21km from Mityana township, and about 5km
from the Nkuru Business and Vocational Training College that John Njendhayo has
built and set up, in the heart of rural Uganda, lies the Namutamba Rehabilitation
Centre (NRC), a rehab centre with vision.
NRC’s focus is providing a range of medical
and para-medical inputs for children living with disabilities, and despite the
predominantly low-tech resources, plus negligible government support, they really
are achieving great things.
The staff team comprises a nurse, a physio,
a primary teacher, someone with occupational therapy experience, two matrons
(one day, one night) and a number of ancillary and admin-related staff.
The children come from all over Mityana
district, and are predominantly too poor to pay for their treatment. But this
isn’t a deterrent to the staff – they treat every child to their best ability
for the medical and associated needs that the child has, and they trust and
pray that the money will come in from donors to pay for it – and it does! Such
faith.
Chatting with the staff, I was asking about
the types of diagnoses that the children have that come to NRC, and also the
obstacles that the staff face in reaching the children in the first place.
Their responses were not that surprising but at the same time it was sad to
hear just what a massive mountain each of the children have to climb, for no
reason of their own.
The main diagnosis that NRC deals with is
osteomyletis – a bacterial bone infection (I think) that can lead to
destruction of the bone, deformity, awful pus-filled wounds that don’t heal,
and associated infections as a result of all the above. Apparently by the time
the child is brought to the Centre for treatment they have usually had the
osteomyelitis for a long time, been seen by several witch-doctors, been
ostracized by the community because of their suppurating, stinking wounds, and
been hidden away as no-one wants to know them.
Other diagnoses include talipes, cleft-lip,
cerebral palsy and hydrocephalus. Nothing unusual there, but what was
noticeable was the lack of resources to deal with the psychological scarring
that so many of the children are trying to cope with. The Centre staff know
that this is an area that they aren’t very well-equipped in, which is good, and
they’d like to get better skilled in being able to deal with this side of
things, but seeing that, and the small range of orthotics, walking aids and
other appliances, it was a big reminder of just how massive is the gap between
health care for the have’s and have-not’s: both at an individual level within
country, and at an international level between rich and poor countries.
The list of obstacles that the children
have to overcome, with their parents on their side if they are lucky, are
similar to those found in many countries around the world:
·
Stigma associated with the
disability
·
Children being hidden away from
the public eye, out of shame, and also out of fear of what the repercussions
might be from others, due to the range of myths and mistruths associated with
disability
·
A common belief that disability
is the fault of the parents - a punishment for past wrong-doings
·
Parents who disown their child,
for a range of reasons, all of which are very sad and can relate to the
survival of the rest of the family, remarriage and non-acceptance by the new
spouse, poverty…..
·
Community disowns the family
·
Witchcraft which is often the
first port of call for treatment of the child, and which in itself can lead to
a lot of extra problems, as well resulting in an acute diagnosis becoming
chronic and much harder to treat.
NRC is planning not just to continue to
provide incredible services to the children in its care, but also to expand its
services to include giving attention to the psychosocial side of things, as
well as parent support groups, and increasing and ongoing community activities
to break down the myths and mistruths associated with disability.
With my ex-physio head on, and my recent
insights gained as a JIGSAW Thornbury Trustee, I can safely say that their
plans are no small ask by any standard; but in faith the team are moving
forwards towards their dreams, and I wish them all the best.
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