Jennie Wilklow, founder of Hope for Anna and Harlequin Divas, joins the 1 Girl Revolution podcast this week to share her own life story, she talks about harlequin ichthyosis and her family’s own journey with it through her daughter Anna, how the Hope for Anna Facebook page started and what led her to start Harlequin Divas, what she’s doing to raise awareness and to help others with harlequin ichthyosis, and so much more. You don’t want to miss this inspiring episode!
6-year-old Lily Hake, founder of The Lilypad Project and the little queen from Michigan doing so many incredible things to help others, joins the podcast to talk about The Lilypad Project – which creates and distributes coloring books to children in hospitals, all of the acts of kindness she does including giving out hugs, paying compliments to strangers, helping people in need, cheering up the elderly, raising money to make sure that other kids are able to afford to eat lunch at school, and so much more. Her amazing mama, Amy, also joins us for part of this episode. Don’t miss this special and inspiring episode of the 1 Girl Revolution podcast!
Erica Hammel’s son Wyatt is a survivor of Shaken Baby Syndrome, and since her son was abused, she has dedicated her life to raising awareness about child abuse and working to pass “Wyatt’s Law” in Michigan and other states, which would created a registry of convicted child abusers. Child abuse is reported every 10 seconds and 5 children die a day from abuse in our nation. It’s about time we did something about it and this 1 Girl Revolution is leading the charge with Wyatt’s Law.
Jenna Haley made headlines a few years ago with the “Bucket List Baby”. When baby Shane was diagnosed with anencephaly, Jenna and her husband decided to make a “bucket list” for their baby and show him the beauty of this world. Jenna joins the 1 Girl Revolution podcast to share her inspiring story.
