Funding and access
How families pay for a Trexo
Most families combine more than one route. Our team helps assemble the paperwork for whichever ones apply to you.
Trexo Theo is a prescription device for patients 12 years and older with cerebral palsy. Funding and coverage decisions are separate from clinical suitability. Indications and safety information.
Four routes
Where the money usually comes from.
01
Insurance and Medicaid
Coverage for pediatric powered exoskeletons is developing in the United States. We help your family and clinician assemble the documentation payers ask for: medical necessity, clinical assessment and recorded session data.
02
Foundations and grants
Many families fund a Trexo through disability and condition-specific foundations. We can point you to the organizations other Trexo families have worked with.
03
Fundraising
Community fundraising covers part or all of the cost for many families. We provide the documentation, imagery and specifications campaigns tend to need.
04
Clinic and school programs
Hospitals, outpatient clinics and school districts can acquire Trexo Theo as shared equipment, spreading access across many children.
What we provide
The documentation payers and funders ask for.
Funding decisions turn on paperwork. We prepare ours so your clinician doesn't have to build it from scratch.
- Device specifications and FDA 510(k) clearance details
- Clinical assessment summary from your child’s treating therapist
- Letter of medical necessity template for your clinician
- Recorded session and step data supporting ongoing use
- Quotes and itemized pricing for your configuration
- Published studies and the evidence packet
Coverage varies by payer, state and plan. Nothing here is a guarantee of coverage or reimbursement. Our team will tell you plainly what we have seen work and what we haven't.
Start with a conversation, not a form.
Tell us about your child and where you are. We'll tell you which funding routes are realistic for your situation.