About the Organization

The Robbie Foundation (RF) is a not-for-profit organization that was founded on behalf of a boy living with cerebral palsy. Robbie’s disability is quite severe in that he is totally dependent on others for all his daily living needs. Robbie has overcome all odds thus far in life and has a very strong “will” in every aspect of his being. In lieu of all that he has accomplished for himself, he expresses an interest and eagerness to help others. The goal of Robbie Foundation is to see the world brought to children who are unable to explore it on their own.

Questions or comments? Feel free to get in touch with us at: robbiefoundation@gmail.com

Robbie Foundation (RF) is a 501(c)(3) Non Profit Organization whose purpose is to improve the quality of life for children living with disabilities.

Our Mission

The mission of Robbie Foundation is to improve the quality of lives for children with special needs.

PURPOSE: The purpose of Robbie Foundation is to support children with special needs and improve their quality of life by: funding adaptive equipment, technology and therapy treatment not covered by insurance; providing art and technology programs to allow access to educational opportunities; offering family support and resources through respite programs, and cultivating awareness of the special needs community.

VISION: A society that values people with a disability, upholds their rights and supports their equitable participation in everyday life.

VALUES: Our decisions and actions are guided by our values that recognize the worth and diversity of all individuals. We act honestly and ethically with our focus on improving the quality of life for these children. Our aim is to reach and provide the best quality service for all children with developmental disabilities.

Robbie Foundation Kids

Photos © HKS Photography

Who We Serve

The Robbie Foundation is dedicated to assisting children with developmental disabilities* (including, but not limited to physical disabilities, speech and language delays, sensory integrated disorders, cerebral palsy, brain injury, autism spectrum disorders, cognitive challenges).  We serve children between the ages of birth and 20 years residing in the state of Maine.  Our primary mission is to fund adaptive equipment, assistive technology, therapy treatment and/or any necessary item not covered by insurance.  By providing such services, our hope is to improve the quality of life for  children with special needs.

*Developmental disabilities are a diverse group of severe chronic conditions that are due to mental and/or physical impairments. People with developmental disabilities have problems with major life activities such as language, mobility, learning, self-help, and independent living. Developmental disabilities begin anytime during development up to 22 years of age and usually last throughout a person’s lifetime.