Little People at The Limes

Little People at The Limes Quality, Inclusive Care and Pre-School Education in a Safe and Enriching Environment.

For all enquires please use the form below-
https://app.famly.co/ #/inquiry?institutionId=90c041c5-ff3b-4333-b3ac-f93e161eae66&hmac=3933adea5f0ae4c148f4bf1ed5fad230d9420205301ac8b52f76a77d20d78b9a&locale=en_GB

💜 CRANIOSYNOSTOSIS AWARENESS MONTH 💜This month, we’re proud to be showing our support by wearing purple, spreading aware...
02/09/2026

💜 CRANIOSYNOSTOSIS AWARENESS MONTH 💜

This month, we’re proud to be showing our support by wearing purple, spreading awareness and raising funds for families affected by craniosynostosis. 💜🎗️

To help us raise as much as we can, we’ve put together this lovely hamper filled with lots of goodies! We also have purple ribbons that we are asking donations for 🥰🎁

But this is about so much more than a hamper…

💜 Craniosynostosis is a condition where one or more of the joints (sutures) in a baby’s skull close too early. It can affect the shape of the head and, in some cases, brain development.

By raising awareness, we hope to help educate others, support families and encourage early diagnosis and access to the right care. 💜

🎁 Want to support us?

You can purchase raffle tickets from the main building, it’s £1 a strip and all the money goes to headlines charity and Alder hay hospital. Please help us spread the word by sharing this post!

Every ticket, donation, purple ribbon and share can make a difference. 💜

Every child. Every journey. Every reason to care.

Together, we can help make a difference. 💜🎗️

Good morning,Following on from our post yesterday and to raise awareness, we have decided to try and raise as much money...
28/08/2026

Good morning,

Following on from our post yesterday and to raise awareness, we have decided to try and raise as much money as we can for two charities. One is the 'Headlines' charity that-

provides support for people throughout their life to overcome the physical, psychological, and social impacts of living with craniosynostosis and rare craniofacial conditions.

facilitates research that seeks to advance understanding, ensure the provision of quality care, and identify the best treatments for craniosynostosis and rare craniofacial conditions.

raises awareness and educates people to improve public understanding of craniosynostosis and rare craniofacial conditions.

And the other is 'Alder Hey Hospital', which does a fantastic job every day and really supported Abi, Steven, and Zach, as well as many other families. We have decided to do a raffle, ask for donations for purple ribbons (these symbolise support), and we will be wearing some kind of purple week commencing 14th September and asking for donations.

We would really appreciate your support, and any donations would be greatly appreciated 💜💜💜

Here is a direct link to Abi’s go fund me page if you would like to donate 💜

Help Abi Kirkby raise money to support Headlines - Craniofacial Support

Last week we attended Domestic Abuse Awareness training delivered by Hope Prevails and HARV. This training gave us an op...
27/08/2026

Last week we attended Domestic Abuse Awareness training delivered by Hope Prevails and HARV. This training gave us an opportunity to gain a better understanding of domestic abuse and prepare us to support and signpost people to the right services.

The course provided us with the knowledge and understanding to become Domestic Abuse Champions.

Our team are committed to continually developing their knowledge and ensuring that safeguarding remains at the heart of everything we do.

Thank you to those involved in delivering the training and for the amazing work that you do💙

Our lovely staff member would like to share her story and raise awareness 💟💜Craniosynostosis 💜With September being aware...
27/08/2026

Our lovely staff member would like to share her story and raise awareness 💟

💜Craniosynostosis 💜

With September being awareness month for Craniosynostosis. Throughout the month I will be sharing a range of different facts and insights to the condition, however, I would like to share Zachary’s story to begin our month.

January 2024. At only 6 months old, we were asked if we had concerns regarding Zach’s head. We did not, however following medical advice we got him checked. Following several consultations and transfers between hospitals. Alder Hey diagnosed our little boy with Sagittal Craniosynostosis. We were given the option of surgery which basically would mean taking apart his skull and reshaping it. We were devastated to say the least! We of course could refuse but ran many risks without it. The waiting game began…

The surgery is only really possible on children older than 18 months and to reduce levels of trauma for the child, the surgeons prefer to complete it while they are still young and growing.

We got the call in December 2025. Zachary was to have surgery in the 22nd. Meaning we would be in for Christmas 😔.

