Logan's Journey

Logan's Journey After my son suffered a devastating brain haemorrhage I am fundraising for private treatment and equ

16/08/2026

💦 Hydrotherapy with Beth at & Eli at 💦

If there’s one place Logan is completely in his element, it’s the water! 💙

Logan absolutely loves swimming and being in the pool, but hydrotherapy gives him so much more than just something he enjoys. In the water, he can move his body in ways that can be much harder for him on land. The buoyancy of the water supports his body and reduces the amount of weight going through his muscles and joints, allowing him to move more freely and work on strength, movement and control in a much more comfortable way.

Recently, Logan has been struggling with scapular winging. This is where the shoulder blade doesn't sit flat against the rib cage and instead sticks outwards, almost like a little wing. It can happen when the muscles responsible for supporting and controlling the shoulder blade aren't working as effectively as they should, and it can lead to weakness, discomfort and difficulties with certain movements.

Hydrotherapy has been a brilliant way for Beth and Eli to work on this with Logan. 💪💦

Because the water supports him, Logan can practise movements with less strain on his body, while the natural resistance of the water helps him strengthen the muscles around his shoulders, back and core. The warmth of the hydrotherapy pool can also help relax tight muscles and ease aches and discomfort.

And the biggest bonus?

Logan doesn't really see it as therapy. 🥰

To him, he's in the water, moving, splashing and having fun — while behind the scenes he's working incredibly hard and making progress.

We've already started to see a real improvement in his scapular winging, so we've decided to continue with further hydrotherapy sessions to build on the progress he's making.

Sometimes therapy doesn't have to look or feel like therapy… and for Logan, the water is definitely one of those places where movement just seems to come that little bit easier. 💙🌊

A huge thank you to Beth at Movement Physio and Eli at Dragons Physio for continuing to find ways to help Logan move, strengthen and progress while doing something he genuinely loves. 🥰

10/08/2026

You can find him in Queen Street 🥰🎶

I didn’t even realise how much the crowd had grown around him until he finished singing… and suddenly they erupted into cheers! 🥹❤️

Such a lovely moment, and one I’m sure he’ll remember for a long time. 🥰✨

25/07/2026

✨ A New Chapter Begins ✨
Some of you may have noticed that our page has a brand new name...
Logan's Journey 💙

When this page was first created, it was to support our fundraising efforts to get Logan to Germany for specialist treatment. Thanks to the incredible kindness and generosity of so many people, we were fortunate enough to make that journey—not once, but twice. We will never forget the support that made that possible.

As the years have passed, so has our journey. Logan continues to grow, amaze us, and overcome challenges we never imagined we'd face. It felt like the right time for this page to grow with him.

From now on, this page will be dedicated to sharing Logan's ongoing journey—his achievements, milestones, challenges, funny moments, and everything in between. But it won't just be about where we are now.

We'll also be looking back at parts of our journey from the beginning, sharing what was happening behind the photos, what we were facing at that time, what helped us, what didn't, and the lessons we learned along the way.

If sharing our experiences can help even one family who is walking a similar path, then every difficult moment we've been through will have an even greater purpose. We hope this page becomes a place of encouragement, hope and support for families navigating life with a child with additional needs.

✨️And finally... we have something very exciting in the pipeline that we've been quietly working on behind the scenes. 🤍 It's still early days, so we're not quite ready to share it yet, but we can't wait to tell you more when the time is right. We truly hope it's something that will make a difference to many other children and families.

Thank you for continuing to follow, support and believe in Logan. Your kindness has carried us through some of our darkest days, and we're so grateful to have you with us as we begin this new chapter.

Here's to Logan's Journey... and everything still to come. 💙✨

22/05/2026

Logan's Soports Day 2026

incredibly proud of Logan at sports day today! 🏃‍♂️💨
Seeing that determination (and that massive smile) on the track was the absolute best.

​Such a brilliant day. 🌞
Logan gave it 100% for his big final races of the year! 🏆
Getting a bit emotional seeing how much he's grown since his very first one here.
​

It’s been a tough few days!On Sunday, Logan became very upset out of the blue. As he cuddled into me, he said something ...
23/12/2025

It’s been a tough few days!

On Sunday, Logan became very upset out of the blue. As he cuddled into me, he said something that shattered my heart into a million pieces:

“Mum, I don’t want to be blind anymore. When will it get better so I can see like you?”

Hearing your child name the loss that you silently grieve each and every day is one of the deepest pains there is.

I celebrate every little win, every milestone and achievement, while quietly battling anger at the unfairness — alongside a constant feeling of helplessness and grief. Living in two worlds at once is something I never imagined, yet here we are.

I told him:
“Your eyes and brain work differently to mine, and that’s okay. You are an amazing superhero who can do things others can’t. You see the world in ways we never will — using your hands, your ears, your clever brain, and your pure heart.
You are a true miracle, and even though I can’t change what’s happened or fix it, I will always help you, protect you, and love you more than words can say.”

I am forever proud to be your Mummy — and prouder still to call you my son 💙

So proud of Logan 💛This week he started reading some CVC words in braille, and the school kindly took some photos of him...
12/12/2025

So proud of Logan 💛
This week he started reading some CVC words in braille, and the school kindly took some photos of him which they shared with me. I’m so happy to share them with you all.

We truly have all of you to thank. Every bit of support, encouragement, and kindness has helped him reach this moment. I will be forever grateful to each and every one of you who made it possible for him to have not just one, but two rounds of intensive therapy. It has made such a huge difference to him.

Thank you from the bottom of my heart. 🌟

06/12/2025

✨ Bursting with Pride ✨
This week my amazing boy, Logan, took part in his nativity play — and he absolutely shone.

He joined in with the dressing up, waited so patiently, played the triangle and the drums during the songs, and best of all… he said his lines so clearly and with so much confidence.

Watching him up there, taking it all in and giving it his all, was a moment I’ll never forget.
So incredibly proud of you, Logan. 💛🎄✨

Address

Cardiff

Website

Alerts

Be the first to know and let us send you an email when Logan's Journey posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Shortcuts

Share

Category