*Reema Narendran *
*06 Feb 2011*

It’s a really exhausting business taking care of someone who is ill, even if
it’s a friend or family member. But if the patient is suffering from
dementia, the difficulties are multiplied manifold.

It starts off innocuously, as a problem of memory. From forgetting small
things, it progresses to forgetting entire chunks of one’s life. Gradually,
the patient loses one faculty after another, ending up completely dependent
on the caregiver even for simple activities of daily living. A person
afflicted with dementia makes enormous, unending demands on the caregiver’s
time and energy, demands that could lead to deep depression in some cases.

A little over two months ago, the Thiruvananthapuram bureau of The New
Indian Express published a story on the plight of a mother-daughter duo
(Baby and Sangeetha). The mother was suffering from dementia and the
daughter was completely exhausted from round-the-clock care she had to
provide day after day, month after month, year after year without
respite. Despite holding a bachelor’s degree in commerce, and a postgraduate
diploma in computer applications, Sangeetha could not go to work. The
Express article brought in money, clothes and even food, but just as ways to
provide respite to Sangeetha were being worked out, her mother died. Alone
with her mother’s body, Sangeetha hanged herself, possibly because of a
deep-seated state of depression.

The physical strain of caring for someone 24 hours a day, along with the
emotional stress, makes it a very complex challenge for the caregiver.
“If there is one disease that affects the caregivers much more than the
patients themselves, it is dementia. While the personality of the patient
gets altered, the family gets socially isolated. Very few relatives drop in
and friends may keep away. The constant demand upon the time of the
caregivers coupled with this social isolation and sometimes poverty can lead
people to commit suicide,” says Sreekanth P Krishnan, secretary of the
Thiruvananthapuram unit of the Alzheimer’s and Related Disorders Society of
India (ARDSI), a secular, non-profit voluntary organisation dedicated to the
care, support and research on dementia. Sreekanth himself was a lone
caregiver for his father, also a dementia patient.

In countries like India, the greater part of caregiving is informal,
particularly by the members of the family. But with globalisation and Indian
families shrinking in size, nuclear families pose peculiar challenges. “In
times of crisis, most caregivers are alone. Even when there is no crisis,
the loneliness eats into them and even though they look all right
physically, they could be victims of depression deep down. The worst happens
when they themselves fall sick,” said Dr Rajagopal, the chairman of Pallium
India, a palliative care organisation based in Kerala. The lack of
specialist medical interventions along with the shortage of specialists such
as psychiatrists, neurosurgeons, psychiatric nurses and social workers
further add to the problem.

An ARDSI study on caregivers of dementia patients has reported high levels
of psychological morbidity, ranging between 40 and 72 per cent. Among older
people needing care, caring for a person with dementia places greater
demands on the caregiver and leads to more strain.
“We found a strong and statistically significant association between the
presence of dementia and psychological morbidity in the carer,” said Leny
Mathew Samuel, programme officer of ARDSI National Office.

On an average, 60 per cent of caregivers showed evidence of adverse mental
health and the prevalence of major depressive disorders was 2.8 to 38.7
times higher in caregivers than in non caregivers. It has been suggested
that the prolonged stress and physical demands of caregiving may increase
their risk for physical health problems.

“The social workers and volunteers in our organisation do try to visit such
families and give them some respite. But we have to admit that these visits
are often far in between. We need to devise some kind of social network to
help out these caregivers, at least so that they do get to interact with
people other than the patient,” said Vijayakumar, programme-coordinator of
Pallium India.

The economic vulnerability of the families who care for people living with
dementia in India is another overwhelming hurdle, particularly for the
families who live below the poverty line. Studies indicate that 23 per cent
of the caregivers cut back on work and nearly a quarter of all caregivers
suffer economic losses as they are unable to fulfill their work
responsibilities.

The components of the cost of care for a dementia patient include the
consultation for the initial diagnosis, medication, at times hospitalisation
and paid care, special food and even house modification.