Zach was put to sleep in our arms, bravely fighting against it with being so scared, causing both myself and dad to leave in tears. 8 hours later (longest 8 hours of my life might I add). Zach was out, awake and asking for mummy ❤️ I couldn’t barely keep it together seeing my little boy all bandaged up but Zach being the bravest little boy simply asked ‘I have Juice?’

Recovery time. Zach was beyond brave and did us all so proud! He took everything in his stride and loved all the attention from the nurses, sweet talking many of them into extra treats! Zach loved having his observations taken, asking about numbers and wanting to help! Frustration hit unfortunately and he pulled his bandage off 😂.

We got to see the scar for the first time. This hit hard but of course, Zach was not bothered in the slightest! We showed them to Zach and explained they are his go faster stripes! To this day Zach refers to his scar this way ❤️

Christmas morning, Zach woke to a sack of presents kindly donated by the hospital and shared his joys with the nursing team. With how well Zach had been and the impressive progress he made in healing. We were allowed to go home mid Christmas morning.

2 weeks following, we needed to clean and care for the wound, Zach got really good at telling us ‘careful my head’.

Today his scar is completely healed, mostly covered by hair and only small sections on show, however his journey is not over. He will continued to be monitored by Alder Hey until he is 15, making sure his skull fuses together properly and no swelling occurs on his brain. Zach continues to amaze us with his bravery and ability to take it all in his stride 🥰

I have shared a few pictures, including a comparison of his head shape before surgery and after as well as how he is today 🙂

27/08/2026

⭐Good luck to our pre-schoolers!⭐

We would like to take this opportunity to say good luck to our Pre-school children who are starting school in September!

We are so incredibly proud of each and every one of you. It has been a privilege to watch you learn and grow into the amazing 'little people' you are.

A huge thank you from all the team to the children and their families for all your support, gifts and kind words.

We wish you all the very best as you begin your school adventures ❤️

We're excited to invite you to our nursery garden party on Saturday 29th of August 12pm-2pm. This is for current parents...
19/08/2026

We're excited to invite you to our nursery garden party on Saturday 29th of August 12pm-2pm. This is for current parents / carers and future families joining us-you must already have a place secured with us.
This will be a great opportunity to talk with your child's keyworker and other members of staff, see your child's room, or maybe visit the room they will be transitioning to soon.
We will have lots of fun things going on, including garden games, face painting and a Bluey and Chase meet and greet!
We hope to see you all there! 🥳

What a fantastic few weeks we've had in holiday club so far!We've been so busy with crafts, baking, walks, park trips, s...
17/08/2026

What a fantastic few weeks we've had in holiday club so far!

We've been so busy with crafts, baking, walks, park trips, swimming and visiting the library.

This week is the last week of holiday club and we have more fun things planned including a trip to Bowland Park!

Over the past few weeks, we have enjoyed exploring our community and going out on trips.We have visited the local parks,...
17/08/2026

Over the past few weeks, we have enjoyed exploring our community and going out on trips.

We have visited the local parks, library and supermarkets. The children have also been out collecting pine cones, sticks and leaves for our natural resources.

Babies have enjoyed trips to Bowland Park and Williamson park where they visited the animals and had a picnic.

We have loved the weather, and while at nursery, have enjoyed lots of time in the garden too ☀️

13/08/2026

Rhythm time- young baby course is returning to Longridge canteen for a 4 week course from 14th September! head over to www.longridgecanteen.co.uk to book your spot!

👶 Rhythm Time's Young Baby Course (0-6months)

What can a tiny baby gain from a music class?

🩷 Boosting brain connections through rich sensory experiences

🩷 Encountering new sounds & rhythms

🩷 Strengthening eye muscles by following shapes & movement

🩷 Practicing tummy time (with fun distractions!)

🩷 Developing an early sense of pulse & timing, which has many benefits to all areas of learning

🩷 Quality time bonding with mummy and daddy!

It's also a fab opportunity for YOU to meet other parents with new babies, socialise, relax, and make friends.

12/08/2026

Address

Berry Lane
Longridge
PR33JA

Opening Hours

Monday 8am - 6pm
Tuesday 8am - 6pm
Wednesday 8am - 6pm
Thursday 8am - 6pm
Friday 8am - 6pm

Telephone

01772780496

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