Our Story

In July 2025 our disabled son Toby took part in a research protocol which has truly changed his quality of life. Neurocytotron needs to be accessible for everyone!

Imagine watching a loved one struggle with the daily challenges of a disability. For many families, this is a heartbreaking reality. However, for our 12 year old son Toby, hope arrived in the form of a groundbreaking research protocol called the Neurocytotron. This innovative therapy has significantly transformed Toby's quality of life, granting him a sense of normalcy we only ever dreamed of.

In July 2025 we were lucky enough to travel to Monterrey, Mexico after raising £35k to pay for the protocol and travel expenses. Toby was diagnosed with  a rare genetic disorder called SYNGAP1,  was non verbal, incontinent and had a severe learning disability with severe behavioural issues. 

4 days into the treatment he was using the toilet. 9 days into the treatment he was saying "wee wee". We went to Mexico with 150 nappies and we used about 20!  He hasn't worn a nappy since. 

He has said new words, his focus and attention has improved and his behaviour has become so much better! 

This protocol improves the life of those with cerebral palsy, dementia, stroke,  brain damage and autism, amongst others. Through travelling to Mexico we have found out that Toby has a spinal cord injury which happened at birth and that this was the reason for his incontinence. This has now been repaired! 

As miracles like these emerge, they often remain inaccessible to the wider community due to various barriers, including availability, awareness, and affordability. Sadly, countless other families who could benefit from the Neurocytotron have not had the same opportunity as Toby. This disparity is unacceptable when a potential life-changer exists.

Developed through years of meticulous research, the Neurocytotron device offers a unique, non-invasive approach that has shown promising results in improving cognitive functions and physical abilities in individuals with disabilities. Its efficacy is backed by data and patient success stories, including Toby's own remarkable journey. Yet, despite these compelling results, the availability of this technology remains severely limited.

We believe it is crucial to make the Neurocytotron accessible to all who might benefit from it. Expanding its reach would allow families across the country, and indeed the world, to access potentially life-altering treatment that could significantly enhance the lives of disabled individuals.

We call on healthcare authorities, researchers, and policy makers to prioritise the integration and funding of the Neurocytotron into public and private healthcare systems. By doing so, we can break down the barriers preventing access and ensure that no family is deprived of the hope and possibility this treatment offers.

Sign this petition to urge decision-makers to act swiftly. Let's push for a world where everyone, regardless of their circumstances, has the chance to access revolutionary therapies like the Neurocytotron. Together, we can make a difference.

We do NOT want your money but we do know of two precious young children with cerebral palsy who are desperate to get to NeuroCytonix one in the UK 🇬🇧 and the other in America 🇺🇸.  Please take a look and if possible, donate to their cause.

https://www.gofundme.com/f/give-vivian-a-chance-at-a-brighter-future​

https://www.gofundme.com/f/fighting-for-amiras-future

To see our full journey and everything we did to raise £35,532 including celebrities like Chris Kamara :

Facebook: https://www.facebook.com/share/195orhffjg/

Instagram:

https://www.instagram.com/the.troublewithtoby?igsh=NWZ2bDJlYWltbmh2

Tiktok :

https://www.tiktok.com/@troublewithtoby?_t=ZN-90FLlSut3lW&_r=1

YouTube:

https://youtube.com/@abirosalie?si=9vaLnaMyoXU4ml8b

X :

https://x.com/TroubleWithToby?s=09

Thanks for reading.  Please sign and share today to especially help our children 🙏 

Craig,  Helen & Toby