Puzzled Butterfly empowers individuals living with lupus and other chronic health conditions through coaching, education, support groups, and community outreach. Whether you’re navigating lupus, autoimmune disease, endocrine disorders, chronic pain, rare conditions, or long‑term symptoms, you deserve support, clarity, and a community that understands.
We recognize the isolation, fear, and uncertainty many people feel when they first receive a chronic illness diagnosis, and we understand the impact these conditions have on loved ones and caregivers. Our programs are designed to help chronic illness warriors build confidence, strengthen self‑advocacy, and actively participate in their own health care. By providing compassionate support and reliable education, we aim to improve health outcomes and enhance overall quality of life.
The Lupus Research Institute reports that “Lupus is one of America’s least recognized major diseases. There are 1.5 to 2 million Americans living with lupus; that’s 1 out of every 185 people. In fact, more people have lupus than AIDS, cerebral palsy, multiple sclerosis, sickle-cell anemia and cystic fibrosis combined; making it one of this country’s most prevalent medical conditions.” Raising public awareness of this reality, and the broader challenges faced by those living with chronic conditions, is a vital part of our mission.
At Puzzled Butterfly, we help individuals find strength, resilience, and hope; one step, one breath, one butterfly moment at a time.
The information provided on this website is for informational and educational purposes only and should not be considered medical advice. Content shared here is gathered from a variety of reputable sources and personal experience, and it may differ from the guidance of your physician or other licensed professionals.
Puzzled Butterfly does not diagnose, treat, or provide medical, psychological, dietary, or fitness advice. Readers should not rely on this information as a substitute for professional care. Always consult a qualified, licensed medical provider, mental health professional, dietitian, or other appropriate specialist for guidance tailored to your specific needs.
I am not a doctor and do not claim any formal medical training. I am not liable, expressly or implicitly, for any emotional, physical, or medical concerns that may arise directly or indirectly from the use of information on this site. Before beginning any new treatment plan, diet, exercise routine, or wellness practice, please consult your healthcare provider.
Thank you for visiting our site and hope you find the information included helpful.

I enjoyed knowing there is another place to get info about lupus. The name is so fitting for symptoms of lupus patients. Butterflies are beautiful n very delicate. Some of the symptoms causes pain from just a touch ; even the thought of a love one wanting to give a hug is devastating. It’s as if the butterfly losing silk. It’s sad to see a love one deal with lupus.
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