Alzheimer’s Foundation of America Congratulates Senate on Passage of Healthcare Reform

New York, NY (PRWEB) December 24, 2009

The following is a statement by Eric J. Hall, president and chief executive officer of the Alzheimer’s Foundation of America (AFA), in response to the United States Senate’s passage today of The Patient Protection and Affordable Care Act:

“On behalf of the Alzheimer’s Foundation of America (AFA), and our more than 1,200 member organizations, we congratulate United States Senate Majority Leader Harry Reid (D-NV), Senate Finance Committee Chairman Max Baucus (D-MT), Senate Health, Education, Labor and Pensions Committee Chairman Tom Harkin (D-IA) and all members of the United States Senate who voted to pass The Patient Protection and Affordable Care Act.

“AFA believes The Patient Protection and Affordable Care Act includes several provisions that will be particularly helpful to individuals with Alzheimer’s disease and related dementias, and their family caregivers. We supported these provisions from the beginning of the Senate’s effort and are grateful to see them included in the final bill:”

“Independence at Home Act demonstration provides home-based coordinated care for high-cost Medicare beneficiaries with two or more chronic conditions, which studies show can reduce healthcare expenditures, improve quality of care and enhance health outcomes.

“Inclusion of ‘detection of any cognitive impairment’ in the new annual wellness exam for Medicare beneficiaries is a new and much-needed benefit for early identification of memory problems or Alzheimer’s disease and related dementias.”

“Direct care training funding over three years will help to establish new training opportunities for direct care workers that provide long-term care services and supports.”

“Geriatric workforce provisions authorize funding to geriatric education centers to support training in geriatrics, chronic care management and long-term care for faculty in health professions schools and family caregivers; develop curricula and best practices in geriatrics; expand the geriatric career awards to advanced practice nurses, clinical social workers, pharmacists and psychologists; and establish traineeships for individuals who are preparing for advanced education nursing degrees in geriatric nursing.”

“The Nursing Home Transparency Act enhances American families’ access to information about the quality of care in nearly 16,000 nursing homes that receive $ 75 billion a year in Medicare and Medicaid funds, and will improve the government’s ability to ensure quality care and better-trained staff at those facilities.”

“Background checks in long-term care facilities for employees with direct-patient access give families greater assurance that their loved ones are safe because it will require these employees to pass a background check for previous criminal activity and abuse.”

“The Elder Justice Act strengthens the network of agencies that investigate abuse and neglect in facilities and in the community, including improving the training of long-term care ombudsmen and state health inspectors, requiring reporting of neglect and abuse, and ensuring that residents are protected when nursing homes close.”

“The CLASS Act creates a disability insurance program financed through voluntary payroll deductions for adults who become unable to perform at least two activities of daily living, and provides a much-needed benefit to help obtain services and supports, while providing disabled individuals more choices and opportunities to live and participate in their communities.”

“In addition, AFA was proud to support Senator Sherrod Brown’s (D-OH) amendment that prohibits insurers from dropping coverage because an individual chooses to participate in a clinical trial and from denying coverage for routine care that they would otherwise provide just because an individual is enrolled in a clinical trial for the treatment of life-threatening diseases. AFA was one of 85 organizations and the only Alzheimer’s disease-related group that supported this amendment.”

“We congratulate the Senate for its historic vote, and we look forward to working with members of the Senate and House of Representatives as the process moves forward to final passage of health reform.”

The Alzheimer’s Foundation of America (AFA) is a national nonprofit organization headquartered in New York and made up of more than 1,200 member organizations nationwide that provide hands-on programs to meet the educational, emotional, practical and social needs of individuals with Alzheimer’s disease and related illnesses, and their families. AFA’s services include a toll-free hot line, counseling, educational materials, a free caregiver magazine and professional training. For information, call (toll-free) 866-AFA-8484 or visit http://www.alzfdn.org.

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Find More Alzheimer Disease Press Releases

Alzheimer’s Foundation of America Announces 2010 College Scholarship Winner

New York, NY (PRWEB) April 22, 2010

“That disease is only for old people. It wouldn’t affect such a young man,” Katherine Henley, 18, wrote. “But it did. And it was my dad.”

With compassion and raw emotion, Henley of Phoenix, AZ has chronicled the loss of her father to early onset Alzheimer’s disease, a rare form of the brain disorder, in an essay written for the Alzheimer’s Foundation of America’s AFA Teens for Alzheimer’s Awareness College Scholarship.

