Showing posts with label death. Show all posts
Showing posts with label death. Show all posts

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, 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:
_______________________________________________________________

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.
______________________________________________________________________
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, March 14, 2012

In The Moment!

As many of you know i have also fought my disease of alcoholism.  The program i joined taguht me to live one day at a time. Taking things as they came and dealing with them without the use of my friend Jonhn Barleycorn. Now I have a disease, Alzheimer's and Frontal Temporal Dementia, which have robbed me of those memories that i was told to keep green, so I would remember my life with JB and the hell that i lived in. Those days and other memories good and bad are all becoming only words to me. They are starting not to carry the pain, joy, saddness, hapiness , etc of my past. Alzheimer's has now forced me to live in only the minute, not even the day, I can do something at 8am and by 8:30am it is gone, not even a memory only a few words exist about it. This is becomming more and more my life. Living only in the moment. I guess that is how we are reallly to live, but this is new and confussing to me. It is about 7pm here and I cannot tell you what I did an hour ago.This fuckin disease really robs you of things and it is taking more faster and faster. But I still have ½ brain cell that refuses to give up, so I can tell you of this journey at least for the moment.

Take care of yourselves.

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

Thursday, March 8, 2012

GOD'S SENSE OF HUMOR

I got the following from a friend you all know i enjoy all forms of humor, I live with me that explains it.

While creating women, God promised men, that good and obedient wives would be found in all corners of the World.


And the HE made the earth round.


I have added some names to my In Memory Of page. I only have the names and dates they were set free, no pictures. I will add anyone's name to this list that you send me that past from any form of dementia. Pictures are nice, but any way we can remember these folks is great.


I am still looking for myself, i just keep missing me. Yesterday for the first time that i can remember Lynn yelled at me. I have to say it schocked me and made me sad. I guess I was taking to long to answer a question and kep on taling about other things and her frustration with me jsust blosommed like a flower. Oh well now it begins.


God Bless,
joe

Wednesday, November 9, 2011

National Alzheimer's Plan Phone Call Results

'via Blog this'

Read and comment. I listened to this entire call and state how i felt. I was interviewed but not made part of the call. After all I have Alzheimer's and am not a caregiver.  Click on title to get the full report.

God Bless,
joe

Tuesday, September 20, 2011

Update on Tests - more doctor appointments.

Well after flunking my 2 hour glucose test with colors, we now have more blood tests we are waiting on, seems Alzheimer's and Frontal Temporal Dementia are not enough to have. We alll konw i cannot spell. have lost many brain cells. I am Bi Polar, I have toooooo much body, now I have Type II Diabetes, Yeah team more fricken meds. The Sleep DR. that did my sleep tests, has me scheduled for pulmenary tests thinks I might have COPD yeah, I will live to be 112 now, thanks a lot. You will love this, I have a motorized cushion to help get my well developed body off the couch into a standing position, yes modern technology to my aid. Still working on the wife to put an elevator in but boy she is stubborn.

I get brain fades now, use to call them brain farts, but then they only lasted a few seconds, these last longer thanb I can remember having them. I was fitted for a back brace to day because I have shrunk almost to grasshopper hieght, have spinal spinousious or something along those lines. The Golden Years that is what they call this, well I am on a hunt for the person that came up with that phrase, I intened to Golden Years all over that person.

At least I have all my body parts, some do not work right, but they are still there. Have all my own teeeth, ok some have crowns, but underneath the construction it is my tooth. I am lucky i still have my sense of humor good or bad (mostly bad) and still can talk with you my family. There are many with Alzheimer's and other forms of dementia that cannot or will not speak out, and that is ok. Because all of us with this disease will be set free each in our own time from this life. I for one can hardly wait.

Well you all be good, if not just do not name it after me.

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

PS Pray for all those who are out there putting their lives on the line for all of us all over this World.

