For Patients and
Families
• Advance Directives April 16, 2009 marks the second annual National Healthcare Decisions Day. On this day, throughout the
country, healthcare providers, professionals, chaplains, attorneys and others
will participate in a massive effort to highlight the importance of advance
healthcare decision-making. To facilitate this process, initiative organizers
will provide clear, concise, and consistent information and tools for the public
to execute written advance directives (healthcare power of attorney and/or living
will) in accordance with their applicable state laws.
• Advance Directives Online Repository in Nevada
Nevada's first online repository for advance directives will allow health care
professionals to retrieve information about their patients’ end-of-life
treatment options. The project is a joint effort of the Nevada Center for
Ethics & Health Policy at the University of Nevada, Reno, and the Nevada
Secretary of State's Office. For further information, please visit
http://www.unr.edu/ncehp/ or call the Nevada Center for Ethics & Health
Policy (775)327-2309.
• American Pain Foundation guide “Treatment Options:
A Guide for People Living With Pain” is a new resource from The American Pain
Foundation. The guide “provides credible, comprehensive information about
medications, psychosocial interventions, complementary approaches,
rehabilitation therapies, surgical interventions and much more.” For a PDF
copy and more information,
www.painfoundation.org
• American
Society on Aging is the largest organization of professionals in the
field of aging. Website resources include publications and educational
opportunities to enhance the knowledge and skills of people working with older
adults and their families.
American Society on Aging
•
Americans for Better Care of the Dying aims to improve end-of-life care
by learning which social and political changes will lead to enduring, efficient,
and effective programs. Their website highlights national news and political
decisions affecting end-of-life care.
Americans for Better Care of the Dying
• Cancer.Net
The American Society of Clinical Oncology (ASCO), launched Cancer.Net,
www.cancer.net,
a comprehensive, physician-approved patient Web site that
provides reliable, up-to-the-minute information on more than 120 types of cancer
and cancer-related syndromes. The site replaces PeopleLivingWithCancer.org and
adds new features, including toolkits to help newly diagnosed patients and
survivors navigate their care. And, regular pod casts give patients a chance to
hear from ASCO experts on a variety of cancer issues, such as genetic
counseling, tobacco use and tips on caregiving. “Good cancer care starts
with good cancer information,” says ASCO President Nancy Davidson, MD.
• CareCommunity is a web-based
community for patients, families and caregivers. This
interactive online community provides peer group and professional support and
compassion, access to resources and in-depth information about life-limiting
illness. This resource may be used
to create social support networks, find local resources, access tools to
organize care activities, and search for answers to care questions.
CareCommunity is part of Enclara Health. For more
information, please visit
www.mycarecommunity.org
• GetPalliativeCare.org is a new palliative care resource
created for consumers that also includes sections for medical practitioners and
policymakers. This new website is easy to navigate and provides clear,
comprehensive palliative care information to patients and families coping with
serious, complex illness. Key components of the site include a palliative care
Provider Directory, a definition and detailed description of what palliative
care is, a three-step process for obtaining palliative care, direct links to
palliative care-related organizations and a brief questionnaire to assist
consumers in determining if palliative care is appropriate for them or their
loved-ones. www.getpalliativecare.org
• Department of Pain Medicine and Palliative Care at
Beth Israel Medical Center offers healthcare consumers and
professionals accurate, reliable information on treatment options, as well
as links to both their integrative pain medicine website,
HealingChronicPain.org, and their Palliative Care website
HospiceNYC.org. Department of
Pain Medicine and Palliative Care at Beth Israel Medical Center
• Hospice Foundation of America offers a general picture of
what to expect before, during, and after the dying process to equip patients and
family with enough knowledge and understanding of the dying process to guide
them through the journey. Hospice
Foundation of America
• MesoLink.org is a site created to provide patients, families and ceregivers with up to date information on mesothelioma. We strive to provide a complete overview of the disease and all aspects of it. This includes general information on the disease, links to other sites and online resources that can provide important mesothelioma and cancer-related information, words of hope and support from those living with the cancer, and a free book by Lorraine Kember, who cared for her husband with mesothelioma. Mesothelioma information for caregivers at MesoLink.org.
