Off to a great start for our
first week in our international practicum! We were placed at the Antiretroviral
Therapy (ART) clinic. This is a clinic that treats people infected with the HIV/AIDS
virus. HIV is much more prevalent in Zambia when compared to back home in
Canada. To put things into perspective, Canada’s prevalence of HIV is 0.5% of
the population; in Zambia, it is 14.3%. This clinic alone treats over 18,000
patients and is considered the largest one in Western Province. There are two
other clinics close by that also treat a large number of people. On our first
day, the clinic saw approximately 500 people!
There are five components to the clinic:
1) Testing and counseling. Patients are either
referred by a Doctor or can come in on a voluntary basis.
2)
Group counseling session, registration, blood
draw, vital signs and weight are taken.
3)
Follow-up with the clinician for an assessment
and antiretroviral (ARV) drug prescription.
4)
Adherence, which goes over possible drug side
effects as well as counseling surrounding safe sex practices and healthier
lifestyle choices.
5)
Pharmacy. New patients are usually only
prescribed two weeks worth of ARV’s and then have to come in for a follow-up.
Usually, patient’s are given 2-3 months worth of ARV’s. A day at the clinic is
an all day event…
During the five days we were
placed in the clinic, we saw a handful of inequities when comparing to the
Western world, specifically with our experiences back home.
ARV’s only became available to
Zambia in 2008; Canada has been offering these drugs since the mid 90’s. The
Western World is also at the forefront of HIV research and has the newest
therapies available to its citizens.
ARV therapy and HIV status is
monitored by CD4 counts and viral loads (both are blood tests). CD4 counts
monitor how well a person’s immune system is doing, and the viral load monitors
where the HIV virus is at. So if a person’s viral load is lower and their CD4
is higher, it means that the ARV’s are doing their job. Both are essential when
monitoring ARV treatment. The WHO recommends treatment be started when a
patient has a CD4 count of less than 500, if a woman is pregnant, if children
are under age five, or if a person is having certain signs and symptoms of the
disease. They also recommend CD4 monitoring every six months.
In Zambia, drug therapy is
started on patients with all of the above, except, rather than starting a
patient on therapy with a CD4 count of less than 500, they don’t start therapy
until their CD4 count is less than 350. This means that Zambians can’t have
access to ARV’s as fast as other patients in wealthier countries. Basically,
they start treatment when their immune systems are lower than the recommended
levels. Many patients are not getting their CD4s monitored every six months.
Many hadn’t had them done in over a year, and for some, it had been longer than
five years. Reasons for this include the number of CD4 machines and trained
staff available, as well as issues surrounding patient transportation to the
clinic. Remember that Mongu is very spread out with many surrounding villages
and it is difficult for many people to travel to the clinic. LGH is also
lacking a functioning viral load machine, so this test isn’t even available.
Lastly, ARV’s can come with
numerous side effects, ranging from nausea, vomiting, and dizziness, to
hallucinations. Back home in Canada, if a patient is experiencing this, drug
treatments can be revised or other medications can be prescribed to help
counter the side effects. In Mongu, that is not always the case. While ARVs and
prophylactic antibiotics are paid for by the government, other drugs are not.
Sadly, these drugs are financially out of reach for most Zambians.
On the other
hand, our week at the ART clinic also showed us a positive side of HIV/AIDS
care that we would have never experienced in Canada. The entire week, one of the psychosocial
counselors working at the clinic had been asking if he could test me (Darien)
for HIV. The entire week, I had laughed
it off and redirected the conversation.
Why? Being tested would involve a
quick prick of my finger, a drop of blood on a pregnancy test-like strip, and a
result within 2-5 minutes. Easy. But when confronted with an offer to confirm
my HIV status, I almost instinctively dug in my heels. A part of me, a big part, it turns out, was
too scared to know. Even though my
chances as a Canadian were 1/50 000 compared to the 1/5 chance faced by any
Zambian.
On Friday, I finally got tested. It took two minutes and the result was
negative, which came as no surprise. But
waiting for the stupid strip to tell me so was the longest two minutes of my
life. The counselor had been bugging me
all week to get tested and my chances were 1 in 50 000.
It got us
thinking about the brave Zambians who voluntarily come into the clinic to be
tested knowing that their chances of testing positive for the notorious human
immunodeficiency virus are 1 in 5.
Chances are, they’ve seen someone die of AIDS. We watched people get tested, and we watched
people test positive. It was
heartbreaking. But as one of the
psychosocial counselors explained, acceptance of a “positive life,” as they
call it, is much more common here.
Whether a person is living a “positive” or a “negative” life, a Zambian
is encouraged to take similar precautions – you are either protecting yourself
or protecting someone else.
This
acceptance reveals a stark difference between Zambia and Canada – my hesitance
to be tested is a prime example. Back
home, people are terrified of HIV; it’s a “dirty,” “terminal,” “incurable”
disease that only “homosexuals and IV drug users” get. Here in Zambia, there are posters encouraging
people to get tested plastered on walls, and patients come in knowing at least
a little about ARVs. In general, myself
and Ali included, the Canadian population doesn’t know that the right ARV
therapy can allow an HIV+ patient to live a quality, full-length life.
The HIV
counseling office was one of the components that impressed us most so far about
the ART clinic. When a person comes in
to the clinic to get tested for HIV, they first sit down with a psychosocial
counselor (PSC). Since most of the
sessions are done in Lozi, the local language, one of the PSCs was kind enough
to role play a session with Ali and I as patients. To be honest, we expected a scripted lecture
in medical-ese about HIV, AIDS and CD4 counts.
What we got was a compassionate, interactive, informative dialogue in
layman’s terms. The PSC picked up on our
learning needs, made sure our questions were answered, and gave accurate,
thorough information without judgment.
The PSC is also the person who administers the HIV test. This seems like a small detail, but by the
time it came to administer the “test,” we felt safe, supported, and
well-prepared rather than overwhelmed and alone.
HIV/AIDS,
stigma or no stigma, is a life altering diagnosis. The long two minutes I spent in limbo and the
week that we have spent surrounded by the victims of this disease has shown us
that. While resources are slim and the
patient volume is immense, the Mongu ART clinic should be proud of the care
they are providing to their HIV+ patients, and Canadians could learn a little
bit about acceptance from the brave people of Zambia.
-
Ali and Darien
Dear Darien,
ReplyDeleteWhat a wonderful story about community, health equity, global citizenship, and learning from our Zambian colleagues you have shared with us. This reminds me of Stephanie Nolan's book on Sories of AIDS that Fay lent me last year before I went to Zambia. You have just added another rich narrative to these sobering, inspiring stories of how people across Africa are facing the threat of HIV-AIDS with courage and wisdom we can all learn from. Hopefully we can also learn how to lessen the inequities of treatment with our own advocacy and knowledge.
Yes, we are lucky in Canada - may we also some day be a country that is better known for our support to reduce the health inequities in our world. Your story is a good step in raising awareness of our need as lucky Canadians to do that.
Onwards,
Tricia