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I. How We Work in Washington. Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services. APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid. We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour. APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
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V. Complaints. Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights. APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.I agree that: A.I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information"). B.APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink. C.APFM may send all communications to me electronically via e-mail or by access to an APFM web site. D.If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records. E.This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year. F.You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
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ECT is a newer treatment for Alz patients with severe agitation, aggression, and depression. It is given in an inpatient hospital setting under general anesthesia.
ECT is a treatment for severe depression when no other alternative treatment has been successful. Alzheimer is a progressive disease. I see no practical use for such treatment for Alzheimer patients. What next, lobotomies?
Having had ECT, I would advise against it. It destroys memory, and that is not what you want for your loved one. Agitation and depression can be helped with medication.
ECT for anyone with memory impairment is returned to barbaric practices.
This from Web.MD
Jan. 28, 2011 -- The recommendations of an FDA advisory panel could mean new restrictions on electroconvulsive therapy --a controversial treatment used by tens of thousands of U.S. patients with severe depression and other mental
The experts urged the FDA not to ease restrictions on electroconvulsive therapy (ECT) for many patients. The agency is reviewing the safety of the treatment and could now require companies to prove to the government that their products are safe.
Electroconvulsive therapy involves the delivery of a series of electric shocks through the scalp to the brain. As many as 100,000 patients receive ECT each year in the U.S., mostly for severe depression or other disorders that do not respond to medications.
ECT machines have escaped strict scrutiny by the FDA largely because they were already on the market when the agency tightened rules three decades ago. The treatment is widely viewed as effective for patients who have few other options. But concerns over long-term safety have prompted new attention from regulators.
ECT Side Effects
Of most concern to the FDA is the risk of cognitive side effects, like memory loss, especially after prolonged use of ECT. While most experts agree that the benefits of short-term ECT treatments outweigh the risks for severely depressed patients, few studies look at the effects past six months, experts said.
Members of the advisory panel on Friday urged the FDA not to reclassify ECT machines as generally safe for patients with several disorders, including schizophrenia and schizophrenia-like disorders, bipolar mania, and catatonia -- a mental state in which patients sometimes are in a stupor.
The panel split on whether the agency should ease restrictions on ECT for patients with severe depression. While ECT was viewed as largely effective, experts said they had little information on how to make it safer.
“I think the data is lacking on how we can better mitigate the risks,” said Jane Paulsen, PhD, a neuropsychology researcher at the University of Iowa.
If the FDA keeps its most restrictive “Class III” designation for ECT, companies would have to submit applications showing their machines are safe and effective. Those may be outdated or may not exist at all for many devices, prompting worries that some machines could be forced off the market.
ECT Side Effects continued...
Some experts worried that the need for new data could hinder access to ECT for severely ill patients who get no relief from other treatments.
“There is no alternative to ECT” for many patients with treatment-resistant depression, warned Wayne K. Goodman, MD, a professor of psychiatry at Mt. Sinai School of Medicine in New York. “I think it would be a mistake to even take the risk of leaving it as a Class III [device] and letting it be removed from market."
New Warnings
Advisory panel members also urged the agency to come up with new, plainer warnings for patients and to improve consent forms spelling out the benefits and the risks. That can be a complicated prospect, since mentally ill patients who are candidates for ECT may not be able to fully understand the risks.
Hundreds of patients have complained to the FDA that they were not informed of the potential for memory loss, cognitive impairments, and other problems before they underwent ECT.
“They did not feel that they were adequately informed,” said Malvina Eydelman, director of the FDA’s Division of Ophthalmic, Neurological, and Ear Nose and Throat Devices. “That certainly was an issue.”
There is nothing new about shock therapy, it's been around since 1937. It works by destroying neuro-circuits and neutralizes aggression. There is a trade off, that being a loss of congnitive function. It will not repair any part of the brain. Post-treatment euphoria is possible, but the Alzheimer's will continue to progress. You will have to sign off an informed consent and have no recourse if the patient is left in a vegetative state.
By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington.
Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services.
APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid.
We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour.
APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment.
You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints.
Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights.
APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.
I agree that:
A.
I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information").
B.
APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink.
C.
APFM may send all communications to me electronically via e-mail or by access to an APFM web site.
D.
If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records.
E.
This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year.
F.
You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
This from Web.MD
Jan. 28, 2011 -- The
recommendations of an FDA
advisory panel could mean
new restrictions on
electroconvulsive therapy --a controversial treatment used by tens
of thousands of U.S. patients with
severe depression and other mental
The experts urged the FDA not to ease
restrictions on electroconvulsive
therapy (ECT) for many patients. The
agency is reviewing the safety of the
treatment and could now require
companies to prove to the government
that their products are safe.
Electroconvulsive therapy involves the
delivery of a series of electric shocks
through the scalp to the brain. As many
as 100,000 patients receive ECT each
year in the U.S., mostly for severe
depression or other disorders that do
not respond to medications.
ECT machines have escaped strict
scrutiny by the FDA largely because
they were already on the market when
the agency tightened rules three
decades ago. The treatment is widely
viewed as effective for patients who
have few other options. But concerns
over long-term safety have prompted
new attention from regulators.
ECT Side Effects
Of most concern to the FDA is the risk
of cognitive side effects, like memory
loss, especially after prolonged use of
ECT. While most experts agree that the
benefits of short-term ECT treatments
outweigh the risks for severely
depressed patients, few studies look at
the effects past six months, experts
said.
Members of the advisory panel on
Friday urged the FDA not to reclassify
ECT machines as generally safe for
patients with several disorders,
including schizophrenia and
schizophrenia-like disorders, bipolar
mania, and catatonia -- a mental state
in which patients sometimes are in a
stupor.
The panel split on whether the agency
should ease restrictions on ECT for
patients with severe depression. While
ECT was viewed as largely effective,
experts said they had little information
on how to make it safer.
“I think the data is lacking on how we
can better mitigate the risks,” said Jane
Paulsen, PhD, a neuropsychology
researcher at the University of Iowa.
If the FDA keeps its most restrictive
“Class III” designation for ECT,
companies would have to submit
applications showing their machines
are safe and effective. Those may be
outdated or may not exist at all for
many devices, prompting worries that
some machines could be forced off the
market.
ECT Side Effects continued...
Some experts worried that the need for
new data could hinder access to ECT
for severely ill patients who get no
relief from other treatments.
“There is no alternative to ECT” for
many patients with treatment-resistant
depression, warned Wayne K.
Goodman, MD, a professor of
psychiatry at Mt. Sinai School of
Medicine in New York. “I think it would
be a mistake to even take the risk of
leaving it as a Class III [device] and
letting it be removed from market."
New Warnings
Advisory panel members also urged
the agency to come up with new,
plainer warnings for patients and to
improve consent forms spelling out the
benefits and the risks. That can be a
complicated prospect, since mentally
ill patients who are candidates for ECT
may not be able to fully understand the
risks.
Hundreds of patients have complained
to the FDA that they were not informed
of the potential for memory loss,
cognitive impairments, and other
problems before they underwent ECT.
“They did not feel that they were
adequately informed,” said Malvina
Eydelman, director of the FDA’s
Division of Ophthalmic, Neurological,
and Ear Nose and Throat Devices.
“That certainly was an issue.”