Winnick Family Foundation Lauds Breakthrough Alzheimer’s Disease Discovery


Beverly Hills, CA (PRWEB) August 10, 2010

The Winnick Foundation was part of a consortium of private philanthropies, universities and federal agencies supporting research that has led to a new discovery that may lead to earlier diagnosis, intervention and monitoring of Alzheimer’s disease. The occurrence of Alzheimer’s disease is becoming more prevalent worldwide as the baby-boom generation ages, but there is presently no conclusive, non-invasive way to diagnose it.

The research was conducted by a team of scientists at Cedars-Sinai Medical Center in collaboration with colleagues from the Weizmann Institute of Science in Israel and the University of Southern California. The team’s findings were presented on July 13 at the International Conference on Alzheimer’s Disease in Honolulu, Hawaii.

Said Gary Winnick, founder and CEO of Pacific Capital Group: “This research brought together some of the finest talents in medicine from Cedars-Sinai Medical Center, the Weizmann Institute of Science in Israel, and the University of Southern California. My family is pleased to be part of that funding group and we all hope that this breakthrough will greatly simplify and speed up early detection of this devastating disease that affects so many millions around the world.”

The scientific team discovered that the same nerve-cell damaging plaque that accumulates in the brain with Alzheimer’s also builds up in the retinas of the eyes. The team has both confirmed this phenomenon in humans and is now perfecting early detection techniques using non-invasive optical imaging procedures in tests with live laboratory mice. The breakthrough suggests the possibility of monitoring Alzheimer’s disease in humans through a similar, simple retinal imaging approach.

Added Gary Winnick: “Earlier studies have suggested that changes in the brain brought in the early stages of Alzheimer’s disease may begin years or even decades before symptoms occur. The results of this new finding suggests that doctors may finally be able to provide earlier, reliable detection and begin in earnest to develop effective remedies for this debilitating disease.”

About the Winnick Family Foundation

The Winnick Family Foundation encourages project-specific programs but also selectively supports capital campaigns and unrestricted gifts to grantee organizations. There is a preference for projects in Los Angeles and New York – or those having an international component.

Foundation naming grants include:

Alzheimer’s Foundation of America Awards Brodsky Grant to Dance Therapy Group


New York, NY (PRWEB) September 15, 2010

The Alzheimer?s Foundation of America (AFA) recently awarded a $ 25,000 grant to the Marian Chace Foundation (MCF) of the American Dance Therapy Association, Columbia, MD, to provide nonverbal communication training to improve interactions with individuals with dementia.

AFA, a national nonprofit organization, awards The Brodsky Grant annually to an AFA nonprofit member organization to create, support or expand an innovative program or service that may be replicated in other communities. The grant honors Bert Brodsky, AFA?s chairman, and his wife, Muriel, for their generosity and outstanding commitment to helping others.

MCF plans to use the funds to refine a pilot program in which dance/movement therapists and adult educators trained caregivers in nonverbal communication techniques. The approach relies on movement and nonverbal behavior to interact with individuals with dementia, who typically lose communication skills as the brain disorder progresses.

“A dance therapist observes the expressive movement of a person and builds on that expressive movement,? said Donna Newman-Bluestein, a dance movement therapist and the program?s principal investigator. She recently completed the nine-month pilot at Friends Village, a continuing care retirement in Woodstown, NJ.

The Brodsky Grant will support the development of a manual and an instructional video to train dance therapists who in turn will teach the approach to caregivers across the country.

In the pilot program, trained caregivers were better able to empower people with dementia to express their needs, and the participants with dementia were more alert, engaged and cooperative, according to Newman-Bluestein. Elements of nonverbal communication include eye contact, facial and vocal expression, and posture and body shaping.

?Most of our nonverbal communication is outside of our awareness, but it?s inside the awareness of a person with dementia. The more we are in touch with our nonverbal communication, the more we can see the effect we have on people with dementia,? said Newman-Bluestein, who has worked with people with cognitive challenges for the past 30 years.

Eric J. Hall, AFA?s president and chief executive officer, commended MCF for creatively addressing this challenge.

?This program offers a critical connecting point. In the absence of a cure for Alzheimer?s disease, it?s incumbent on all of us to look for innovative and positive ways to meet the changing needs of people with dementia,? Hall said.

