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Andrea was diagnosed with Grave’s and Thyroid Eye Disease (TED) in 2016. It took her almost seven years to regain her health and get her life back on track. Thanks to new treatment options and therapies she is now able to live her best life. The journey to get there however, was not an easy one. She has lived through the pain, frustration, confusion, and loneliness that are all associated with a disease diagnosis. She shares her story today to help others along their journeys and bring about meaningful change. Find out from real patients what life with chronic disease feels like. The invisible pain, the insurance battles, and the hidden full-time job "being sick" entails, can feel like too much at times, and it is a weight you shouldn't have to carry alone. It is so important that patients with rare and chronic diseases are heard. Follow patient stories detailing life with lupus, multiple sclerosis, thyroiditis, Thyroid Eye Disease, Chron's, RA, and other complex diseases. Are you an infusion patient that wants to help shed light on the chronic disease journey? Reach out to the Infusion Access Foundation team at [email protected] so we can hear your story and help you find the right pathway to be really heard. Infusion Access Foundation (IAF) is a community of patients united to protect access to treatments that you get at a clinic, such as infusions and injections. We support each other across all diseases and advocate with one voice that reaches policy makers.