Thursday, September 15, 2011

What AAAAAAAHHHH RUUUUUSSSSHHH

Yesterday when I was younger, i wnt and had a large amount of blood taken for tests. Now I am a child of the night seeking out dinner.  I had a two hour glucose toleratnce test, WOW.  I was hungry as hell then they gave me the water to drink, filled with what tasted like sugar, but I am not sure what was in it. Well now I felt fine, they drew my blood at one hour and the world was ok, at the seceond and final hour the world was a bit different. I felt like i was as drunk as a skunk I could not walk without help. Funny how the floors and walls move by themselves. I truly was wasted have not felt like that in decades, nor do I want to again. Should get results within the week. Had to wait until today to catch you all up, yesterday just was a RUSH all day, no one wanted to leave me but everyone had to go somewhere, I ate alot and slept and by late evening I was in better shape. Today is ok, i just hurt all over, feel like i was used as a punching bag, i am big enoungh and well stuffed.

I still wonder why this disease is not working the same with me as others, it seems all the physical parts are rapidly come down, but although not fully functional, my brain seems to be somewhat alive. I do have problems doing complicated things, this is one of them, but there are times that things seem crystal clear, then they go to hell in a hand basket. Really drives me nuts. But Lynn in her loving and gentle way reminded me today that I never do anything the way I am suppose to. Marriage what a wonderful thing. Try it you may like it, I tried three times, until I was taught how to behave myself.

Stay well and take care of yourselves.  Love You All!

God Bless & Keep You & This 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

Sunday, June 26, 2011

Goodbye Mr. Peter Falk!

Dear Peter,
Thank you for the years of Columbo and many other movies that you so entertained us in. You will always be remember for that wonderfully prestine kept car, your Gentlemen's Q dress and your mild manner of investigating.  Yes I was a fan.  You are now free from this bastardly disease, yes I am jealous I am still awaiting my freedom.

Only wish that you and your family would have choosen to go public loud and clear and beat the drum loudly for all of us that suffer.  You could have done so much for us. I know it is hard to let people know, but our closet needs to be smashed so that folks know there are real faces and voices behind this disease.

But rest in peace now and enjoy your freedom, walk with the Lord my friend Peter.

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

Friday, June 17, 2011

Hi All.

Well i decided to do as my Dr. requested i went and saw a neurologist today. Met one with some brains actually, she feels that the meds they have for us are really of no value, she has yet to see them help anyone. Smart lady.  She has determined after trying to kill me that I have orthostatic tremors. The meds i am on are supposed to help these, right, we have added one to the list, we will see. However she referred me to another of her spieces  that is supposed to have this as their specialty. We went over my PET scan that i had had and finally got a real discriptive  telling of my brain, it showed considerable damage, loss or destruction if you will to both side temporal lobes and the frontal, and other abnomalities. Of course she did not know the other abs is my most wonderful sense of humor, did not have the heart to tell her.  As she did those reflect tests, it sounded like she was beating on cement on my knees. did not do well on rest of the things, but that is the way it is. Her only thoughts at this time to help me to stop shake rattle and rolling, is the possibility of DEEP BRAIN STIMULATION!!!!!! Who knows what monsters that might awake. Oh well we will see what her cohort has to say.
To all you DADS (Dads Against Diapers) you have a wonderful Fathers' Day.

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

PS. for those who followed my great KOI adventure, my two prized KOI died this week. Buggers they got out of here beforre me.

Saturday, June 11, 2011

Getting SStuck In time.

I am becomming more confused eac day. I sit here to write and just draw a complete blank. I feel that thi journey is getting rather rocky and bumpy now. When i started this blog, which seems like centuries to me, i was filled with a fire and a passion that was overwhelming me. You all know how i feel that we who suffer from Alzheimer's, Lewy Bodies, Parkinsons, Frontal Temproal Dementia, Vascular, etc. do no have a voice for us, i still feel that way, i do not want some so called expert, caregiver, reasearcher, etc. speaking for me and telling how terrrible this is and the problems and heartbreat they feel caring for us. Hell that does not put a voice or a face to us, to u yes, us no. Like it or not, WE hold the key to this disease. We have the answer, not you, we live it, why are we not asked, why are we not the experts, why is it not us that talks to the media and the big stars to tell the story? You do not know this side at all.  When it started for me it was small slices of my life taken each day, those slices have grown steadily until they are now steak size. The passion is still there to tell the story, but the fire is just a glow now. I feel like i am talking to me on my left side, i am deaf in my left ear, i feel like my blog has lost it's thunder and no longer reaches out and is heard. Yes i hear from folks once and awhile but not much anymore, I cannot begin to tell you how lonely it is inside my mind what is left now. I cannot realy even talk about things much anymore. Hell the fire and fuck the world attitude  has tempered down, I am understanding how the others that were in the hbo documentaroy felt and relate lmore to the world they became to know.
My niece died thursday, she was in her forties, i feel for her husband and three sons, but more for her mother and father, see we are to die before our children not out live them.
This is becomming way to much, there are things i want to do, but i forget them or just plain have no motivation to do them. I rarely sit by my ponds any more, my interests seem to becoming less daily about anything.
Well until i remember you are out there again take care of yourselves.

