I asked if I could hold him. She nodded her head and handed
over her one and a half year old baby boy to my open arms. His eyes were open
but he did not see or focus on my face. His hands were in continual rhythmic
motion. His mouth made baby sounds and noises. His soft skin and chubby body
filled my lap. He smelt strongly of urine and I wondered if my lap was getting
wet from his damp shorts, but I didn’t care. This little precious one was in my
arms.
We were talking with his mama about the surgery that he’d
had months ago in the previous Mada outreach. She was ‘very satisfied’ with his
scar as it was hid amongst his curly black hair. She said he was ‘more accepted’
in society now, but she was saving up finances for a surgery to ‘fix him’
because he wasn’t walking yet and wasn’t doing things other children his age
were doing. I think a little piece broke off my heart when I heard that. It was
a comment that I have heard so many times in different countries throughout
Africa. Yet again, I explained to his mama that her precious little boy could
not be ‘fixed’ with a surgery. It was just the way he was and that in my
country we also have boys and girls the same as hers, who cannot be ‘fixed’
with a surgery. The most important thing that she could do for him was be a
good, loving mama and I already knew she was because I had seen her care for
him in our hospital with my own eyes. My heart yearns for her, knowing the hard
road she will continue to walk in a country without government help or even
support groups for disabled children.
~
Little girl J was brought to the chair next to me. She sat
down timidly, keeping her head down, feet swinging because they didn’t touch
the ground. Her grandmother sat down on the chair beside her, rubbing her rough
hands together nervously. Her feet were bare and it was clear to me that she
was a woman who knew how to work extremely hard. The translator told me that
they were from a village far away. We introduced ourselves and we asked them a
few questions.
Little J has a tumour growing from the right side of her
face. It had been growing for one year and had already split the skin on the surface,
causing fluid to occasionally leak out and run down her neck. At 11 years old,
J is small with no body fat to speak of. Despite her young age she sat so still
and bravely while I stuck a needle in her arm so that she could have a scan.
Even when the doctor looked at her and poked around the tumour, she was so
brave. My background knowledge tells me that the results we’ll get back from
the tests will tell us that she is not a candidate for surgery on the ship, but
my heart screams for the opposite.
~
At the end of the day in the screening tent I turned around and
saw a large stack of envelopes sitting on the table. It looked like fan mail. I
asked Jas what it was. She told me it was the pile of photos and referrals that
the day crew at the patient assembly site in town brought back to the ship EACH
DAY. There would have been more than 60 photos of all areas of people’s bodies
that had a problem or pain, that they would like a doctor to see and remove the
lump or cure the pain. We looked through each photo and put them in piles of problems we could potentially help and those we couldn’t. There were some photos
that were really heartbreaking. Among them, a baby with hydrocephalus that needs a
shunt placed that we cannot do and neither can any other hospital in this
country and a young girl with terrible scoliosis who needs a spinal fusion which
we cannot offer. The pile of photos went on and on; a pile of papers that cried
out ‘Help us!’
~
We arrived in Madagascar on Sunday 30th August
after further unforeseen delays at sea. My last post was about waiting
and I had a bit of a laugh because I got further practice less than 24 hours
after it was written, when I thought we were finally on our way!
The M/V Africa Mercy in port, Tamatave. |
Since we’d been so delayed, we hit the ground running and
had cleaned and set up the whole hospital in 5 days, with many thanks to our
alumni Malagasy day crew and 60 brand new nurses.
The last couple of days I have spent with the screening team
or doing maxillofacial evaluations. I have seen patients waiting for surgery
and patients who have had surgeries. I have seen the faces of those who are
daring to hope that this is the chance they have been dreaming of or prayed for
and I have seen the smiling faces of those who have had successful surgeries
and despite some still facing challenges say that they are now accepted in
their community and are satisfied with their surgeries. Many of them still do
not look ‘normal’ and require further surgery for improvement, yet they are not
complaining. I am just amazed at these Malagasy people who continue to flaw me
with their selflessness.
Mercy Ships hospital team 2015 Mada2 |
The first surgeries of the Mada2 outreach began yesterday.
The patients were outnumbered by the nursing staff as a handful of the new nurses got to
work their first shifts in a place that many of them have dreamed about coming
to. I love watching the new nurses in their new environment which is so normal
and comfortable for me (it should be after 5 years!) I love watching them fall
in love with the people and patients in the ward, knowing that they will never
be the same after this experience. Mercy Ships is a place that you just can’t
walk away from and be the same person. Despite the fact that this is now my 7th outreach with Mercy Ships, working and living here continues to change me, stretch me and mold me into a better person. So, I say, let the outreach begin!
No comments:
Post a Comment