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02/06/2012 08:18 PM
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News and Events

Ian has recently been diagnosed with Autoimmune Urticaria, making it impossible for him to attend SJS kids week. He is scheduled to attend the Boston Foundation for Sight in March 2012. In the meantime, Ian is back at school and enjoying being with friends again and we have begun fundraising for travel costs associated with his upcoming treatment. Meanwhile, our research for the treatment of Ocular Surface Disease continues. We are excited to announce that we are making progress in the design and development of a material that can be used to treat many diseases of the cornea, eliminate pain and restore vision. We will keep you up to date as new information becomes available.

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Articles or advertisements referring to specific programs, services and/or products do not constitute endorsement by the Milne Stevens Johnson Syndrome Society. Articles involving medical conditions, treatment protocols or procedures are not intended to be medical advice. ALWAYS consult with a physician regarding your condition or any changes you may be considering to your current treatment program.

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