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

Wednesday, June 8, 2011

Gingrich to Alzheimer’s Association Advocacy Forum attendees: "We should be able to come together to address Alzheimer’s"

May 16, 2011
Former Speaker of the House and Alzheimer’s Study Group Co-Chair Newt Gingrich addressed more than 600 advocates to begin the second day of the Alzheimer’s Association Advocacy Forum. Throughout his hour-long remarks, Gingrich encouraged advocates to speak out and share their experiences with elected officials.
"The Constitution says, 'We the people,' not 'We the legislators,'’" said Gingrich. "One of my goals here today is to assure you that you have every right and responsibility to go out and tell elected officials what is going on. You are the living embodiment of the Alzheimer’s issue."
Gingrich emphasized several themes, including the ongoing need for bipartisan support of the fight against Alzheimer’s — an issue he embraced when serving as co-chair of the non-partisan Alzheimer’s Disease Study Group (ASG) with former Nebraska Senator Bob Kerrey. 'Alzheimer’s should be a totally bipartisan issue," said Gingrich. "Alzheimer’s does not just affect Republicans or Democrats, liberals or conservatives. It affects Americans. Therefore, as Americans, we should be able to come together with no partisanship to address Alzheimer’s."
Gingrich highlighted the high financial cost of Alzheimer’s disease to Americans both now and in the future. He emphasized the need for investment in Alzheimer’s research — and the potential cost savings if methods of treatment or prevention could be realized.
"Between now and 2050, Alzheimer’s will cost the American government an estimated $20 trillion," said Gingrich. "Yet today, Alzheimer’s research is grotesquely underfunded. We need the scientific community to tell us the optimum they could invest in the next 10 to 15 years. What could they do if they had the resources they needed to save lives and save money?"
To conclude his remarks, Gingrich shared his overall optimism that the dream of a breakthrough in Alzheimer’s research and awareness is on the horizon.
"I’ve seen things change," he said. "Every generation of Americans has been allowed to dream, and every generation has seen some of their dreams come true."
Following a brief question and answer period, advocates left with much to discuss.
"Anyone who is standing up and advocating, I respect," said Suzette Armijo, an Alzheimer’s ambassador from Mesa, Ariz. "He understands the impact of this disease. He has big dreams and broad ideals when it comes to this issue. It shows us as advocates that there are people on Capitol Hill who have those feelings. It gives us hope."





 
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Saturday, May 28, 2011

Alzheimer's, The Blessings Of!!!!

I can hear you all now, joe is going on the rampage with this one. Well you are wrong. You all know the crap side and so do I, but you do not know the, morbid as it sounds, the blessings that come with this death sentence.
1. You know you are not nuts.
2. Death is no longer a fear.
3. You get to forget your resentments.
4. You no longer hate someone, because you forget them.
5. You meet new people daily.
6. You talk to stangers more frequently.
7. You do not have to be stylish in your dressing any longer.
8. You forget to tell people to fuck themselves, hence you may not swear as often.
9. If you smoke you make forget to or where you placed the things, spend all day looking for them and go to bed saying the hell with it, and never having smoked.
10. Nine could work for drinking.
11. Wake up each morning with a new woman or man in your bed, This One We All Like, even you.
12. Forget you annoying relatives and neighbors.
13. Forget to turn on the TV, but yet you watch it.
14. Have conversations with people who know what you are saying, but no one else can see them.
15. Forget you hate vegetables and even try them now.
16. Get to have some one else change your clothes, what fun that coould be.
17. Take a bath when you damned well feel like or think you may need one.
18. Won't discuss the toliet training that you forgot, you caregivers might not find that so enjoyable.
19. Your new eating habits that help you loose wieght, no 20.00 for 20lbs., you just forget what food is for.
20. One day the World and all of its' Bullshit suddenly stop for you.

