Short Story
I was nominated to join the Warrior Troop and now I am on the Waiting List for my NillyNoggin EEG Cap!
I am SO excited to receive my NillyNoggin cap!
I’m even more excited to be part of the Warrior Troop at Hannahtopia.

The Troop is made up of amazing warriors like me – kids and adults who face medical challenges every day. Hannahtopia helps us by bringing fun, color and comfort to our lives. Creating positive happy moments. Happiness is SO important – it helps with the healing process!

My medical condition requires me to get EEG tests that are very medically sterile looking and often scary.

Sometimes an EEG is worn for days, in public, and people often stare. The NillyNoggin covers up this scary medical look. It puts a positive, happy twist on the EEG procedure that some of us have to get a lot. The NillyNoggin cap is comfortable and colorful! Lots of people will come up to talk with me ’cause it’s so cool! It will also give me confidence and comfort!
I am so excited to receive my NillyNoggin!
Can you help me? I’m on the Waiting List for my NillyNoggin.
There are A LOT of other amazing warriors waiting as well. If we can raise $50 then my NillyNoggin cap will be sponsored and I won’t have to wait!
Plus if we work together we can achieve even more! If we raise over $50, we can help sponsor NillyNoggin caps for other warriors on the Waiting List!
I would really like to help my warriors in the troop. I know what it means to fight every day and it’s easier with a troop of warriors fighting alongside me.
This is My Story
In 2010 we were in a horrible accident the day after my daughter turned 3 her seatbelt broke and ejected her from her booster. She suffered a brain injury and wasnt expected to live let alone walk or talk. 2 years later she was in school and started having spells they called them one so bad she fell. Took her to the e.r and they rushed an MRI and got the diagnoses of seizures stemming from the brain injury. She has overcome everything the docs have said she wouldnt do. She walks talks plays and is 13 now. Shes had epilepsy for 8 years now.
Chloe B.
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$40
Funding Goal -
$0
Funds Raised -
Campaign Never Ends
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