Getting medical information is essential to significant disease patients. Unfortunately, Taiwan has not been able to provide satisfying communication channels in terms of medial information. Today, with the arising of new media, patients today have a chance to search for help through Internet. However, by doing so, they are under the pressure of criticize from doctors and more than often they encounter biased images on televised media. It is especially true toward female SLE patients, who are suffering the stigma of their media usage and stigmatic media images. To find out the truth behind the stigma, we held a focus group of female SLE patents. We investigated their behaviors of media usage and responses toward biased media images. We concluded that female SLE patents are just the opposite of what our society think: they process online information carefully; they never try to replace doctors with new media; they clearly indicate Internet can provide them certain functions that can’t be found in our traditional media systems. We hope our findings can serves as a bridge between patients and doctors. This study can become a new step forward to erase the stigma which patients have to face in terms of media usage and stigmatic media images.