Showing posts with label seniors. Show all posts
Showing posts with label seniors. Show all posts

Saturday, July 21, 2012

Oceanside's Cultural Art Center

Should you happen to be in Oceanside, CA on Saturday 7/28/2012 the center is having what is called "Write On", event.  Featuring the authors that live in Oceanside. More info Click Here!!!!!

Bet you cannot guess who will be there. So if you are out and about that day stop by.

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

Friday, April 13, 2012

Sadness in one's life.

This has been a hard week for me. My bird died Easter night. I was the only one that could handle her, very picky with people. Her leaving has really messed me up, i come down in the morning and go to uncover her and feed, water, bird talk all that knid of stuff and no cage. At night I want to cover her and say goodnight again no cage or bird. She had been ill and sitting with me at nights for long periods cuddeling and sleeping, i knew time was near, but never expetced feeling this lost over it. I look forher cage and it is not there. Change is not good for me anymore I have problems with it now. I find I am angrier inside now than ever, but I fight not to let it out at others, i just leave the room come st here at this beast and do nothing or go in my bedroom and just lay there for awhile. I find the tremors and my balance worsening daily my head seems to be screwe on sideways this crap has to endlife really is beginning to suck big time. well that is the hand i have drawen and have to play.

Take care of yourselves.

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

Wednesday, December 7, 2011

My Life and Times With Alzheimer's.

I havenot posted is sometime. I have not been around for sometime. My brain has been on Jupiter and I on Pluto. Last few weeks have been very trying and uncomfortable for me.  I am not used to being sick alot, but I guess I have no choice in the matter. Also  have become more i guess you would say going in different directions while triing to go forward. Things are finally catching up.  I am getting more and more losst in each day, for get talking to people that is becomin a chore. I still can come here and tell you how shitty it is getting.Iknow that we hada howuse full on Thanks Giving and I have been not with it since then at least. We are dog sitting or I guess we are seeing if we will be keeeping my one daughters dog for a whilce since the are moving. Just another thing to get under foot. So far thisis becomming a rather crappy holiday season, and it is nobodies fault. It is just my constant companion Alzheimer's moving in the heavier furniture for its final push however long that may take.

To my friends in Israel, you asked for my father and mother's names well real hard on the father, Joseph, my moms name was Muriel.  Both have been gone for sometime, my mom over38 years and my day close to23 years. I have been very touch lately by those in other countries that have written me and I am glad that they are part of this family of ours.

I want you to know that Yolanda Sanmartino who was in the HBO Documentary is still alive and with us and of course me. We are the only tow left from Memory The Loss Tapes, and at least two of those fetured in the Caregiver part have past. Friends keep me posted. Out of 10 people seen and spoken of in the documentary only two of us are left that I am aware of. This show was done in 2008 and released in 2009 mid year. So in that short period of time 3½ years, eight have passed and most all in the 8 year or less time span. I keep being told how this disease affects people dirrerntly and I am aware of that but it still claims us when it has finished us. But what sweet freedom afterwards.

Everyone says that there is nothing good about Alzheimer's or other forms of dementia, wellI am here to tell you that it has put me at peace about dieing and that is good, it also is starting to rid me of not only good memories but many of the ones that causea great deal of pain and let me tell you that is good.

Well my head is staring to wander and hurt, take care till next time.

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

Thursday, August 4, 2011

I wonder why I bother to share my Journey!


As many of you know i get rather testy at times and just fell like saying to hell with it, you do not need to know this or how I feel.  Then i get an email like the one tha follows, this is why I keep trying to give us a voice.  Parts are edited since it came to my private email so no name of way to tell who it is from. But i did write back to the person, took me a short time then longer. I asked for a pic and name and dates for my memory page, but like soooooo many of you i receive nothin back. I post the pics so people will know that these folks lived, they gave, they touch others lives and that should be celebrated. well to the email i am getting on my soap opera box. by the way this has been on my todo list for sometime, i am quick.I was asked if i filled out the facebook form, YOU BET YOUR SWEET A__, I did.
____________________________________________________________________

