Calebs Trio of Hope

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Calebs Trio of Hope Supporting children with palliative cancer diagnosis our own hero Caleb is our driving force SC051825

29/10/2026

Thinking of one of the families we recently supported with a memory grant sadly they gained their wings too soon and today is the service.
The passing of a child never gets any easier sending our love and strength to all the childs family and friends đź’”

We are delighted today that Kiltwalk 2027 dates have been announced as we know it’s a firm favourite of our supporters 💛...
22/10/2026

We are delighted today that Kiltwalk 2027 dates have been announced as we know it’s a firm favourite of our supporters 💛

If you are thinking about registering sign up using the link below by choosing your preferred location and help raise funds for Caleb’s Trio of Hope 💛

We can’t wait to see you all again taking part in this fantastic event 💛

https://www.thekiltwalk.co.uk/events/glasgow

https://www.thekiltwalk.co.uk/events/aberdeen

https://www.thekiltwalk.co.uk/events/dundee

https://www.thekiltwalk.co.uk/events/edinburgh

Hi everyone not long until our Christmas ladies day. Get the girls together and come down to the Glenhead Tavern in Dunt...
20/10/2026

Hi everyone not long until our Christmas ladies day. Get the girls together and come down to the Glenhead Tavern in Duntocher for an afternoon of fun, dancing, Prosecco, cocktails Tombola and raffle.

If you have purchased tickets already they will be handed out this week.
Or pop in to the Glenhead tavern in Duntocher and purchase then from behind the bar 🎶🎅

03/10/2026
03/10/2026

We spent a fantastic afternoon supporting the team at FORMA who took part in Battle Cancer today for the charity.
Great team effort from everyone, I may well join in next year.

Thank you for choosing to support our charity the team managed to raise an incredible ÂŁ295 this will be put towards our Christmas projects to purchase pantomine tickets for our oncology families.

If anyone wishes to donate you can do so using the link below

https://www.justgiving.com/page/char-p-1790621420945?utm_medium=FR&utm_source=CL

Today marked another milestone in Calebs journey its been exactly 4yrs since he stopped his last chemotherapy and yester...
01/10/2026

Today marked another milestone in Calebs journey its been exactly 4yrs since he stopped his last chemotherapy and yesterday we had an oncology appointment and his scans have gone to 6months.
Today we had a follow up appointment with his neurosurgeon and we discussed how much of a miracle he truly is to think we were told he wouldnt see turning 5 to now being almost 11 in a few months is nothing short of a miracle. We are incredibly grateful we get to see each and everyday we do
From the incredible doctors to the wonderfull world of research we are incredibly lucky, and its with a special thanks to his incredible surgeon removing the tumour for a second time and us being able to participate in a trial drug that we have seen these years.
Despite Calebs ongoing issues/long term side affects that we deal with everyday he still gives us the biggest smiles,determination and sheer resilence.
We are incredibly grateful to everyone whom has played a part in Calebs journey as we know things could have been very different.
Todays picture (shared with permission) of Caleb today with Dr Roddy O'Kane who we owe his life too and Calebs journey through the years 💛💛💛

Tonight draws a close to Childhood Cancer Awareness Month but for families living with this diagnosis it never ends each...
30/09/2026

Tonight draws a close to Childhood Cancer Awareness Month but for families living with this diagnosis it never ends each and everyday they watch and pray their child gets through the gruelling treatments sadly in many cases the treatments arent enough.
Approximately 36 children are diagnosed EVERY WEEK In the UK with cancer.
250 children here in the UK DIE from childhood cancer each year,that equates to 5 children each and EVERY WEEK this is sadly seen as rare however for every family we represent this is arguably the most frustrating sentence cancer is not rare to these families its never ending destruction.
We aim to try to raise as much awareness as possible and to try to support these families as much as we can.Whilst we may not always be continously updating on our socials please be assured we are quietly working behind the scenes as we also continue to navigate our own families personal journey through this awfull illness đź’›
Thank you for reading,sharing and supporting our posts each and everyday đź’›

Tonight the Titan crane in Clydebank is lit up in gold to represent Childhood Cancer Awareness month.
Thank you to Marie McNair MSP and West Dunbartonshire Council for their support in representing all the children who are fighting or completed treatment and for the ones who are sadly taken too soon 💛💛💛

May is brain tumour awareness month.One of our reasons why we created our charity was to help fund brain tumour awarenes...
13/05/2026

May is brain tumour awareness month.
One of our reasons why we created our charity was to help fund brain tumour awareness and research after our own son Caleb was diagnosed age 3 with a rare aggressive brain tumour we never knew much about brain tumours until it entered our family’s life.
Brain tumour signs to watch out for in children are as follows:_

Symptoms and Diagnosis Symptoms in children can be varied and often mimic other illnesses, leading to longer diagnosis times (median over 3 months).

Parents should watch for:Headaches:Particularly if persistent or waking the child. (Caleb had this over a period of 4days however at the age of 3 he shouldn't know what a headache is so should have been red flagged at A&E which sadly it wasnt)

Vomiting: Especially in the morning.(Caleb violently vomited every 30mins over 12hrs when he first took ill)

Vision/Eye Changes: Blurred vision, diplopia (double vision), or involuntary eye movements.

Behavioral/Physical Changes:

Fatigue, lack of motivation, balance issues

(Caleb started to walk inwards towards his pram in the weeks leading up to his diagnosis we didn't think anything as he was a late walker due to being premature and at the time he had a weakness in his left hand side which had been picked up previously)
On relapse Caleb had Fatigue signs as he started to sleep a lot more.

(ataxia), or regression in milestones.

Head Size: Increasing head circumference in infants.

If you ever have these symptoms present in a child please go with your gut we got sent home 3 times and on the 4th I demanded he be looked at if I hadn't he would have gone home to die as he had sadly already started heomaraging and nobody had picked up on it.

This is why we need better education in GP surgeries and A&E as sadly too many times children are overlooked and deemed as rare however despite this Brain tumours are the leading cause of death in cancer for the under 40s children being included in this statistic.

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Clydebank

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