Through the project, Invisible No More! the Invisible Disabilities Association is bringing awareness, compassion and belief to millions living with debilitating conditions, shining a light on the “invisible” and making these valuable, incredible people Invisible No More!
This video features the story of Leeza Gandley who lives with Dysautonomia, CFIDS and other complications. Leeza was a student of Pharmacy (Pharm D. Program) and Medicine (M.D. Program) before she became sick and had to leave school before completing her studies. Leeza shared, “Now I utilize that knowledge in navigating the healthcare system — not only for myself, but also as a Patient Advocate for others.” Visit Leeza’s YouTube Channel, She Who Feels.
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The Invisible Disabilities Association (IDA) encourages, educates and connects people and organizations touched by illness, pain and disability around the globe. Formerly known as The Invisible Disabilities Advocate, IDA was founded in 1997 and incorporated in 2004 as a 501(c)(3) non-profit. IDA reaches out through our websites, projects, articles, pamphlets, booklet, social network, resources, videos, radio interviews, seminars, events and more! Get the word out! Share a link to our articles and pages with Google Plus, Facebook, LinkedIn, Twitter and through Email by clicking on the Share link. Leave a comment!
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i have gastroperisis…i cannot eat more then two bits of food without getting sick…i havnt kept food down in over two and a half years…i lost 80 pounds before the doctors deciced it wasnt all in my head…i eat most of my food thru a feeding tube…i dont look sick most the time but other days i cantt get out of bed becasue im malnutriotioned of in too much pain to move …..but as thye outside world says…you dont look sick…welcome to my world of feeding tudes and liquid food and one more person saying …just eat something youll be fine…….