Susan and John McFadden discussed how we are
all aging together and there are challenges as well as opportunities we are
facing as a result. At the turn of the
20th century, the average life expectancy for men and women was
47. In the 21st century, the
age average life expectancy increased to 80.
Nationally, by the year 2030, approximately 1 out of 5 people will be 65
and older. At the age of 65, 1 in 7-8
persons already have Alzheimer’s disease or some other form of dementia. By age 72, about one third of us will have
some form of measurable cognitive decline.
At age 85, up to one half of all people will have some form of
dementia. There is a critical shortage
of geriatricians and geriatrics psychiatrists in this county. There are also few potentially effective
medications on the near horizon to slow the progress or prevent dementia. Dementia is a progressive impairment
in memory, cognitive and the ability to reason.
Alzheimer’s disease is a category within the term of Neurocognitive
Disorder. Changes in the brain happen
before symptoms occur/show-up on an average of 2 years before the diagnosis of
dementia. What do you do after you have
been diagnosed with dementia? You may be
prescribed with some pills to slow the progression but you may also find
yourself excluded from your social networks.
When one is excluded there is physical and social pain. People with chronic pain are more anxious
about the commitment of social partners.
Higher levels of social support are associated with lower levels of
chronic pain. People with more physical
pain tend to be more prone to hurt feelings about social exclusion. Three
examples of how social engagement can have a measurable effect on the symptoms
of dementia include therapeutic touch reduces restlessness and agitation, group
exercise program slowed the decline in dementia and participation in a group
cognitive stimulation improved cognitive test scores. Memory Café’s are all about reducing social
pain and improving the feeling of inclusion. They are a place where persons
experiencing memory loss can share their experiences with one another. The Nun
Study of Aging and Alzheimer's Disease shows that nuns experience no form of
dementia while alive. Is it due to
intellectual stimulation, diet, exercise, live for God and not themselves,
their routine or their love and support from others? In the UK, there is a joint initiative
between members of various Rotary Clubs who have recognized the need for
increased support in the community for families affected by dementia (REPoD –
Rotary Easing the Problems of Dementia).
England
has National Heathcare that includes paid respite professional care each week
in the home and psychiatrist visits in the home. There are Memory Café’s, Singing for the
Brain, monthly tea dances and restaurant outings available with others with the
diagnosis and those caring for them versus isolation and abandonment. Social connections can slow the progression
of the disease. Each Memory Café has
their own rituals such as the greeting, singing a song at the beginning and
parting, snacks/tea, memory exercises, sticky darts, raffles that pay the cost
of refreshments, etc. Most people in England
live within an easy reach of 2-3 Memory Café’s that meet every other week for
about 2 hours. Susan and John’s goal is
to start 5 Memory Café’s in the Fox
Valley . They will be looking for volunteers and
financial support. Singing is often still pleasurable and possible deep in dementia. Many can still sing if they are accompanied
by music. In the Singing for the Brain
programs, each member is greeted in song, refreshments are served and it is a
social time. Outings can also help to delay
the progression of the disease. The goal
is to create a flourishing community in which all members, including those
experiencing progressive memory loss, along with their care partners and
friends, can enjoy rich, full and joyous lives.
More people in the U.S.
turn 85 than are born each day. We need
to educate those who regularly interact with older people in how to practice
patience and hospitality and offer inclusion hospitality to persons with memory
loss in community organizations. An
educated community is one that no longer fears or stigmatizes dementia, whose
institutions extend hospitality and inclusion to persons with dementia and has
the capacity to provide a correct and early diagnosis that permit persons to
make the nine affirmations. 1. I was diagnosed early. 2. I
was diagnosed early so I can make good decisions and provide for future
decision making. 3. I can get treatment and support best for my
dementia and my life. 4. Those around me and looking after me are well
supported. 5. I am treated with dignity and respect. 6. I
know what I can do to help myself and who else can help me. 7. I
can enjoy life. 8. I feel part of a community and I’m inspired
to give something back. 9. I am confident my end of life wishes will be
respected. I can expect a good
death.
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