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Home » Archive by Category "Lupus Story"
Lupus Story

“Meet my ‘SuperwoMOM’”

  • May 1, 2025
  • Posted by author-avatar Hope for Lupus
  • 0 comments
26 Aug
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 beca...

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Lupus Story

Lupus Story: Kat Hizon

  • May 1, 2025
  • Posted by author-avatar Hope for Lupus
  • 0 comments
26 Aug
Six years ago, I was diagnosed with Systemic Lupus Erythematosus: a chronic, autoimmune disease wherein the immune system mistakenly at...

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Lupus Story

“A Light in the Midst of Darkness!”

  • May 1, 2025
  • Posted by author-avatar Hope for Lupus
  • 0 comments
26 Aug

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…

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Lupus Story

The Story Of The Lost Girl

  • May 1, 2025
  • Posted by author-avatar Hope for Lupus
  • 0 comments
26 Aug

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…

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Lupus Story

My Lupus Journey

  • May 1, 2025
  • Posted by author-avatar Hope for Lupus
  • 0 comments
26 Aug

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…

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Lupus Story

Lupus Story: Tiffany Uy

  • May 1, 2025
  • Posted by author-avatar Hope for Lupus
  • 0 comments
26 Aug
“Lagi ka na lang naoospital ah.” “Bakit parang lagi ka na lang pilay?” “PWD ka? Ano ba disability mo?” “If you’re so sick, why don’t yo...

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Lupus Story

From Weakness into Strength

  • May 1, 2025
  • Posted by author-avatar Hope for Lupus
  • 0 comments
26 Aug
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,...

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Lupus Story

What It’s Like to Lose Your Hair at 19

  • May 1, 2025
  • Posted by author-avatar Hope for Lupus
  • 0 comments
26 Aug

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…

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