See we have to look at the bright side once and awhile. So I am sick, I am allowed, brain confussion, cannot seem to find the darn thing.  Have fun, be good to yourselves.

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

Tuesday, May 10, 2011

Yesterday i had blood drawn for tests for my physical next week. Then I spent the rest of the morning with my phsycologist . It was interesting, i have seen mim for nearly 7 years or so with breaks. We were talingi about the so called new advances in Alzheimer's and the new guide lines for diag. and treating. Funny part about it is as we talked he remembered I had said most of this years agao. And it has been posted on this blog in various forms over the years. I dound that all to be interesting that these so called experts only needed to talk to me or someone like me with the disease to get these startling new ideas and would have cost nothing. But what the fuck do we know, we are sick and mindless. But it does add credability to sites like mine, that we know what they cannot figure out.
I had another doctor write me recently, and the gist of what he said as I could understand it and questioning him on what he said is that he basically in simple terms agrees about the profession, and pharma companies, they all have their heads up their collettive asses and only promote drugs for money sake, because no matter how you want to cut it, the drugs DO NOT WORK! It is still about 8 years from diag. to the end drugs or no drugs. Our paper here had an article today about a former mayor, whose wife was diag. 7 years ago and just died. I know we hear about the 15 to 20 year sufferers, but they only exist because someone was smart enough to notice it in its infancy stages. The ten or so years of true EOA which most pros call DDSS, my term for Distraticed, Depressed, Stress, Syndrome.
I have my moments, what is difficult is getting what is in my brain cell, down to my fingers and then getting them to type what it is that is their. I have to do it quickly or if I think to long ( 5-6  seconds) it is gone and never gets said.
I know from some mail i got i insulted the Alz.org, but i want you to know that was intentional. Yes they help caregivers, they have done shit for me and I have contacted them many times. Even my local San Diego Chapter, who I gave copies of my book to for their lending library. And they wanted me to help with things and with the State, YES YES YES i said. Their ultimate answer and reuests have been complete silence, and I have heard this from others, including some Drs. I know their are good people working for them and my attack if you will is not on them, but what seems to be an organizzational lax of understanding the sufferer. Oh yes they know it is not pretty, but it does not seem that they have the first idea of the real terror in our minds and the loneliness and the difficulty we have telling anyone, because we know you do not know or understand this hell, you are not in it.
Time to shut up, i am getting to angry and feel like telling most everyone out there to fuck off, but we are family and I need you and I think you need me also while I can spout off and make some sense.

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

Friday, April 29, 2011

Alzheimer's = Millions Survivors = ZERO

Yep that is the score. Now what do you want to do about it. NO CAUSE - OF COURSE NO CURE - & MEDS THAT DO NOT DO MUCH.  Yes now they say it starts, the brain shrinking, 10 years before first diagnosis. New three stages, shrinkage, mild to moderate loss and final stages. These brilliant morons, sorry that is what they are, have confirmed everything I told my physchologist over 6 years agao. What these folks call Early Onset is not, it is mid stage.

I have been fighting the fight for years now, daily. I have lost on a daily basis. What is it that people do not understand? This Disease KILLS.............  When does the truth get told over the media, we are not mentally ill people we suffer from a deadly disease, get with it people.

I have grown tired of the battle and tired of trying to help the word get spread and fighting my own decline, I no longer have the physical or mental or emotiooonal strength or will to continue to fight. So no more from me. only that which I can remmeber happening each day and coming forth and trying to tell you, no more fight no more argumment, my time to rest has come, it is time for others to pick it up. People only want to hear from those that are nicey nice, well you all know me simple and raw to the point.

