Showing posts with label sleep apnea. Show all posts
Showing posts with label sleep apnea. Show all posts

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

Wednesday, August 8, 2012

Thanks to You & Health Line.

Because of your support, comments, ideas and postings and sometimes out right YELLING at me, and we know how calm a peaceful I am, not:: Health LIne has chosen this blog as one of it's top 25 for 2012, the bage is on the side. I read you else was chosen and what tickles me is that I know most of the folks and follow their blogs, and I say to them good going. Belosw is what Health Line wrote on their site:
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Living With Alzheimer’s

Meet Joe. As funny and frank as it gets, his Living With Alzheimer’s blog is making waves. Both inspirational and incisive, his wit and laid-back approach to life somehow make it easier to grapple with the challenges brought by dementia.
Joe is no stranger to the effects of Alzheimer’s, but he faces the difficulties of the disease and makes the battle less painful – and certainly less isolating – by adding humor and casual grace into the mix. Stop by to give Joe some virtual applause for leading the way to a future of dignity, perseverance, and hope for everyone with dementia.
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I like the casual grace part.  Thank you all, my ego is out of control right now, but what the hell I feel good this day.

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

Wednesday, June 6, 2012

5 Awesome Smartphone Apps That Every Caregiver Needs


as always we do not promote or recommend any products, you are the ultimate decision maker in you purchases. we try to bring things to aide and possibly be of use to you.

Sure, your smart phone might be a great way to fling disgruntled birds at thieving swine, but it can also be just as useful in helping you care for an elderly parent or a special needs child. Right now, more than three in ten households report that at least one person has served as an unpaid caregiver. Taking this into account, developers have begun to release a wide variety of apps that can make providing care much easier. From scheduling medications to tracking lost loved ones, there’s almost no limit to what these programs can do. So if you have a dependent at home, you should definitely consider downloading these 5 apps.
1)    Med Helper - $3.99. Med Helper provides caregivers with the most comprehensive medication scheduling suite on the market. Available for the Android and iPhone, the app tracks medication, treatment and appointment schedules for your loved one. In addition to alerting you when it’s time to give a patient their pills, Med Helper Pro also tracks your prescription inventory and lets you know when it’s time to get a refill. It even creates a log of past doses that you can export and show to your healthcare professionals. If providing medication is part of your daily routine, this is one app that you need to get.
2)    ICE - $3.99. ICE, by development firm Appventive, is a high-tech “In Case of Emergency” app. It functions just like the diabetic bracelets that people use to inform medical workers about their condition, but the app can convey very detailed information. With just one click, EMT staff or other medical professionals will know the person's conditions, emergency contact numbers and insurance information. You can include phone numbers for doctors, information about allergic reactions and special instructions. Though the app is currently exclusive to the Android operating system, look for it to expand to the iPhone soon.
3)    Pain Care – Free. When you're sitting in the doctor's office, it can be difficult to remember every single thing you wanted to say about how you've been since your last visit. Pain Care, the winner of the “Project HealthDesign,” says it for you. The app, which is available for free on Android, Blackberry and iPhone, is a kind of pain management journal. A pain slider allows patients to rate their level of pain as well as its duration, location, triggers and more. In-depth information like this gives your doctor a clear picture of your condition over time.
4)    GPS Tracking Pro – Free. Caring for a family member who is suffering from Alzheimer’s or dementia can be difficult, especially when they start losing track of their surroundings. A simple walk alone can quickly turn into an emergency if your parent or grandparent forgets how to get back home. The GPS Tracking Pro app will allow your family member to retain their independence by keeping tabs on their location 24 hours a day. Just load the free app onto their Android or iPhone, and you'll be able to track their location from your phone or computer.
5)    Brainwave Tuner - $2.99. Brainwave Tuner can be a useful app for those who suffer from fits, migraines, insomnia and other stressful conditions. Binaural acoustic therapy aims to help people achieve a more relaxed state of mind by coaxing brainwaves to entrain with a gently pulsing audio source. Brainwave Tuner projects special ambient sounds through headphones to help relieve pain and induce sleep. The app is currently available for iPhone and Android phones.
Being a caregiver isn't easy, but these apps can make looking after a loved one with special needs much less trying than it used to be. Apps like these turn your smartphone into an emergency device, a medication scheduler or an acoustic therapy device at the touch of a button, and as technology continues to advance, these apps will only become more helpful. So check out your operating system’s app store today and download a few that you think might be useful in providing care for your family or loved ones. For such a small price, they can be a big help. 

hope you enjoy this and find some useful inforation. You can tell i did not write this, you can read it.

