Development that deserves full support — regardless of diagnosis.
NNMCCD is a membership organisation for families of neurodiverse children and the clinicians who work with them. We build the structure to study and share what clinical practice shows — translating international research into practical guidance families can use.
The evidence exists. The parent testimonies exist. What is missing is the structure to test this systematically — safely, rigorously, together. Food is something every child eats every single day. It is the foundation.
"Diet does not make a difference." — that is what we are told. And yet the entire world of nutrition science says the opposite. For a child with autism — suddenly diet does not matter? Really?
"Yes — autism. But also: no sleep, chronic constipation, ADHD, food selectivity." Constipation, allergies, sleep disorders — these are not autism. They deserve separate clinical attention. A diagnosis is a starting point, not the full picture — and there is still much to investigate.
"We spent thousands on tests. We got the results. And then — silence. Nobody could tell us where to start, what it all meant, or what our child should simply eat every single day."
NNMCCD did not begin in a boardroom. It began in a clinic — in Oslo, in the same consultation, repeated hundreds of times: "What else can we do, Paulina?" We saw the same pattern, again and again — and decided to build something that could outlast any single appointment.
Mother of Nahili. She refused to accept that a diagnosis was the end of the road — and pushed for something more systematic than what the system offered. Her family's journey became one of the founding stories of NNMCCD.
Representing the Somali community in Norway — where autism is disproportionately common, and where families too often face this journey without adequate support or cultural understanding. Layla bridges communities that the system does not yet reach.
A Polish mother living in Norway for many years, raising a son with autism. She created ABC after diagnosis — a practical parent guide for families who have just received a diagnosis and don't know where to start.
NNMCCD did not start in an office. It started in the clinic — with these families, and with the same question asked over and over: what else can we do? These stories are the reason this organisation exists.
We are honest about what is ready and what is still being built. What we offer today is grounded in real clinical experience. What we are building will be tested, documented, and shared — because that is the only way this work earns the weight it deserves.
We are not asking for donations. We are building a membership organisation — one that belongs to the people who believe in it.
Have questions before joining? Read the FAQ →
For families who want to be part of this community, have a voice in what we build — and help us understand what your child needs.
For companies and organisations who want to support the programme — and be recognised as partners in the work.
200 NOK / year · via Vipps · cancel any time
NNMCCD is open to partnerships with organisations working in ASD, ADHD, epilepsy and paediatric neurodevelopment — patient organisations, clinics, universities and NGOs. We bring clinical expertise, a multicultural family community, validated data infrastructure, and grant documentation. You bring institutional reach and credibility.
Partnership can mean shared educational content, joint grant applications (Dam-stiftelsen, EEA/Norway Grants, Nordforsk), or formal research collaboration. We are in active dialogue with organisations in Norway, Poland, Finland and Sweden.
An organised community of families, clinicians and researchers — that is what gives this work the weight it needs. Join at the beginning, when your voice shapes what we build.