ghost writterbut person requests to stay in background.

Hope you enjoy and find use in this as we continue this journey.

God Bless & Keep You & This Country of Ours!
joe (ir) 

Thursday, May 3, 2012

Welcome to Our World, Bobby Vee.

Bobby Vee was a pop singer in the 1960s, diagnosed with Alzheimer's a year ago, he is now 69. See not an old farts disease. I welcmoe him to this World of Ours so that he knows, should he ever read this blog that he is not alone he now has a family of millions and growing by the minute.  So welcome friend.
I also learned last evening, I think it was, that my Son-in-laws father has been diagnosed with Stage 1 Alzheimer's six months ago. They just found out. The man is I think 10 years my junior.
Looks like what we have said all along from the beginning of this blog, Alzheimer's is not jus an old persons disease. Which the Alz.org finally in recent weeks has said, some folks are just slower than others.
My day has just been a day, mostly sleeping this morning, finally getting on this beast and ready to go off somewhere else.
If you do not want to comment, you can just rate a post, check interesting, thank you and what ever the other one is. At least that will let me know that the posts are read. Thanks for being there for me.

God Bless & Keep You & This Country of Ours!
joe