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!
Help Me Feel like a Rockstar!
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.
And Just a Bit More About Me
Our little one has the sweetest smile and kind heart . He loves his iron man and woody and buzz. He enjoys play cooking and having fun adventures with his family. He loves his big brother and they enjoy playing games together.One Sunday morning changed our lives. We awoke to a nightmare. Axl screamed and turned blue . We were in shock . Out of nowhere he began to shake and crazily for a moment as a health care workers I was relieved . I thought he wasn’t breathing and we’d lose him,if this is a seizure it’ll just pass right? .That quickly changed as the seizure didn’t stop. It kept on for 5 min. Fast forward to almost a year now we’ve been in and out of hospitals our longest stay with 6 days with an EEG. He had to undergo IVs different scans the poking the late nights not being able to sleep in a hospital that he wasn’t familiar with people he didn’t know. Countless tests doctor’s appointments and let’s not mention the different medications that we’ve had to try because some weren’t working. We go in one med and he’d have a different type of seizure then the doctor would put us on another and he’d have another different type of seizure we were at our wit’s end until we found an amazing doctor who gave us encouragement and faith. In this time I’ve seen him cry I’ve seen his blue eyes turned so red from fear and hurt. But nonetheless he still has the most beautiful smile and kind heart. He loves everybody he meets. He is our miracle from God and we adore him.
