Erin Murphy Welch

Hello and thank you for visiting my website!

My name is Erin, and I love creating books about our differences and the importance of acceptance and inclusion because of them. 

I’m a mother of three and I began writing the series “Little Bluebird” shortly after my daughter was diagnosed with a rare genetic disorder, called FoxP1 Syndrome. FOXP1 syndrome is considered a rare disease that is caused by a mutation or change to the FOXP1 gene. The gene is located on chromosome 3 and includes the instructions or “recipe” for making the Forkhead BOXP1 protein. As a member of a family of transcription factors, it is vital in regulating the expression of other genes. FOXP1 controls when and how specific genes affect the development of the nervous system, along with many other systems. When a gene like FOXP1 does not function properly it can lead to a wide range of developmental delays and medical needs.

As my daughter got a little older, I noticed that when we would go to the park, store, etc., children would ask questions. I love when children ask questions! It got me thinking about their curiosity and how important it is to educate children about their peers with special needs. So, I decided to write a story about a little bird with a visible disability-a shorter wing. The understanding that not all disabilities are visible is very important to me, but Emmi (Little) Bluebird is a wonderful conversation starter for the little ones. 

Through the power of storytelling, particularly involving a little bird with a disability, I strive to promote kindness, acceptance, and an understanding of diversity among children during their favorite story time. 

Thank you for taking the time to learn a little bit about me. I hope to continue to share more of myself and my books with you! 

-Erin