Florida #100Kchallenge Virtual Walk to End Lupus Now

Erin and her 3 sons (Kallen, Dane and Connor)
Erin and her 3 sons (Kallen, Dane and Connor)

Erin's Pack

Welcome to Erin's Pack fundraising team page.

Erin was diagnosed with Lupus at 19 after showing signs and symtpoms for over a decade. Despite her illness, Erin became an ESE Specialist for Broward Schools and had 3 boys, the loves of  her life...Kallen, Dane and Connor. Erin ran out of treatment options, even clinical trials and passed away suddenly at 34 due to heart related lupus complications. Her pack walks in her memory and to make sure no one else loses a loved on to this disease. 

Imagine a day when doctors can say, "There is a cure for lupus". Until that day though, there is work to be done. That's why we are taking action in the fight against lupus. Join us as we participate in the Lupus Foundation of America's Walk to End Lupus Now! in [city] to raise critical funds for the estimated 1.5 million people living with lupus in the United States.

Will you join our team and help us reach our fundraising goal? You’ll be supporting the Foundation's efforts to improve the quality of life for all people affected by lupus. You can also support by making a secure contribution on our walk page. Every single dollar counts!

Did you know?

  • Lupus is a mysterious and misunderstood autoimmune disease. It strikes without warning, affects each person differently, and has no known causes or cure.
  • Lupus symptoms can be severe and highly unpredictable and can damage any organ or tissue, from the skin or joints to the heart or kidneys.
  • While lupus can strike anyone at any time, 90% of people living with lupus are women. Women of color are at especially high risk. 
  • Only one drug has ever been developed and approved by the US Food and Drug Administration specifically to treat the disease.


Together, we can solve the cruel mystery of lupus. Join our team today and support our efforts! 

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