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support - share - experience

   
  • Home
  • About Little Hiccups
    • About Us
    • Welcome Pack
    • FAQ
    • Meet The Team
    • Awards and Certifications
    • Supporters and Affiliates
    • Policies and Procedures
  • How We Support
    • –
      • Stay n’ Play
      • Family Fun Days
      • Parent/Carer Events
      • Hydrotherapy
      • Physiotherapy Support
      • Accessible Yoga Sessions
    • –
      • All Terrain Buggy Hire
      • Travel Bed Hire
      • Stabilo Bagel Hire
      • Counselling
      • Compassion Packs
      • Mosaic Trail
    • –
      • Max Card
      • Educational / Informative
      • The Principle Trust Holidays
      • Ison Harrison Solicitors – Making a Will
      • Other Information
  • Get Involved
    • Volunteering
    • Fundraising
    • Corporate Sponsorship
    • Charity Lottery
    • Will Legacy
    • Give As You Live
    • Nectar Donate
    • Donate
  • Upcoming Events
    • All Events
    • Family Fun Days
    • Parent/Carer Events
    • Stay n’ Play
    • Educational / Informative
    • Fundraising
    • Annual Charity Ball
  • Blog
  • Contact
  • DONATE
  • Store
    • Shop at Little Hiccups
    • Cart
    • Checkout
  • Login
    • Login/Register
    • Update My Details

support - share - experience Here to support and guide you Finding out that your child has an additional need or disability can be overwhelming. Little Hiccups is here to support and guide you through it all. Find out more support - share - experience Here to support and guide you Finding out that your child has an additional need or disability can be overwhelming. Little Hiccups is here to support and guide you through it all. Find out more

Welcome to Little Hiccups

Little Hiccups is an award-winning, Leeds-based, parent-led support charity dedicated to helping families with children who have disabilities or additional needs. Founded by parents who understand the unique challenges of raising a child with complex needs, we provide a safe, inclusive, and welcoming community where families can connect, share experiences, and access vital support.

In 2005, Linsay, the founder of Little Hiccups gave birth to her little boy, full of the joys of becoming a parent and filled with all of the dreams and aspirations for their lives ahead…. those dreams were shattered just a few days afterwards as they very nearly lost their boy. They spent the following weeks in PICU before finally bringing their son home, only to keep returning to the LGI as the extent of his injuries came apparent. Jack had been left with scarring all over his brain, resulting in him having severe cortical visual impairment, he cannot sit, stand, hold up his head, or use his hands. He cannot speak (though he can certainly vocalise and express his teenage strops! He is fed via a gastrostomy, has a very difficult to treat form of Epilepsy called Lennox Gastaut Syndrome which means he has 20-30 seizures a day of every different kind and his condition is life limiting. All that said, he is the most loving and inspirational boy we have ever met.

The journey he has taken Linsay on since then has been a roller coaster. He is also the inspiration behind Little Hiccups. In fact, he is the reason behind the Little Hiccups name. The name came about because when Jack was first born he appeared to be having ‘little hiccups’. We later found out they were seizures  and this was the start of our journey and in 2009, Little Hiccups was founded.

Our mission is to ensure that no family feels isolated. We offer a wide range of services including accessible family events, sensory-friendly activities, and inclusive play sessions that are tailored to meet the needs of children with disabilities. These events are designed not only for fun but also to foster social inclusion and build confidence in both children and their families.

In addition to our events, we provide practical support such as equipment lending, signposting to relevant services, and emotional support through peer networks. We also work closely with local authorities and healthcare providers to advocate for better services and accessibility.

Little Hiccups is committed to creating a world where all children, regardless of ability, are celebrated and supported. Our work is made possible through the dedication of our volunteers, the generosity of our donors, and the resilience of the families we serve.

Am I eligible to join Little Hiccups?

Little Hiccups is a charity that supports families that have a child(ren) under 18 with additional needs or a disability.  The Education Act 2002 defines ‘additional needs’ as:

“the new concept of additional support needs refers to any child or young person who, for whatever reason, requires additional support for learning. Additional support needs can arise from any factor which causes a barrier to learning, whether that factor relates to social, emotional, cognitive, linguistic, disability, or family and care circumstances and learning environment.”

Our remit as a Charity is to support additional needs that are specific to a disability, regardless of whether or not they are registered disabled or have an official diagnosis.

