Kaydence's Fight

08/14/2025

So KJ made the middle school softball team!!!!!!!

The New Providence Lady Mustangs Softball team fundraiser begins tomorrow. It’s super easy to purchase online and you get your coupons electronically. The team receives 50% of everything sold. You don’t have to live in Clarksville, you only need to know where your nearest Krispy Kreme is!!

Click the link below to order your dozen, or purchase from your favorite Mustang softball player.

*If you waited until TODAY, August 14th to make your purchase, our team will be entered in a daily contest for today only. If our team receives the most orders today, we could win additional money for our program.

Thank you in advance for supporting your Lady Mustangs Softball Team!

groupraise.com/oc/61145/5TB2TL

Help New Providence Lady Mustangs Softball fundraise by ordering delicious Krispy Kreme Digital Dozens today! Enjoy mouth-watering dozens & share to support their Krispy Kreme Fundraiser!

05/30/2024

Now that KJ is epilepsy free, it is time to tackle some of the other health issues. One of her biggest issues is migraines at the moment. We saw a new neurologist tonight and she said her migraines are trigger point related to her hEDS which is hard to treat with meds. She’s too young for nerve blocking treatment, and there are only a couple options after that. The first option is a device called Cefaly. It is not covered by insurance. Wish us luck.

Cefaly Homepage

04/26/2024

Got some good news today….
After 10 years of challenges and seizures,
KJ IS EPILEPSY FREE!!!
She has officially had a normal EEG after many many abnormal EEGs. 💜

Now we are on a long journey with AuDHD, hEDS, beta thalassemia trait and severe migraines…

04/08/2024

Always 🩵

02/11/2024

For those with kids like mine, Valentine’s Day is tough because KJ doesnt really like sweets and G doesnt really eat lol. We also have friends with t1d so candy isnt always our go to. This has a bunch of amazing ideas that are non-candy.

Discover even more ideas for you

12/06/2023

We officially got hit with a school bug. Hoping she gets over it soon because sick pr***en = a coughing whiny big child who thinks she’s smarter than you who won’t rest. 😭 I love her so I’ll let her cough on Patrick pillow not mine!

07/29/2023

07/07/2023

Kj had her first MRI today without anesthesia. So proud of her. 💜

07/06/2023

Some of you may remember the horrible times Vanderbilt put us through… I wish we had sued back then.

Just finished watching "Take Care of Maya" on Netflix and it left me speechless. This documentary tells the powerful story of a young girl battling a rare illness and her mother's unwavering determination to find a solution.

As Maya's health deteriorates, her mom travels to Mexico and finds a doctor who offers a temporary relief for her excruciating pain. But upon returning home, a devastating hurricane strikes, bringing back Maya's suffering and forcing them to rush to Johns Hopkins in Florida.

However, instead of support, the hospital takes Maya away from her mother, deeming her unfit and dismissing her concerns. Heartbroken, Maya's mom fights to regain custody and understand the treatment given to her child. The injustice she faces drives her to unimaginable despair, and it's a heartbreaking turn of events.

This documentary highlights the struggles faced by parents of special needs children, reminding us of the strength and resilience they possess. It's a call to all moms and caregivers—whether dealing with special needs or not—to trust your instincts and advocate fiercely for your children.

Incredibly, the real-life family behind this story is currently suing Johns Hopkins Hospital, seeking justice for what they went through. This serves as a reminder that we must stand up for what is right and protect our loved ones no matter the circumstances.

To all the amazing moms out there with special needs children, you are superheroes. Keep pushing forward, never give up, and remember that you have the strength to overcome any challenge that comes your way. We are here to support each other, because together, we can make a difference.

06/10/2023

KJ is on her way to allstars! If you want to help out is my Venmo and $sarahbring is my cash app. If you want to help out but don’t have either of those, academy sports gift card is appreciated too since she needs a full uniform and sliding gear. Our first districts game is June 30th and if we make it to States, it’s July 17th. Thanks for all the support!! 🥎♥️

06/06/2023

Kaydence officially made ALLSTARS!!!!!! Even with her broken arm she’s still practicing with her team every day. So proud of this girl. ♥️♥️♥️