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10 AIDS and the
Church: When Church Members Need Help

Exploding Exploding myths
Caring for church members
Infection usually
survives conversion AIDS
time bomb in the church AIDS
in the church office Can
you keep a secret? People
with AIDS may leave your church Big
leaks can start slowly Now
is the time to prepare Openness
can bring release Practical
care at home 1.´Show you still
care 2.´Maintain friendship
3.´Listen to the questions
4.´Open your home 5.´Draw
others in 6.´Seek expert
help 7.´Be ready
for the long haul 8.´Fear
of death can be worse than death itself 9.´Support
the carers too 10.´Be
ready to help around the clock at the end

CHAPTERS: Introduction
1
The Extent of the Nightmare 2
What's so Special about a Virus? 3
When Cells Start to Die 4
How People Become Infected 5
Questions People Ask 6
Condoms Are Unsafe 7
Moral Dilemas 8 Wrath or
Reaping? 9
Some Life and Death Issues 10
When Church Members Need Help 11
Others Need Help Too 12
Saving Lives 13 Needle
and Condom Distribution? 14
Special Issues in Poorer Nations 15
A Ten Point Plan for the Government 16
A Global Christian Challenge Appendix
B Appendix C
Appendix D
Note: This chapter of The Truth about AIDS
by Dr
Patrick Dixon is the original text as published by Kingsway
in 1994 updated 2002 and may be reproduced with acknowledgment.
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How are you going to care for people with HIV in your church, especially
when people in churches may still be worried about things like the
communion cup? How are you going to look after church members dying
at home?
Exploding myths
(return to index)
Priority number one must be to get educated. Church leaders need
to be up to date and well informed. Books, conferences and visiting
speakers are all ways to achieve this. Even a ten-minute presentation
as part of a Sunday service can be long enough to bring home the
impact of AIDS, if done by someone with personal experience of the
illness, possibly from an organisation working in the field as a
Christian agency.
Church congregations need clear information about risks, the communion
cup and about social contact. They also need clear teaching on some
of the ethical issues involved. Teaching needs to be given about
God's accepting love, as well as his standards, emphasising the
need to care unconditionally, challenging prejudice and judgementalism
(see Chapter 8).
Caring
for church members
(return to index)
We tend to think of AIDS as something out there rather than a problem
within, yet AIDS is also marching into the church. Any growing church
which is seeing people come into faith, with lifestyles changing
and lives transformed, is likely to find imported HIV sooner or
later.
Infection
usually survives conversion
(return to index)
It is sobering to think how many of your congregation have come
into faith in the last ten years. Conversion or a rediscovery of
faith can happen gradually or suddenly, but infection always remains,
barring God's intervention in a miracle of healing.
AIDS
time bomb in the church
(return to index)
As we have seen, someone who joined a church in 2003 may have been
unknowingly infected in the mid 1990s. The person may still be perfectly
fit and well today. In a few years' time the person may be a recognised
leader with many responsibilities. One day the person may come to
you looking obviously unwell after having been afflicted with various
medical problems for some time. Now he's tested positive for HIV.
This scenario has already become a very common scenario in
many African nations. The pastoral implications are huge when you
have a congregation which has mushroomed from maybe 500 to 5,000
in five years and you realise that up to a fifth of your adult members
could be carrying the virus.
AIDS in
the church office
(return to index)
It is a huge step for someone to tell you they have HIV or AIDS.
In many cases it means revealing intensely personal things about
the past; things which have been prayed over and forgotten years
ago. This is in addition to the shock of coming to terms with a
future death from AIDS. It often seems particularly tragic when
someone who has made a fresh start has to pay such a very personal
and public price for what happened so long ago.
Such tragedies can tear churches apart, with people asking over
and over again why God has not chosen to heal the person after the
greater miracle of life-changing conversion.
Can you keep
a secret?
(return to index)
Once someone in your church has told you they have HIV or AIDS,
a journey has started which will probably have a profound effect
on you and the church over many years. Confidentiality is important.
