It has been an uphill, hard, tolling, exhausting and difficult battle, but I continue to fight. I promised myself when I was diagnosed in 2023 that I will not allow this illness to take my strength or define who I am. 
 

I was fortunate to meet Mikaela, someone who understands the daily battle, the indescribable symptoms and constant doctors appointments and hospitalizations. We decided to join forces and battle it together. 

It is now that time again to walk with us in this fight. Rather virtually or in-person, we welcome, appreciate and embrace the support and love you all continue to shower us with. Please help us to continue to fund research for our treatments to manage, tackle and be the FLYEST LUPUS WARRIORS WALKING!