Additionally, based on the insights and advice she gave
us regarding the final stages of the disease, I will be contacting Hospice Care
next week to see if they can evaluate mom’s situation. As you know from reading
this blog for just the short window in which I’ve been writing it, Mom’s
situation has been changing dramatically and all the facets which are
identified as part of the final stage are notably present and escalating in
mom’s case. I know that’s now what we want to hear, but it is what I’ve been
seeing. It’s also what the caregivers who help us have been seeing, based on my
questions to them about her situation, as referenced below in the letter.
Here is the letter:
“I don’t have any literature to send with the prevention
issues I talked about. I do want to clarify though, these are only ways that we
can REDUCE risk factors for, and hopefully delay onset and/or slow progression
of Alzheimer’s disease. The hope/thought is that if we can keep the “disease
pathways” healthier, we can slow the progression or onset of disease. We cannot
change our genetic risk factors, but we CAN do something about managing
vascular risk factors i.e.
Avoid developing Type II diabetes: through lifestyle management like daily
exercise and a low fat/low sugar diet, avoiding high glycemic index foods –
things that the body breaks down quickly into simple sugars, like a popsicle vs
low glycemic index foods, like an apple, that take the body longer to break
down therefore avoiding big peaks of both blood sugar from eating the food and
the insulin that is produced in response to those big spikes of blood sugar.
Our data shows that just 30 minutes of aerobic exercise will reverse, at the
cellular level, insulin resistance ( pre-diabetes) for 24 hrs!..exercise is
very, very powerful medicine!
Manage high blood pressure: again, through lifestyle management of diet
and exercise. Watch foods with hidden sodium (canned soups, sauces etc). If you
have been prescribed blood pressure meds, take them.
Manage high cholesterol: again, through lifestyle management of diet
and exercise. Have yearly fasting cholesterol labs taken. If you’ve been
prescribed a cholesterol lowering medication, take it. I use Red Yeast rice
tabs from Costco. My cholesterol is borderline high, but has stayed steady for
the 5 years I’ve been taking Red Yeast rice. I also have very high HDL’s, which
are especially protective for women.
Manage and REDUCE stress levels: Chronic, high levels of stress are really bad
for brain health. When your body is in a constant state of stress, you are
releasing the “fight or flight” hormone, cortisol. We know that constant high
levels of cortisol in the body cause an inflammatory response (because you are
NOT supposed to have any hormones as a constant in your body, they work on
peaks/valleys) that not only affects your body but your brain. We know that
these inflammatory responses in the body (including your body’s response to
high blood pressure, high cholesterol, type II diabetes) are damaging to both
body AND brain.
To answer your question about mom’s increasing sleep
time, could be winter time affects but also could be her body slowing down as
her disease progresses. Your caregiver is probably picking up on some more
clues with your mom’s behavior than just the increased sleeping and decreased
alertness. The fact that she is spending most of her time sleeping may very
well mean she is moving toward the end of her life. However, with this damned
disease, sometimes it’s just hard to tell. When she starts to have significant
decrease in wanting to eat or drink, along with the increased sleeping, you are
probably nearing the end of her life.
It would not be unreasonable to get hospices services in
now, to offer emotional/ physical/ spiritual support for your mom AND the
family/caregivers. If her PCP believes she meets hospice criteria i.e.
increased sleeping, decreased verbal interaction, bladder/bowel incontinence, (
and some others that I can’t remember right now) I would highly recommend it.
FYI, she may well rally with some hospice team care, then no longer meet
hospice criteria and then get pulled off of hospice!...Alzheimer’s patients
often “graduate” from hospice care, then when they start to decline again (
which they always do), then they can go back on hospice. Hospice benefits do
NOT end after 6 months of care. Folks just get re-certified as meeting hospice
criteria (via the PCP/hospice team agreeing that they meet criteria again) and
go back on. It is an old wives tale that you only get 6 months of hospice care,
simply not true. That being said, her PCP and Providence Hospice, may NOT agree
that she meets hospice criteria at this time. Hospice is used far too late in
far too many cases! It’s a wonderful service
and highly recommend it, especially for end stage Alzheimer’s patients.”
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