Description
The Ice Cream Cone NillyNoggin EEG Cap is designed specifically for the EEG medical procedure. It assists in protecting the leads from wandering little hands as well as adds a fun, colorful cap to cover-up the ‘scary’ look of the leads. It is comfortable, breathable, cool and snug. Handmade in the USA of imported fabric – 95% cotton, 5% spandex. This Ice Cream Cone NillyNoggin EEG cap is popular with those who love sharks, crabs, starfish and well all those cool ocean creatures! The caps are one size fits most from child to adult. Care Instructions: machine wash warm, line dry. May iron if needed. Some shrinkage may occur. We recommend you wash the Nilly Noggin prior to use.
Learn How NillyNoggin Caps Improve the EEG Experience for Kids
“Thank you for creating this product. It makes going through a difficult situation so much easier on both the patient and the caregiver. It was hard emotionally for me to see my boy with all those wires. So much of what we’d experienced with seizures came flooding back. The NillyNoggin humanizes the experience. My boy went from looking like a science experiment (his words) to being Adam, a playful child with a condition we’re trying to understand.”
Angela
Many parents have praised the NillyNoggin EEG Cap. Parents report it has been very helpful in distracting their child from the EEG setup and study. Once the leads are placed, the cap is placed on the child’s head over top of the leads. The cap helps keep the leads in place and deters the child from touching the leads. The caps are also fun and colorful which helps to distract from the procedure allowing a better result. I highly recommend this one-of-a-kind cap!
Dr. Shelley Williams, MD
“Rylee just turned 12 and was diagnosed with BRE at age 6, and then ESES at age 8. The ESES had been hard to manage and has required frequent med changes and trials which come with frequent EEGs. She has had ambulatory EEGs about every 3 months for the past 2+ yrs. NillyNoggins have given Rylee back comfort and dignity while she is around family and friends during testing, and makes her feel fashionable! Thank you Heather and Hannah for all you do for Epilepsy Warriors!”
Rylee P
