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November 24 2020 3.09pm

New Palace Minute: Royal Variety Performance 2018

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View cp forever's Profile cp forever Flag south london 03 Jun 18 2.29pm Send a Private Message to cp forever Add cp forever as a friend

Thank you wonderful and laugh out loud...hope you get the full amount for Katerina.

 

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View bexleydave's Profile bexleydave Flag Barnehurst 03 Jun 18 2.38pm Send a Private Message to bexleydave Holmesdale Online Elite Member Add bexleydave as a friend

This post has been merged from a topic called 'youtube' by Guntrisoft

Errr......

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Bexley Dave

Can you hear the Brighton sing? I can't hear a ******* thing!

"The most arrogant, obnoxious bunch of deluded little sun tanned, loafer wearing mummy's boys I've ever had the misfortune of having to listen to" (Burnley forum)

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View mezzer's Profile mezzer Flag Main Stand, Block F, Row 20 seat 1... 03 Jun 18 3.51pm Send a Private Message to mezzer Add mezzer as a friend

Very, very good Bubbs. Thank you.

So hope it goes well with your daughter.

 


Living down here does have some advantages. At least you can see them cry.

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View Bubbs's Profile Bubbs Flag Edinburgh 04 Jun 18 4.31am Send a Private Message to Bubbs Add Bubbs as a friend

What can I say... As a family we are just totally overwhelmed by the amazing support, kind wishes and generosity of everyone. Thank you just doesn’t even come close to covering it.

What an unbelievable bunch you are.

 


'Better stop dreaming of the quiet life 'cos it's the one we'll never know'

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View Stirlingsays's Profile Stirlingsays Online Flag 04 Jun 18 6.27am Send a Private Message to Stirlingsays Holmesdale Online Elite Member Add Stirlingsays as a friend

Very very good.

 


'I can't stand innuendo. If I see one in a script I whip it out immediately.' (Kenneth Williams)

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View rollercoaster's Profile rollercoaster Flag Cornwall 04 Jun 18 5.43pm Send a Private Message to rollercoaster Add rollercoaster as a friend

The Palace Minute just seems to get better every time, absolutely superb, well done Bubbs and thanks.

 

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View Lyons550's Profile Lyons550 Flag Shirley 05 Jun 18 4.56pm Send a Private Message to Lyons550 Add Lyons550 as a friend

Donated Bubbsy...another great effort sir and a more than worthwhile cause.

 


The Voice of Reason In An Otherwise Mediocre World

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View est1905's Profile est1905 Flag 05 Jun 18 5.20pm Send a Private Message to est1905 Add est1905 as a friend

Originally posted by Bubbs

A Palace Minute No.28

End of Season Royal Variety Performance

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Supporting Katerina

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Hope you all enjoy my latest Palace Minute offering. Been doing this nonsense for eight years now believe it or not, and have had so much enjoyment making them. It has never been my intention to profit from them – the pleasure has come from all the very kind comments and appreciation they have received.

However, my personal situation is such that I’ve decided to use the Palace Minute to raise funds for my three year old daughter Katerina who has Fragile X Syndrome. In summary, it’s a genetic disorder that causes a wide range of learning, emotional and behavioural challenges. Medical science now are very clear on the causes of Fragile X, and there is now a lot of work and research going on all over the world to find effective treatments and ultimately a cure.

One of the world’s leading specialists in Fragile X, is a neurodevelopmental doctor in California. We flew Katerina out to be assessed by her last December, and she has set up a treatment plan that she believes will have a positive impact on her future. Unfortunately, this is not something she can access here in the U.K due to lack of funding concerning research into the condition.

Early intervention is absolutely essential in these disorders in order to make a real difference to the future of children affected; and so as a family, we are taking the big step and travelling back to the States to receive this specialist medical treatment and therapy. We have been in touch with other families who have undertaken similar intervention from this doctor and medical centre, and have all reported back very positively about the differences it’s made to their children affected with Fragile X.