The Pioneer Fund Contributes $1.5 Million Gift To The Brain Research Foundation For Atypical Dementia Research

Chicago, Illinois (PRWEB) October 7, 2010

The Brain Research Foundation (BRF) and The Pioneer Fund today announced a $ 1.5 million endowment to study atypical dementia. ?The Pioneer Fund?s generous contribution ensures substantial research will continue to advance the understanding of atypical dementia,? said BRF Executive Director Terre A. Sharma, Ph.D. ?The funding of this endowment comes at a critical time and means that the tremendous potential of early stage research will continue to be explored.?

Atypical dementias are unusual cases of dementia related to a variety of underlying pathologies, including atypical Alzheimer?s disease, frontotemporal dementia, dementia with Lewy bodies, and prion disease, among others. Because these types of cases are not as common, research has not pursued them as vigorously as typical dementia. However, much can be learned from these less common conditions that could benefit people suffering from both typical and atypical dementia.

A private family foundation, The Pioneer Fund was established by Helen M. McLoraine and her mother, Mabel Green Myers, in 1962. The Fund was created to support medical research, higher education scholarship assistance, and youth social welfare. ?We are very encouraged by the innovative work that the Brain Research Foundation supports and are confident that our grant will serve to further the understanding of atypical dementia,? stated a representative of the Pioneer Fund.

In 2006, Dr. Lawrence Pottenger, a University of Chicago orthopedic surgeon and Ms. McLoraine?s cousin, died as a result of complications due to early onset Alzheimer?s disease. His wife was instrumental in connecting the Brain Research Foundation with The Pioneer Fund to create this endowment to research atypical dementia. This work will be led by Dr. James Mastrianni, Associate Professor of Neurology at the University of Chicago, who was Dr. Pottenger?s doctor.

About the Brain Research Foundation

The Brain Research Foundation funds innovative neuroscience research that expands understanding of how the brain works, and provides educational programs for researchers, families struggling with debilitating brain disorders and the general public. The Foundation plays a critical role in the scientific process by funding seed grants that are the starting blocks to discovery, allowing scientists to prove the feasibility of their projects and produce data that will make them eligible for larger government and institutional funds.

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Sigma Kappa Foundation Partners with Celect for New Website and Donation Portal

Evanston, IL and Indianapolis, IN (PRWEB) January 18, 2011

Celect today formed a new partnership with Sigma Kappa Foundation to build a brand new enterprise website for the organization, complete with administrative communication tools and a private social network.

With the new website and communication platform, Sigma Kappa Foundation will refresh its web presence with a professionally designed, easy-to-navigate website. Celect?s backend solution will ease internal communications for Sigma Kappa Foundation while offering potential donors a simple way to submit charitable donations.

?Celect?s design experience will help us present a refreshed, visually attractive web presence through our main website,? said Lisa Fedler Swiontek, Executive Director of Sigma Kappa Foundation. ?The ability to collect donations directly through our site enables us to contribute to the causes that move us the most, like Alzheimer?s disease research and leadership development.?

The Celect platform is a website solution developed by Celect for member-driven organizations, including Greek chapters and alumni groups, which gives organizations a markedly unique ability to manage their websites without extensive technical knowledge. The new website and administrative solution combines features that build community, enhance communication and foster commerce with the ability to present a professional, cohesive brand identity across the web.

Sigma Kappa Foundation is a 501(c)(3) nonprofit organization whose mission is to lead, educate and inspire Sigma Kappa members and society through educational programming and philanthropic endeavors. Since its inception, the Sigma Kappa Foundation has granted more than $ 1 million for Alzheimer?s disease research ? now our nation?s seventh leading cause of death ? and offers educational and leadership grants and scholarships.

About Celect

Celect develops customized websites equipped with private social networks and online management tools for fraternities, sororities, councils, churches, student groups and other community-based organizations. Serving more than 2,000 organizations and nearly 1.1 million unique members, Celect strives to redefine the way organizations unite, communicate, promote and monetize. For more information, visit http://www.celect.org.