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

Monday, April 4, 2011

Click Me Find Out Those of Fame That Died from Alzheimer's

To those that went before me, I am trying to give you a voice as well. The title is a link to a listing of those who of fame have died from AD.  And Still the medical profession and sorry for this Alzheimer's Association have done crap to help us. Lot of studies, lots of meds, NO CAUSE, NO CURE & MEDS THAT DO NOT REALLY WORK!!!!  Only true diagnosis, cut the brain open at death.

The closer i get to the end the angrier i get at this world of ours, 2nd most dreaded disease and who talks about it. So Called Experts, who really have no idea what we with it go through, WHY?, because they do not listen or ask they know it all.

Everything causes it and everything can cure or hault it, in the end all this fails, we just fucking die. Cancer Society song is Happy Birthday, great for the survivors which there are millions.  Alzheimer's new song, So Long It has Been Good To Know You!!! no survivors.  Yes there is anger in me today, not for myself but for those that do not speak out without concern for hurting peoples feelings and not being polically correct.
I stand at the gate to this World of Dementia and I put out my had to each that enters every 70 seconds, to welcome them, to tell them they are not alone regardless of the failures of their fellow man to really help them.

Go ahead an rip me a new one. I am ready, but when you do prove me wrong and show me that ONE SURVIVOR.

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

Thursday, February 17, 2011

Click on This Title

This post is from the Alz.org, forum.
click the title for the post.
Joe

Friday, February 4, 2011

For Those Who Can Still Walk!!!!!

Yes this disease even takes that away from you. I know I have griped abouut the brain going away, but it seems my feet and legs are developing a mind of their own now. Several times I have falleen and trip and got hurt, but never thought of how AD is affecting me in that way.  Well the other day I had some sense knoccked into me. I was putting away the garbage cans, tuff duty right? We let me tell you it can be, putting the last can away I was practicing walking backwards, front ways not that good, try something new: Well I check where I was going turneed back around, steppped out of my sliper, apparently steped on my foot, you got it I went on a trip. My rather robust bottom slammed on the walk way, my back hit the pavers and this empty head of mine proceeded to put a rather nice looking dent in the one metal storage shed we have.  I have to admit the shed looks good it now has character. Me I have character to, back hurts like hell, my head hurts, the crack in my bottom has widened and I have been advised by my keepers, that maybe I should not do that anymore. You loose one freedom after another with this crap.

Until we meet again, take care of yourselves. I hold walking classes every Tuesday at 1pm PST.

God Bless & Keep You & This Country of Ours!!!
joe (the marathon walker)

Thursday, February 3, 2011

From The Mountain Tops - WE WILL BE HEARD!!!

From: Alana Rogers <ARogers@Biosector2.com>
To: JosephPotocny@yahoo.com
Sent: Thu, February 3, 2011 7:57:16 AM
Subject: National Family Caregivers Association Joins 7 Summits Climb for Alzheimer's 

Dear Joseph,

Knowing your interest in Alzheimer’s disease and family caregivers, I wanted to share with you a recent update on The 7 Summits Climb for Alzheimer’s: Memories are Everything campaign. 

To kick off 2011 – The Year of the Family Caregiver – the Alzheimer’s Immunotherapy Program of Pfizer Inc. and Janssen Alzheimer Immunotherapy today announced the addition of the National Family Caregivers Association (NFCA), an organization that empowers family caregivers to act on behalf of themselves and their loved ones, as a supporter of The 7 Summits Climb for Alzheimer’s: Memories are Everything campaign. 

NFCA joins the campaign just as alpine mountaineer and Alzheimer’s disease advocate Alan Arnette successfully summitted Aconcagua in Argentina, his second climb of the 7 Summits.  From the top of the summit, Alan dedicated his Aconcagua climb to family caregivers of loved ones with Alzheimer’s (you can listen to his audio dispatch here:http://www.alanarnette.com/blog/2011/01/29/audio-dispatch-from-aconcagua-5/). 

As you may already know, Alan is seeking to climb the 7 Summits, the highest peak on each continent, in order to help raise awareness of the enormous financial and personal burden Alzheimer’s places on people with the disease, their family caregivers and society.  With two summits completed in just a few months, Alan is well on his way to achieving his ambitious goal. 

