Short Story

I am on the Waiting List for my NillyNoggin EEG Cap. It will help me during my EEG testing! Please help me reach my goal.

I am so excited to receive my NillyNoggin!

And an added bonus,

if I go above and beyond my goal, we will help other Warriors battling epilepsy! How?

Once I reach my goal of $50, every $50 over that will support other Warriors wishing for a NillyNoggin!

I would really like to help others battling neurological conditions. I know what its like to fight every day and having something to help us get through stressful testing with a smile and help us feel like a rockstar is priceless.

Let’s work together and help sponsor NillyNoggin EEG Caps for more warriors battling epilepsy!

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! This cap will help ease my anxiety and make life easier on everyone involved with my care.

Liam was born at 31 weeks with bilateral grade 4 IVH and Dandy Walker Variant, he only has 25% of his cerebellum which contributed to him having Spastic Quad Cerebral Palsy and Intractable Multi-focal Epilepsy.
He is truly a fighter, he has fought from day one over coming obstacle after obstacle. He is the happiest child with a smile that lights up a room and personality to match. He has a chocolate Labrador retriever sidekick named Dug and they are always into something. Liam is non verbal, non mobile and partially deaf but he does have a gait trainer and he goes where ever he wants and usually playing chase with Dug. I wish that I had half of his energy. He is such an inspiration to not only me and his daddy but to everyone who meets him.

Liam P.

by Heather Shuker

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Heather Shuker

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