Hello, My name is xxxxxx, and I'm a nursing student studying in xxxxxxxxxx, xxxxxx (Canada).  I watched The Alzheimer's Project documentary, and was very touched by your story.  I know you have probably heard this from so many other people who have read your story online, or watched this same documentary, but I would like to thank you so much for contributing your own experiences and stories to helping understand and find a cure for Alzheimer's.  I was asked to write an essay for one of my courses at school on anything I wanted related to disease and disease concepts.  I chose Alzheimer's because my grandfather passed away from A.D. 10 years ago.  I never had the chance to really get to know him, since his diagnosis occurred when I was only 2 years old.  By the time I was old enough to have memories of my own, he had already progressed to the very late stages of the disease.  He only spoke Italian, which I did not, thus I had very limited communication with him.  My memories with this man consist of visiting him at the nursing home, where he stared at me with blank eyes. I fed him and walked him around, and told him stories.  When he passed away, I felt like a part of me had been ripped out of my chest, and it was difficult to accept that I had not known him better, and could do nothing about that. I appreciate hearing from someone who can recount his own experiences with this disease. I do not have personal experience with this disease, and was only an observer to something that took away someone I loved.  However, I believe that it takes great strength to explain what it feels like to go through something that takes away from the person you have grown to become.  I do not know what has happened to you or your family, or if you crosses "the line" since the documentary was filmed. I would only like to thank you, quite simply, for giving me a story that my grandfather never was able to. So thank you, truly, from the bottom of my heart.

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

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

Saturday, May 21, 2011

Alzheimer's Folk Do Not Want To Talk About It!!!!

This is actuaaly about denial this post. I read on caregiver sites, other blogs and comments on mine, "how do I get mom or dad to admit they have Alzheimer's, they are in denial".

Well my point of view, you just don't. What is the big deal if they say Yes dam it I have Alzheimer's. Does that validate YOU in some way. Frick they know something is wrong, wake up. Your job as their caregiver is TO BE THEIR FOR THEM, not to make them agree to having Alzheimer's. We know we have a problem and it will get worse.

Yes I am yelling at you. Imagine yourself being handed a DEATH SENTENCE, that is what Alzheimer's is. Would You go around skipping down the street saying oh goody I have Alzheimer's; or do you think you just might keep your mouth shut and go about your business the best you could? That is what I choose to do and many folks that I know that have the disease have choosen to do. But I tell you on this blog what is happening to me so you get some insight into our world of frustration, terror and brain fog. I do not know how everyone feels, but i do not consider myself any more important than anyone else with this disease, we walk together.

Forget whether your patient, loved one, etc. accepts or talks about having Alzheimer's. They have it, is not that enough said? Help them do not hoover and smother them, be there and not in their face. As you can tell this denial shit getss to me, because I wonder who really is in denial, the person with the disease or the person saying that one is in denial.

Enough of my ranting.

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

Sunday, April 3, 2011

Alzheimer's - The Miss Understanding of Many People

What follows is a statement made of Caring.com by a supposed, i use the term very loosely and with distain, 20yr Professional Caregiver.  Persons words just prove what I have said here, we are not understood and we need a voice, and not from the professionals.  My response to this very ill informed ass and Lynn's is there also.  Pleaase understadn that most of the people on Caring.com are really people who care and are trying to undeerstand and get good information not this type of pure crap and idiocracy.
"it's an illness, it's difficult but it's not ugly, horrible, demeaning, cruel.
i know that no-one i ever look after ever could remember my name, but i remember theirs. and i walk beside them. that's what caregiving is. it's not oppositional, it's walking beside who this person actually is now. it's about forgiving them for their illness."
Frena wrote the above. Well maybe if you had the disease Lady, you might just find out how ugly, horrible, deameaning, cruel and damnable it is. See I suffer from it, so do not hand me that load of crap. And i do not need yours or anyone elses forgiveness for me having this disease. Expert you are not, you do not live in this world. I and over 5 million people at present in thsi countyr of orus do.
Joseph
/this is Joe's wife, Lynn, I am surprised that he was very calm in the response to your letter. This is a disease. It is ugly and horrible. Nobody wants to loose their minds and that is what happens with Alzheimer's. I do not know of anybody that has this disease who needs to ask for forgiveness from you or anybody else. The people who have cancer which is a disease don't ask for forgiveness why should the people who have Dementia. Maybe you need to rethink your profession.


Read more: http://www.caring.com/questions/tell-parent-she-has-alzheimers#ixzz1ITq5Jin3



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

Monday, March 21, 2011

A different world

I know or at least think that many thought testifying in court was a big deal. But I had an attorney that ledd me through it, the entire eveidence package in fron of me and a judge that was just supper and helped everytime i sat therre with a blank and confused look on my face. Trust me that is why it took two days for me. Mr. Computer Brain, buned out circuits.

