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Lupus

warriors

United!

Happy Business People, Women Empowerment and Diversity Team, Collaboration and Motivation, Employee Engagement and Support in Startup Office. Laughing Group, Female Friends and Marketing Agency Staff

no one does lupus alone

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Registration opens 9/15 for

Lupus Gala

Event date: November 12,2023

2023

Events

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Registion for Lupus Gala opens 9/15

Event date:November 12, 2023

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who we are

We are a a nonprofit organization, who is dedicated to improving the quality of life of lupus patients by providing financial assistance, promoting awareness, and offering educational programs.

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Our Story

Founder and Executive Director Ashley Diehl was diagnosed with mild lupus at age 24. The early years of living with lupus presented with mild symptoms and little affect to regular life. 10 years later that Ashley's lupus took a nose dive and began to completely disrupt her life. Her rheumatologist diagnosed her with mild-moderate lupus, skin lupus and lupus nephritis as well as alopecia. None of which she had previously dealt with. Debilitating pain, extreme fatigue, miserable rashes, hair loss and inflammation in her kidneys are just a few her new "normal" symptoms. As a way of making lemonade out of lemons, Ashley founded Lupus Warriors United to allow her experiences to help others, to spread awareness and make sure no one does lupus alone.


What is lupus

According to the Lupus Foundation of America:

Lupus is a chronic (long-term) disease that can cause inflammation and pain in any part of your body. It’s an autoimmune disease, which means that your immune system β€” the body system that usually fights infections β€” attacks healthy tissue instead. Lupus most commonly affects your:

  • Skin
  • Joints
  • Internal organs, like your Kidneys and heart

Because lupus affects many parts of the body, it can cause a lot of different symptoms.


Who is affected By lupus?


Anyone can develop lupus.

However, certain people are at higher risk for lupus, including:

  • Women ages 15 to 44
  • Certain racial or ethnic groups β€” including people who are African American, Asian American, Hispanic/Latino, Native American, or Pacific Islander
  • People who have a family member with lupus or another autoimmune disease


9 out of 10

people with lupus are women.

-Lupus Foundation of America


photo credit KWSO 91.9

Awareness

Awareness= validation for lupus warriors and eventually a cure

What we fight for

family/friend support

How to walk along side a loved one with lupus

financial support

Living with lupus is expensive, we want to help

Community

No one does lupus alone

Meet The Team

Ashley Diehl

founder/ executive Director

Brenda Diehl

Relations Director

Gina Parker

Event Specialist

How to get involved

Volunteer Group

Volunteer

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We need YOU! From organizing events to packing swag bags to setting up chairs, if you are willing, we have something for you!

Donate

donate

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from $5-$500 We always appreciate your generosity!

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Attend our formal gala

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Register for Lupus Gala

November 12, 2023

Contact us

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Lupus Warriors United


lupuswarriorsunited@gmail.com


417-294-0710

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