I have a patient with psoriasis who recently had a terrible flare when she had to stop Raptiva. For a month she didn't want to be in public because people would stare at her or ask her questions about her rash that bothered her.
Have you ever encountered this? If so, how did you handle it? Did you say something sarcastic? Tell them to mind their own business? Use the opportunity to explain what psoriasis is and why they should be contributing money for ongoing research? Share your experiences.
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