Two years ago, lupus became a part of my story, but it didn't define me. Instead, it ignited a fire within me to fight, to advocate, and to inspire others to do the same.
Receiving a diagnosis of lupus in 2021 was a pivotal moment in my life. The initial shock and uncertainty gave way to a deep-seated determination to take control of my health and my future. I realized that lupus might be a part of my journey, but it wouldn't dictate my destination.
The journey hasn't been easy. There have been days of debilitating fatigue, painful flares, and frustrating setbacks. But with each challenge, I've discovered inner strength, resilience, and a growing community of support.
Lupus has taught me to appreciate life's simple joys: a quiet morning, a beautiful sunset, or a warm conversation with loved ones. It's shown me that every day is precious and that every moment counts.
As I navigate this new reality, I've become passionate about raising awareness and advocating for others affected by lupus. I've connected with fellow warriors who inspire me with their courage, humor, and determination.
My diagnosis has become a catalyst for growth, self-discovery, and purpose. I've learned to prioritize my well-being, listen to my body, and celebrate small victories.
To those who may be facing a similar diagnosis or challenge, I want to say: you are not alone. Your story is not defined by your condition. You are strong, capable, and resilient.
Lupus may be part of my story, but it will never be the ending. Instead, it's a chapter that's fueled my passion to live, to love, and to inspire.
I am joining thousands of people across the country for the Walk to End Lupus Now®. I hope that you will join me either by lacing up your sneakers or by donating to my fundraising page.
You can make a difference by donating to help me reach my personal fundraising goal and support the Foundation's efforts to improve the quality of life for all people affected by lupus! A generous contribution of $25 or $55 can make a definite impact. What’s more, if your employer offers a Matching Gift Program to employees, you may be able to double your contribution with just a little bit of paperwork. Trust me, it’s worth the effort! 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.
Lupus is hard to diagnose, but the Lupus Foundation of America is working to make life easier and more comfortable for the estimated 1.5 million people living with lupus in the United States. Together, we can solve the cruel mystery of lupus. Thank you for your generosity!