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

Monday, May 21, 2012

As The Door Closes.

sounds like a soap opera, but that is what is happening to my life. My eldest and her group were here the other day and when I said goodbye to my granddaughert who is 9, she aaid grandpa why don't you call me that name anymore when we leave and i did not know what she was talking ablut and asked her, she said oh it is ok grandpa, you just don't remember things anymore. That kind of hit home as to she understands and can see the changes taking palace. My daughter and I think it was the same day told me she missed me and i was really lost on that one. I just looked at her and she told me she misses how we would jokw around and that i do not do that much anymore but she understood that things were getting harder for me. It almost felt like she said goodbye while she still could. Right now i feel like shit and am not in a good place, which seems to becoming normal. Oh well It is What it Is.

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) 

Saturday, November 12, 2011

Have not written you all in awhile!

Yes i am still here, unfortunately. We now use pad on the bed, you know that song Old Man River he just keeps rolling on, well he does we and where he decideds to.Most of my momments are fuzzy now and fewer and fewer clear days. One of our family (this means all of you) recently lost there love one to Alzheimer's. I am still waiting for a picture name and birth date and date set free to post on memory page.  I guess it maybe to hard, believe she has been diagnosed with Alzheimer's or som form of dementia just recently what a bitch life can be. Well i guess it is what it is. Have read some new studies that contradict the last 100+ years of the possible cause of Alzheimers. I need to post them for you all. They kind of boost my ego what is ledft of it showing what my doctor and i felt was right that they had the wrong path basically. Problem is I sit down to do thes things and forget why I am at my computer.My days consist of very little since i do not leave the house oftern and I sit down and the next thing you know i am waking pup hours later, i cn not control it I fall asleep while talkin even. Ihave held my own for sometime nowbut the disease is doing its job and catchin me pretty fast now.

I am no longer sending emails to people who could help raise our voice and face to the public, they just do not care my feelings, i get back auto reply emails, wel when it strikes home I guess they will be some of the loudesss to yell, and never look back at the chance they had to hep raise our voices.i will be taking my book off of my site for free shortly nobody really seems to want it either, so sounds like i am on a pitty pot, i guess i am, i have fought and fought and yelled been nice even9that took courage) and still nothing so you will only hear fom now on as i cn remember to let ou know how life is.

Thank all of you for being there for me.
God Bless & Keeep You & Tis Country of Ours!
joe

Thursday, September 1, 2011

Yes It Is ALZHEIMER'S AWARENESS MONTH!

That means that i expect all of you to make people aware of us.  If need be take an Alzheimer's suffer out and about so people can see our faces and that we are REAL people. As much as you mya thnik many people still do not know about us, the disease yes, the faces no hide them away.

I have a challenge for all of you. GET MY BOOK FREE, just pay shipping and hanlding hell it is even signed, except the digital copy. After the cost of mailing the rest goes to Alzheimer's Disease Reseaarch Foundation. I get nothing, even on the sales my royalties go to them. You reall want to help well here is an eay way. You can even give the book to friends to view and follow. Only have about 5 hard backs, about 75 siftcovers, but can sen ou a hell of alot of digital copies. Yes I am assking for you to put you money to wor.  This book cost me thousands of dollars to get published, i never expected to get rich or my money back, let alone sell more than 2 or 3 books. Well giving them away and my royallties will never pay for the printing, have sold more than 3 though. Those in other countries i still charge what is on the list, although it cost not only the shipping you pay, but double thatn. So you money does not get donated since i go in th whole on it. But the message gets out and that is what my blog and book are all about.

Remember us this month, it is Our Time To Be Known!!!!

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

Friday, August 26, 2011

Alzheimer's, Sleep Apnea, Early Onset Alzheimer's and Medications!

