Our sweet little Nico has been a fighter since the day he came into this world, and likely long before that! We also know he has a lifetime of fighting ahead of him.

Although his genetic syndrome still doesn't yet have a name, he's got a long diagnosis list, countless hospital visits, IV's, X-rays, MRI's, blood draws, and meds worthy of his own official Team Nico!

These shirts are to:

1) Show support for our little Nico!

2) Raise awareness for the rare white matter disease community - those with official diagnosis and those still waiting for answers.

3) A great reminder to raise awareness that not everyone eats by mouth, that some kiddos use buttons to communicate, and that not all brains are the same - and that's beautiful!

We've selected for all proceeds to go to a local charity here in MN that supports kiddos with 4H Leukodystrophy. One of the many white matter conditions we have learned about during our journey to a diagnosis.

We would love to see pictures of you supporting Nico that we can add these to his memory book and show him how loved he is!