As we have seen already, we live in harsh times when it comes to
AIDS. Violence, discrimination, verbal abuse and hostility are common
reactions in many nations from an intolerant minority; common enough
to create an atmosphere of tension and fear if the diagnosis becomes
known.
A diagnosis of AIDS or HIV infection is sensitive information which
may need to be kept strictly confidential for a long time. You may
be able to create a supportive environment in the church. However,
churches are by their nature public groups meeting in public places.
Anyone can turn up to meetings and new people join. You cannot be
certain how one or two on the edge of things might react, especially
those who perhaps have not been Christians very long or who have
deep personal problems of their own.
People
with AIDS may leave your church
(return to index)
I remember talking recently to a mother with a young child. She
told me that she had moved 100 miles away from her church after
the news that she had HIV gradually spread. She said the church
had been caring. She had felt accepted and cared for by the leaders
and supported by her home group which met in someone's house during
the week.
Unfortunately, once her situation became widely known in the church,
she began to notice a change. She felt people were avoiding her.
No one wanted to have her child to play any more. No one wanted
to share the communion cup with her. She felt isolated, insecure,
rejected and afraid. After a few weeks she left. I am pleased to
say she is now happily settled elsewhere.
Her story made me think. The same could so easily have happened
in my own church or in any church for that matter. Much of the supposed
rejection could have been her own hypersensitivity and insecurity,
but it is quite likely that one or two may have made inappropriate
comments, or behaved in a hurtful and unkind way.
For these reasons we need to address the issue of who is told before
the event, rather than working out a policy an hour after realising
someone has HIV. Do all the leaders need to know at this stage?
What about their spouses? If one person in the church knows, will
others be told---`just for prayer, of course'?
Big leaks
can start slowly
(return to index)
News may leak gradually before an explosion occurs. Take the situation
of four senior leaders who know, each confiding in one other person
over the next six months. Each of the new four also confide in one
other, while the four leaders also tell two or three others. The
result is that in just twelve months at least fourteen to sixteen
people already know. After the second year the number knowing has
grown to twenty, and by the third year to twenty-five.
One day a conversation is overheard by someone else who very likely
tells another ten in as many days. By the end of the month people
at work have found out and are saying they will refuse to co-operate
unless the person is laid off. The result could be loss of job,
loss of income, public humiliation and a big question mark: Does
every other person in the church know?
Now is
the time to prepare
(return to index)
Churches for whom all these things are quite new and unfamiliar
need to prepare now, before someone turns out to have HIV. Perhaps
someone in your church is already infected, but he or she---or you---has
yet to find out. Sometimes I am asked to speak to a church because
the leaders are now aware of someone with HIV who is becoming unwell.
They realise people are going to guess soon and they want help now,
so when people find out there will not be any panic. It would have
been better to have visited the year before.
It can be hard to know when to widen the network of those who are
aware of the situation. The timing and occasion are best determined
by the person with HIV. The process becomes easier if one or two
new people are told at a time, before involving larger groups. Often
the person with HIV feels anxious about possible reactions. As each
person is found to be accepting, warm and encouraging, it helps
to overcome the big lie which says that people will reject once
they know.
This fear of being known is a curse because it robs and destroys
friendship. Whenever someone lives under the shadow of discovery,
there will always be deep insecurity. It is only as we find people
still love us despite our failings that we begin to see and feel
what the love of God is like.
Openness
can bring release
(return to index)
The more open we can be, the more AIDS becomes normalised as a
part of our suffering world, and in turn the easier it is for others
to be open in the future. More importantly, the more open we are,
the easier it is to organise help. So in general it makes
sense to be as open as possible, given all the constraints of the
local situation and culture, and all the cautions above.
One rule of thumb if you are unsure how to proceed is is to operate
on a need-to-know basis. And as illness develops, the need to know
becomes gradually greater for a larger circle of people.
Practical
care at home
(return to index)
The needs of those with AIDS living in the community are in many
ways exactly the same as the needs of those with other kinds of
illness. There is always the need for friendship, but often the
greatest needs are practical. It is easy for barriers to form and
for people to feel a burden, unable to ask for help. On the other
hand, wanting to help can make us feel awkward and embarrassed,
not knowing what to say or do.