Alan was his mother’s caregiver during the time she lived with the disease and knows only too well that the burden of caring for these people often falls to family members and friends:
·         In the U.S., an estimated 10.9 million unpaid caregivers see to the daily needs of people struck by Alzheimer’s
·         In 2009, these caregivers provided about 12.5 billion hours of care 
·         Caring for a person with Alzheimer’s can be overwhelming, and research shows that caregivers themselves are often at an increased risk for depression and illness
·         In the U.S. the indirect and direct costs of caring for people with Alzheimer’s are estimated to be more than $ 100 billion a year

Alzheimer’s disease, the nation’s 6th most deadly disease, gradually destroys a person’s memory and ability to learn, reason, make judgments, communicate and carry out daily activities like bathing and eating.  Alan hopes to raise $1 million to go directly to the Cure Alzheimer’s Fund™, and now NFCA to advance Alzheimer’s research and provide support for family caregivers, respectively. 

You can follow Alan’s journey and encourage people to donate to his cause by visiting www.Climb4AD.com orwww.Facebook.com/Climb4AD.  Additional information is included in the press statement below.  Please let me know if you have any questions or would like to speak with Suzanne Mintz, president and CEO of NFCA, or with Alan.

Best,
Alana

Alana Rogers
Biosector 2
450 West 15th Street, 6th Floor
New YorkNY 10011

212.845.5627
212.845.5650

*****************************************************

Below please find press statements issued on February 3, 2011 by Janssen Alzheimer Immunotherapy and Pfizer Inc. of the Alzheimer's Immunotherapy Program about The 7 Summits Climb for Alzheimer’s: Memories are Everything campaign.

National Family Caregivers Association Supports Advocate in His Mission to Raise Awareness of the Burden of Alzheimer’s Disease

SOUTH SAN FRANCISCO (February 3, 2011) – Janssen Alzheimer Immunotherapy, together with its collaborator on the Alzheimer’s Immunotherapy Program, Pfizer Inc., is pleased to announce the addition of the National Family Caregivers Association (NFCA), an organization that empowers family caregivers to act on behalf of themselves and their loved ones, as a supporter of The 7 Summits Climb for Alzheimer’s: Memories are Everything campaign.  NFCA joins the campaign just as alpine mountaineer and Alzheimer’s disease advocate Alan Arnette successfully summitted Aconcagua in Argentina, his second climb of the 7 Summits.  Through this campaign, Alan is seeking to climb the 7 Summits, the highest peak on each continent, in order to help raise awareness of the enormous financial and personal burden Alzheimer’s places on people with the disease, their family caregivers and society.  In addition, he hopes to raise $1 million.  The funds he raises will go directly to the Cure Alzheimer’s Fund™, and now NFCA to advance Alzheimer’s research and support for family caregivers, respectively.  It is estimated that more than 5 million Americans have Alzheimer’s and approximately 10.9 million unpaid caregivers see to their daily needs.

“The NFCA’s participation in this campaign spotlights the vital and expanding role of the Alzheimer’s caregiver, which is why we are so glad they have joined this effort,” said Stef Heylen, MD, Chief Medical Officer and Head of Research and Development for Janssen Alzheimer Immunotherapy, on behalf of the Alzheimer’s Immunotherapy Program.  “Through their participation in the 7 Summits campaign, NFCA will be able to reach even more family caregivers, providing education, support and a public voice.”

Prior to Aconcagua, Alan summitted the first of the 7 Summits -- Mt. Vinson Massif, the highest peak in Antarctica -- in December.  Coming up in April, Alan is planning to summit Mount Everest, the highest peak in the world.  The Alzheimer's Immunotherapy Program of Janssen Alzheimer Immunotherapy and Pfizer Inc. is funding Alan’s climbs so that all money he raises from donations will go directly to the organizations he has selected.  You can track Alan’s progress or make a donation to one of his chosen charities by visiting www.Climb4AD.com or www.Facebook.com/Climb4AD.

