Linda Kanner was diagnosed with MS in 2007. She had an awareness of the disease through an Uncle, but her official diagnosis still took twenty years after first presenting symptoms to a medical professional. Shortly after this, Linda became a member of the board of The Accelerated Cure Project for MS. She also now serves on the iConquerMS Governing Board.In this interview, Linda recounts her first symptoms and how, despite MS being the "definitive sickness" in her family, it still took her a while to recognize these symptoms for what they were. She also reminds patients that no one is more expert in their bodies than they are - so if you're going through your own diagnosis journey keep going until you get an answer. Visit iConquerMSVisit the Accelerated Cure ProjectInterview by Laura KolaczkowskiEdited by Steve Woodward at The Podcasting EditorPodcast artwork by Jackie Zimmerman at Queen of GSDBackground Music is “Old Photos” by Olexy Support of this project is made possible through the generosity of Janssen Pharmaceutical Companies of Johnson & Johnson.

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