Anna Regina Banatin MD / Rheumatology

10/05/2026

Calamba Medical Center is marking with a striking purple lights display — A symbol of hope for our Lupus Warriors.

08/05/2026

Day 2
Come Join Us

07/05/2026

See You at CMC Tower

23/04/2026

with Us at Calamba Medical Center

14/04/2026

World Lupus Day Online Summit
This May 9 , let’s unite virtually to raise awareness, share knowledge, and support those living with lupus.

✨ Tune in and be part of the event
📅 Date: May 9
🕒 Time: 8 am -12 nn
📍 Online – watch from anywhere

Don’t miss this chance to learn, connect, and make a difference!

👉 Save the date and join us live!

01/01/2026

Happy New Year

13/11/2025

Get on your Feet 💜

We’re getting ready for the Lupus Fun Walk — a day of fun, inspiration, and spirit!

Lace up and walk, laugh, and shine with others who share your journey.

The FUN begins at 530 am🧡

🎶 Music • Fun 😄 • 🧃 Refreshments • 💜 love and Support

20/07/2025

hey Lupies! Come Join Us in A Celebration!
RSVP please❤️

10/05/2025

https://www.facebook.com/share/p/1EGeYzoNnK/?mibextid=wwXIfr

# is a lifetime autoimmune disease where in the immune system fights back against the body's normal and healthy cells. It can affect different parts of the body, including the skin, bones, heart, lungs, kidneys, blood and brain.

Though there is no known cure at the moment, doctors, particularly rheumatologists, can manage the symptoms with the use of immunosuppresants like steroids. But since steroids can bring a whole plethora of side effects, doctors try to bring the dose to the lowest possible. Other medications are used to spare the patient from taking high dose of steroids, such as hydroxycloroquine.

Due to it's unpredictability, no two lupus journey are the same. But through seeing the doctor regularly, complying with medications, avoiding sun exposure, managing stress better, and living a healthy lifestyle, people with lupus may and can achieve low disease activity and remission.

We urge all who are living with lupus, their families, friends, and doctors to strive hard to make the government recognize the unmet needs in lupus healthcare, and push forward reforms for better lupus policy and care.

Learn about SLE patient charter: https://worldlupusfederation.org/a-charter-to-improve-care-for-sle-systemic-lupus-erythematosus/

10/05/2025

https://www.facebook.com/share/p/16JBdZ5uLq/?mibextid=wwXIfr

Happy World Lupus Day!
As we celebrate the strength, courage, and voice of every Lupus warrior. You are seen. You are heard. You are not alone.

Let’s keep the conversation going, because awareness doesn’t stop after one day.

KICKOFF EPISODE OF THE SKIN IMMUNE WELLNESS SERIES!

📍 WORLD LUPUS DAY SPECIAL
🗓️ May 17 (Saturday)
🕢 7:30 PM
📡 LIVE ONLINE

Beyond the Flare: Living and Thriving with Lupus

Tired of medical talk you can’t relate to? This one’s different.

Join us as we talk about the real deal of living with lupus—straight from someone who’s been through it, and a doctor who is an expert on it.
With:
👨‍⚕️ Dr. Evan Glenn Vista – Rheumatologist & top lupus expert
👩‍🦱 Robelle Tanangonan – Lupus warrior & patient advocate

✔ Real stories
✔ Real tips
✔ Real hope

📲 Watch it live:
FB: Psoriasis Philippines
FB: Wellness Weekends Philippines
YT: PsorPhil Channel

This is your sign to tune in. First episode pa lang, solid na.

23/03/2025

Got Gout?

ctto: GoutEdicationSociety