Showing posts with label crossing. Show all posts
Showing posts with label crossing. Show all posts

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

# # #


Saturday, January 2, 2010

Better Late Than Never.

I know I am a day late and a dollar short but; HAPPY NEW YEARS TO YOU ALL. I want to thank all of you that have followed my blog, sent me coments, emails, good and thos not so. Even the ones I had to have interpreted for me or replying with , WHAT? See you need to keep it simple and clear for me, my one time brain cell hsa shrunk to about ¼ of its size this past year.

My family and I hope and wish all the best for you and yours in the coming New Year and years to come.

For me 2006 was not as good as 2005, 2007 got a little worse, 2008 things got on the move, and last year 2009 this disease reallly started to make itself known. So things being what they are I would imagine 2010 is going to be interesting as I trudge this happy road of Alhzeimer's and FTD.

For now take care catch you on the other side.

God Bless You & This Country of Ours!
Joe

Sunday, November 8, 2009

A Request

Many of you may not know, because the media does not care this is NATIONAL ALZHEIMER'S AWARENESS MONTH. Let your local papers know, let us see if they have the balls to say anything.

Again I ask for pictures, birth year and year of passing of loved ones that died from this damnable disease. Two of you have heard. They need to be remembered for they are the faces of Alzheimer's.

(Yes I used spell checker, so I cheated)!

If you like this blog I ask you to click on the Wellsphere voting Icon on the right and vote for it. I know that many on Wellsphere do not necessarily like it, I am not a caregiver or dr. I just suffer from the disease and try to tell how my life is deteriorating and getting worse as we move to my physical death. Yes the 7th leading cause of death. Probably if death certificates showed the real agent that caused death I am sure that it would be higher. Most to feared diagnosis so it is said, is you have Cancer and You Have Alzheimer's. Help me spread the word Please.

Till next time thanks for your thoughts and help.

God Bless You & This Country of Ours!
Joe

Tuesday, December 30, 2008

This Pretty Well Sums It Up!

The folowing is form some friends of mine, slightly more mature than I and walk in my World. Though I forget many of a friend until I get an email, it still amazesss me that you can grow to love and care about those you have never seen or shared a spoekn word with.

HOW TRUE IT IS

Another year has passed
And we're all a little older.
Last summer felt hotter
And winter seems much colder.

I rack my brain for happy thoughts,
To put down on my pad,
But lots of things, That come to mind
Just make me kind of sad.

There was a time not long ago
When life was quite a blast.
Now I fully understand
About 'Living in the Past'..

We used to go to friends homes,
Baseball games and lunches.
Now we go to therapy, to hospitals,
And after-funeral brunches.

We used to have hangovers,
From parties that were gay.
Now we suffer body aches
And sleep the night away.

We used to go out dining,
And couldn't get our fill.
Now we ask for doggie bags,
Come home and take a pill.

We used to travel often
To places near and far.
Now we get backaches
From riding in the car.

We used to go out shopping
For new clothing at the Mall
But, now we never bother...
All the sizes are too small.

That, my friend is how life is,
And now my tale is told.
So, enjoy each day and live it up...
Before you're too darn old!!

HAPPY NEW YEAR
& thanks for making my days enjoyable by your Blog and e-mails funny or sad .

Wally & Delores

God Bless You & This Country of Ours!
joe

Monday, November 3, 2008

Dropped Call * Dead Zone

This is how I feel in the World of mine, like a droppped call or just the buzzing on the line. The thoughts are there but the connection to the jaw finds a dead zone. No messeages come or go out. It gets frustrating as you talk and sudddenly the line goes dead and your jaw stops and you look at the person and you choke up trying to get the words out and suddenly even the thought is gone. Emptiness in the brain cell. It happens when trying to write on this blog, I sit and have things to say and then the brain, fingers and keys on the keyboard become strangers. I go nowhere without someone with me, not good idea. Now the family worries because of the heart problems, I just look at it as one moore thing to add to the list, someday I will get through the list and have to start over, why, because i won't remember the beginning of it, so I will not know if I got to the end. This all makes perfect sense to me. But then so does waxy ear build up, whatever the hell that means. I know I do like hearing from folks who stop by and take the time to read my babble, strange humor and other things.

If you want to know about me truly, read my post, A Warriors Lament, it tells about me from beginning to where I am at now.You may not understand it, but I do and that is what matters to me. Well for now have fun and be kind to yourself.

God Bless You & This Country of Ours!
Joe

PS: VOTE TOMORROW - I HAVE ALREADY.

Friday, May 9, 2008

Crossing The Line

Some of you may have read in other entries of mine of that line that those thaat live is this World of Mine cross. Itt is that point where you cease to be who and what you are and become another entity, if you do not physicallly pass on. Yes they say this is gradual and can take many years, true but sure, it can happen in a day. Here today gone tomorrow. I have over the years since joining this ever growing community of those with dementia have seen it take place just that way. One instance my wife told me of a fellow at one of the sites she works at who has been reading my blog and hopefully gainnned some insight and comfort that he was faultless. HIs mother was fine the one day and the very next (24 hours later), knew crap, nota and required suddenly 24 hour care. So many I have communicated with that suffer have had this take place with them, because I speak (this form) with their loved ones and caregiverss and they tell me of this suddeness. What say you perverers of great wisdom and knowledge, what is that "Duh". MY own life is growing shadowier, forgetting we said grace at dinner, turning on this beast, conversations in the middle of them, physically becoming a poster child for damage of the year or how to screw up your body in one simple lesson. My time is coming when ?????? but it is on its' way. I have told my family the day will come as long as I have any ability to think as who I am, that I will kiss them all and say goodbye and be gone. I believe I have the right to passon with some of me in tact and with some dignity. I refuse to have my family see me lying with my face in my food, as I have seen from working in Assisted living homes when doing computers. Looking into the trap souls of those folks through their eyes made my decision along time ago shoulod I ever be blessed with this disease. There is no cure and most likely will not be one, until they whoever they are talk to US and really learn. For their knowledge of the brain fits in the head of a pin. Bye for now until next time be good to yourselves.

God Bless You and This Country!
Joe