“2011 marks the Year of the Caregiver, and as such, we are thrilled to join Alan in his efforts to raise awareness about Alzheimer’s and the burden it places on family caregivers,” said Suzanne Mintz, president and CEO of NFCA.  “We applaud Alan for his commitment, perseverance and tireless advocating for the AD community.”

Alzheimer’s disease is the sixth leading cause of death in the United States, with another person newly diagnosed every 70 seconds.  The burden of caring for these patients often falls to family members.  Last year, these family caregivers provided about 12.5 billion hours of unpaid care.

Alzheimer's Immunotherapy Program
The Alzheimer's Immunotherapy Program of Janssen Alzheimer Immunotherapy and Pfizer Inc. is an equal collaboration committed to researching and developing selective products for the treatment and/or prevention of neurodegenerative conditions, including Alzheimer’s disease.

The Alzheimer's Immunotherapy Program believes that it is possible to reduce the burden of disease through early intervention in the illness.  It is dedicated to delivering comprehensive and integrated solutions that help address the needs of people impacted by Alzheimer’s disease.

Its research focuses on the beta amyloid hypothesis.  Scientific evidence supports the idea that preventing the accumulation and/or promoting the removal of beta-amyloid may have the potential to slow the progression of Alzheimer’s disease and help preserve function in people with the disease.  This theory is being tested inclinical trials.
                                                                                                         
Janssen Alzheimer Immunotherapy
Janssen Alzheimer Immunotherapy is researching, developing and commercializing selective products for the treatment and/or prevention of Alzheimer’s disease.  Janssen Alzheimer Immunotherapy is based in Dublin and has R&D facilities in South San Francisco.

National Family Caregivers Association
National Family Caregivers Association (NFCA) envisions an America in which family caregivers lead full and productive lives, free from depression, pain, isolation, and financial distress.  NFCA provides family caregivers support, education, and a public voice.

Cure Alzheimer's Fund
The Cure Alzheimer's Fund is a non-profit public charity established to provide funding for targeted research into the causes of Alzheimer’s disease.  The Cure Alzheimer’s Fund exists exclusively to fund targeted research to hasten the slowing, stopping or reversing of Alzheimer’s disease.

MEDIA CONTACT:
Ellen Rose                                                                                                           
Office: 650-794-2546
Mobile: 650-491-4901
erose@janimm.com                      
____________________________

National Family Caregivers Association Supports Advocate in His Mission to Raise Awareness of the Burden of Alzheimer’s Disease

NEW YORK (February 3, 2011) – Pfizer Inc., together with its collaborator on the Alzheimer’s Immunotherapy Program, Janssen Alzheimer Immunotherapy, is pleased to announce the addition of the National Family Caregivers Association (NFCA), an organization that empowers family caregivers to act on behalf of themselves and their loved ones, as a supporter of The 7 Summits Climb for Alzheimer’s: Memories are Everything campaign.  NFCA joins the campaign just as alpine mountaineer and Alzheimer’s disease advocate Alan Arnette successfully summitted Aconcagua in Argentina, his second climb of the 7 Summits.  Through this campaign, Alan is seeking to climb the 7 Summits, the highest peak on each continent, in order to help raise awareness of the enormous financial and personal burden Alzheimer’s places on people with the disease, their family caregivers and society.  In addition, he hopes to raise $1 million.  The funds he raises will go directly to the Cure Alzheimer’s Fund™, and now NFCA to advance Alzheimer’s research and support for family caregivers, respectively.  It is estimated that more than 5 million Americans have Alzheimer’s and approximately 10.9 million unpaid caregivers see to their daily needs.

“As the number of people diagnosed with Alzheimer’s increases over the next few decades, so too will the burden of this devastating disease on family caregivers, which is why continued resources and support are essential,” said Gregory Rippon, MD, MS, Senior Director, Specialty Neuroscience, Clinical Development & Medical Affairs, Pfizer, on behalf of the Alzheimer’s Immunotherapy Program.  “We are excited that NFCA has joined this effort, as their participation expands the reach of the 7 Summits campaign to focus on this critical audience.” 

