Persatuan SLE Malaysia HQ

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Persatuan SLE Malaysia HQ Persatuan SLE Malaysia was formed in 1994 to provide support for people living with Systemic Lupus Erythematosus (SLE), an autoimmune disorder.

Apply to be a member at https://forms.gle/6H75FqcR89oYcEGh7. Systemic Lupus Erythematosus (SLE), or Lupus for short, is an auto-immune disorder where the body makes antibodies that attack the person’s own tissues. Persatuan SLE Malaysia (PSLEM) or the Malaysian SLE Association helps to empower people with SLE to live a full and meaningful life despite having a chronic disease. PSLEM is registered with the Registry of Societies Malaysia to provide social and psychological support and financial assistance to SLE patients. Our Secretariat is based in Petaling Jaya, Selangor, while six Chapters (support groups) have been initiated in the States of Penang, Kedah, Johor, Terengganu, Sabah and Sarawak. SLE patients who wish to be members of Persatuan SLE Malaysia can register here https://bit.ly/3nWpIHz Membership is free for SLE patients while non-patients pay RM50.00 for life membership. For non-patients please register here http://bitly.ws/vRLx

Kekal aktif walaupun hidup dengan lupus boleh menjadi cabaran! 💜 Cuba senaman berimpak rendah dan lakukan dengan perlaha...
18/08/2026

Kekal aktif walaupun hidup dengan lupus boleh menjadi cabaran! 💜 Cuba senaman berimpak rendah dan lakukan dengan perlahan dan konsisten untuk meningkatkan kekuatan otot dan fleksibiliti, sambil menjaga sendi daripada cedera. 🧘‍♀️✨ Berbincanglah dengan pakar reumatologi anda untuk maklumat lanjut!

Staying active with lupus can be challenging, but it’s possible! 💜 Try low-impact exercises, and perform them slowly and consistently to boost muscle strength and flexibility while protecting your joints. 🧘‍♀️✨Speak to your rheumatologist to know more!

Learn more at https://unlockinglupus.my/.

Lupus causes tissue damage and illness by attacking the individual's own tissues. It has been suggested that we visit a doctor if we have symptoms of lupus.

Esok di TV3 MHI!
17/08/2026

Esok di TV3 MHI!

rLiving with lupus nephritis can feel isolating, but stories from public figures like Selena Gomez, Nick Cannon, and Mau...
11/08/2026

rLiving with lupus nephritis can feel isolating, but stories from public figures like Selena Gomez, Nick Cannon, and Maurissa Tancharoen Whedon remind us that no one walks this journey alone. 💜

Their experiences highlight the importance of awareness, support, treatment, and learning how to care for ourselves through each stage of lupus.

Read more at: https://www.mylupusteam.com/resources/celebrities-with-lupus-nephritis-and-how-they-cope-with-symptoms?utm_source=iterable&utm_medium=email&utm_campaign=lupus_roc&mht_token=BAhJIhZwc2xlbWhxQGdtYWlsLmNvbQY6BkVU--092e71beebd6b7970511350eb2756f46660f3da9984a46cd3676f95377c241af

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Living with systemic lupus erythematosus (SLE) can feel isolating. If lupus has caused kidney damage and you’ve been diagnosed with lupus nephritis, you mi

It's starting this week! ✨ If you haven't yet, do join our safe space on the internet for patients to connect, share exp...
10/08/2026

It's starting this week! ✨

If you haven't yet, do join our safe space on the internet for patients to connect, share experiences, and receive emotional support from other Lupus Warriors. 🫂

Bermula pada hari Isnin ✨

Mari sertai safe space kami di mana pesakit SLE boleh berhubung, berkongsi pengalaman, dan menerima sokongan emosi daripada Pejuang Lupus yang lain. 🫂

🗓️ Date: 10 - 13 August 2026
🕒 Time: 8.30pm - 9.30pm
📍 Platform: via Zoom

Click the link to register 👉🏼 https://forms.gle/7G2SZqwmP1KqWHig8

Untuk Borang BM, klik pautan untuk mendaftar 👉🏼 https://forms.gle/RNauAdsg59cdjArB8

Let's support each other and find strength together. We look forward to seeing you there!

Mari kita saling menyokong dan mencari kekuatan bersama. Kami berharap dapat berjumpa anda di sana!

Hi everyone! 👋🏼 Our monthly “Share & Care” is back!

🗓️ Date: 10 - 13 August 2026
🕒 Time: 8.30pm - 9.30pm
📍 Platform: via Zoom

Click the link to register 👉🏼 https://forms.gle/7G2SZqwmP1KqWHig8

Untuk Borang BM, klik pautan untuk mendaftar 👉🏼 https://forms.gle/RNauAdsg59cdjArB8

Come join our Online “Share & Care” Session ✨ This is a great opportunity to connect with fellow lupus warriors, share experiences, and receive support in a compassionate and understanding environment 🫂Feel free to register for your preferred language and time slot.

