INTERVIEW: Morgan Villano & Ichthyosis

Published: March 24, 2021, 4 a.m.

We are back for another Because We are Strong episode this week.\xa0 We are chatting with Morgan, the mother of a rare disease fighter and a mom on a mission to raise awareness about her daughter's condition. Morgans daughter Addison has Lamellar Ichthyosis, a rare genetic skin disorder that is present at birth and occurs in about 1 in 200,000 people.\xa0


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