In case you are wondering what the big earth movement in Oceanside was on i think Thursday, it was the shifty old whale here hitting the deck as I tripped and fell over the cat. Not so nimble anylonger. Good thing have exxtra extra padding on my butt.. However ever since then I have been really having difficulty talking and trying to make sensse of things. Lynn says my face is lost when we talk or i look at her. Really i am lost and really do not like what is going on.

Have found out in round about ways why my voice is not listened to or my book received, I am just not gentle, kind and nuturing in my telling of this fucking disease. I guess i need to be more politically correct I think is the phrase, well bite my ass, there is nothing grand and wonderful of about having this disease. I have one thing for me though, I stand at the gate to the world of mine and about every 70 or so seconds I get to greet a new friend, shake their hand and hug them and welcome them to the darkside.

Dr. Joe Sivak will be in Long Beach in April promoting his book and Lynn and i hope to be able to make it up there to see him and maybe harass him a little those physcs need it.

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

Thursday, March 3, 2011

Who Am I Now?

I no lonegr know wo Joe is. It is like i have become two different people. Actually the same but in two different worlds.  I feel like the Joe I was is sitting up in the balcony at a play. And i see the actors on the stage and they are me and those I know, but I am no longer part of their world or they mine.The world they are in, i am all screwed up in and walkand talk in circles. But the Joe in the Balcony is who he once was, this is getty scarey now. I knew things would happen but not this. I am starting to progress faster each day and it is harder to get here to write and tell you.  I have a new computer, an all in one, so only a screen sits on my desk. all is wireless, mouse, keybaord, internet and i have a remote. built in webcam and mic, touch screen, boy can i scrtew things up with this. The voice recogn. prog. andme are having a battle, it spells worse then me. Once I get it down if I do.My posts will be written by it, so you will get all he what the f***ks and things as I forget where I am and doing.

Will be making book available soon in digital format for everyone around the world to get. have to addd to my buy button.and stuff.

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

Tuesday, February 15, 2011

Posting On This Blog

Only one rule to those invited to post, must be on dementia any type and you are free to be explicit. If a caregiver your thoughts, what you have learned, what you see, etc. One always has something to say even if it is I cannnot take this crap anymore.

Please check out the In Memory Of page udates. If you want a love one added, use email form on bottom, or email me at jolynn1@cox.net  I need name, birth year, date set free and a picture.

This is our home please join in. If you would like to be able to post here using above guidlines let me know? Remember abuse the priviledge and u will be cut off and so will your post. You know language is not always a criteria here, but honesty is.

I have had the honor of speakinnng to Alan Rodgers, the nut, who is climbing the 7 highest summits on each connntinent for Alzheimer's Awareness. I call him a nut because he climbs these mountains, me I fall down them. He is going to keep us in the looop. He has reached over 20 million people already through the presss coverage and talk shows he has been on.  Alzheimer's took his mother about 1½ yrs. ago, so this is his mission and is takking us with him.  May God go with you Alan.

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

Sunday, February 13, 2011

Because of You!

Yes because of you my every growing famliy out there we have made progress>
As you may or may not know their are something close to approaching 100 million sites on the Internet world wide. When I started the story of mine and asked you to join in this blog was number 57,xxx,xxx million something in standing. Well we are making an impact somehow, because it is as of today 927,085 in standing, Good JOb you guys. Out of the 10's of million in the US, we are now listed as 190,851, I am so humbled by what you have done.

Also thanks to those who have purchased my book.  I truly hope you enjoy and pass on the info to others. Now on the other hand me being a very tiny little bit mercenary - tell your friends to buy it and have them help spread the word as well.

I am going to invite more to post here soon. My haze is starting to get heavy and is keeping me from my job to let all know, how really crappy I feel. but yesterday I was a ball of fire, was so busy donig things, were it came from is beyond me.  Today different story.

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

Friday, December 31, 2010

A Victory!


Thank You!

Dear Joe,

Soon, we expect President Obama to sign the National Alzheimer's Project Act into law. This is the largest legislative victory in many years for the Alzheimer cause, and you made it happen. We look forward to working with all of the various agencies to ensure this law is enacted in the spirit in which it was drafted.

