22/05/2026
Lots of fishies....sea animals 🐟🐠🐙🦀🦞🦞🐋🐢🐢🪸
The kids enjoyed thumb printing & drawing the fins & tails...well done!!🙆♀️💯💥🎉🤗
10/05/2026
Jono Lancaster was born on October 31, 1984, in West Yorkshire, England. He was born with a rare genetic condition called Treacher Collins Syndrome. This condition affects the way facial bones develop, leading to visible differences in appearance.
Just 36 hours after his birth, his biological parents left the hospital. His adoption file stated that they were “horrified by the child’s appearance” and felt no emotional bond with him. After this, Jono was placed in foster care.
In 1990, when he was five years old, he was officially adopted by Jean Lancaster, a social worker. She gave him a loving home and supported him fully, no matter how he looked. Her care played a big role in shaping his confidence and strength.
However, growing up was not easy for Jono. He faced severe bullying at school because of his facial differences. Despite this, he did not give up on life or himself. Over time, he turned his pain into purpose.
As an adult, Jono became a public speaker and disability campaigner. He travels around the world sharing his story to inspire others and raise awareness about facial differences. In 2017, he co-founded the “Love Me Love My Face” Foundation to support people with Treacher Collins Syndrome and similar conditions.
In July 2023, he published his memoir titled Not All Heroes Wear Capes, where he shares his journey of rejection, love, and self-acceptance.
12/04/2026
Thank you to our parents for coming to our Parent Teacher Meeting end March 2026. Your child has grown & learnt so much since beginning of the year! 🥰👨👩👧👦
18/02/2026
Xin Nian Kuai Le! Have a Blessed Chinese New Year 2026!!🍊🍊🍊
09/02/2026
Learning all about Aa.
The 3yo having fun doing lots of activities on Aa.
18/02/2026
09/02/2026