Dr. Fayanne Lim - Internal Medicine, Rheumatology

13/07/2026

01/06/2026

Learn more about medications in lupus

11/05/2026

This Lupus Awareness Month, let’s continue to 💜

Behind every smile is a lupus warrior fighting battles we may not always see.

As rheumatologists, we continue to advocate for awareness, compassionate, and individualized care.

To every lupus warrior — you are seen, heard, and never alone. 💜

From Luneta Park and Davao City!

28/04/2026

Sa darating na May 9, Saturday, 8AM to 12NN, inaanyayahan namin ang lahat ng Pilipinong may Lupus, ang inyong mga pamilya at kaibigan, at lahat ng Pilipinong nais makilahok, sa Kaunaunahang Filipino Lupus Patients' Summit.

Ito ay gaganapin online, via Zoom, at mapapanood din ito ng live sa LUISA - Lupus Inspired Advocacy.

Kabilang sa mga speaker ay mga kilalang Rheumatologists at ibang espesyalista na dalubhasa sa pag-aalaga ng Lupus. Ito rin ay inorganisa upang malaman kung ano-ano ang ginagawa ng ating mga doktor, ng pamahalaan at ng mga nagsusulong para sa kapakanan ng kalusugan ng mga Pilipinong may Lupus.

Para magregister, pumunta lamang sa bit.ly/FilipinoLupusPatientSummit o i-scan ang QR code na nasa poster.

Kung kayo ay may katanungan, mag-email lamang sa [email protected] o magmessage sa page.

Ang aming taos-pusong pasasalamat sa mga katuwang upang maganap ang Summit:
- AstraZeneca Philippines, Inc (silver sponsor)
- Medinfinity Inc (in-kind sponsor)
- IPCA Philippines (in-kind sponsor)

Ang 1st Filipino Lupus Patients Summit ay nabuo sa pagsasasama-sama ng mga sumusunod na grupo:
- Lupus Inspired Advocacy of Rheumatology Educational Trust Foundation, Inc.
- Kidney Alliance Philippines Inc.
- Live, Love and Hope Lupus Support Group
- Mariposa Lupus Support Group
- Hope for Lupus Foundation

27/02/2026

Rare Disease Day is celebrated annually every February 28 (or February 29 during leap year). Rare Disease is defined as disease affecting less than 1 in 2000 people. In the Philippines, we celebrate National Rare Disease Week every last week of February through Presidential Proclamation No. 1989.

In Rheumatology, we deal with different rare diseases such as Scleroderma, Idiopathic Inflammatory Myopathies, Primary Systemic Vasculitis, Juvenile Idiopathic Arthritis, Juvenile Systemic Sclerosis, Still's Disease, Behcet Disease, and other rare rheumatic diseases. 2026

26/02/2026

Sharing our updated schedule and hospital affiliations ☺️

✔️ Internal Medicine / Adult Diseases
✔️ Arthritis, joint pain, and muscle pain
✔️ Rheumatologic and autoimmune diseases (e.g., lupus, rheumatoid arthritis)

20/02/2026

🗣🗣🗣

We are all connected to someone who lives with a rare disease – whether a family member, friend, neighbour or coworker. Yet, for too long, rare diseases have been overlooked in global health policies, leaving over 300 million people worldwide without adequate support, diagnosis, or treatment.  
  
That’s why the World Health Assembly (WHA) Resolution on Rare Diseases was so critical. By recognizing rare diseases as a global health priority, the paves the way for stronger healthcare systems, increased research, and better access to life-saving treatments. It is a call for equity—ensuring that no one is left behind simply because their condition is considered rare.  
  
But the Resolution is just the beginning. Help support the rare disease community by urging policymakers, healthcare leaders, and global institutions to commit to tangible actions that improve the lives of those affected by a rare disease. Together, we can drive change and create a future where people with rare diseases receive the care and recognition they need and deserve. 
  
Because rare diseases affect all of us.
Join us in making sure that HealthforAll leaves no one behind.

11/02/2026

👂👂👂

Let's Mung-GO to the Philippines this coming APLAR Midterm! Check out the APLAR-AYR IG page as well. (https://www.instagram.com/aplar_ayr/)