08/19/2026
🙏Let's show Mason some love everyone🤟😎
Quick update and request for everyone who sees this🤍🤍🤍
Would you mind checking to see if you have “liked” Mason’s page AND “followed” it? If you have not done one or the other, would you please do so? 🙏🏽
We are wanting to show Mason that there are still ppl interested in HIM and his struggles(he is checking the page himself now🥹). It really does help push Mason’s page to other ppl’s news feed…which helps us spread awareness and gets more prayers sent up🙏🏽☦️
Mason is doing “better”, but we still have a couple things that need to be addressed before we can be discharged. ❤️🩹
I had to make the drive back home to Cayde yesterday evening and met him and Dad at urgent care. Thankfully, he tested negative for “all the things”, so we are battling an ugly virus. 😔 My littlest mister just needed his momma!
This life is not easy nor desirable. It’s not pretty and fun. My personal page is no longer filled with all the “happy” experiences, family pics, and milestones. For the most part, it’s rarely utilized. It’s simple, really. I don’t see the point 🤷🏻♀️ Mason’s page is where I can POSSIBLY help make a difference for others.
I am not giving in. I’m just warming up.
This hospital stay has been quite eye opening to the failures of the Oklahoma Healthcare System and this
Momma is ready to start talking about it.
I am going live today! YEP, you read that right. Not sure when, that depends on Cayde’s needs.
The past two years have wrecked my confidence in my abilities I know I excel in.
NOT ANYMORE! I have been fighting my way back to “see myself”, again.
This hospital stay felt like it was going break me. BUT, once I walked into our house last night, I suddenly felt quite the opposite.
I felt grounded and laser focused!!!!
This stay gave me some of that confidence back. 🥹❤️🩹🙏🏽☦️
We know Mason better than ANY medical professional. It is not acceptable for specialist’s(ie Neurology, Neurosurgery, etc) to take a quick look and “sign off”.
NO! There are new symptoms that have largely been ignored by the specialists that COULD help figure out the piece of the puzzle that is missing. Why not find the missing piece while in a controlled environment? At this stage, Mason is not medically manageable at home. Soooo, here we are in MEDICAL LIMBO, again💔
Parents/caregivers should not have to pay and use PROFESSIONAL AI tools to help figure out what’s wrong with their loved one’s and what the DOCTOR’S are missing. And, quite frankly, if they all lack the empathy to dig in and actually figure it out…maybe THEY need to use all their FANCY AI tools to check themselves and their ego’s! Not all patients fit into the box they try to shove them into. Where is the “personalized” approach to the care plan? Why. at a teaching hospital, can they NOT dig in? MAKE IT MAKE SENSE!
I do not like having to be the momma honey badger, but I’m not afraid to unleash the beast if need be. 🤷🏻♀️
Lord, have mercy on me!🙏🏽🙏🏽🙏🏽
