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 Jodie Akers, a young lady in the United Kingdom who lives with POTS (Postural Orthostatic Tachycardia Syndrome). In the midst of her challenges, Jodie loves to encourage and educate others through her YouTube Channel and her website, POTS Awareness.
UPDATE: Jodie’s story was published in the Derby Telegraph on November 28, 2011. Jodie wants to make people aware of her life-altering and rare illness.
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