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Related Alzheimer Disease Press Releases

Father Of Three Internationally Abducted Children Illegally Taken To Japan Inspires Parents Everywhere According To The I CARE Foundation


New York, NY (PRWEB) November 09, 2011

Bruce Gherbetti, a loving father living in Vancouver with his three children when they were targets of international parental child abduction to Japan has inspired parents around the world by his unbowed acts and unconditional love and devotion to reunite with his children, who were illegally abducted from Canada and taken to Japan by the children’s mother according to individuals at the I CARE Foundation.

Similiar to the United States, international parental child abduction is a crime in Canada.

According to court papers filed with the Vancouver, British Columbia Supreme Court (FP20097642) it took Mr. Gherbetti nearly 23 months to find and then travel from Vancouver to Japan’s Fukushima Prefecture, where remarkably, he was able to locate and reunite with his three young children who previously were illegally removed from Canada in September, 2009. In the absence of his children, Mr. Gherbetti lived a life of great pain and worry: the Fukushima Prefecture is a small town located approximately 30 miles away from Fukushima Dai-ichi, Japan’s tsunami-maligned ‘Nuclear Power Plant Number One’ located in the disaster stricken towns of Okuma and Futaba. On March 11th, 2011, after an earthquake categorized as a 9.0Mw caused the creation of a deadly Tsunami, with waves reaching over 14 meters high, Japan and its citizens quickly went from a country straddled with the crisis caused by the earthquake and tsunami, to inevitably, a country that will be long-scarred due to the nuclear disasters that ensued.

Despite the hardships that Bruce Gherbetti had had to endure, which include the pain of not knowing where his children were or when he would see them again, the father of three traveled down every possible road until that road lead him to the Fukushima Prefecture, and into the loving arms of his three daughters. Unfortunately for Mr. Gherbetti, a reunification with his children was not what the children’s abducting mother had in mind, and if fact, “she wanted to erase Canada from the children’s memories.”

Mr. Gherbetti reunification with his daughter may appear to be short-lived; however, for the hundreds of thousands of parents around the world familiar with the criminal act of international parental child abduction, Bruce Gherbetti tremendous effort to let his children know he loves them and desires to be a part of their life has provided hope and inspiration for targeted parents of abduction everywhere. Mr. Gherbetti commented, “My children, Rion, Lauren and Julia are delightful, precious and very dear to me. I was a loving father who was involved in every aspect of their upbringing until they were so unjustly internationally abducted to Japan. They need to know that I am alive, that I love them, and that I want to be with them. I don’t know what they have been told. I don’t know what they believe or what they know at this point. I just want to arrive and give them the opportunity to see that I am here and to be a part of their life. In coming to Japan, I am fighting for my children’s human rights. Rion, Lauren, and Julia have a fundamental human right to see and know their father and their grandmother, their uncles and aunts, and their cousins in Canada. And it is my intent to ensure that Japan allows for this to happen.”

Mr. Gherbetti’s first reunion with his children lasted only 30 minutes and occurred when his former spouse was not home: the children were being watched by their Japanese grandmother.

Since this time, Mr. Gherbetti has stayed in Japan, where he intends to do everything legally possible to see and be a part of his daughters’ lives, while also being proactive in changing Japan’s incomprehensive laws that essentially make it near-impossible for one of the parents of divorce (typically the father) from enjoying any rights of custody or access to their children.

Mr. Gherbetti realizes that what he is fighting for is his children’s rights to know and receive the love of both of their parents. “None of this is about me, this is about my children,” he says. “I feel what she has done is essentially denied them knowing half of who they are. It is not fair ? it is simply not fair.”

Peter Thomas Senese, a child abduction prevention advocate and a father who successfully reunited with his abducted child in accordance to the Hague Courts commented, “Bruce Gherbetti has empowered and inspired so many individuals within the parental child abduction community through act. Once his plans were secure, this loving father, who lives for his children, made a careful plan – including making sure his children knew he was alive and that he loved them – and left his home of Canada, ready and willing to start a new life in a foreign country so that he could be in his children’s lives. When considering the political and legal atmosphere for Bruce in Japan, his willingness to endure whatever he must in order to be in his daughters’ lives tells a story of remarkable love. A love I hope one day soon his children will embrace.”

Bruce Gherbetti commented, “I know what it is to struggle without a father ? to make your way in this life without the competence and guidance of a father. It made me realize that if I am ever in the position where I have children, I just want to emulate what he was able to give me. He was a very good man ? a good father.”

