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Ester Charlestin

Finding out I had Lupus at the age of 22 was devastating. Lupus isn’t only a silent disease but also a costly one. I have started Channel My Lupus to focus on awareness and helping those in financial need living with Lupus, or as I like to call them, Lupus Warriors. A Lupus Warrior is someone living with Lupus who decides to live despite the debilitating daily struggles that come with the conditions. I have been battling this chronic autoimmune disease for the past 10 years and have overcome so many obstacles. Common symptoms of Lupus are low-grade fevers, severe fatigue, all-over-body rashes, joint pain, and shortness of breath. I’ve dealt with all of these in addition to night sweats, ulcers, and loss of appetite, and I have undergone two hip replacements. I regulate my symptoms now with a constant intake of medications.

Going through so many battles, I wished I had someone to guide me along the way. As a Lupus Warrior myself I would like to provide an outlet for those who need to express themselves in a world that often turns a blind eye to this unseen battle. Support is crucial, I’ve tried to do this alone but I now understand I must have more than just me. I am beyond thankful knowing that friends, family, and strangers are willing to come together to make a difference.