While in some cases of mild dementia there need to be brighter lights and
non-skid bathroom floors, even moderate dementia demands better safety
arrangements, a high commode for example, and severe dementia calls for
special bed with siderails, bed pans, throw-away nappies, and so on.
Reduced family incomes and increased out-of-pocket payment for care takes a
toll, increasing the economic vulnerability and making the poor poorer.

*Global projections*
Global projections estimate that 24.3 million people have dementia today,
with 4.6 million new cases every year. This will double every 20 years to
reach 81.1 million by 2040. The rate of increase is predicted to be three or
four times higher in developing areas than in developed regions.

*Barriers to dementia care in India*
* 3.7 million people with dementia and very little specialist manpower to
manage them
* Stigma of the disease
* Lack of awareness, a feeling that nothing can be done
* Lack of policy initiatives for people with dementia
* Poor awareness even within the medical fraternity
* Lack of funds for dementia services, research and training
* Lack of training and support
* Considering memory problems as a normal part of ageing

*An expensive disease*
A landmark report on the Global Economic Impact of Dementia jointly authored
by Anders Wimo of the Karolinska Institute, Stockholm, Sweden, and Martin
Prince of the Institute of Psychiatry, King’s College London, reveals that
dementia exacts a massive toll on the global economy.

The report reveals that the worldwide costs of dementia exceeds one per cent
of global GDP at $604 billion. If dementia care were a country, it would be
the world’s 18th largest economy. If it were a company, it would be the
world’s largest by annual revenue exceeding Wal-Mart and Exxon Mobil. The
number of people with dementia will double by 2030, and more than triple by
2050. Reports from individual countries such as the UK suggest that
Alzheimer’s is one of the costliest illnesses, yet research and investment
is at a far lower level than for other major illnesses.

Alzheimer‘s Disease International (ADI), an international federation of
Alzheimer associations throughout the world, has urged the global community
to take the following immediate steps:
* Central and state governments should act to make Alzheimer‘s a top
priority and develop national plans to deal with the social and health
consequences of the disease. Several countries have moved forward to develop
national plans, including France, Australia and England. It is critical for
other governments to follow suit.
* Governments and other major research funding agencies must increase
research funding to a level more proportionate to the economic burden of the
   condition. Recently published data from the UK suggests a 15-fold hike is
needed to what is spent for research into heart disease and a 30-fold
increase is necessary to reach parity with cancer research.
* Governments must develop policies and plans for long-term care that
anticipate and address social and demographic trends and have an
explicit focus on supporting family/ caregivers and ensuring social
protection of vulnerable people with dementia.
*  The scale of what is facing us elevates this to a global challenge, which
must be addressed as a top WHO priority and on the G-20/ G-8 agenda.
Financial burden on providers

A detailed economic analysis of any disease or health situation is quite
limited in India. Even then, it has been inferred that an individual caring
for a person with dementia in an urban area needs approximately Rs
10,000-14,000 a month, and that the minimum amount needed to manage one
person with dementia would be Rs 42,585 a year.

As much as 56.5 per cent of the cost would be due to informal care
(primarily as money not gained by the caregiver who could have been
otherwise employed and/or money paid for outside help), while nearly
one-third of the cost would be due to direct social cost (such as
transportation costs, day-care costs, residential care costs) and about 12.3
per cent would be due to the direct medical costs (cost of the medication,
consultation, investigation and hospitalisation).

As the disease progresses, there will be a proportionate increase in cost
and estimates indicate that during the average seven years of life for a
person with dementia in an urban area, the total cost of care would be Rs
9.6 lakh.

As per this model, India currently spends as much as Rs 16,000 crore a year
for the care of persons with dementia. As the number of dementia patients is
set to double from the current 3.69 million to 7.61 million in 2030, the
cost of care is also set to double. Assuming a nominal five per cent annual
inflation, the actual cost of care would treble by 2030.

*[email protected]*

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