Moti Me Family

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Moti Me Family

Supporting young children with developmental delay disabilities in achieving their milestones.

13/01/2026

Children helped us design our product 💛

By spending time with them, listening to their needs and watching how they move and play, we shape our prototypes around what actually works.

Every tweak, every idea, every improvement comes from real moments like these 🌟

11/01/2026

Sometimes kids just need a little help finding their calm 💛

These simple, playful techniques can be a lovely way to support regulation, breathing and focus - especially during busy or overwhelming moments. Take a look at the image for a few easy ideas you can try together 🌿✨

05/01/2026

Jesy Nelson’s recent post about her twins has opened up an important conversation around Spinal Muscular Atrophy (SMA) 💛

SMA is a rare genetic condition that affects muscle strength and movement - and while many families live with it quietly, awareness matters.

More awareness leads to earlier support, better understanding, and families feeling less alone.

Sending so much love to Jesy, Zion and their families, as well as every parent navigating a diagnosis, questions, appointments and unknowns. We hope that these facts help to spread some awareness 🤍

04/01/2026

🐘 Meet Elfie the Elephant

This is Elfie - the sweetest elephant with the biggest heart 💕

Elfie loves routines, cosy moments and grounding activities that help children feel safe, supported and ready to learn.

Whether it’s practising balance or finding calm on a busy day, Elfie is always right there with a gentle nudge of encouragement 🐘💛

28/12/2025

Mia has made incredible progress 💪
..Using an early-stage prototype in photo 1, to our 2025 prototypes in photo 2! We have absolutely loved following Mia's journey - a true inspiration 🌟

Antonia (Mia's Mum) has says:

"Since trialling the second time we are now able to use the prototype on her tuff tray to encourage her to weight bear at the same time as using it. We love how the app allows us to change how many spots are being used. Especially as Mia has global development delay alongside her Angelman Syndrome so we can develop her control over matching different colours once she masters one, two etc."

"She has learnt how to control a squat from standing as well since using the prototype as it has given her something to bend down for when she’s practising her standing."

23/12/2025

Christmas doesn’t have to be busy to be magical ✨

Simple activities, gentle routines and moments of connection can make the holidays feel special for children with additional needs 💛

Saving this one for some cosy festive ideas? 🎄

21/12/2025

Every child has individual needs... which is why customisation is so important to us 💫

We have designed 3 friendly animal characters that can be used as part of our product!

Based on the child's goals, abilities and animal preferences, they can select their favourite to work with:

🦒 Giraffe - Single handed gripping

🐘 Elephant - Large loopy ears for easier grip

🐒 Monkey - Pinch grip practice

18/12/2025

Sometimes we rush through the day without noticing the little victories - the tiny moments that actually took so much effort ☁️

A deep breath, a small step forward, a moment of calm… it all counts 💛

What was your quiet win today?

14/12/2025

If you’ve ever felt this way… it doesn’t mean you’re failing.
It means you care 💛

04/12/2025

I recently learnt more about hydrocephalus after speaking with Nora, Mum of Rayan 💛

I was inspired by their journey and knew I had to help raise more awareness about this condition.

So today we are sharing these 6 facts about hydrocephalus so more families feel informed and supported 🧡

💙 💙 ❤️

Address

The Studio
Loughborough
LE113UZ

Website

https://www.motimefamily.com/

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