Hope for Lupus – Foundation

Lupus

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Building A World

Without

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Our Story

Lupus affects over 5 million people worldwide, yet so little is known about the condition that it baffles medical professionals until today. This lack of awareness leads to countless misdiagnoses and deaths – deaths that could have been prevented had more people been armed with the correct information.

The Hope for Lupus Foundation seeks to change all that. It envisions a world without lupus and aims to shed light on the disease to help people win the fight against lupus.

ABOUT US

What is LUPUS?

Lupus is more common in young women, and the first symptoms are usually felt in their 20s to 30s.

Find out now

Our Projects

HFL produces exhibits, seminars, publications, and several activities that are mostly free of charge.

Donate NOW

Your donation goes to indigent lupus patients who are in need of medical assistance.

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Our Instagram

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Our Publications

“Living Better with Lupus” is a self-help book written by Rep. Em Aglipay-Villar, Dr. Angeline Magbitang-Santiago, Dr. Evelyn Osio-Salido, and Dr. Geraldine Zamora. The book is now available in all National Bookstore and Fully Booked outlets!

PERSONAL EXPERIENCE

Lupus Story

Many people call it “the disease with a thousand faces.” Contrary to what others think, lupus is not rare; but the condition can be different from person to person. Its manifestations and symptoms...

This isn’t the first time I’m talking about what it’s like to live with an illness. I’ve spoken about it as a speaker in talks to getting interviewed. I’ve even talked about it with someone...

No human is perfect. We all have strengths that we are proud of and weaknesses that we try to hide. But instead of hiding our weakness, what if we embrace it? Using your own weakness...

In 2010, I was diagnosed with Systemic Lupus Erythematosus and life was never the same. When I entered UP I thought I could adjust to the stress and handle a minimum workload of 15 units...

Hi, my name is Cecille Luna 34 years of age. My battle with lupus started 13 years ago. To be exact, i was diagnosed with SLE in 2004 and eventually develop to Nephritis Lupus in 2006...

It was summer of 2006 when I started to feel something was wrong. I began losing my hair for no apparent reason. I had rashes all over my face and arms. I had pain all over my body...

I knew myself very well then, but right after I learned that I had “LUPUS”, Things changed as though they will never be the same again, never again...

Six years ago, I was diagnosed with Systemic Lupus Erythematosus: a chronic, autoimmune disease wherein the immune system mistakenly attacks the body’s tissues and organs...

When my mom was diagnosed with Lupus in 2000, she never obliged us to take care of her or accompany on her checkups and activities because we were so young then. I never really understood...