Japan is a country that has never returned one American or Canadian child-citizen back to the child’s country of original jurisdiction and is known to be non-cooperative to alienated parents seeking to reunite with their abducted children. In fact, Japan is the only G-7 member nation that has not signed the 1980 Hague Convention on the Civil Aspects of International Child Abduction which was established to protect the rights of defenseless children who have been internationally abducted by returning them to the country of original jurisdiction. Recently, Japan has made a commitment to ratify the Hague Convention; however no time-table has been established, nor will Japan’s anticipated signature allow for past abduction cases to be retroactively aligned with the treaty’s provisions.

“I think there is a cultural issue at play here,” he says. “When the marriage fails, as far as I understand it, in Japan, traditionally access and contact with the left-behind parent is viewed as an inconvenience. It is so completely different from our Western philosophies ? that children have the right to know both their parents, a right to know their whole family.”

At the time of his children’s abduction, Mr. Gherbetti sought assistance from the Canadian government. Mr. Gherbetti commented, “The Canadian government, though well intentioned, is unwilling to press these issues with the government of Japan, preferring instead to try to improve trade volume between Canada and Japan and not jeopardize it by demanding that Japan live up to its treaty obligations under the UN Convention on the Rights of the Child which they ratified on March 22, 1994 and Canada has also ratified.”

Joel S. Walter, a father and attorney practicing international family law in New York City commented, “Mr. Gherbetti’s decision to travel to Japan, where it is my understanding, he intends to stay so that his children will know his love speaks admirably of the man Bruce obviously is. His interests are directed toward his children. He clearly wants what is best for them, and that clearly is having such a loving and devoted father in their life. And undeniably, as a parent myself, when I come to learn of the dedication of men like Bruce, it inspires me to be the best parent I can be, too.”

Eric Kalmus, Co-founder of the Japan Children’s Rights Network stated, “Mr. Gherbetti’s children are at the mercy of a court system that does not involve trained psychologists, nor consider the possibity of child abuse by a Japanese parent when rendering decisions. It is apparent that the love he shares with those girls has not, and will not be shattered by Japans lack of proper children’s rights protection. Japan must make swift change to their antiquated family law system so that loving families like the Gherbetti’s are not ripped apart by the abuse of parental abduction.”

Bruce Gherbetti stated, “Japan needs to change domestic law in order to have a joint custody system post separation and divorce. Japan must sign the 1980 Hague Convention on the Civil Aspects of International Child Abduction in its present form without amendment and comply with the spirit and intent of the convention. Japan must resolve all outstanding cases of international child abduction as they have said they will not make their accession to The Hague Convention retroactive. Lastly, Japan must ensure to enforce the new domestic law as currently police will not get involved in parental abductions claiming that they are ‘family matters’.”

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For use of any photograhps, please contact Simon Scott at:

rotty007(at)gmail(dot)com or via cell phone: +81-80-3053-1843

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FAIR Foundation CEO Asks, “Is there Greed in both National and Local HIV/AIDS Organizations?”


Palm Desert, California (Vocus/PRWEB) April 01, 2011

The FAIR Foundation?s President and CEO, Dr. Richard Darling, asks that you decide and he offers the following information:

Nationally, taxpayers have spent well over one third of a trillion dollars –yes, a trillion–on HIV/AIDS, including over $ 3,000 per HIV/AIDS patient on bio-medical research annually versus less than $ 200 for virtually every other illness.

The Department of Health and Human Services has only one HOPWA program that has spent billions on providing housing to patients. Does HOPWA stand for ?Housing Opportunities for Patients with Alzheimer?s?? No, the lucky beneficiaries of this federal program are AIDS patients.

Billions more are spent annually on HIV/AIDS by others, including the 50 states, pharmaceutical companies and non-profit organizations such as the Bill and Melinda Gates Foundation.

Darling asks, ?How successful has all this funding been?? His answer: ?Extremely successful?the plummeting HIV/AIDS death rate nationwide is exemplified by the 99 percent decrease in deaths of California?s newly infected HIV/AIDS patients from almost 10,000 in 1992 to less than 200 in 2009.?

“Our government’s top HIV researcher and the physician who oversees the annual $ 3 billion HIV/AIDS research budget, Anthony Fauci, MD, admitted years ago that their success is ‘breathtaking’ with HIV patients who ‘look and feel well, and are leading very productive, very gratifying lives.’?