Yes I have Alzheimer's and Sleep Apnea seems to go with it. I was first diagnosed back in the mid 1990s, remember the old times. Had my test again, well now what took place, well went for my findingss or whatever want to call them, appiontment was for 10:30AM as usual had the normal 15 min. delay, that turned to 30 mins. at whch time the wifey got involved as to what was going on, well 45 min after my appt. time taken back had blood pressure, which was rissing, taken and my wieght. Seated right in front of the Dr. office and told it would be about 2 mins. and I was next. Well, he comes out and takes in three people who needed an interpeter ahead on me.  Now you all know the high esteeenm i hold the medical field in, so you can guess what took place, the Dr. was told directly what I thought and so was his entire staff and all the patients heard, you know i hold nothing back. Well with contrite voice and approach the ass called me later in the day and was so apppologitic that I wanted to vomit. I still gave him no respect or quarter. Apparently my SA is not very bad, so time will tell on the front.

Early Onset Alzheimer's diagnosis is a MYTH it does not exist people. Only if they tell you 10 or so years before. One of our family members (part of this family on the blog), husband was diagnosed with EOA from reading her blog and things it seems to me to be about a year ago.  He is now in mid stage, gee from EOA to mid stage in 1 to 2 years no way. We are generally diagnosed in mid stage, because the HealthCare providers do not want to TAG us as one of THOSE people. But if you have cancer, aids, heart disease, herpes, well yeah we can tell you normal folks get those diseases.What I am trying to say in the stage play here, is we are still not to be talked about and I see and hear it all the time.  Everything is to help the caregiver, Time To Listen To Us, we hold the key let us give it to you. Are we not people, do we not cry, do we not feel pain, do we not feel the frustrations of loosing our memories and control over our bodies? Bet your sweet ass we do and are.

I take 80mg of Fluoxetine (prozac) a day to handle my mood shifts and anger, also take 20mg of Crestor to manage my cholesterol ( diet and exercise has never worked, liver is to efficient at producing this little bugger), 300mg of Gambapentin (Neroutin) to manage moods, seizures and the neropathy that I have so I can walk and feel in my hands, take .5mg of Cholozapam (Kolonipin) twice daily to help with my St. Vidas Dance, the tremors and shakes probably will be increased because it helps with sleep temmors and REM Behavoral Disorder.

None of the so called slow the process drugs, sorry tried no help and most people I know have gotten no real benefit from them. Have hadt tow reallly top neurologists say no to them because they have not seen them help anyone in their practices. You know the drugs, Aricept, Namenda, Exerol and the rest. I have written I believe in past posts about these drugs.

Well this is a lot for me, I feel like I am preaching, probably I am and it is to the choir, no one that counts is listening, you all know this is not directed at you.

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

Thursday, August 18, 2011

Alzheimer's and Sleep Apnea.


Yes aliens came and got me and did wierd things to me. I loved it. Wired for the night and sleep test should get results on next earth visit. My doctor says that in his practice in sleep studies that he has found that sleep apnea is a precursor to different forms of Dementia, including Alzheimer's. This i find interesting and have looked into this and their seems to be some validaty to this thought process.

To all that have bought my book thank you, I am sure the Alzheimer's Disease Research Foundation appreciates you also. All funds I receive from my book are donated to them. I will be posting the new amount shortly. I cannot thank you all enough for helping to find the cause.

I was on the Natioanal NAPA Alzheimers Comference call on the 5th i think it was. Have to say i was less than impressed.  Most callers  (practically all) just wiened about there not being financial help for them to take care of THESE PEOPLE almost all used that terem. I think i said it before if not i will say it now, we who suffer this disease are just to be put off to the side.  I am one of THESE people and deserve more thought than we are given.  Only two ladies had any brains on that call, as far as i am concerned.  They both spoke about their mothers getting Alzheimer's in their late 40's and early 50's and dieing within 5 years. They feel and I agree whole heartedly with them that the studies should not be for onlyl those 65 and older,  THEY (yes thos who know it all) have to realize that this disease starts much sooner than 65, I knew at 50 something was wrong but it took years to get any health provider to really listen. I was asked what I wanted to say off the air, you know the screening process, and I told them we need a voice and as i continued, you guess click and back to toe conference, that just depens my distaste for ALZ.org, and many of you know I do not hold them dearly at all.

Will let you all know the outcome of my alien abduction and expierements after they return on Monday to talk to me again.

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