Building a greater understanding of neurodivergence
Finally understand what you're seeing.
The SenLife Strengths and Needs Pre-Assessment: four weeks of structured evidence, reviewed by a clinician, discussed with you in a 30-minute call, with a written report you can take to school and your GP.
“With SenLife and our clinicians understand what is happening for your child and how you can best support them now.”
No payment today. Places offered in order of priority.
NICE recommends assessment begins within 13 weeks of referral. The reality is often years. The pre-assessment doesn't replace that assessment, it supports you while you wait.
How it works
Track your daily diary
Fill in your SenLife daily diary and behaviour profile. Aim for at least 4 weeks of entries — real days, not perfect days.
Complete the questionnaire
A structured question set informed by recognised screening frameworks, done at your own pace.
We build the evidence report
Your diary + answers become one clear picture: patterns, triggers, strengths and needs — in plain English.
30 minutes with a clinician
A SenLife clinician will review all your data and discuss it with you; what it means and what to do next.
What you walk away with
A written report you can share with school, your GP and assessors
Clear guidance on whether formal assessment looks right — and which pathway fits what you're seeing
Practical language to advocate for reasonable adjustments now
Support & strategies you can start immediately — while you wait
“The whole process from start to finish was great. The app is simple to use and the voice note option is a game changer! I’ve shown the evidence during AFI meetings and plan to use all the evidence and documents from our clinician in his EHCP/DLA meetings too. Our senco was super impressed with the digital reports and said they were a helpful overlook to our day to day life at home.
I’ve sent and suggested it to so many families, and have told my own EYFS complex needs class parents how useful the app is and process.
It’s really nice to have a professional tell us what we have also thought for a while in regards to diagnosis for Otis, especially given we could be waiting up to another three years for his community paediatric appointment.
We will continue to use the app going forwards too.”
Jemma
Mother to Otis
“Can I just say how helpful this report is for us and would be for any parents waiting for a diagnosis.
Having all the diary info, questionnaire and our conversation summarised into one document helps reassure us that we should trust our parental judgement and we know our child.
Although not an official report, this report lays out everything in one document that we can use it to start getting support for Rose, instead of waiting for an official diagnosis. Something we know can be an uphill battle.
All SEN parents need this app, I just wish it was around or I knew about it 7 years ago when I was struggling to understand what was going on with my older son.
More people need to be aware of it and I certainly will be sharing it to any SEN parent I know!
I will continue to use it and enter info each day! I particularly like the reminders to complete it each day, as I do sometimes forget.
Thank you for this report and everything the app does for SEN parents. It’s an amazing resource.”
Ginny
Mother to Rose
Launching October — 20 places
Each family gets clinician time, so the first cohort is capped at 20 — and these first 20 places are at half price, £150 instead of £300. Join the waitlist now — priority goes to families who are ready, including those already building their diary in the app.