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 $40 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 $40, 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.

Shane was born a month early at 3 mths old he started physical therapy at a lil over a year old we noticed something was off we were sent to neuro test after test they kept telling me nothing was wrong Aug 8th of 2019 he kept having what they were calling episodes he turned super pale an said momma i need to go to the doc i rushed him to the hospital they done eeg an all kinds of blood work 2 weeks later at his neuro appt we found out he carries the pol g genes we still don’t have all the answers but at his 3rd eeg they seen seizure activity an told me i had been right all along hes now on seizure meds but stil has mini episodes and were still waiting on more extensive genetic test they done.

Shane B.

by Heather Shuker

  • $40

    Funding Goal
  • $40

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Heather Shuker

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Name Donate Amount Date
Anonymous $40 February 15, 2021