With a new Congress convening in January, we're eager to build on the momentum from this victory and hope that you'll join us. As we prepare to launch our 2011 legislative priorities we are asking you to please consider making a donation so we can continue the fight against Alzheimer's disease. A donor has graciously stepped forward and offered to match all gifts made to the Alzheimer's Association by December 31, 2010, up to $10,000. So we need your support now to allow us to continue our efforts to advance research, as well as vital care and support programs in the upcoming year.
Please Donate!
As leaders in the fight against Alzheimer's disease, you already know the stark realities:
  • 5.3 million.  Americans who are currently living with this disease, with that number expected to skyrocket to as many as 16 million by mid-century.
  • January 1, 2011. That's when the first baby boomer hits the age of 65, entering into an age of increased risk for developing Alzheimer's.
  • 0.  The number of people today with access to a means to prevent, cure or even slow the disease.
Yet our nation has lacked a national strategy to address this crisis. Thanks to your help, that stops now.  Throughout this year you have called on Congress, written the President, and signed the Alzheimer's Breakthrough Ride Petition to ask that our nation address this crisis. You made a difference and soon our nation will make a commitment to fighting this disease.

Thank you for all that you do and Happy Holidays.

Sincerely,

Robert Egge
Vice President of Public Policy
Alzheimer's Association
 
 
The Alzheimer's Association is the leading voluntary health organization in Alzheimer care, support and research. Our mission is to eliminate Alzheimer's disease through the advancement of research; to provide and enhance care and support for all affected; and to reduce the risk of dementia through the promotion of brain health.
 
  © 2010 Alzheimer's Association. All rights reserved.
Alzheimer's Association National Office, 225 N. Michigan Ave., Fl. 17, Chicago, IL 60601
www.alz.org | 800.272.3900

As you read you will see why I received this email.  Yes a victory to a point, I am not sure what. But I want you to pay particular attention to the part I highlighted in RED. How many times have I said the same. When do you folks raise your voices, This is a Call To Arms. We the Walking Dead need your voice to be heard loud and clear and without stopping.

God Bless & Keep You & This Country of Ours!
joe
http://LivingWithAlzhiemers.wordpress.com

Tuesday, December 28, 2010

Hello to all as we near the end of this year. I am still in February I have no idea where the rest of this time has gone or what has happended. As some of you know I attend a 12 step group and have for centuries to fight my disease of alcohol and am still sober some 37 years. I was at a ongoing meeting on Christmas Eve, we have what they call marathon meetings around certain holidays to add extra support, what made this special to me and has caused me to wonder if we have the stages of AD right, yes we have it starts and you die correct, but the inbetween seeems to be not so straight forward. I know I have written on my blog the stages, others have, Alz Org has, but you folks, my experience and what happended Christmas Eve tell me in my mind at least that there is no set inbetween stages actually, that we experience similiar things to a greater or lesser degree as suffers. I man shared at the meeting that his father had passed in the last week from AD and he was happy for him and said how he felt. I fortunately had the oppportunity to talk with the gentleman after the meeting, hugged him and told him I was glad his dad had been set free. We looked at each other and I know he was confused, hell I know that feeling, so I gave him my card that has my book info on it. We talked about how his dad was diagnosed about 3 years ago with it, for most of the time he was level had some problems then came the LINE CROSSING, 4 months ago when we knew no one and went downhill and died in the 4 month period from AD. He and I feel the same if we can prevent ourselves (he does not have it yet) from getting to that line to end it before. He saw the suffering of his father and the destruction on the family and does not want to go through that or put the family through it. Unfortunately his mother is at some point in the disease, where?????? Another lady joined us and told about her parents dying from AD a number of years ago and as I listened I could hear that her parents did not follow the so called stages either. Yes they had portions of them but kind of out of order. I see that in myself and think what master mind is comming up with this stuff. Maybe we need to revist how the disease really progresses, the middle part, we know that it starts and then we die. I know for me this is long, but I was very much touched and moved by these folks, I could see their suffering, but they were able to understand to a point my side. Especially when we talked of how they could get away from it and here I was at this meeting still getting support to help me not drink and I brought along old Mr. AD, i cannot get away from it not even a second.

Well I need to shut up, take care of yourselves and if I forget, Have A Very Happy New Year one and all.

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

Monday, October 4, 2010

Locked In Time.

While this is still in my brain cell, the wife and I were talking last night, we are strange we do that. We were discusing yesterday and tomorrow.  To me there is no longer a tomorrow, it does not exsit and she asked me if I wanted it to come and I said not really or something like that. It just seems that tomorrow does not matter anylogner to me. Yesterday, well that is not 24 hours ago to me, but it seems like centuries and having no meaning. Lynn says I am in a time warp, who knows. All I know or thik I know is that time for me is right now, not 10 minutes from now or past just right now. It is a strange feeling, I guess my ½ brain cell is on overload.

