Book Description

I was diagnosed with Systemic Lupus in 2008, after a year of pain and confusion in my body. When I first heard of my diagnosis I felt extremely vulnerable, broken, lost and helpless. I desperately looked for messages of inspiration and hope as far as my new diagnosis was concerned but I was unsuccessful. Over time though, armed with more awareness about lupus, I realized that almost every side effect of the disease and the medications could be managed (and counteracted in some cases), and I began to feel like I could regain much of the energetic life I once had. Since lupus is based on inflammation, I learned of the triggers that cause inflammation at a physical, emotional and even spiritual level and started to put together an action plan to restore balance back into my body. This enabled me to regain a sense of confidence and I began to work more effectively with my doctors and care team to create a wellness plan for me, which was a great source of empowerment. Having lived through a complete transformation from weakness to empowerment and even gaining a deep sense of gratitude for all that lupus has inspired in my life, I wanted to share everything I have learned, in an objective way by allowing the reader to follow me on my journey. I have listed every bad judgment as well as every success through my experience as a way to support self-discovery in others touched by lupus. I'm a firm believer that we need to be our biggest advocates and having all the information around us, empowers us to make better decisions toward our own well-being. By sharing my journey, I hope others can avoid a lot of the fear, panic, confusion and despair that often comes with this diagnosis. I also hope to relay an alternate perspective about facing chronic illness: in my experience, lupus has shaped me in ways I never imagined and through it I have a deeper sense of inner peace and balance and I sincerely look to my lupus as being my greatest inspiration. I hope to be that message of inspiration and hope that I looked for, unsuccessfully, when I was first diagnosed.