Here is a brief outline of ten practical steps that any church
can take to support a church member, most of which also apply in
many ways to caring for others in the community. This is not a definitive
guide. Many of the basic principles of care are valid in different
cultural and economic situations, but other aspects require adaptation.
The greatest help is often the simplest: things that anyone
can do, whether they live in Manhattan apartment in New York, or
in a house of corrugated iron and plastic on a rubbish tip in Brazil.
It doesn't cost money to be kind.
1.´Show you
still care
(return to index)
Someone with HIV is likely to feel especially vulnerable after
telling you the news, or just after knowing someone else has told
you. What will the next meeting be like? Will there be a smile,
a hug or an awkward turning away? People may say it does not make
any difference, but is that really true, or are they just pretending?
Surely I am a liability, an embarrassment, a burden on the church?
Go out of your way to express appreciation, acceptance, love, care
and support in those first critical days.
Learn about the illness so you are well informed and can help others
later on who may be struggling with ignorance.
2.´Maintain
friendship
(return to index)
Try to maintain as much normal life as possible. The person who
has HIV will probably want to carry on as usual rather than be dragged
down by thinking about the illness all day long. Be sensitive to
changing physical needs, moods and feelings about the future. It
is perfectly normal for people to swing from optimism to pessimism,
from grand plans to the depths of despair, from acceptance of the
situation to denial.
This is just part of the process of adjustment to grief and loss.
Often we think of grief as an emotion triggered by the death of
someone we love. However, grief is a process of adjustment triggered
by losses of any kind. As we have seen in earlier chapters, the
losses for someone dying with AIDS are numerous and often devastating.
Loss of health; loss of memory, sight, physical comfort, sleep,
control over one's body; loss of future plans, ambitions, hopes
and dreams; loss of friends, family, job, physical attractiveness,
energy; loss of independence and freedom; loss of future; loss of
life on earth. It is no surprise, then, to find people oscillating
between denial, anger, sadness and acceptance, or with mixtures
of all four. AIDS can be a heavy burden to carry.
3.´Listen
to the questions
(return to index)
The Psalms are full of heart cries towards God. Why is this happening
to me? What is God doing? This seems so unfair. Questions and statements
like these are cries of pain and anguish which need a listening
ear rather than a trite reply. The person may just want you to sit
and listen while feelings are expressed. There are no simple answers
to human suffering, as Job's friends discovered.
Anger can often be directed at others such as members of the family,
neighbours, friends, doctors, nurses, volunteers and members of
the church. Anger and sadness are closely linked. They can both
be a part of the process of grieving for a life that has been unexpectedly
shortened. The anger may be directed at you too. It is important
not to take such rejection too personally, and to continue to offer
friendship.
Sometimes anger can become a test of friendship. You may be on
trial yourself. Is your love great enough to keep coming back? In
the meantime, while offering continued support, there may be another
who is better placed to maintain the closest links.
4.´Open your home
(return to index)
Be ready to offer a meal, a place to stay or sit quietly during
the day. Often a change of environment can help not only the person
who is unwell, but also the other carers. Many with AIDS have no
real homes or families. Many have been effectively orphaned by their
condition, or by previous circumstances. Many are living on their
own, or with friends, in situations where dying at home may be difficult,
or impossible. As we open up a network of homes and relationships,
we are offering new choices to people who may feel they have none.
5.´Draw others
in
(return to index)
In our desire to preserve confidentiality, to care and to protect,
it is easy for intense relationships to develop, and to reach a
situation where `lock up' occurs. It is easy as a carer to convince
yourself that no one understands the person better than you, and
that you alone have an `inside track' on the situation. You want
to be involved in all decisions; to be present at every discussion.
It is easy to have mixed feelings about others becoming involved.
Yet that very intensity can become more than the relationship can
bear when illness develops.
