This survey helps to gather information on the benefits of MindBlown! Cystic Fibrosis learning kits. You and your child's feedback is extremely helpful as we continue developing projects, improve past kits, and prepare to present to other CF centers so they may use our kits to help educate their patients and families.
The first six questions are for the parent or caregiver. The final two questions are for the child to answer. If you have more than one child who completed kits, please fill out multiple surveys.
Additional comments, questions, and feedback can be sent to Torie at victoria.miele@hitchcock.org or 603-650-0226.
Thank you for your time!