Latar Belakang PDK Selayang

SEJARAH PENUBUHAN:

PDK Selayang (Pusat Pemulihan Dalam Komuniti Selayang) telah ditubuhkan pada 1hb Sept 1991, oleh sekumpulan ibubapa kepada kanak-kanak kurang upaya (pada masa tersebut dipanggil sebagai kanak-kanak istimewa) yang mana anak-anak mereka telah dinafikan hak untuk menerima pembelajaran wajib dari aliran perdana sekolah.

Pada 29 Oktober 2017, Pertubuhan Pemulihan Dalam Komuniti Selayang (Pertubuhan PDK Selayang) telah didaftarkan sebagai sebuah Badan Bukan Kerajaan (Non-Gorvermental Asoociation-NGO) dengan Pendaftar Pertubuhan Malaysia Cawangan Selangor.

Bermula dengan 15 orang kanak-kanak kurang upaya kelas diadakan sekali seminggu pada setiap hari Sabtu dari jam 8:30 pagi hingga 1:00 tengahari, dengan dilatih oleh seorang Petugas PDK (panggilan Cikgu PDK pada masa tersebut) iaitu Puan Noraini Othman.

Hari ini PDK Selayang telah berkembang pesat dengan jumlah pelatih OKU PDK seramai 84 orang melalui beberapa program iaitu Kelas Harian EIP, Kelas Harian LPV, Kelas Harian Pemulihan Perubatan (Pemulihan Anggota, Pemulihan Pertuturan dan Pemulihan Carakerja), Lawatan ke Rumah dan Program Rumah Kelompok (lelaki).

Kumpulan Sasar Utama:
OKU (Orang Kurang Upaya)

Kumpulan Sasar Tambahan:
Anak-Anak Yatim, Kanak-Kanak Kurang Bernasib Baik, Ibu Tunggal/Ibu Tinggal, Warga Emas dan Keluarga Miskin (dari lingkungan kumpulan sasar utama)

Kelas Harian EIP:
5 hari/minggu; Isnin-Jumaat; 8:30am-12:30pm.

Kelas Harian LPV (Latihan Pemulihan Vokasional):
5 hari/minggu; Isnin-Jumaat; 9:00am- 4:00pm.

Kelas harian Pemulihan Perubatan pula dijalankan seperti berikut:

Pemulihan Anggota:
3 hari/minggu; Isnin, Rabu danJumaat; 8:30-11:30am; untuk OKU dari keluarga miskin dan berpendapatan rendah.

Sabtu & Ahad pula dikhaskan kepada OKU yang keluarganya mampu bayar penuh kos pakar (OKU dari keluarga kaya).

Pemulihan Pertuturan:
2 hari/minggu, Rabu dan Jumaat 8:30am- 12:00pm; untuk OKU dari keluarga berpendapan rendah dan miskin dan hari 2 hari dalam seminggu dikhaskan untuk OKU dari keluarga kaya yang mampu membayar kos pakar.

Pemulihan Carakerja:
3 hari/minggu; Isnin, Rabu dan Jumaat; 8:30-11:30am; untuk pelatih kanak-kanak; 2:30-4:00pm untuk pelatih remaja PDK.

Program Lawatan ke Rumah:
2 kali/minggu; Selasa (2:00-4:00 petang) dan Sabtu (9:30am-12:30pm). Berdasarkan keperluan dan persetujuan dari ibubapa/penjaga untuk kehadiran Petugas PDK di kediaman mereka.

Program Rumah Kelompok (Lelaki):
Menempatkan seramai 4 OKU yang telah bekerja. (telah ditamatkan pada Januari 2015)

Pengurusan:
PDK Selayang yang ditadbir-urus oleh Jawatankuasa Pertubuhan Pemulihan Dalam Komuniti Selayang yang mana barisan Jawatankuasa terdiri dari ibubapa/penjaga OKU, Masyarakat Tempatan dan seorang OKU

Kakitangan:
Seramai 12 kakitangan berkhidmat di PDK Selayang yang diketuai oleh Penyelia PDK iaitu Puan Noraini Othman, (sila lihat
side menu).


Sunday, February 13, 2011

New technology to detect Alzheimer’s disease developed by US scientists

WASHINGTON: University of Texas Southwestern Medical Center scientists have helped develop a novel technology to diagnose Alzheimer's disease from blood samples long before symptoms appear, Xinhua news agency quoted the centre as saying in a press release.

This preliminary technology, which uses synthetic molecules to seek out and identify disease-specific antibodies, also could be used eventually in the development of specific biomarkers for a range of other hard-to-diagnose diseases and conditions, including Parkinson's disease and immune system-related diseases like multiple sclerosis and lupus, the researchers predict.

"One of the great challenges in treating patients with Alzheimer's disease is that once symptoms appear, it's too late. You can't un-ring the bell," said Dr. Dwight German, professor of psychiatry and an author of the paper that has been published in journal Cell.

"If we can find a way to detect the disease in its earliest stages before cognitive impairment begins we might be able to stop it in its tracks by developing new treatment strategies."

Because patients with Alzheimer's disease (AD) exhibit immune system activation and neurodegeneration in several brain regions, researchers in the study hypothesized that there may be numerous antibodies in the serum of affected patients that are specific to the disease and can serve as a biomarker.

Antigens substances such as protein from a virus or bacteria that triggers an immune response traditionally have been necessary for the discovery of antibody biomarkers.

It has been impossible previously to identify an antibody (a type of targeted immune molecule) without first knowing the antigen that triggers its production.

The new study, however, challenges conventional wisdom and uses synthetic molecules (peptoids) rather than antigens to successfully detect signs of disease in patients' blood samples.

These peptoids have many advantages; they can be modified easily and can be produced quickly in relatively large amounts at lower cost.

The adaptive immune system is thought to be a rich source of protein biomarkers, but diagnostically useful antibodies remain undiscovered for a large number of diseases, Dr. German said.

This is, in part, because the antigens that trigger an immune response in many diseases are unknown.

The technology behind this discovery is essentially an immune-system reader, which is designed to pick out antibodies without knowing in advance which ones to look for.

The researchers used a combination library of several thousand peptoids to screen serum samples from mice with multiple sclerosis- like symptoms as well as from healthy control mice.

The particular peptoids that retained more antibodies from the blood samples of the diseased animals were identified as potential agents for capturing diagnostically useful molecules.

The investigators then examined serum samples from six AD patients, six healthy patients and six patients with Parkinson's.

Three peptoids were identified that captured six times the IgG antibody levels in all of the Alzheimer's patients when compared to the control group or to the Parkinson's patients.

Two of the peptoids were found to bind the same IgG antibody, while the third was shown to bind to different antibodies meaning there are at least two candidate biomarkers for AD.

Using an additional set of 16 normal control subjects and 10 subjects at the very early state of AD, the three candidate biomarkers identified AD with 90 percent accuracy.

"The results of this study, though preliminary, show great potential for becoming a landmark," said Dr. German.

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