As the situation unfolds, it is wise to draw others in. As a church
leader myself, I feel it is vitally important that at least one
member of the church leadership is closely involved, providing pastoral
support to the person and to the carers, spotting signs of pressure
or difficulty and helping to find ways through.
At every stage you will need the backing of the person concerned
to involve others in this. If this is constantly blocked at every
turn, you may have some hard talking to do. I have seen many situations
break down at home, with people landing up in hospital simply because
no one was willing to think seriously about the future.
6.´Seek
expert help
(return to index)
At some stage or other you are going to need expert help. It is
all very well providing emotional support as a friend, but when
events unfold you may need extra professional advice and support
either from a clinic or from a community service. It may be that
there is no local service available in which case even telephone
advice can be helpful.
Community care varies from country to country, but the trend in
many places is towards caring for people in the community. Neither
the richest nor the poorest nations can afford to keep people with
AIDS in hospital when they do not need acute medical care.
As we have seen in Chapter
1, anxiety can produce many of the symptoms of early HIV illness,
and as in other areas of medicine it is possible for people to convince
themselves and others that they have HIV when there is no evidence
of this. Because medical confidentiality is so strict in many nations,
it is only possible for health care professionals to obtain confirmation
of diagnosis after written permission from the person concerned,
and even then it can be difficult. However, such confirmation is
important . Fraud and deception are not unknown, in order to get
extra attention or material help.
7.´Be
ready for the long haul
(return to index)
Both those with HIV and those who care for them can be bewildered
by rapid changes in the illness. One week there may be such a marked
deterioration that they assume the end must be near, while the next
week things may be back to their usual state. AIDS is a disease
of ups and downs. People can be close to death, yet recover with
prompt treatment, and be home again. People with AIDS are living
longer in many countries with improved treatment, as we have already
seen. Therefore it is wise to plan for a level of support that may
need to be sustained for a long time.
People often ask me when the end will come. The answer is that
no one knows, although we can often be certain about one thing:
death is not here yet. With onset of new symptoms it is natural
for everyone to become anxious. I often say to people that although
it is true they are going to die of this illness, barring a miracle
or a sudden new discovery, it is also true that they are not dying
at this moment. We can often look back and see that maybe over the
last few days things have actually improved a little.
One of my greatest joys has been seeing people begin to make realistic
plans again: a last holiday, a project to complete, friends to see,
a place to visit. Our aim is to redeem time; to give back dignity,
freedom and choice. That is why expert care is so important. When
it comes to practical care, nothing is more rewarding to me than
something as simple and important as being able to give someone
their first good night's sleep in months, so that the following
day can be enjoyed.
8.´Fear
of death can be worse than death itself
(return to index)
Remember that the process of dying can be far more worrying to
people than death itself, particularly if the person is sustained
by the hope of eternal life. Common worries can include losing control
over bowels or bladder, becoming mentally feeble with loss of memory,
becoming disabled and confined to a wheelchair, losing hair as a
result of chemotherapy for cancers, having to be washed and dressed
by another.
Other worries can include the fear of uncontrolled symptoms of
pain, breathlessness or other kinds. Finally, there is also the
fear of losing control, of others marching in as strength fades,
and of the wrong decisions being made.
The way to deal with these fears is to address them, and to try
to discover what lies behind them. I remember someone asking me
one day whether he would suffocate to death. There was real fear
in his eyes as he gripped my arm waiting for the reply. Before answering,
it occurred to me to ask why he was asking the question and, even
more importantly, why he asked today when I was visiting so regularly.
The answer tumbled out that he had woken in a terrible fright the
previous night in the middle of a nightmare. He had seen himself
lowered into the ground in a coffin while still alive. Despite his
shouts and his hammering on the sides of the box, they had covered
him with earth. He had suffocated to death.
We were then able to talk about the dream, and I was also able
to promise him first that he would not suffer from feelings of suffocation
if he developed a pneumonia, and secondly that death when it did
come would be certain. No one would suddenly whisk him away. He
could remain in the house for some time. As a result of the conversation
he felt at peace and the fear never returned. It is an important
principle to find out what lies behind a question before wading
in with an insensitive and immediate response.