Darling points to further evidence of success: HIV/AIDS activist Elton John, whose AIDS Foundation has raised many millions of dollars for his cause, stated on the American Idol TV show that HIV ?is not a life-threatening disease anymore? and rock star Bono, while asking for more money for HIV/AIDS in TV ads, states that HIV patients need to take just two pills a day to stay alive; two pills that cost only 40 cents.

Darling inquires, ?Is there greed in local HIV/AIDS organizations??

In Palm Springs, CA the Desert AIDS Project (DAP) competes with neighboring charities for every dollar available from local residents. Why, in Darling?s opinion, is that inappropriate? While charities work hard for a few thousand dollars at local events, DAP’s 2008 IRS Form 990 shows that they have already received $ 11.8 million in receipts, including $ 7.5 million in grants, contributions and program service revenue with a large staff of 100 for only 2,200 patients. The 990 also shows $ 3.6 million in salaries and benefits with a Director?s total compensation of $ 200,000. Dr. Darling suggests it is informative that DAP also has an art collection that has a book value of $ 1 million dollars.

Integrated Wealth Management (IWM) is the Title Sponsor for the Kraft Nabisco Ladies Professional Golf Association?s 1st major tournament being held this week in Rancho Mirage, CA. IWM uses local charities to sell tickets for the event?the charities compete with each other with their sale proceeds returning to the charity. DAP is presently competing with all local charities in this event even though IWM had already donated $ 150,000 to DAP in 2008, 2009 and announced recently they are increasing their gift to DAP?the new amount: $ 1 million dollars. Darling offers this question: ?Would it not have been appropriate for DAP to disclose to the competing charities that it had already received this significant funding from IWM with DAP?s subsequent withdrawal from the event so that the few thousand dollars available in ticket sales would go to other local charities that are not so blessed??

In Darling?s opinion, DAP rubs salt further into the wounds of every other neighboring charity by using their treasure chest of funds to run regular, lengthy TV ads in which their CEO, David Brinkman, states ?funding has been slashed? while urging all local citizens to support DAP, presumably with more funding. Darling adds, “Of course, no other local charities can afford such expensive television advertisements.”

Darling questions if the DAP?s Board of Directors, including representatives from Bank of America, Desert Regional Medical Center, Union Bank & the Episcopal Church know that DAP is fighting so hard for every local penny that could benefit other financially strapped charities, including youth clubs, homeless shelters, and those that help crippled and abused children, even though DAP is receiving such immense funding from federal and local governments? If so, Darling believes they should be ashamed of themselves if they allow it to continue.

Darling points out that DAP rings the register again with their annual awards banquet (in 2009 over $ 500,000 of expense with George Hamilton and Joan Collins listed as headlining stars this year). During the 2010 event, the IWM President & CEO, Jim Casey, who is also a DAP Board member, seemingly contradicted Brinkman?s assessment in the TV ads of their financial condition when Casey stated ?even in the worse economic times in history, we are set to have the most successful fundraising event in Desert AIDS Project history.? Casey then announced IWM?s $ 1,000,000 donation to DAP.

Darling suggests it may also be informative to look at other local groups that are the beneficiary of exorbitant funding for HIV/AIDS and offers the following example: ?The San Francisco AIDS Foundation?s IRS Form 990 reveals $ 19.4 million in grants, $ 7.8 million in salaries including CEO Mark Cloutier’s total compensation of $ 247,893 and many others receiving over $ 150,000.?

Darling asks, ?Has Dr. Fauci or any local HIV/AIDS organization been willing to entertain the suggestion that they are receiving a disproportionate amount of taxpayer dollars, refused it or offered to have it redirected to other illnesses? The mantra of the HIV/AIDS industry is that their disease is special because it is infectious, that you and everyone in your family, even grandparents, should fear this disease and therefore even more money should go towards battling HIV/AIDS.?

?The truth, as stated by the Centers for Disease Control and Prevention (CDC), is that the only people at risk from this PREVENTABLE disease are men having sex with men, IV drug users and heterosexuals having sex with those with HIV or those at risk of having HIV.?

Darling concludes by stating that it is time to add the HIV/AIDS industry to those in need of cutbacks by our Congresspersons during these tough budgetary times. He recommends that a significant portion of HIV’s overflowing treasure chest, which includes President Obama?s 2012 budget request of $ 28 billion for this one illness, should rightfully go towards helping patients and research for illnesses other than HIV.

