Gladiator X Project

A Repost from 4/8/25

The Beauty
Pure Innocence
Thru a child’s eyes

Charlotte, you were heavy on my mind the other day.
You are a FORCE!

, one ripple at a time and you continue to create waves. Waves of IMPACT!

April 7th (Charlotte Figi Day in Colorado)
Read from 4/7
Stories were shared
Our family story is on GXP Facebook as well as what led to us moving forward w/ Medical Ma*****na forever holds a special place in our 🖤

X will forever have a young mind d/t the significant impact on his cognition.

X’s story (a part of a medical J article & Natl. Webinar)
He has quality days & that is huge given his diagnosis’s
Seizures today-some weeks worse than others. He’s on 3 different blends of MM tincture, along w/ other meds

We are very passionate about others eyes being opened to the possibilities of MM for the pediatric population

It is not a cure

We do not see many characteristics of autism now.
Years ago it took both of us to put his shoes on. He used to be fearful to leave the house. His aggression and impulsiveness were unmanageable. There is so much MORE that the MM has helped with beyond his seizure burden.

Let’s OPEN our eyes to the possibilities for the usage for kiddos w/ other neuro-developmental diagnosis’s. They take ‘big time’ medication. It’s not an answer but it’s worth being an option.

Xavier is now 13. It will be exactly 6 yrs, the week of 4/21, that he’s been on his MM. We met w/ his medical team on 4/19/19 to move forward w/ MM. It was a day that shook me to the core. One of fear, hope and desperation.

WE have been given the opportunity to MEET and interact with OUR son once seizures, aggression & impulsivity calmed down. We still have HARD days w/ outbursts w/ Xavier. They are short and he is redirect able. We have been given time to learn better approaches as well. We get to work with him vs against.

Because of YOU Charlotte.....
Because of YOU Paige......
Our kiddo is living quality days .....
There’s a calm to this Storm
Thank YOU!

Please learn more about Charlotte Figi

A Force that has unveiled the beauty of a plant

Your energy
Your spirit
FOREVER a piece of so many

Wrapping up …….
Infantile Spasm Awareness Week:
December 1-7

WHAT IS INFANTILE SPASMS?

Infantile spasms is a rare and particularly severe epilepsy syndrome that typically begins within the first year of life. Infantile spasms is characterized by subtle seizures which can have large neurological effects, potentially leading to developmental delays and cognitive and physical deterioration.

Sadly, many primary care doctors and parents are not familiar with the signs and symptoms of infantile spasms. So, many children with infantile spasms do not receive treatment during the critical window within the weeks and months after the emergence of symptoms.

Please see: https://www.cureepilepsy.org/get-involved/awareness-days/infantile-spasms-awareness-week/