I was diagnosed with lupus in July of 2020. My journey with lupus and autoimmune actually began in 2018, after my recovery from a rare hip surgery called Periacetabular Osteotomy. After I graduated college and began my career, my symptoms quickly progressed. After numerous tests, doctor appointments and many unanswered questions, I received the news that I had lupus.

My journey with lupus has been challenging to cope with both mentally and physically. I have struggled with accepting the necessary lifestyle changes that those with lupus are forced to make. I have felt isolated, scared and concerned for my future. As an active and ambitious person, I have to remind myself to put my health first. Despite my difficult journey, I have learned about the power of positive thoughts and the impact that positivity can have on both my mental and physical health. Although I have days that I struggle, as most people with lupus do, I remind myself of my strength and ability to persevere. Lupus has taught me how to appreciate and focus on the good, rather than the bad. With the help of my amazing support system, including my dog Gracie (who never leaves my side)I can get through the most difficult days.

After receiving my lupus diagnosis, I began researching and came across the Lupus Foundation of America. Ever since, LFA has provided information and resources that have helped me navigate through this difficult time. I participated in my first Walk to End Lupus Now with my family and of course, Gracie, last year. I was so happy to be a part of this amazing cause and even though it was virtual, I still felt connected and supported.

The Walk has enabled me to connect with the lupus community and for that, I am very grateful. The Walk is empowering and gives me the encouragement I need to push through the bad days. I am looking forward to participating in the Walk to End Lupus Now again this year, surrounded by my family and friends.