This site is dedicated to men, women and children around the world that have been diagnosed with Lupus and also for those who might just want to learn more about the disease.

Have you or someone you are close to recently been diagnosed with a form of Lupus?
This site is designed to give you the information you need to know, including:
*  symptoms
* latest information on treatments
* statistics
* videos discussing specific Lupus topics
* personal stories from Lupus Patients
* an Anti-inflammatory Information and Recipe section
* Lupus events that are taking place
* and more!

We hope this site broadens your perspective on the disease. It has been my own experience that when I mention to some people that I have Lupus, I am greeted with the same responses: “You have what?”, “How do you spell that?”, “Is it contagious?” Learning as much as we can about the disease equips us with answers and information that we can share with those who do not know a lot about Lupus.

The team at LSG has taken on the task of getting the word out there, and we hope you will join us. We need to be as informed as we can about the disease so that we can educate our community. Who knows…the next person we meet and discuss the disease with might be a future doctor or researcher who comes up with the cure!

Please join me and the Lupus Survival Guide team in a global effort to find a cure and offer assistance and support to patients and their families.

Enjoy the time you spend at this website.  We look forward to your comments and emails.

I hope today is a wonderful day for you!

Marisa Zeppieri-Caruana
Founder of LSG -Board Member Lupus Foundation of America S.E. Chapter
LupusSurvival@aol.com