English Childminder, Hilversum.

English Childminder, Hilversum. Qualified in childcare since 1995, over 20 years of experience, registered childminder since 2008.

Having qualified in the UK in 1995, i worked within various schools and childcare settings before setting up my own childminding business in November 2008. Providing English daycare for International families living in and around Hilversum.

Our little Spider-Man! Rocking his hearing aids, My little mindees have all been fascinated by them too
25/08/2022

Our little Spider-Man! Rocking his hearing aids,
My little mindees have all been fascinated by them too

💖
05/04/2022

💖

WCAT Ambassador Thomas recently celebrated his 9th ‘Happy Heart Day. His mum, Alison, tells us more.

‘This is a day that is celebrated a lot within families whose children where born with congenital heart defects. It celebrates the anniversary day of a child’s open heart surgery.

The date of a child’s open heart surgery is a huge milestone in a family’s life.
Without these heart surgeries children could go into heart failure and would not survive.
Its such a monumental moment that the thoughts and feeling that you have as a parent stay with you your entire life.
This is why many families choose to turn it into a celebration.

We mark every year with a small party for Thomas, joined by family and friends who supported us at the time of his surgery.
Thomas looks forward to this day every year.

Thomas is now 9, and he is questioning why he has his “brave” - the scar down the centre of his chest which was caused by his heart surgery. We feel that his heart surgery was such a significant moment in his life and he should understand what happened and how he got his “brave”. So this year we created a photo storybook of his first year, as it was quite medically complex. The book includes a simplified explanation of his heart defect
and lots photos of him during his first year, especially the 4 months he spent in hospital and his heart surgery time. We have included in the book a photo of him with his surgeon and the ICU Drs and nurses who looked after him.

Without their expertise, dedication and care Thomas wouldn’t be here.
We called the book “How I Got My Brave”

05/03/2022

Me and Thomas doing Wouldn't Change a Thing Saturday Signs
Windmill /Mollen

21/02/2022

Great video showing children with Down syndrome Can learn more than one language. 🤩🇬🇧🇳🇱🇵🇷🏴󠁧󠁢󠁷󠁬󠁳󠁿🇮🇹🤩

🥰⭐️🥰 SO PROUD ⭐️🥰⭐️Thomas is so happy to be an Ambassador again for Wouldnt change a thing.  🥳🥳🥳When I fist started look...
20/01/2022

🥰⭐️🥰 SO PROUD ⭐️🥰⭐️

Thomas is so happy to be an Ambassador again for Wouldnt change a thing. 🥳🥳🥳

When I fist started looking for online groups like it was definitely for me it was was my way of me reaching out asking for support and advice of other parents.
But then we found Wouldn't Change a Thing and the charity has had a massively positive impact on our lives.

Over the last few years he got so excited doing videos and really wanted to make them.
Last year he started to tell people about wouldn’t change a thing - apparently in school whenever he has iPad time he watches all the WCAT videos, school have even subscribed to the YouTube channel 😂
But the moment I realised just how proud Thomas was to be involved with WCAT was watching the National Diversity Awards last year and his reaction when he saw them nominated and then Winning was priceless

So we are all made up that he’s staying on as ambassador again. 💖

We are delighted that 2021 WCAT Ambassador Thomas is joining us again as an ambassador for 2022. Thanks to mum, Alison, for introducing him again this evening.

‘Thomas is 9 and from a British family who live in the Netherlands.
He lives with his mum Alison, dad John and 14 year old brother Daniel.

After a standard pregnancy, Thomas was born via emergency c-section. His first 6 months where medically difficult, including a 5 week NICU stay, where doctors diagnosed Down syndrome and AVSD (a heart condition).
He had heart surgery at 16 weeks and diaphragmatic hernia surgery at 20 weeks. He also had pulmonary hypertension and a feeding tube till he was 10 months old.

But this didn’t stop him! Thomas has always been determined and full of life.
He defied every obstacle and smashed every hurdle put in his way.
He has this way of grabbing people’s attention and hearts; his smile lights up the room, he’s loving, kind and fiercely empathetic, he can read people’s moods better than most adults.
He is fun and mischievous, he makes friends wherever he goes, he loves singing, dancing, playing football, playing with his brother and his brother’s friends, who all look past his Down syndrome only seeing a cool, funny little boy.

He also loves a challenge!
His biggest challenge has been learning a second language. Thomas has attended a Dutch SEN nursery since he was 3 years old, he transitioned to SEN school when he was 6.
When he first started at nursery there was concern over his language acquisition skills, but within weeks he was signing in Dutch.
Within a year he was speaking words in both English and Dutch. He’s now 9 and still has a small speech delay, but over the past 6 months we’ve seen huge jump in both languages.

We’ve been involved with Wouldn’t Change a Thing for a few years. Thomas is so proud to be involved with Wouldn’t Change a Thing, he recognises the logo, he gets excited whenever there is a new project, he can name children and parents he’s never met, but he “knows them” from the videos and stories.
He tells people he’s an ambassador. I think he just loves the feeling of be represented.
One of his 2021 highlights was watching The National Diversity Awards, he was so excited and cheering when they announced Wouldn’t Change a Thing winners.

We couldn’t be prouder of him, he’s everything we could have asked for and more.’

28/10/2021

October is Down Syndrome awareness month
But it is also Augmentive and Alternative communication month.,

Here is Thomas showing off his bilingual skills

So very proud tonight! Well done to everyone at Wouldn't Change a Thing 💗🥳🥳🥳💗Challenging perceptions and smashing outdat...
17/09/2021

So very proud tonight! Well done to everyone at Wouldn't Change a Thing 💗🥳🥳🥳💗
Challenging perceptions and smashing outdated stereotypes of Down Syndrome!
Proud that Thomas is part of this amazing community 🤩🤩🤩

Congratulations to all involved at Wouldn't Change a Thing!!! You are the WINNERS of the Community Organisation award for Disability at the National Diversity Awards 2020!!

Wouldn’t Change A Thing (WCAT) started with a video, created for World Down Syndrome Day 2018, that took social media by storm. 50 Mums | 50 Kids | 1 Extra Chromosome became one of the most popular not-for-profit viral videos of all time, racking up in excess of 500 million views to date and popularising the hashtag: .

The video made such a positive impact on modernising mainstream perceptions of the condition that some of the parents involved set up Wouldn’t Change A Thing to continue the mission. It has now grown to include a multi-skilled, passionate group of people from all over the world.

They create projects to challenge outdated perceptions which are devised to be uplifting, emotive and positive; offering insights into how enjoyable life for all those associated with the condition can be. They now have a combined social media following of 50,000.

Fantastic!!

Adres

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