AZ Butterfly Warriors

AZ Butterfly Warriors Ultimately improving quality of life for those affected. Butterfly Warriors is a Lupus Advocacy, Awareness & Education Page. There is NO CURE.

(480) 572-0088

Dedicated to creating a meaningful impact, Butterfly Warriors works to raise awareness, advocate for, support, and empower individuals and families battling lupus. Lupus is a chronic, autoimmune disease where your immune system attacks healthy cells, tissues. It can effects any part of the body (your joints, skin and organs causing inflammation and damage. Lupus is painful, debilit

ating and destructive and can be fatal. As a lupus ambassador and patient myself I know firsthand the impact this disease can have on the lives of not only the people living with lupus but also on the family members who are helping care for them. I AM NOT A DOCTOR/HEALTHCARE PROFESSIONAL. All content on this page is provided for informational and educational purposes only. It is not intended as medical advice. Always consult a qualified healthcare professional regarding any medical condition or treatment.

May is Lupus Awareness Month Taking Plaquenil/Hydroxychloroquine?👁👁👀👁👁👀👁👁👀👁👁👀👁👁👀Protect your vision. Lupus can affect ma...
05/28/2026

May is Lupus Awareness Month

Taking Plaquenil/Hydroxychloroquine?
👁👁👀👁👁👀👁👁👀👁👁👀👁👁👀
Protect your vision. Lupus can affect many parts of the body. This includes your eyes. People with lupus may develop symptoms that affect your vision.

Lupus Awareness is more than just the month of May. We want to continue to educate, empower, and mobilize communities ar...
05/27/2026

Lupus Awareness is more than just the month of May. We want to continue to educate, empower, and mobilize communities around lupus awareness all year long — not just during Lupus Awareness Month in May.

Lupus already affects every person differently, but research shows Black women are disproportionately impacted — both in...
05/26/2026

Lupus already affects every person differently, but research shows Black women are disproportionately impacted — both in how often lupus occurs and in how severe it can become.


No two lupus journeys are the same. Race, culture, and our lived experiences deeply shape how we access healthcare, spe...
05/26/2026

No two lupus journeys are the same. Race, culture, and our lived experiences deeply shape how we access healthcare, speak up for our needs, and thrive.
💜🦋🐺

PLEASE SHARE Lupus is a massive global health challenge with an estimated 5 million people affected worldwide. Here's ...
05/25/2026

PLEASE SHARE
Lupus is a massive global health challenge with an estimated 5 million people affected worldwide.
Here's a global lupus resources directory organized by country and region, including major lupus foundations, advocacy organizations, and support websites from around the world.

Research Creates HopeEvery breakthrough starts with research. Research is essential to improving treatments, understandi...
05/24/2026

Research Creates Hope
Every breakthrough starts with research. Research is essential to improving treatments, understanding lupus, and finding a cure.

You Don't Have To Fight Alone Living with lupus can feel isolating. Lupus impacts physical, emotional, and mental health...
05/23/2026

You Don't Have To Fight Alone
Living with lupus can feel isolating.
Lupus impacts physical, emotional, and mental health. Support systems are essential. If you or someone you love is struggling with adjusting to living with lupus check out the websites below.

NAMI (National Alliance on Mental Illness) https://www.nami.org

Lupus Foundation Support Groups https://www.lupus.org/resources/support-groups

Mental Health America https://mhanational.org

Psychology Today Therapist Finder https://www.psychologytoday.com

Your skin is your body's largest organ and its first line of defense against infection. Your mouth is the front door to ...
05/22/2026

Your skin is your body's largest organ and its first line of defense against infection. Your mouth is the front door to your entire body. When you protect your body from outside germs, you minimize immune stress and lower your risk of painful flares.

Living with lupus is an unpredictable, daily battle. But no warrior fights this disease entirely alone. Today, we want t...
05/21/2026

Living with lupus is an unpredictable, daily battle. But no warrior fights this disease entirely alone. Today, we want to honor the incredible caregivers who stand by us through every flare-up, appointment, and tough mental health day.

Caregivers are the quiet backbone of the lupus community. They manage medication schedules, coordinate with doctors, and handle the invisible burdens so we can focus on healing. Most importantly, they offer a safe space when the physical and emotional exhaustion peaks.

To every lupus caregiver out there: Thank you for your strength, your patience, and your endless love. Please remember to take care of yourselves, too. You matter just as much as the warrior you support. Tag a fierce caregiver in the comments to show them some love today!💜


Men with lupus face unique challenges related to their health and well-being. They may encounter misconceptions that lup...
05/20/2026

Men with lupus face unique challenges related to their health and well-being. They may encounter misconceptions that lupus is primarily a women’s disease so advocating for their health, finding knowledgeable healthcare providers, and managing their medications effectively is vital. Each person’s experience with lupus is unique, and these challenges can vary. If you’re a man with lupus, consider joining a support group to connect with others who understand your journey. Check out were my fellow warriors Dion Langley and Emmitt Henderson III address living with lupus from a male perspective.

Shout out to my newest followers! Excited to have you onboard! Deidra Perez-Scruggs, Filiti Lomaloma, Cynthia Rodriguez,...
05/20/2026

Shout out to my newest followers! Excited to have you onboard! Deidra Perez-Scruggs, Filiti Lomaloma, Cynthia Rodriguez, Louna Louna, Jess Wright, Terrie Barrows Crawford, Jenny Vaccarello, Emmanuel Ferreira, Mya Lynn Slayden, Ranata Henry, Laura Woodson

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Gilbert, AZ

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http://www.lupus.org/, https://worldlupusfederation.org/

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