I got a comment from a young lady in Romania and she was worried about her English. Well is was perfect and really young one, this is not the place to worry about it. As you read you will see what I mean. I welcome you and the other new folks I have heard from to this World of Mine. You never know waht will come out of my brain, and neither do I.

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

Thursday, September 30, 2010

TO BE CONTINUED-------------

Well I am back today. Hope you all are well.  My day is a bit foggy and slow, but that is how things go. It is cool and rainy here, rain part very unusual for us, but welcomed.

Now tehn since you have wiated with great anticipation, pounding hearts and sweaty palms here is what is going on. First can you guess why the title to this post? Bet your wrong.

Living With Alzhiemer's (A Conversation if You Will), is in the process of being published. All of you have made this possible and have contributed in one way or another to it. Hopefully it will be out before xmas 2355, you know how slow and forgetful I can get. The Book as it is called, is not a novel or such, it is our conversation we have had over the last 4 years I think. Completely unedited and to the point. Yes it is this blog in print, comments and all, except the side materials as they appear.

So to you all Thank You, for your support, caring, sharing and just being there as I make this journey.

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

Tuesday, September 28, 2010

I Can Take Directions???????

I was told do not shoot the refrigerator.  Last hunting trip it was still alive and well. I just look straight in and not at the botoom creatures. They call but I do not listen I just hear them, kind of like your kids do.

Went and saw my shrink today and we changed meds again, or actually I did.  Told him the last stuff he gave me I think it was lats month was at the hazardous waste dump. It ripped my system apart. Back on the old stuff, feeling fine, except have to get the old poop train back on track and the fund dissolver as well.

having fun refinishing a cedar chest, of course my friened Bobby had to sand the thing, otherwise it would have had mountain ranges and gorges in it. He did a beautiful job on the sanding. Yess my staining and varnishing shills are excellent except the stuff makes me loopy, just what I need.

To all of you who visit here and leave your comments, I deeply appreciate them. You who claim to have nothing to say, I say bull, HELLO works well. Nothing important to add, the fact that you stop by, say hello or whatever is important to me and the rest of this world family we have created.So do not be shy.

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

Tuesday, September 21, 2010

What is in YOUR Refrigerator?

A few years ago we had the kitcehn remodeled. New Honey Oak Cabinets, with black nobs with dark cherry wood centers, the walls in a chocolate color, and a Brazilian Cherry Hardwood Floor, Black Stove & Microwave and a Black & Stainless Steel Dishwasher.  Then there sat6 are very old but working fine White Refrigerator. So for years you know who has been bitching for one to match, yes me. Well we just purchased a new one. Reasons, much more energy efficient then are 15 year old one, quieter, it has crushed ice a must for me, but most importantly it is BLACK and matches the decor. Happy am I, yes, except for opening it.

You see the last one the bottom drawers were solid and you could not see what was in them. This one they are CLEAR and you see everything. So what you say, well let me tell you there are creatures in those bins. I open the door and they stare at me, I know they want me. I cannot look at them, sill y yess, but that is how my brain reacts to them.Lynn just says Joe, get over yourself and deal with it. Not so simple, things like this are creeping into my life now and I can only wonder what lies ahead. The part of my brain that still understands logic laughs at me, but there is that growing part that sees and witnesses strange things and seems to have more control. The stuff in thre drawers seems to have eyes and moves when I look at it, not anyone else, just me and that is what really counts is how I feel about it.Well I guess I will just have to outfit myself for hunting when I go to the refrig that way I am prepaired for any attack.

Thank you all for being here for me.

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


PS: PLEASE NOTE IN MEMORY OF PHOTOS NOW HAVE THEIR OWN PAGE!!!!!!!!

Monday, June 28, 2010

My Forum

This is my forum to tell you how I feel and for you to talk back to me. It has always been my goal to make this not just about me, but about those that travel my journey before and after me. For you that care for us to tell how you feel. For those who contribute to leave posts on their take and views. I personally feel that my time to the line is close and I am having difficulty battling that.While I fight it, I know inside and have accepted the fact the fight is lost, but I am an honory bastard and just have to fight for the sake of it, win or loose does not matter, I just will not give this disease the satisfaction it wants. It is going to have to stomp on me and its shoes are getting heavier. Sometimes my posts are less than kind, but this is not a kind disease and I am trying to make people think about us in this world as real people not someone in a looking glass. This is my only forum to do that in. I feel caged and somewhat worthless at this point and that feeling will probbably woresen as time goes on. Well so much for now.

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