Meet Tucker

Tucker came into this world fighting.

Born at just 32 weeks and 1 day after an emergency delivery, he weighed only 3 lbs 15 oz. In those critical moments, his tiny brain likely experienced a lack of oxygen and blood flow—the leading cause of cerebral palsy in premature babies.

For the first six months, everything seemed okay… and then suddenly, everything changed.

Tucker was diagnosed with infantile spasms, followed by quadriplegic cerebral palsy, cortical visual impairment, epilepsy, and speech delay.

But those diagnoses don’t define him.

They don’t show his joy.

They don’t show his determination.

They don’t show the way he works every single day for things most of us never have to think about.

Tucker doesn’t walk or talk yet—but he fights for every bit of progress. Through intensive therapies, stem cell treatments, functional neurology, and daily exercises, he continues to prove that he is capable of more.

He loves Mickey Mouse, music, counting, and being around people.

And through it all—he is the happiest little boy.

Now we have another opportunity to help him keep moving forward.

None of these therapies—or the travel required—are covered by insurance. But they are giving Tucker something priceless:

a chance to grow, to improve, and to reach his full potential.

If you feel led to donate, we are incredibly grateful.

If you can’t, sharing Tucker’s story is just as powerful—it helps us reach someone who can.

Tucker has already overcome so much.

And we truly believe he still has so much ahead of him.

Thank you for believing in him.

Thank you for standing with us.

And thank you for helping us continue to fight for Tucker’s future.