This week we were honoured to have the amazing Erin on our podcast sharing her incredible journey with daughter Luella who has a rare form of Epilepsy known as Infantile Spasms.

In this episode we discuss Erin's birth story, Luella's initial diagnosis and the journey she and her family have been on for the past two years.

Erin and her Husband Dave are the most incredible parents and have left no stone unturned when it comes to treatments and therapies for their daughter Luella. A huge thank you to Erin for opening up to us in this episode and sharing her and Luella's story.

Erin and Dave are currently raising money for research into Luella's condition, and we encourage all of our listeners to head to their fundraising page to make a donation. You can access the page at www.lululoveproject.com/donate

You can also follow Erin and Luella's journey on instagram @little.lulu.love

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