Dr. Richard Darling is the Founder, President & CEO of the FAIR Foundation, a national organization with thousands of members in all fifty states. FAIR?s Missions and goals are fair and equitable bio-medical research funding for all diseases, new organ-donor policies to reverse America?s organ donor crisis, promotion of organ donation and preventive health education to reduce the need for donor organs. FAIR?s Board of Directors includes 29 transplant surgeons, medical directors and patient advocates.

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Related Alzheimer Disease Press Releases

Carol Ann Sanders Foundation – We Rose to the Occasion for Alzheimer’s!

(PRWEB) February 25, 2005

The Carol Ann Sanders is an advocate of the Alzheimer’s Association and works as an independent fundraiser to support various programs related to the disease and advance research efforts to find its cure.

Artwork featuring roses from the photography of David A. Sanders is the cornerstone of the Foundation’s fundraising efforts. To complement its signature rose collection, they are introducing a new line of photography capturing many of nature’s feathered friends including Trumpeter Swans and Canadian Geese.

In addition to the convenience of the web, the Carol Ann Sanders Foundation will also display high-quality artwork at numerous regional fine art and craft shows throughout the year. Hand in hand with raising funds, the goal of the Carol Ann Sanders Foundation is also to provide literature and present brain-teaser games to raise awareness of Alzheimer’s disease, its symptoms, and what can be done to prolong the onset.

Working closely with the Minnesota –North Dakota chapter of the Alzheimer’s Association, the Carol Ann Sanders Foundation will bloom into a positive resource in the crusade against Alzheimer’s.

http://www.carolannsandersfoundation.org

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Alzheimer?s Foundation of America Releases New DVD on Preventing Falls


New York, NY (PRWEB) July 22, 2010

The Alzheimer?s Foundation of America (AFA) recently released ?Preventing Falls: Practical Steps to Reduce Fears and Risks,? the latest DVD in AFA?s ?Your Time to Care? series of educational programs for family caregivers, in the hopes of helping caregivers reduce their own risk of falls and prevent their loved ones from falling.

Falls are a very common and life-threatening occurrence and are particularly worrisome for caregivers of individuals with Alzheimer?s disease, a brain disorder that primarily affects people older than 65. In fact, according to federal government statistics, one out of three individuals over the age of 65 will experience a fall, resulting in 20,000 deaths annually.

?What’s really important to know is that a fall is preventable,? said Laura N. Gitlin, Ph.D., one of the experts featured in the DVD and director of the Center for Applied Research on Aging and Health, Thomas Jefferson University, Philadelphia.

With this in mind, ?Preventing Falls? provides insight into why dementia intensifies the incidence of falls and offers practical strategies from experts and family caregivers on how to reduce risk factors, including communication techniques, home modifications and lifestyle changes.

Among the caregivers who share their concerns, Judy Earnest provides care for her 85-year-old mother who has Alzheimer?s disease; she is worried that her mother?s gradual loss of coordination and balance will lead to a devastating fall and that that may prompt Earnest to break her promise to keep her mom at home.

?She’s never really been steady on her feet, but more so I think is, is her not realizing she can’t do all the things she ever did,? said Earnest. ?I just don?t want her to get hurt.?

In the DVD, P. Murali Doraiswamy, M.D., co- author of ?The Alzheimer?s Action Plan,? noted that dementia very often affects coordination and balance as it progresses. ?Cognitive impairment substantially increases the risk for falls anywhere from about two to eight fold,? he said.

The DVD, which was funded in part with a grant from Novartis Pharmaceuticals, is available on AFA?s E-store at http://www.alzfdn.org or by calling 866-232-8484. Other topics in the ?Your Time to Care? DVD series include wandering and medication management.

Alzheimer?s disease results in loss of memory and other cognitive functions, and is the seventh leading cause of death in the United States. An estimated one to four caregivers care for each person with the disease.

The Alzheimer?s Foundation of America is a national nonprofit organization based in New York City that focuses on providing optimal care to individuals with Alzheimer?s disease and related illnesses, and their families, and unites 1,400 member organizations nationwide that provide hands-on programs. AFA?s services include a toll-free hot line with counseling by licensed social workers, a free caregiver magazine, and National Memory Screening Day. For information, call 866-AFA-8484 or visit http://www.alzfdn.org.