Prior to Aconcagua, Alan summitted the first of the 7 Summits -- Mt. Vinson Massif, the highest peak in Antarctica -- in December.  Coming up in April, Alan is planning to summit Mount Everest, the highest peak in the world.  The Alzheimer's Immunotherapy Program of Janssen Alzheimer Immunotherapy and Pfizer Inc. is funding Alan’s climbs so that all money he raises from donations will go directly to the organizations he has selected.  You can track Alan’s progress or make a donation to one of his chosen charities by visiting www.Climb4AD.com or www.Facebook.com/Climb4AD.

“2011 marks the Year of the Caregiver, and as such, we are thrilled to join Alan in his efforts to raise awareness about Alzheimer’s and the burden it places on family caregivers,” said Suzanne Mintz, president and CEO of NFCA.  “We applaud Alan for his commitment, perseverance and tireless advocating for the AD community.”

Alzheimer’s disease is the sixth leading cause of death in the United States, with another person newly diagnosed every 70 seconds.  The burden of caring for these patients often falls to family members.  Last year, these family caregivers provided about 12.5 billion hours of unpaid care.

Alzheimer's Immunotherapy Program
The Alzheimer's Immunotherapy Program of Janssen Alzheimer Immunotherapy and Pfizer Inc. is an equal collaboration committed to researching and developing selective products for the treatment and/or prevention of neurodegenerative conditions, including Alzheimer’s disease.

The Alzheimer's Immunotherapy Program believes that it is possible to reduce the burden of disease through early intervention in the illness.  It is dedicated to delivering comprehensive and integrated solutions that help address the needs of people impacted by Alzheimer’s disease.

Its research focuses on the beta amyloid hypothesis.  Scientific evidence supports the idea that preventing the accumulation and/or promoting the removal of beta-amyloid may have the potential to slow the progression of Alzheimer’s disease and help preserve function in people with the disease.  This theory is being tested in clinical trials.

Pfizer Inc.: Working together for a healthier world™
At Pfizer, we apply science and our global resources to improve health and well-being at every stage of life.  We strive to set the standard for quality, safety and value in the discovery, development and manufacturing of medicines for people and animals.  Our diversified global health care portfolio includes human and animal biologic and small molecule medicines and vaccines, as well as nutritional products and many of the world’s best-known consumer products.  Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time.  Consistent with our responsibility as the world’s leading biopharmaceutical company, we also collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 150 years, Pfizer has worked to make a difference for all who rely on us.  To learn more about our commitments, please visit us at www.pfizer.com.

National Family Caregivers Association
National Family Caregivers Association (NFCA) envisions an America in which family caregivers lead full and productive lives, free from depression, pain, isolation, and financial distress.  NFCA provides family caregivers support, education, and a public voice.

Cure Alzheimer's Fund
The Cure Alzheimer's Fund is a non-profit public charity established to provide funding for targeted research into the causes of Alzheimer’s disease.  The Cure Alzheimer’s Fund exists exclusively to fund targeted research to hasten the slowing, stopping or reversing of Alzheimer’s disease.

MEDIA CONTACT:
Victoria Davis
Global Media Relations         
Office: 212-733-3227
Mobile: 347-558-3455

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Tuesday, February 1, 2011

My 300th Post - Mercenary This Time

As you may or may not be aware I have self published my blog through Xlibris Publishing and it was released in 10/2011. On the right hand side of my blog, yes I am promoting, hell I have to pay for this some how, you will find a new spot to buy my book, directly from me and I will even sign it for you. I got a limited supply from Xlibris at special pricing. The price includes any taxes and shipping costs for the price. If need be I will send Uncle Louie after you.
Some Humor Today:


EXERCISE  FOR PEOPLE  OVER 50
Begin by standing on a comfortable surface, where you have plenty of room at each side.
With a 5-lb potato bag in each hand, extend your arms straight out from your sides and hold them there as long as you can. Try to reach a full minute, and then relax.
Each day you'll find that you can hold this position for just a bit longer. After a couple of weeks, move up to 10-lb potato bags.
Then try 50-lb potato bags and then eventually try to get to where you can lift a 100-lb potato bag in each hand and hold your arms straight for more than a full minute. 
(I'm  at this level.)
 
 After you feel confident at that level,  put a potato in each bag. 

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