We're a family. Just like yours.
Teanexia was born from a real story: ours. Today it supports thousands of families who, like us, are looking for guidance, clarity and someone who understands the journey.
A diagnosis. A flight. A decision.
We're a family of four. Our youngest son, Benjamin, is six years old and has level 1 autism. We found out when he was two: first it was a hunch, then an assessment, and finally a diagnosis that changed everything we thought we knew about our future.
It wasn't easy. But instead of freezing, we made a decision: move from Argentina to Spain, specifically to Málaga, looking for a health and education system that could give Benjamin the best tools for his development. Spain has solid public resources for autistic people: social security, the early-intervention centre network, school integration programmes, benefits like the autism allowance. We knew that in theory.
Reality was very different. When we arrived, we found information that was completely scattered. Every region has its own procedures, its own deadlines, its own way of naming the same things. To access a benefit, you first had to know it existed, then find the right guide for your region, then decode the administrative language, and finally gather documentation nobody had properly explained.
What weighed on us most wasn't the bureaucracy. It was the isolation. We didn't know anyone who'd been through the same thing. We didn't know who to ask whether the school was required to have a special-needs teacher, or what to do when the health centre took months to refer us. The answers existed, but they were hidden in scattered forums, private WhatsApp groups, conversations we couldn't have because we didn't know the right people.
One day, after finally finding the information we needed thanks to another family who'd been through exactly the same thing six months earlier, we asked ourselves: why can't this all be in one place?
"What weighed on us most wasn't the bureaucracy. It was the isolation. We didn't know anyone who'd been through the same thing."
That's how Teanexia was born. Not as a business project, but as a human response to a real problem. We wanted to build the space that would have saved us months of anguish: a place where autism information was brought together, explained in plain language, organised by region, and backed by a community of families who'd already walked that road.
Today, Benjamin is six and thriving. He's still in therapy, still at a school that includes him, still surprising us every day. And we're still here, building the tool that would have changed everything for us if it had existed when we needed it most.
At its core, Teanexia is a love letter to every family standing exactly where we once stood. Because no one should feel like they're figuring out autism alone.
What we believe in
Clear information
We know how hard it is to find the right information at the right time. That's why we bring it together, simplify it, and explain it without jargon.
Real community
The experience of a family who's already been through this is worth as much as any report. Here, that knowledge is shared and reaches whoever needs it.
Empathy above all
We know what it feels like to get a diagnosis and not know where to start. Everything we build comes from that place.
Constant improvement
Teanexia grows with the families who use it. Every question, every suggestion and every story helps us build something better.
Will you join us?
Every family that joins makes Teanexia more complete. Your experience could be the answer another family is searching for today.