There is something about seeing/hearing someone else’s experience with lupus that resonates and lets you know that it’s not just you.
We’ll share stories, as permitted by the warriors who share them, in hopes that they’ll encourage and strengthen others who need their guiding words.
We also present Warrior Tales, your story in your own words, in a short video clip. If you’re comfortable, you can answer 2-3 questions about your experience with lupus. We do the recording/editing and post it to our YouTube channel and Walk to End Lupus Now page.
Maria D.
I was diagnosed 13 years ago, but had been living with the symptoms for about 15 years. It was certainly 5 years when I began to take notice of symptoms and sought a rheumatologist due to family history.
I was dismissed and had to endure many problems like endocarditis, headaches, and pancreatitis before I was officially diagnosed 5 years after that dismissal.
I have:
- learned my triggers
- how to manage my stress
- and listen to the needs of my body.
I’ve also learned to prioritize my health in order to be able to do the things I love and take care of the people in my life that depend on me. I have become a women’s champion in self care, raising awareness and empowering women to advocate for themselves and others.
I say listen to your body if you feel something is wrong. Keep looking for the answers; it may take a minute, but once you get the answers, the healing process can begin.
Be informed.