Killaloeโ€™s Thinking Toys has walked away with the leadership prize from the 2022 Lean Business awards.

The prestigious award show, which took place in Croke Park last month, gave a prize to Thinking Toys for an overall organisational change in their business. The award is a recognition of Thinking Toysโ€™ 18 years in the business of sensory specific products.

The company began in 2004 after its founder รine Conacur realised how few toys were available for her daughter Ailis and other children with special needs. โ€œAilis was born in London with a condition called Sturge-Weber syndrome. Essentially, she had very bad epilepsy and devlopemental delay. Then we moved back to Ireland, and Iโ€™d be buying things from England, America, Europe because I wasnโ€™t able to source things in Ireland for her,โ€ explained รine.

โ€œWhen she was eight or nine and in school, I was looking for a part time job around school hours and Michael, my husband, whoโ€™s an accountant, said youโ€™re always giving out about lack of resources why donโ€™t you do something about it. I thought thatโ€™s a great idea so thatโ€™s where it started, just as a little number for me and within two years Michael had joined me because we were just flat out,โ€ she said.

Almost two decades later the business has turned into one of Killaloeโ€™s most successful enterprises with nine people employed in the business including Ailis, now 26, who works part-time with them.

Despite all the time that has passed รine says mainstream toy retailers still donโ€™t cater well for those with special needs. โ€œI donโ€™t think [mainstream retailers] quite grasp it but I suppose itโ€™s two fold really, as a parent starting out youโ€™re bewildered and youโ€™re suddenly hit with a lot of language, โ€˜fine motor skillsโ€™, โ€˜growth motor skills, โ€™visual perceptionโ€™, โ€˜sensory perceptionโ€™, you name it youโ€™re hit with it and it kind of takes you a while to get your head around what that actually means for your child. So, thatโ€™s what I try to do with my website, Iโ€™ve tried to set it up so that the parent can easily find out what the child needs. Then the other thing weโ€™ve done is getting the pitch right for your child, a lot of kids with special needs will have poor fine motor skills and an OT will continuously tell you to do threading activities. So, you might go into a regular toy shop and find threading activities but they tend to be at the higher end of ability, so what I do is start off at the easiest level of threading and work it step by step so you can move your child along. Thatโ€™s what I think is one of the biggest problems, for our kids you need to break the activity down into easily achievable steps and itโ€™s about having those all in one placeโ€.

For รine the most important thing is to meet your child at their pace, โ€œone thing I always say to parents is that you follow your childโ€™s lead, you canโ€™t force your child to do a jigsaw especially if theyโ€™re visual perception skills are weak. What you have to do is make the jigsaw interesting to them, it doesnโ€™t matter if you do all the pieces and they do one piece, thatโ€™s success. Like with Alis when we began with connect four, she was just posting the pieces in, but I was happy because she was having to pick them up and grasp them and then post them. Then I moved her on to doing little patterns like three red, two yellow, three red, two yellow, and see if she could copy that and now youโ€™re sequencing. Then when she was nine or ten because she loved that game and was very comfortable with it I thought her the rules and now sheโ€™s 26 and we call her the connect 4 queen because she will beat you hands down, so with our activities if you can pull them into it you can get longevity out of themโ€.

Despite the business growing extensively since its beginnings of selling toys from a physical shop to now supplying parents, schools, and HSE therapists throughout the country online, รine has no plans to take the business out of her native Killaloe, โ€œItโ€™s great [being in Killaloe], I can walk to work everyday thereโ€™s no travel time. After Ailisโ€™ surgery and diagnosis, my family were all back here and I remember I was awake one night, I couldnโ€™t sleep, and then the next morning I said โ€˜Mick I want to go home but I want to go home to my home, Killaloeโ€™, he had no say in itโ€.

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