About - Lupus Lyfe

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Hi, Im Britt!

Welcome to my lupus blog! I am a lupus warrior who is on a mission to spread awareness and inspiration to those living with lupus.

I currently work as a graphic designer and digital marketer for an advertising agency by day and am a passionate blogger by night. I recently became a contributor on The Mighty, where I hope to spread even more awareness and hope to those living with an autoimmune disease.

My Story

I was diagnosed with lupus in April of 2016 after many years of suffering from various symptoms. I have learned many things over the last few years and look to share my lupus blog life with others!

I am also diagnosed with Trigeminal Neuralgia and Fibromyalgia. In November of 2019, I was recently diagnosed with Stage 1 Clear Cell Renal Cell Carcinoma and proud to say that I am cancer free at this time!

I am a wife- serious kudos to my husband for somehow dealing with me for almost 14 years 🙂 and I am the mom of two wonderful boys.

I love exploring new places and new food! I am a serious coffee addict and have a newfound love for life.

You can read more about my lupus life here:

Join me on this lupus adventure and welcome to my Lupus Lyfe!

Lupus Advocacy:

I have proudly served as an Admin since 2018 for what I personally believe is the best lupus support group on Facebook.
Lupus Warriors SLE Support Group was founded by inspirational lupus warrior and advocate Venissa Pillay. She is an amazing woman who works incredibly hard to provide a safe and informational lupus support group. With over 25k members worldwide, if you are looking for a legit support group for lupus, join her group! I would love to see you there!
As of 2019, I am a Lupus Patient Leader for WEGO Health.