Within this remit, Little Hiccups does not want to put a label on what classes as an ‘additional need’ or  ‘disability’ as the definition and range is so broad. Our emphasis will instead be on whether the family feels they need the support of the group.

We are however, completely self funded so need to ensure that the monies raised are getting to the right families that need the support the most. Consequently, we ask that families are honest and decide themselves that they feel that they are in need of the support of Little Hiccups.

Very occasionally we may have to admit that Little Hiccups is not the right environment for a particular child or family at that time; where this is the case, we will work with the family to find another suitable provision if possible.

We also ask that new members read our Behaviour Statement before joining. By joining Little Hiccups you are agreeing to abide by the Guidelines.

How We Can Support

Find out all the ways we can support you in your journey.

Find Out More

Register With Us

Register with us for free and access the fun.

Register Now

Stay n’ Play

A relaxing atmosphere where your child will be allowed to play and discover the world at their own pace.

Book Now

Family Fun Days

A weekend Family Fun Day out and about on a monthly basis for all the family. Our goal is also to show that there are no limits to having fun!

Book Now

Max Card

The Max Card is a discount card for foster families and families of children with additional needs.

Buy Now

Donate

Little Hiccups is a Registered Charity (Charity Number 1170147) and relies 100% on charitable donations, fundraising and grants to keep running.

Donate Now

Charity Lottery

Join our Charity Lottery! Only £1 a ticket.

Find Out More

Fresh from our Blog

Neurodivergent children’s parents call for support
October 17, 2025

Image caption,Louise Moller’s son was diagnosed as neurodivergent when he was five years old ByKit…

Read More
Collaboration in Rehabilitation: A Day of Insight and Inspiration at Horizon Leeds
October 17, 2025

Linsay Medica and Noel Davies-Atack had the pleasure of attending the Collaboration in Rehabilitation conference,…

Read More
Christmas Drawing Competition 2025
October 16, 2025

Get the pens and pencils ready! Entries are now open for our annual Christmas Drawing…

Read More
Free Harewood House Access for Little Hiccups Families!
October 14, 2025

We’re delighted to announce that Harewood House has gifted Little Hiccups 250 Community Access Cards! These cards offer free entry to Harewood House, Gardens and Grounds — a fantastic opportunity for our families to enjoy one of Yorkshire’s most beautiful and inclusive venues.

Read More
Sensory Fun at Lush – A Halloween Treat for Little Hiccups Families!
October 13, 2025

Yesterday, we had the absolute pleasure of joining Lush at the White Rose Centre for…

Read More

What our families say

  • In a world where disabilities are judged at Little Hiccups there are no judgments, no boundaries, no limits – just happy smiling children being able to access and enjoy life experiences that without Little Hiccups they might not ever get the chance to try.

     

     

  • We just wanted to say a huge thank you to you lovely ladies for the care package we received last week! I’m not sure how you found out but it was a welcome surprise… Your kindness made me cry happy tears! Thank you xxx

  • Photo of family on The Principle Trust Holiday“Our holiday was amazing and it gave us the opportunity to relax between constant appointments and new diagnosis. We have created some fantastic memories and we feel ready to take on the next few months.  A massive thank you to Little Hiccups and The Principle Trust.

     

     

    Laura

Our Awards and Certifications

Fundraising Regulator

View All Our Awards and Certifications here

Our Supporters and Affiliates

Get to know us

Little Hiccups is a Leeds based support group that has been set up by parents who have children with additional needs.

Through personal experience they recognise the importance of allowing the parents and families of a child with a disability the opportunity to meet people in similar situations, to make friends and support each other.

Important Links

Terms and Conditions
Privacy Statement
Use of Cookies

Contact Info

  • Little Hiccups
  • c/o The Barrowbys, 170 Barrowby Lane, Garforth, Leeds, LS25 1NG
  • 07831230741
  • info@littlehiccups.co.uk
  • https://www.littlehiccups.co.uk

Charity Details

Little Hiccups is a Company limited by Guarantee - Company number 09692276

Little Hiccups is a Registered Charity
Charity Number 1170147

Blog

  • Neurodivergent children’s parents call for support October 17, 2025
  • Collaboration in Rehabilitation: A Day of Insight and Inspiration at Horizon Leeds October 17, 2025
  • Christmas Drawing Competition 2025 October 16, 2025
  • Free Harewood House Access for Little Hiccups Families! October 14, 2025
  • Sensory Fun at Lush – A Halloween Treat for Little Hiccups Families! October 13, 2025

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