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About The PIC Foundation

We are a charitable organization dedicated to improving the quality of life for Protein Intolerant Children (PIC) and their families. We are a chapter of the Partnership for Cures, a 501c3 organization that funds research to promote faster cures for sick children.

As parents of protein intolerant children, we are navigating very muddy waters. We have found that not much is known about protein intolerance nor how to treat it and live with it. There seems to be a lack of standardized treatment methods in the medical profession leading to much confusion for families and much suffering for children. We hope to change all of that.

Our mission is to improve the lives of protein intolerant children and their families by providing information, resources, support forums, and by promoting public awareness and supporting medical research.

We plan to fulfill this mission by accomplishing the following goals:
  • Empower families
  • Become the number one source of information for families and medical professionals
  • Promote early diagnosis and treatment
  • Promote awareness and education in the public and the medical community
It is our hope that this website will serve as a solid source of information to help families make educated decisions about caring for their protein intolerant infant/child.

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