Psoriasis Association Of Malaysia

23/03/2026

Fear of judgment turns moments of joy into moments of avoidance.
No one should feel unwelcome because of a health condition.

It’s time to replace stigma with empathy, understanding, and support—especially during moments meant for togetherness.

21/03/2026

Semoga Hari Raya ini membawa kebahagiaan, ketenangan, dan keberkatan buat anda serta keluarga tercinta. Didoakan juga agar rezeki kita semua terus dimurahkan, dipermudahkan dalam setiap urusan, dan sentiasa dilimpahi kejayaan.

Selamat Hari Raya! Maaf Zahir dan Batin 🕌💜

12/03/2026

The Psoriasis Association Of Malaysia continues to explore every possible avenue to engage with the government in advocating for increased budget allocation for psoriasis care and treatment.

In response to the previous article, we have provided a comprehensive explanation of the challenges faced by patients living with psoriasis, including the physical, emotional, and social burdens of the condition. We also highlighted how access to appropriate medication can significantly improve patients’ quality of life, enabling them to live healthier and more productive lives.

Through continued dialogue and advocacy, PAM hopes that greater attention will be given to the needs of psoriasis patients, particularly in ensuring better access to effective treatment and support within the public healthcare system.

The Psoriasis Association of Malaysia says a dedicated biologics programme can help prevent disability, restore productivity, and significantly improve the lives of Malaysians living with severe psoriatic condition.

10/03/2026

Thank you Dr Dr Siti Mastura Muhammad for raising the issue on behalf of Psoriasis Association Of Malaysia at the parliament.

Sometimes the small steps we take can lead to meaningful outcomes when guided by consistency and persistence. In time, and with faith, things will unfold as they are meant to.

MOH spent RM17.35 million on psoriasis biologics in 2025, up 46.7 per cent from 2024, and plans to seek RM29 million more from M*F for six biologic medicines. Biologics are needed for a small group of patients with difficult-to-control disease.

03/03/2026

We are deeply saddened by the passing of our dear friend Eugene. His unwavering dedication and compassion made him one of the pillars of psoriasis advocacy—not only in Malaysia, but across the Asia Pacific region. Eugene’s work touched countless lives, and his spirit will continue to inspire us.

Our heartfelt condolences go out to his family and to the Psoriasis Association Of Malaysia. May his memory be a source of comfort and strength.

03/03/2026

Dear Loved Members,

We are deeply saddened by the passing of our beloved Past President, Eugene Cross.

For 36 remarkable years, Eugene devoted himself wholeheartedly to serving the psoriatic community. His unwavering dedication, selfless leadership, and uplifting spirit inspired many to step forward and serve alongside him. His impact on our community is immeasurable.

Even while facing serious health challenges, Eugene continued to contribute tirelessly, demonstrating extraordinary courage and commitment until the very end.

We extend our heartfelt condolences to his family and loved ones during this difficult time. His legacy will live on in the community he helped build and the many lives he touched.

Funeral details will be shared once confirmed.

May he rest in peace.

With love greetings,
Psoriasis Association of Malaysia

22/02/2026

Rare Disease Day – February 28

Over 300 million people worldwide live with a rare disease — that’s about 1 in 25 people.

Many know the most common form of psoriasis — plaque psoriasis or psoriasis vulgaris, which causes itchy, flaky patches. But psoriatic disease is a spectrum, with several lesser-known forms.

About 3% of people with psoriasis develop pustular psoriasis, including:
🔸Generalized pustular psoriasis (GPP) – a life-threatening condition where the skin becomes intensely red, painful, and can peel in large areas.
🔸Palmoplantar pustulosis (PPP) – painful inflammation on the hand palms and feet soles.
🔸Acrodermatitis continua of Hallopeau (ACH) – affecting fingers, toes, and nails.

Other rare, serious forms include:
🔸Erythrodermic psoriasis, characterized by fiery red skin across the body, increased heart rate, severe itching, and temperature changes.
🔸Arthritis mutilans – a severe, deforming form of psoriatic arthritis.

This Rare Disease Day, we stand with everyone living across the psoriatic disease spectrum, along with their families, friends, and caregivers.

💜 Join us in raising awareness for every form of psoriatic disease.

👉 Read more here:
https://eu1.hubs.ly/H0rZJRT0

09/02/2026

The Psoriasis Association of Malaysia (PAM) is truly happy and deeply thrilled to be part of a meaningful milestone — the signing of a Memorandum of Understanding (MOU) with the Ministry of Health (MOH). 💜

We were honoured to witness the newly appointed Director-General of Health, YBhg Datuk Dr Mahathar, officiating and signing the MOU alongside fellow Non-Communicable Disease (NCD) organisations. Alhamdulillah, this formal partnership brings us great joy and marks an important step forward in strengthening collaboration for the NCD community in Malaysia.

Through this MOU, PAM proudly reaffirms our commitment to advancing holistic psoriatic care, recognising that living with long-term NCDs often involves complex challenges, including comorbidities and psychosocial impact. We are excited to work closely with MOH and our NCD partners to address both physical and mental well-being.

19/01/2026

Walk wit us for a care - Truly thankful to every volunteer who showed up with open hearts and positive vibes for our very first event. Your time, energy, and support made this walk meaningful and memorable. From planning to walking together, you proved how powerful community can be. Small steps, shared smiles, and a cause that brought us together beautifully.

03/01/2026

Reflecting on 2025. Reimagining 2026 💜🧡

31/12/2025

In conjunction with World Psoriasis Day 2025, over 30 Parliamentarians across political divides pledged their personal support for improving psoriatic care during a special awareness exhibition organised by the Psoriasis Association of Malaysia (PAM) — held for the first time at the Parliament Building 🇲🇾

Their handwritten messages on our art canvas symbolised solidarity, empathy, and a shared commitment to patients living with psoriatic disease.

This year’s theme, “Psoriatic Disease & Comorbidities: Understanding the Domino Effect,” reminds us that psoriasis is more than a skin condition — it is a lifelong autoimmune disease linked to serious health complications and social stigma.

Grateful for the meaningful engagement, open dialogue, and growing awareness at the highest level of leadership. Together, we move closer to early diagnosis, holistic care, and better access to treatment for all psoriatic patients.


disease

23/12/2025

# Throwback: PAM is honoured to be invited to attend a discussion with the Director-General of Health, Datuk Dr Mahathar. We represented the community to highlight that pustular psoriasis is a rare disease, alongside psoriatic arthritis, and the importance of inclusion within Malaysia’s rare disease framework.

This meeting marked a positive step forward, with MOH acknowledging the role of patient-led coalitions and strengthening coordination towards translating the National Rare Disease Policy into action. United voices, patient-centred advocacy, and meaningful collaboration remain key as we move ahead.