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.

Haven started having Infantile Spasms at 4 months old. She is now diagnosed with intractable seizures from a rare genetic disorder called Spata5. She is 2 years old and living her best life! Enjoying all of her firsts and spreading awareness of epilepsy, infantile spasms, and Spata5.

Haven S.

by Heather Shuker

  • $40

    Funding Goal
  • $155

    Funds Raised
  • Campaign Never Ends

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Heather Shuker

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Name Donate Amount Date
Buddy Cain $40 January 21, 2022
Mandy Lindow $40 January 21, 2022
Victor Williamson $40 January 21, 2022
Anonymous $10 January 21, 2022
Anonymous $25 January 21, 2022