Although it is a massive upheaval and huge financial consideration, me and Mrs Bubbs feel we can’t let this opportunity to make a real difference to Katerina pass us by. So, hence, using my Palace animation to try and fund the large medical bills, travel costs and living expenses while out in the States. We would hate to look back in 10 years time and think we missed a chance to make a real difference to our daughter’s life.

Creating a fundraising page has not been an easy decision, as asking for help does not feel comfortable for me; but I realise that my daughter’s welfare and well-being is what is most important… and anyway, Mrs Bubbs said she’d kill me if I didn’t put to good use the ‘hours and hours’ spent making these ‘childish’ animations for you ‘sad sad’ people, to help our daughter.

Please know, there is absolutely no obligation to contribute – the fact this and the other ‘Minutes’ have hopefully made you chuckle over the years has been enough for me. But if you are able to donate, no matter how small, we as a family will be truly and massively grateful.


Thank you

Nick Timotheou (Bubbs)


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Bubbs my son was suspected of suffering from Fragile X as a new born baby. The doctors said he had many symptoms at the time. After tests (as you'll be well aware the blood test takes months) he was given the all clear. During which time I read a few books on the condition and prepared for the worst. My boy as it turned out is healthy and strong. My heart goes out to you and your family for the challenges you will face daily. I very much hope your daughter gets a successful treatment that she deserves.

 

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View Stirlingsays's Profile Stirlingsays Online Flag 05 Jun 18 5.38pm Send a Private Message to Stirlingsays Holmesdale Online Elite Member Add Stirlingsays as a friend

Donated, good luck with this.

 


'I can't stand innuendo. If I see one in a script I whip it out immediately.' (Kenneth Williams)

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View Y Ddraig Goch's Profile Y Ddraig Goch Flag In The Crowd 05 Jun 18 6.53pm Send a Private Message to Y Ddraig Goch Add Y Ddraig Goch as a friend

Donated


Good luck and this was an absolutely fantastic laugh loud Palace Minute.

 


the dignified don't even enter in the game

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View daneagle's Profile daneagle Flag Bromley 08 Jun 18 11.04pm Send a Private Message to daneagle Add daneagle as a friend

Haven’t been on here for a long time. Thank you bubbs for your very funny videos I love them. I have donated as much as I can. I really hope you get the full amount as quickly as possible.#cpfcfamily x

 


Why, for the love of god why!!!!!!!!!!!!!!!!!!!!!

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View Bubbs's Profile Bubbs Flag Edinburgh 10 Jun 18 4.08am Send a Private Message to Bubbs Add Bubbs as a friend

Originally posted by est1905

Bubbs my son was suspected of suffering from Fragile X as a new born baby. The doctors said he had many symptoms at the time. After tests (as you'll be well aware the blood test takes months) he was given the all clear. During which time I read a few books on the condition and prepared for the worst. My boy as it turned out is healthy and strong. My heart goes out to you and your family for the challenges you will face daily. I very much hope your daughter gets a successful treatment that she deserves.

Thanks so much for that. And so glad to hear about your son. It must’ve been a huge relief.

Funnily enough, it was the opposite experience for us; Fragile X wasn’t suspected, and and her developmental delay was put down to the ridiculous amount of infections she picked up in the first 2 years of her life. Even when our Dr said she was testing for it she told us not to worry as she very much doubt she has it as it’s so rare...so hearing the news came as quite a bombshell.

Yes, the daily struggle and constant worry is almost indescribable...you honestly wouldn’t wish it on your worst enemy, but here we are and you just have to stay positive for your kid and make the best of the hand you’ve been dealt. As devastated as we were when receiving the diagnosis, me and Mrs Bubbs have been so proactive everyday to try and push little Katerina along and tease that potential out of her. Obviously, reading everything and anything on the subject is all part of it. That’s how we found out about this top specialist in America and the promising work she’s been doing with other children with Fragile X.

Can I just take this opportunity again to thank all the Holers who have contributed so far. Can’t describe how grateful me and Mrs Bubbs are to you all.

 


'Better stop dreaming of the quiet life 'cos it's the one we'll never know'

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