HOPE for Skye: Sanfilippo Children's Foundation

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HOPE for Skye: Sanfilippo Children's Foundation HOPE for Skye is dedicated to Skye Robson who has Sanfilippo Syndrome. It's part of a wider 'Hope' campaign of the Sanfilippo Children's Foundation.

Skye "Nongnaphat" (Angel) Robson,
(written by Mark Robson)
Both our children were born in Bangkok, where I lived for 12 years working in the adventure travel industry. It was during this time that I met my wife, Wanna, or as she is known "Daeng". Thai people believe that evil spirits are attracted to young children, so in order to confuse them children are given two names: their official name and a nickname. Whilst we did not carry on this tradition with our children, we did give them a western name as a first and Thai name as their middle names to truly represent their heritage. Our son, Luke, was given his grandfather’s name “Winai” and our daughter, Skye, was given the Thai name “Nongnaphat”, which means Angel. In 2012, when Luke was 3 and Skye was 2, we relocated back to Melbourne, Australia. I had decided it was time for a career change and had been successful in an application to do a Master of Teaching at the University of Melbourne. Upon reflection, it is around this time we started to suspect something wasn’t right with Skye’s development, as the only word that she could say with any consistency was “No”. We thought that she was just taking her time and would be fine in the long run. As time progressed, this didn’t happen. We were referred by the local community nurse to a Speech Therapist and a programme being run through the local community centre. This required my wife to take Skye along to sessions on a regular basis with other parents. Not long into the programme, Daeng’s sister lost her battle with cancer and she returned to Thailand for a few weeks to be with family. As a result, Skye did not continue the programme. At the time, we were still not overly concerned as we were confident she would catch up in her own good time and we could always re-enrol in the programme. The year rolled on and I finished my course and was lucky enough to gain employment at a school in Ballarat. Daeng and I had discussed relocating to a regional centre as we saw an opportunity for a good lifestyle for our family, not to mention a more affordable one! Luke started kindergarten and then moved onto Prep at the local primary school in 2014. In the same year, Skye started at the local Kindergarten. As time passed, she seemed to stand still while other children around her continued to develop. It was now that we started to get concerned. We were lucky enough to be referred to our wonderful paediatrician, who was determined to find answers to what was causing Skye’s delay. Following a barrage of tests, we had an appointment with her in July 2014. All the discussions to date had been around enrolling Skye at the Special School to do a year of Prep, with the hope that she would catch up and be in a position to attend the local primary school the following year, possibly repeating Prep. Our story is the same as everyone else’s battling this disease: we walked into that appointment with a slightly delayed child and walked out with one who was terminally ill. Our world came crashing down, we were stunned. My wife is Thai, born in Kanchanaburi, Thailand and I was born in Melbourne, Australia. This condition has been traced back to the Dutch… and the odds of us both being carriers is, well… crazy. A trip to the Metabolic Clinic at the Royal Children’s Hospital the next day and a blood test confirmed that Skye has MPS III B. To compound matters, my wife lost her hearing completely only 3 weeks before we received the diagnosis. She had been having issues with her hearing since our daughter was born and it had got to a point that she required hearing aids. She was suffering from a cold and blew her nose one night, which resulted in her hearing disappearing altogether. She is currently waitlisted for a Cochlear implant. This has presented challenges, particularly when it comes to communication between Mum and daughter. Since Skye’s diagnosis we still have times where tears are shed, but we are determined to bring her love, happiness and quality of life not to mention to seek out a cure. At the same time, we have our son Luke to raise, who is an amazing big brother to Skye; always looking out for the welfare of his little sister. Luke and Skye are our little Angels and always will be.

Today’s the day- Childhood Dementia Day! Let’s double those donations. As we are still running Steps for Skye this month...
22/09/2026

Today’s the day- Childhood Dementia Day! Let’s double those donations. As we are still running Steps for Skye this month, we are able to double donations for our fundraiser 💜💜 so grateful!

Donate here - https://www.childhooddementia.org/fundraisers/teghanhenderson/steps-for-skye-2026

Today is Childhood Dementia Day. Donate today and have twice the impact - all donations are DOUBLED.

Over the last month you've heard about Angelina, Caleb, Eddie, Hannah, Noah, Thomas and Toby. Some are living with childhood dementia today. Some have died. Every one of them is why we're saying it plainly: We Can't Wait.

We can't wait for early diagnosis of the 145+ conditions that cause childhood dementia. We can't wait for more research into this group of conditions. We can't wait for treatments and improved survivorship. We can't wait for children and families to have the right supports around them every step of the way.

