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Every epilepsy warrior should have the option to wear a NillyNoggin EEG Cap during EEG testing
So you have options! Purchase one or fundraise for one through our Warrior Troop Program!
Are you here to help epilepsy warriors get their NillyNoggin EEG Cap?
Choose from one of the following options!
Hannahtopia, where BRAVE RESILIENT STRONG Warriors get their gear!
Because we feel that these Warriors – these kiddos who face medical challenges and their families who support them – have earned their stripes and they deserve to be pampered and treated as such!
The girl behind Hannahtopia and the NillyNoggin EEG Cap
Hannah is a beautiful young lady inside and out. She’s a pretty cool 20 year-old young lady who has severe intractable epilepsy in the form of Lennox Gastaut Syndrome. As a result, Hannah has suffered from 100,000+ seizures, leading to multiple developmental delays. Severe epilepsy has presented her with many challenges in life; however, we do our best to try and focus on the positive, savor each day, and push hard to make it to the next day!
Check out other cool products we sell!
We sell products that have made our lives ALOT easier! Products that are colorful, comfy, functional, and well just plain awesome! From Adorable G-tube Covers to oversized colorful Incontinence Pads and more!
Wear, Wash, Repeat!
We’ve designed the NillyNoggin EEG Cap to be washed and re-worn over and over for when you need repeat EEG’s.
Brave Resilient & Strong
What people are saying about the NillyNoggin EEG Cap!
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!
Warrior Mom Ryan P ~ worn at Duke University in Durham, NC
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, Pediatric Neurology, UPMC Children’s Hospital of Pittsburg
The NillyNoggin helped my son have easier EEG experiences at ages 5 and 7 because it covers up the medical tape and wires which can look a little scary for children. I purchased one in his favorite color and he did such a great job wearing it for 3 days during both EEGs. He was even able to go to his homeschool group with the other kids. When Lucas looked in the mirror he was not afraid to see what was on his head.
Warrior Mom Katie P ~ Ambulatory EEG
Why We Created the NillyNoggin EEG Cap
Making a difference in the life of a child that struggles from seizures is our passion!
NillyNoggin at UNC
UNC Children’s – North Carolina Children’s Hospital created this video showing the NillyNoggin EEG Cap in action after receiving a large donation of NillyNoggin’s!
Bulk Orders for Hospitals and Non-Profit Epilepsy Organizations
Are you a hospital or a non-profit that supports Epilepsy? Contact us to discuss how we can get NillyNoggin EEG Caps to your Warriors!
Help Build the Warrior Troop!
Share our information with your epilepsy support, neurologist, EEG team, local epilepsy non-profit, other warriors and their family and friends. You could also share their information with us and we would be more than happy to reach out to them directly. Let’s build this troop together so that all Warriors have an opportunity to wear a NillyNoggin EEG Cap and bring a bit of happy, comfort and confidence to their EEG Process.