Myoku matters

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Selamat bersara Tuan Hj. Khir selepas perkhidmatan cemerlang selama 38 tahun. Kehilangan pasti kami rasa di JPOKU. Semoga Tuan Hj Khir sentiasa bahagia bersama keluarga tercinta. Take care. All the best

Penglibatan Pegawai KPWKM, JKM, JPOKU, AJK & Penyelia PDK Semenyih dalam ASEAN Hometown Improvement through Disability-Inclusive Communities Model mulai 7-9 Mac di Bangkok anjuran ASEAN, APCD dan JAIF.

Mesyuarat JPOKU bersama Malaysian International Dance Organization (MIDO) pada 8 Mac 2019 @ JPOKU. Harap lebih ramai OKU akan menyertai para dance.

Mesyuarat JPOKU bersama Malaysian Invisible Illnesses Association (MIIA) pada 8 Mac 2019 @ JPOKU

Lawatan YAB TPM ke SK Putrajaya Presint 9(2) & Pelancaran Kad OKU baharu mengikut sub kategori pada 7 Mac 2019. Terima kasih semua pihak yang menjayakan program ini.

Mesyuarat JK Penubuhan Independent Living Centre (ILC) pada 6 Mac 2019 @ JPOKU, Aras 6, KPWKM

JPOKU dijemput sebagai panel Sesi Town Hall sempena Bengkel Memperkasa Persatuan Sukan Kebangsaan (Para) anjuran Majlis Paralimpik Malaysia (MPM)

Bengkel Pemurnian Garis Panduan Pendaftaran OKU Bil.1/2019 pada 27 & 28 Feb 2019. Terima kasih kepada semua pakar perubatan KKM, pegawai KPM, pegawai KPWKM, pegawai JKM dan wakil2 NGO yang membantu JPOKU menjayakan bengkel ini.

Rare Disease Day takes place on the last day of February each year. The main objective of Rare Disease Day is to raise awareness amongst the general public and decision-makers about rare diseases and their impact on patients' lives.

The campaign targets primarily the general public and also seeks to raise awareness amongst policy makers, public authorities, industry representatives, researchers, health professionals and anyone who has a genuine interest in rare diseases.

Building awareness of rare diseases is so important because 1 in 20 people will live with a rare disease at some poinRare Disease Dayt in their life. Despite this, there is no cure for the majority of rare diseases and many go undiagnosed. Rare Disease Day improves knowledge amongst the general public of rare diseases while encouraging researchers and decision makers to address the needs of those living with rare diseases.