A close-up perspective on Aids in Nigeria
On September 24th, 2010 The Clare Champion covered Emily Price's story. See the article.
It is a fairly common experience for teachers in Ennis to have children
in their class from Nigeria and other Sub-Saharan African countries.
When I heard I had won a travel award to visit Nigeria, I was pleased to
get the opportunity to learn more about the life experiences of some of
my pupils. EIL Intercultural Learning, the organisation who gave me the
award, is an Irish not for profit organisation, which provides
intercultural learning opportunities for about 2,000 people annually.
I
set off for Nigeria with very little idea of what to expect. Like most
people in Ireland, I was aware of the unrest in Nigeria and my
perception was that it could be a dangerous country but nothing could
have prepared me for the wonderful warm welcome I received. I was
immediately stuck by the eagerness of everyone I met to make my stay in
Nigeria worthwhile.
Almost everybody in the country speaks English
but Yoruba is the tribal language spoken in the south-west where I
stayed. An aspect of Nigerian life, which took some getting used to, is
the passion that people display when they communicate. In most
conversations people would greet each other warmly, shout at one
another, talk animatedly and laugh.
I travelled extensively in the
south-west and with other volunteers to Kano in the north of the
country. The transport consists of okadas (Chinese-made mixtures of
scooters and scramblers that are as noisy as vuvuzelas) and minibuses
that are so riddled with rust that a heavy rain may cause them to melt
into the mud below. The only time I felt unsafe throughout my visit was
when these vehicles danced dangerously around oncoming traffic due to
the potholes that engulf half of the road. Believe me, it puts a whole
new perspective on complaining about the state of Irish roads.
Since
Nigeria is the most populous country in Africa, with a population of
154.7 million (UN, 2009), it is an extremely diverse country. The people
identify themselves primarily through their tribe, rather than
nationality. It is a bit like Irish people closely identifying with
their county but on a much larger scale. Ireland’s presence in Nigeria
is unmistakable, from the GAA tops donated by Irish charities that adorn
the children on the street to the newly constructed HIV/Aids clinics
and orphanages and, of course, the Guinness signs which are seen
everywhere.
I worked with Living Hope Care, an organisation that
provides care and support for people living with HIV and Aids and
orphaned and vulnerable children. There were 33.4 million people living
with HIV at the end of 2008 (UNAIDS). EIL provided me with training
before I travelled, during which time I learnt that being HIV positive,
or having HIV disease, is not the same as having AIDS. Many people are
HIV positive but don’t get sick for many years. As the HIV disease
continues, it slowly wears down the immune system. Without treatment,
two-thirds of adults infected with HIV are likely to develop Aids within
10 years of being exposed to HIV. Unfortunately, in Nigeria this period
is much shorter, as people are exposed to tuberculosis and parasitic
diseases such as malaria.
Antiretroviral (ARV) medication can prolong
the time between HIV infection and the onset of Aids. Unfortunately, as
I learned in Nigeria, these medicines are not widely available in
poorer countries around the world and millions of people who cannot
access the medication continue to die. The clear message from the
training is as relevant to people in Ireland as those in Nigeria. It is
important for people to know their HIV status and to protect themselves
and others from this virus. The only reliable way to discover if you are
HIV positive is to get a blood test, which can detect infection from a
few weeks after the virus first entered the body.
Those of us who
have access to information regarding HIV/Aids have a duty to use this
information in order to reduce the spread of the disease in Ireland.
This
can be such a simple task for Irish people when compared to the
experience of Shaio, an amazing volunteer with Living Hope Care. She
herself was living positively with HIV and had suffered unbelievable
prejudice from the community as a result. When she was pregnant, she was
aware of her HIV status and was determined to take precautions to
protect her unborn baby from contracting the virus. However, when she
was in labour she was refused entry to a maternity clinic because they
were aware of her status. She then travelled to another clinic and in
order to save her baby’s life, she withheld her status from the
mid-wife. Throughout the labour she ensured that the mid-wife took all
the necessary precautions to protect herself and the baby. The delivery
was successful and a few hours after giving birth, Shaio washed all the
surfaces and the bed and equipment with the bleach she had brought in
order to protect others from the virus. She later ensured that the
midwife received training from Living Hope Care on HIV and Aids.
Others
I met travel over an hour, crammed into old buses on treacherous roads,
to receive their ARVs, check-ups and to have secondary infections, such
as TB, treated, as there is nowhere in their state that provides the
drugs. At the hospital, those with TB and other air-borne diseases are
required to wait outside in the unbearable heat.
Once, at night, we
had to rush to the hospital where a mother lay exhausted, malnourished
and frantic for her baby to receive the drugs, which are more effective
the sooner they are administered. The baby had been born a few weeks
premature and because of the poor conditions of the maternity clinic,
was going to have to vacate the bed and building within a few hours.
Another
experience that will always stay with me is the time I had to rush to a
run-down maternity health clinic to administer drugs to a baby born to a
mother who was HIV positive. These drugs are ARV prophylaxis drugs,
which means that they attempt to prevent mother-to-child transmission of
HIV. The reason our NGO had to deliver this treatment was that the
maternity clinics did not have access to the drugs, as they are not
provided by the State. Therefore, it was necessary to travel to a
hospital in a neighbouring state to register during pregnancy to receive
the drugs. Our NGO kept the drugs until the baby was delivered, as they
must be stored in a fridge, something most our clients did not
otherwise have access to. In Ireland, this baby would have been in an
incubator. However, in Nigeria it was sent away from the overcrowded and
understaffed maternity clinic despite its vulnerability.
This
experience brought home to me in a very real way the inequalities of
access to healthcare. Poor people receive poor treatment. In the Global
South, one-third of women have HIV positive babies (UNAIDS). Sadly, it
has been recorded that “An estimated 500,000 mothers die from
pregnancy-related causes each year; at least eight million suffer
life-long health problems linked to pregnancy and childbirth”.
Every
two weeks, regardless of how sick our clients were, it was necessary for
them to spend an entire day travelling and waiting at the state
hospital in the city of Ibadon to receive their drugs. While waiting to
see the doctor, I asked a woman if I could take her photograph, after
she had spoken to me about her life story.
“Once she said I could, I
took my camera out of my bag and immediately chaos ensued as the group
of about 30 people sitting with us jumped up and ran out of view. I
reassured the group that I would not take any photographs, as aside from
this woman, nobody else wanted anyone to learn of their HIV status.
This fear was a result of living in a community and a world, which
stigmatises those living with HIV/Aids.
Nelson Mandela said, “Many
people suffering from Aids are not killed by the disease itself. They
are killed by the stigma and discrimination surrounding everybody who
has HIV and Aids.”
Emily recommends that anyone interested in overseas voluntary work should check EIL’s website at www.eilireland.org/.