9.´Support
the carers too
(return to index)
Sometimes all the attention can naturally fall on the one who is
ill, ignoring those giving most of the support. Sometimes partners,
children, other family and friends can unexpectedly run out of steam.
Things can become too much, juggling job, other responsibilities
and the needs of someone with AIDS. An effective early warning system
is vitally important. Often it's the case that very young children
are having to do most of the day to day caring.
Those doing all the work need to know they too have someone who
is special to them, watching out for their own needs, stepping in
with practical help, sharing the load, providing a shoulder to cry
on, and being a friend in times of trouble. The greatest help is
often practical. You could spend an hour a day counselling a carer
who is near breaking point when the time would be better spent sitting
in the home for a morning or an afternoon so the carer can go out.
Perhaps you can take the person who is unwell out for the day, or
have the person to stay for a night or two, possibly longer.
Do not wait for people to shout for help, as they will often tell
you much too late. Keep in touch regularly, even when things seem
to be going very well. Time can fly by. Write a note to yourself
in the diary when you are going to telephone next or drop round
again.
Be honest about your own needs, to yourself and to others. You
are a special person too in God's eyes. He loves you too. Allow
yourself to be vulnerable. Let the right people see when you too
are feeling the strain and are hurting inside---obviously you need
to be careful not to share too widely, nor to dump your own emotional
needs on someone who is ill, or on the main carer. Maybe you will
encourage someone when they see that you are human too. Be ready
to say no, to draw the line, to have recovery time of your own.
That is why it is a good idea to involve a few others. You never
know just when you will need their support.
10.´Be
ready to help around the clock at the end
(return to index)
You will need to be well-organised if the person wishes to die
at home. It is likely that the last day or two, or even longer,
will be quite harrowing. There may be a need for a continuous presence
in the home, in addition to professionals coming in and out. You
may need to identify a few sensible friends who would be willing
to help on a rota basis, and who are acceptable to the person who
is ill. The main need is likely to be for the sort of help that
a caring relative would provide, to help in various practical ways.
On the whole, the care approach is the same as would be taken locally
for any illness, whether you are living in Kampala or Bangkok or
San Francisco. The only thing you need to take extra care about
is exposure of skin to body secretions. Spillages of blood or other
secretions should be wiped up wearing a pair of gloves. The easiest
thing to do is mop up using disposable paper towels, and then to
soak the area for two or three minutes with a freshly-made solution
of one part bleach to nine parts water. The area can then be cleaned
in the normal way (see Chapter 5).
Gloves are not needed at other times. As we have seen, intact skin
is an excellent barrier to HIV. Even if there is some skin contact
with secretions, infection is most unlikely to occur unless the
skin is damaged. It is wise to cover cuts with a waterproof plaster
before going into the home.
Although this may all seem rather daunting, it is most unlikely
that you will be managing on your own. In many countries you will
find community nurses and other health care workers are also providing
support and advice. In other places, churches have found themselves
having to develop their own community services because there is
nothing available in their area.
When the moment of death comes, those in the home can feel uncertain
as to what to do. There is no need for great activity when someone
dies. The normal cultural rituals can be observed, remembering that
secretions from the body will still be infectious. There may be
one or two who need to be contacted, and would like to be able to
say goodbye before the person is taken out of the home.
I want to look now at extending our care from our own church to
the wider community. Should we? Can we?
Exploding
myths Caring for
church members Infection
usually survives conversion AIDS
time bomb in the church AIDS
in the church office Can
you keep a secret? People
with AIDS may leave your church Big
leaks can start slowly Now
is the time to prepare Openness
can bring release Practical
care at home
1.´Show you still care
2.´Maintain friendship
3.´Listen to the questions
4.´Open your home 5.´Draw
others in 6.´Seek expert
help 7.´Be ready
for the long haul 8.´Fear
of death can be worse than death itself 9.´Support
the carers too 10.´Be
ready to help around the clock at the end
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