Your donations will help drive these changes forward.

Today, every donation is doubled, dollar for dollar, up to $150,000, thanks to the Hooper Shaw Foundation.

Donate now and play a part in changing the future for childhood dementia and the 2 Australian babies born every week with one of these conditions. We Can't Wait.

www.childhooddementia.org/wecantwait

$11,600 raised and a lot more to go 💜https://www.childhooddementia.org/fundraisers/teghanhenderson/steps-for-skye-2026
16/09/2026

$11,600 raised and a lot more to go 💜

https://www.childhooddementia.org/fundraisers/teghanhenderson/steps-for-skye-2026

Meet Teghan and Skye. Skye has Sanfilippo syndrome, a form of childhood dementia. Teghan, with fellow carer Bree, has cared for her for almost 12 years.

In 2020, they challenged 15 people to walk 15,000 steps a day for a month. 6 years on, Steps for Skye has raised over $135,000 for research, care and advocacy - for all kids with childhood dementia, not just Skye.

This September, Teghan and the team are back, and the challenge is open to everyone. Inspired by their story? Pick a challenge, ask 15 people, and see what happens.

Sign up for Steps for Skye 2026: https://www.childhooddementia.org/register/steps-for-skye-2026/

Every donation made on Childhood Dementia Day, Wednesday 23 September, will be matched up to $150,000 thanks to the Hooper Shaw Foundation. Double the impact, one day only.

We are getting closer !! 13 days until Steps for Skye 2026. Don’t forget to sign up 💜💜During the past 6 years, over $135...
19/08/2026

We are getting closer !! 13 days until Steps for Skye 2026. Don’t forget to sign up 💜💜

During the past 6 years, over $135,500 has been raised for Sanfilippo Syndrome. Let’s not stop now 👊🏼

Donate here - https://www.childhooddementia.org/fundraisers/teghanhenderson/steps-for-skye-2026

WE ARE BACK in 2026!! 💜💜
With a little change… Steps for Skye will be this SEPTEMBER.

Just think warmer weather, easier steps 🤪
15,000 steps a day, solo or in a team!

Link below takes you to sign up (and donate) so get ready for a big month ahead.

https://www.childhooddementia.org/event/steps-for-skye-2026/home

WE ARE BACK in 2026!! 💜💜With a little change… Steps for Skye will be this SEPTEMBER.Just think warmer weather, easier st...
19/07/2026

WE ARE BACK in 2026!! 💜💜
With a little change… Steps for Skye will be this SEPTEMBER.

Just think warmer weather, easier steps 🤪
15,000 steps a day, solo or in a team!

Link below takes you to sign up (and donate) so get ready for a big month ahead.

https://www.childhooddementia.org/event/steps-for-skye-2026/home

That’s a wrap on Summer holidays. Our beautiful girl turned 16, explored the beach, went to lots of cafes (her new favou...
28/01/2026

That’s a wrap on Summer holidays. Our beautiful girl turned 16, explored the beach, went to lots of cafes (her new favourite thing!), enjoyed time with family and friends and now ready to head back to school 🤍🎉☀️

Steps for Skye 2024 !! 🌟 🌟 We are back for our 5th year and we can’t believe last year we hit the big $100,000. We can’t...
29/07/2024

Steps for Skye 2024 !! 🌟 🌟

We are back for our 5th year and we can’t believe last year we hit the big $100,000.
We can’t wait to see what this year brings.

- Firstly, sign up solo or in a team and walk 15,000 steps a day for the month of August to raise much needed funds for Sanfilippo Syndrome, a form of Childhood Dementia which my darling Skye suffers from.

- Secondly, share your links and start fundraising for funds to go towards research into this rare disease.

- Thirdly, have fun and step every day from 1st August until 31st August. Yes we know August is a very cold month but it’s a challenge and nothing as challenging as what Skye goes though each day.

Lastly, the wonderful Stitch Nest has put together some merchandise for us with profits raised going towards Steps for Skye. We hope you love them as much as we do 🤩💜 Any questions just message me, yay let’s go !!

Sign up (scroll down on page) - https://www.sanfilippo.org.au/event/view/2024-steps-for-skye

Buy Merch - https://www.stitchnest.com.au/collections/steps-for-skye

Donate - https://www.sanfilippo.org.au/fundraisers/teghanhenderson/2024-steps-for-skye

Address

Ballarat, VIC
3350

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