Let's support each other and find strength together. We look forward to seeing you there! ✨

Sesi sokongan ini adalah di mana anda dapat berhubung dengan pejuang lupus yang lain, berkongsi pengalaman, dan menerima sokongan dalam persekitaran yang penuh belas kasihan dan pemahaman 🫂

Mari kita saling menyokong dan mencari kekuatan bersama-sama. Jumpa anda di sana! ✨

Help advance lupus research.Researchers are studying an investigational medicine for lupus. Adults with moderate to seve...
06/08/2026

Help advance lupus research.

Researchers are studying an investigational medicine for lupus. Adults with moderate to severe lupus may be eligible to join.

Your participation could help researchers better understand lupus and future treatment options.

Visit the link below if you are interested in partaking in our clinical trial! https://www.facts.clinicalresearch.my/condition/joints

Hi everyone! 👋🏼 Our monthly “Share & Care” is back! 🗓️ Date: 10 - 13 August 2026🕒 Time: 8.30pm - 9.30pm 📍 Platform: via ...
01/08/2026

Hi everyone! 👋🏼 Our monthly “Share & Care” is back!

🗓️ Date: 10 - 13 August 2026
🕒 Time: 8.30pm - 9.30pm
📍 Platform: via Zoom

Click the link to register 👉🏼 https://forms.gle/7G2SZqwmP1KqWHig8

Untuk Borang BM, klik pautan untuk mendaftar 👉🏼 https://forms.gle/RNauAdsg59cdjArB8

Come join our Online “Share & Care” Session ✨ This is a great opportunity to connect with fellow lupus warriors, share experiences, and receive support in a compassionate and understanding environment 🫂Feel free to register for your preferred language and time slot.

Let's support each other and find strength together. We look forward to seeing you there! ✨

Sesi sokongan ini adalah di mana anda dapat berhubung dengan pejuang lupus yang lain, berkongsi pengalaman, dan menerima sokongan dalam persekitaran yang penuh belas kasihan dan pemahaman 🫂

Mari kita saling menyokong dan mencari kekuatan bersama-sama. Jumpa anda di sana! ✨

We are pleased to share that donations made to PSLEM are now tax-exempt. 💜Your contribution not only supports lupus awar...
28/07/2026

We are pleased to share that donations made to PSLEM are now tax-exempt. 💜

Your contribution not only supports lupus awareness, patient education, and community support efforts, but may also qualify for tax exemption in accordance with LHDN guidelines.

👉🏼 Click here to donate: https://www.lupusmalaysia.org/support-donate

Thank you for continuing to stand with the lupus community in Malaysia.

Persatuan SLE Malaysia sets up educational booth @ Making Lupus Visible at Hospital Putrajaya. The event  featured publi...
23/07/2026

Persatuan SLE Malaysia sets up educational booth @ Making Lupus Visible at Hospital Putrajaya. The event featured public talks on SLE, patient journey sharings and an exercise session in conjunction with World Lupus Day 2026.


Keradangan lupus dan kerosakan salur darah boleh mempercepatkan risiko jantung. Oleh itu, pesakit lupus mempunyai risiko...
21/07/2026

Keradangan lupus dan kerosakan salur darah boleh mempercepatkan risiko jantung. Oleh itu, pesakit lupus mempunyai risiko serangan sakit jantung yang lebih tinggi pada usia muda.🫀 Berbincanglah dengan pakar reumatologi anda untuk maklumat lanjut!

Lupus-related inflammation and damage to blood vessels can speed up heart risks. Therefore, people with lupus have a higher risk of heart attack at a younger age.🫀Speak to your rheumatologist to know more!

Learn more at https://unlockinglupus.my/.

Lupus fatigue is real, and it can affect work, family, movement, and daily life. 💜 Olympic soccer champion Shannon Boxx ...
14/07/2026

Lupus fatigue is real, and it can affect work, family, movement, and daily life. 💜 Olympic soccer champion Shannon Boxx shares a gentle reminder for those living with lupus: focus on what you can control, build your support system, and give yourself grace on the harder days.

Read more at: https://www.mylupusteam.com/resources/fighting-lupus-fatigue-tips-from-soccer-pro-shannon-boxx?utm_source=iterable&utm_medium=email&utm_campaign=lupus_roc&mht_token=BAhJIhZwc2xlbWhxQGdtYWlsLmNvbQY6BkVU--092e71beebd6b7970511350eb2756f46660f3da9984a46cd3676f95377c241af

Shannon Boxx is a three-time Olympic gold medalist and a World Cup champion with the U.S. Women’s National Soccer Team. She was diagnosed with systemic lup

Address

3rd Floor, Bangunan Sultan Salahuddin Abdul Aziz Shah, 16 Jalan Utara
Petaling Jaya
46200

Opening Hours

Monday 09:30 - 17:30
Tuesday 09:30 - 17:30
Wednesday 09:30 - 17:30
Thursday 09:30 - 17:30
Friday 09:30 - 17:30

Telephone

+601110617672

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