Current Need / Intensive Therapy

Charli can't walk, or sit up on her own. This is not her ceiling. It's her starting line.

We're raising $9,000 to give her three weeks of intensive therapy during the window when her brain is most ready to learn. Every dollar, whether through a direct gift or a shop purchase, goes toward making it happen.

Three weeks One concentrated therapy block
Four hours Therapy each day
Five days Therapy each week

Funding

Where the $9,000 goal stands

Total Raised
$5,195
$9,000 goal

$3,805 still needed.

Goal $9,000
Parents Have Contributed $4,500
From The Shop $195
Individual Donations $500

Why Now Matters

There is a window, and Charli is in it now

There is a window in early childhood when the brain is at its most adaptable, when neural pathways are still forming, still listening, still ready to be shaped by experience. Charli is in that window right now.

Intensive therapy during this stage is not a miracle promise. It is something more honest than that: it is showing up, day after day, with skilled therapists who know how to turn repetition into progress and effort into ability. It is giving Charli's brain the kind of repeated input it can use most effectively right now.

We are not chasing guarantees, because no one can offer those. We are chasing the chance to look back and know we did everything we could while the door was wide open.

That door will not stay open forever. But it is open now.

Charli working in her stander.
Most kids her age are learning to run. Charli is learning to stand, and it's one of the hardest things she does all day. Her stander helps her bear weight through bones that would otherwise grow brittle and fragile, and keeps her joints and muscles from tightening into positions her body was never meant to hold. She should not have to fight this hard just to be upright. But she does, and she does not quit.
Charli supported upright in a gait trainer or harness.
Her legs do not carry her yet, so mine do. Strapped into a walking harness between her dad's legs, Charli gets to feel what movement is supposed to feel like: the weight shift, the rhythm, the forward motion. Love is doing the work that muscles cannot. This intensive is built to take moments like this and turn them into ability.

At Now I Can

What the intensive looks like

Right now, Charli cannot walk. She cannot sit up on her own. These are the starting points, not limitations, but the specific skills we are asking therapy to help build.

We are raising funds to take Charli to Now I Can Foundation in Orem, Utah, a nonprofit clinic founded by parents of a child with cerebral palsy who traveled to Poland searching for better therapy, then brought what they found back to the U.S. so other families would not have to make that same trip.

What makes Now I Can different from the weekly therapy Charli currently receives is the intensity and the method. Their program puts children in therapy four hours a day, five days a week, for three straight weeks. Instead of one short session a week where progress inches along, this is full immersion, where each day builds directly on the last.

Now I Can uses a specialized orthotic suit, a soft, wearable system of strategic supports that helps teach the brain and body correct patterns of posture and movement while providing resistance, strengthening, and sensory input. For a child like Charli whose brain has difficulty communicating with her muscles, this suit works to retrain those connections from the outside in.

The therapists there are trained in hands-on techniques that work to override incorrect neurological signals and create new pathways that help children move in ways they have never moved before.

This is not a single technique applied on repeat. Now I Can's therapists build a customized plan around each child, combining suit therapy, vibration therapy, neurodevelopmental treatment, and flexibility work, all tailored to what Charli specifically needs to work toward sitting, standing, and eventually walking.

This kind of intensive repetition has helped children sit, stand, and walk for the first time. Families often describe more progress in three weeks of intensive therapy than in many months of traditional weekly therapy.

Your donation goes toward something specific and concrete: three weeks, four hours a day, with a team that specializes in helping children like Charli build the skills that weekly therapy alone cannot reach.

Why This Plan

Built for kids like Charli

We did not pick Now I Can at random. We picked it because it is built for kids like Charli.

Now I Can specializes in children with cerebral palsy and neuromuscular conditions. Their therapists are trained in neuro-developmental treatment, suit therapy, and techniques specifically designed to create new neural pathways in children whose brains struggle to communicate with their muscles. Charli cannot walk. She cannot sit up on her own. These are not problems that a general pediatric PT clinic sees every day, but they are exactly what Now I Can's team works on, every day, with every child who comes through their doors.

The program's Intensive Model of Therapy was originally developed in Poland and brought to Utah by Now I Can's founders, parents of a daughter with cerebral palsy who saw their child make more progress in weeks of intensive work than in years of traditional weekly sessions. They built the clinic so other families would not have to fly overseas to access it. We do not have to either.

Now I Can is in Orem, Utah, driving distance from us. That matters. It means we are not spending your generosity on flights, rental cars, or the kind of logistical overhead that quietly eats into a fundraising goal. We load up the car, we bring what we need on our backs, and the money goes where it should: into Charli's therapy.

Every dollar of this fundraiser has a short, direct path from your hands to a room where Charli is working with a therapist who knows exactly what she needs.

Charli riding comfortably in a backpack carrier.
She cannot walk beside her dad yet, so she rides.
Thank you to everyone whose love carries her.

How To Help

Three clear ways to support Charli

Donate directly

The clearest path is a direct gift to Charli through the CalABLE link.

Shop with purpose

The current plant inventory gives another concrete way to help.

Share the page

Even if you are not able to give today, you may know someone who would want to help.

Questions You May Have

Answers to common questions about this need

Why not just continue with weekly therapy?

Weekly therapy matters and Charli will continue it. But one hour a week has limits.

Now I Can's intensive model puts Charli in therapy four hours a day, five days a week, for three weeks, the kind of concentrated repetition that gives her brain the chance to form new movement patterns while they are still fresh from the day before.

Families consistently report more progress in three weeks of intensive therapy than in a full year of traditional sessions.

Why Now I Can specifically?

Now I Can was founded by parents of a child with cerebral palsy.

Their therapists specialize in the exact challenges Charli faces. They work daily with children who cannot sit, stand, or walk independently, and they use suit therapy, neuro-developmental treatment, and vibration therapy tailored to each child.

They are in Orem, Utah, driving distance from us, which means your money goes to therapy, not airfare.

What does the $9,000 cover?

The intensive therapy program itself, travel to and from Utah, lodging for three weeks, and the everyday costs of keeping our family stable while we are away from home and work.

We have chosen a drivable destination and a nonprofit provider specifically to keep overhead low and put as much of every gift as possible toward Charli's time in therapy.

Is a specific outcome guaranteed?

No, and we would not insult you by pretending otherwise. Every child responds differently.

What we can tell you is that Charli is young, she is in the window when her brain is most adaptable, and this program is specifically designed for children with her diagnosis.

We are not chasing a miracle. We are chasing the chance to look back and know we did everything we could while the door was open.

What if you raise more than the goal?

Any additional funds will go toward follow-up therapy and the equipment Charli needs to continue building on whatever progress she makes during the intensive.

Nothing will be wasted.

Can I help in ways other than money?

Yes.

Sharing this page is one of the most valuable things you can do. Every share puts Charli's story in front of someone who might be the person to help.

We would also welcome meals, childcare support, or encouraging notes, the small things that keep a family going during a hard season.

Ready To Help

Support Charli in the way that fits you best

Direct donations and shop purchases both help support this need.