Mesothelioma Cancer Center operates Asbestos.com which is committed to providing the latest, up-to-date information to visitors in hopes of spreading awareness about the dangers of mesothelioma. This website offers a one-stop resource on all asbestos issues ranging from occupational exposure to mesothelioma treatment options. This center offers comprehensive and cutting edge information for people who have received a mesothelioma diagnosis.
National Hospice
and Palliative Care Organization is the largest nonprofit membership
organization representing hospice and palliative care programs and professionals
in the United States. The organization is committed to improving end -of -life
care and expanding access to hospice care with the goal of profoundly enhancing
quality of life for people dying in America and their loved ones.
www.nhpco.org
• PBS Documentary Caring
for Your Parents is Online for Viewing
Produced, written, and directed by award-winning filmmaker Michael Kirk, Caring
for Your Parents is a moving two-hour special that draws much-needed attention
to this universal reality. The program aired on April 2 and is now available for
online viewing and also will be available on DVD for $19.95. The first
90-minutes of the documentary underscores today's struggle to keep parents at
home, tensions between siblings, and the complexity of shifting caregiver roles
through an intimate look at five American families. In the end, the documentary
contends that successful caregiving requires one primary ingredient ‒ love.
Immediately following the broadcast. Dr. Art Ulene leads "A Conversation About
Caring." This half-hour panel discussion offers concrete advice and guidance on
how to start the conversation, often the most difficult step in caregiving.
http://www.pbs.org/wgbh/caringforyourparents/watchonline/index.html
• Palliative Dementia Care Resources
Palliative Dementia Care Resources (PDCR) was established in 2006 to provide resources and information to help people make decisions about end-of-life care and services for individuals with dementia. PDCR is committed to advancing quality end-of-life care for individuals with advancing dementia and serving as a resource for family and professional caregivers. Created by Polisher Research Institute and funded by the Farber Family Foundation, PDCR guides professional and family caregivers to news, educational materials, and organizations related to palliative care for individuals living with advanced dementia. In addition, PDCR provides a forum in which family and professional caregivers exchange views, identify needs and possible solutions.
• Reclaiming the End of Life is a nonprofit,
nonpartisan New Hampshire-based projected designed to make bold changes in
caring for frail elderly, serious ill persons of all ages, and family
caregivers. Formed to use the New Hampshire presidential primaries and the
national spotlight they command to engage candidates in a national conversation
about how they plan to address the unmet needs of this large and increasing
population of Americans. The Initiative's movement is based on four
phases: Collecting voices of the New Hampshire Citizens, spring/summer 2007;
Making voices heard by presidential candidates, fall 2007; Monitoring the
issues, ongoing; Sharing what is learned/spring 2008.
www.reclaimtheend.org
• The Family Caregiver Handbook, created by researchers
at the MIT Workplace Center, is a “gateway” to key elder care
organizations across Massachusetts, but much of the information is applicable to
caregivers in any state. http://web.mit.edu/workplacecenter/hndbk/toc.html
• The Friends of St. John the Caregiver is an international
Catholic organization addressing the growing needs of family caregivers by
providing spirituality, information and resources to individual caregivers
www.YourAgingParent.com; training and educational material to dioceses and
parishes
www.CatholicCaregivers.com; and a membership association offering spiritual
support for those who need care, those who give care, those who assist others
giving care.
• U.S. Living Will Registry ® This
registry allows for on-line registration of an advance directive and/or organ
donor information,
U.S. Living Will Registry ® - Living Will and Advance Directive Registry
Tools
• Internet-Based Scheduling Calendar service for friends, family, colleagues,and neighbors to assist loved ones in
need is now available through a joint effort of Project Compassion and Lotsa
Helping Hands. The free, internet-based, private calendar can be designed to coordinate specific task
needs of a patient and family, such as meal coordination and delivery;
transportation to and from medical appointments and commitments; as well as
other tasks necessary to help life run more smoothly during an illness or
crisis. Participating volunteers simply log on and sign up where they can help,
http://www.project-compassion.lotsahelpinghands.com.
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