Handayani Center Responses to Follow-Up the Efforts for Handling PMIB Children Suffering from Heart Disease
PURWAKARTA (June
16, 2022) – The Ministry of
Social Affairs through Handayani Center will follow up on the handling of PMIB
children diagnosed with heart disease. In April 2022, the Minister of Social
Affairs, Tri Rismaharini, assisted the repatriation of 34 Troubled Indonesian
Migrant Workers (PMIB) from Saudi Arabia. Arriving in Indonesia, all PMIB
received full attention of the Minister.
All UPT (Technical
Implementation Unit) belonging to MoSA immediately carry out an assessment
process to determine the identity, condition, and needs of PMIB. "Handayani"
Center Jakarta, conducted an assessment of several PMIB who are domiciled in Karawang
and Purwakarta Regencies.
Nia (40), is a
PMIB from Purwakarta Regency has been to and from work in Saudi Arabia 4 times,, and has 3 children, one of whom is married. Her husband works as a farmer and does other odd jobs.
Nia doesn't want
to go back to work abroad because of the increasingly worrying physical
condition of her third child, Salsa (8). "I give up", Nia complained
when asked if she wanted to return to work abroad or not.
Salsa is known to
have heart disease. Since she was 3 years old, she often looks out of breath when
she breathes, and cannot play like other children because she will feel weak if she
does too much activity.
When an
examination was carried out at (Public Health Center) Puskesmas, Salsa had
spots on her heart. Not receiving intensive care, when she was 5 years old,
Salsa had a high fever, blue mouth and nails, and difficulty breathing.
Initially, when she was examined by a local midwife and was declared
malnourished because her weight was below the average children as usual.
Her father checked
Salsa to the hospital. By taking advantage of the paid BPJS card service every
month.
The doctor stated
that Salsa must be given surgery immediately. However, due to the lack of
complete medical equipment at the hospital, the doctor suggested that she
should be treated intensively at the Jakarta Hospital with adequate equipment.
Due to lack of money,
Nia's husband only took care of Salsa traditionally and gave medicine that must
be consumed for 6 months. But unfortunately, it was not continued after 4
months of taking the drug. Even today's BPJS has not been paid until the
arrears are quite large.
"Thank God, finally I can take my child to Jakarta for treatment assisted by MoSA," said Nia.
In the next action, Handayani Center will coordinate with related parties so that Salsa can still get an education despite her conditions and limitations.