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The Leprosy
Institution (Leper Settlement as it
was then called) was first located
at 5th Mile, Rock Road, Kuching. It
accommodated about 70 patients. In
1917, a fund in memory of the late
Second Rajah Sir Charles Brooke, was
set up and generously supported by
the public. With the funds
collected, it was possible to build
a new Settlement at Satang Island.
This was desirable as the patients
were becoming a public nuisance by
begging in the streets and involved
in other activities such as
gambling, etc.
In 1924,
the buildings, houses, stores,
dispensary and others were completed
and the patients were moved to the
new settlement. Unfortunately this
site was found to be unsuitable
because during the Landas season,
supplies, communications, rations
and other necessities were extremely
difficult. This prompted a move to a
more suitable sanctuary.
In October
1925, the patients were shifted back
to the mainland to the present site
at 13th Mile, Penrissen Road. This
new place was found to be ideally
suited for the location of the
settlement. In 1926 more permanent
buildings were constructed by the
patients themselves as 'Gotong
Royong Project' from timber and
other building materials brought
from Satang Island. In the same year
(1926) the Government took over full
responsibility of the settlement,
but it was still named as Rajah
Charles Brooke Memorial Leper
Settlement.
In 1940,
permanent administrative block and
hospital wards were built which
could accommodate about 40 patients
who needed proper medical and
nursing care due to acute illness,
ulcers and complications. Since then
progressive expansion and
improvements continued to take place
until 1962. The present Institution
consists of the following
infrastructure:-
Administrative Block
3 Wards
buildings
11
Dormitory Barracks
State
Leprosy Control Centre Building
complete with Computer and Record
Rooms
Outpatient
Department
building/Laboratory/Pharmacy/Kitchen/Laundry
M.C.H.
Clinic/Workshop/Canteen
Mortuary
Generator
House
Fire
hose/pump house
7 Staff
Quarters/Barracks
1 MO
Bunglow
Places of
Worship : Chinese temple/SPG
Churches/Surau
Trainee
Hostel
Community
Hall/Occupational Therapy
Unit/Classroom
Kindergarten
The
settlement was renamed in 1962 and
since then is known as Rajah Charles
Brooke Memorial Hospital with a
total of 62 acreage.
Since its
establishment, R.C.B.M. Hospital is
the sole Leprosarium providing
leprosy care to patients not only
from Sarawak, but also from Sabah,
Brunei and Kalimantan Indonesia. At
its peak occupation, the patient
population was as many as 500 plus.
The Sarawak
Leprosy Control Programme was
launched in June 1974. Since then,
with the decentralization and
integration of leprosy care into the
general medical services, the
patient population has progressively
declined over the years. This was
because compulsory admission by law
of a leprosy patient to R.C.B.M.
Hospital was abolished and R.C.B.M.
Hospital was and is that of Referral
Hospital for:
|
(i) |
High
infectious cases that cannot
be effectively managed in
their own environment. |
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(ii) |
Patients
with complications and
reactions that cannot be
managed at peripheral hospital
level. |
|
(iii) |
Patients
for intensive phase of
Multiple Drugs Therapy 'Regime
(MDT) (especially those coming
from Bahagian Kuching) |
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(iv) |
Patients
requiring special
rehabilitative services. |
Since the launching of Leprosy
Control Programme until today a
total of 1512 cases are being
registered and only 590 are still
receiving treatment while the rest
were either cured or died of old
age. It is assumed that there are
about 2000 cases of leprosy in
Sarawak.
Leprosy Treatment In Sarawak
Before
1940, leprosy was thought to be an
incurable disease. The first
medicine introduced for Leprosy was
Chaulmogra oil injection extracted
from the fruit of the Hydnocarpus
trees. However it has been found to
have no medical value. The greatest
advance made in the treatment of
leprosy came in 1949 with the
discovery of Dapsone, a derivative
of Sulphones and was first
introduced to this Hospital in 1951,
after which a number of leprosy
patients were cured and discharged
from the hospital, thus warrant
unnecessary admission to
leprosarium. However in 1972 other
medicines have since been discovered
which are also effective for the
treatment of leprosy, there being
Lamprene and Rifampicin used
as dual therapy with Dapsone.
In 1986
W.H.O. introduced the use of these
three drugs i.e. Dapsone, Rifampicin
& Lamprene (Ethionamide) and
termed as Multiple Drug Therapy
Regime, which are very effective and
thus accepted as National Therapy.
Now a total of 173 cases are on MDT,
while 94 cases are on surveillance
and 417 cases are either on Dual
Therapy on Monotherapy.
Leprosy as a Disease
It is
caused by Mycobacterium Leprae, a
gram positive bacilli, invading only
the skin and peripheral nerves. It
is infectious and contracted through
prolonged intimate contacts with the
patient, but it is NOT HERIDITARY
and its incubation period is
about 2-7 years.
Natural
body resistance of an individual
will determine the severity of the
disease, thus the early sign of the
disease (Indeterminate) may just
disappears if the body resistance is
high.
According
to W.H.O. definition there are only
two types of leprosy namely
Paucibacillary and Multibacillary,
which can be recognised with the
following signs and symptoms:-
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White/Red
patch or patches over the skin |
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Loss
of sensation over the white
patch(s) |
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Now
sweating over the white
patch(s) |
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Swollen
and painful peripherals nerves |
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Presence
of Mycobacterium Leprae in
skin smears or skin biopsy |
LEPROSY IS CURABLE AND TREATMENT
IS FREE
EARLY DETECTION PREVENTS DEFORMITY
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Members
of PAN-BORNEO COMMUNITY
PROJECT COMMITTEE
Rtn. Michael Hii (Project
Chairman),
Rtn. CP Chua Teck Kheng
(Deputy Chairman),
Rtn. Ee Guan Teck & Kho
Ping (Members),
Hj. Mohamad Ismail b. Hj.
Gusta
(Hospital In-Charge). |
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The
Multi-Purpose Hall built in
1954. |

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