Avarni-Mae’s Journey

Avarni-Mae’s Journey Avarni-Mae’s Journey � Fighting T Lymphoblastic Lymphoma Leukaemia at just 2 Years old.

🎗️🧡AVARNI-MAE’S JOURNEY UPDATE 🧡🎗️Yesterday was another incredibly tough day for our little warrior. 😔🧡Avarni-Mae was st...
04/09/2026

🎗️🧡AVARNI-MAE’S JOURNEY UPDATE 🧡🎗️

Yesterday was another incredibly tough day for our little warrior. 😔🧡

Avarni-Mae was still spiking temperatures roughly every 4 hours, and her CRP had risen to 190, showing just how much inflammation her little body is fighting at the moment.

She has also been having some really bad stomach pains and has been throwing up quite a lot. Because of how much pain and discomfort she has been in, the doctors have put her onto a constant morphine PCA to help keep on top of the pain and keep her as comfortable as possible.

The doctors also think she may have mucositis, which could be contributing to the pain, sickness and difficulty she is having at the moment. She is pooling her saliva and not swallowing very much, which is another indication that her mouth and throat are really struggling. 💔

She also needed a blood transfusion last night, as her blood counts continue to be very low. It was an incredibly difficult night, and unfortunately, there wasn’t much sleep to be had because of the stomach pains and how unsettled she was. 😢

But amongst all of the difficult moments, today has brought us some little positives to hold onto. 🧡

Her CRP has come down from 190 to 174, which is a step in the right direction. Her blood cultures have also not shown anything growing as of yet, which is reassuring, although she is still being very closely monitored and treated because she continues to spike temperatures.

She has needed another platelet transfusion today, as her platelet levels remain very low. She is still spiking temperatures, but thankfully the spikes are now lasting longer than the 4-hour mark, rather than happening as frequently as they were.

And then there is the news we have been waiting so desperately to hear… engraftment is starting to happen. 🥹🧡

Her numbers are slowly starting to come back, which means her new cells are beginning to appear and her little body is starting to show those first signs that the transplant is taking hold. It is still very early, and she has a long road ahead of her, but seeing those numbers slowly rise gives us the biggest glimmer of hope.

She is still incredibly poorly, still fighting infections and complications, and still has so much to get through. But today, we are choosing to focus on the little positives. A drop in CRP. Blood cultures still showing nothing growing. Longer gaps between her temperature spikes. And, most importantly, those first signs of engraftment.

One day at a time. One blood result at a time. One transfusion at a time. One tiny step forward at a time.

We are so unbelievably proud of you, Avarni-Mae. You continue to show us just how strong our little warrior is. 💗🎀

Please keep our girl in your thoughts and prayers as she continues to fight her way through this incredibly difficult part of her journey. 🙏🏻

Come on, Avarni-Mae. Keep fighting, beautiful girl. Your body is starting to do exactly what we have been praying for. 🌸💗

🧡🧡 UPDATE ON AVARNI-MAE 🧡🧡Avarni-Mae’s Journey 🎀It’s been a really rough night for our little girl. Throughout the night...
02/09/2026

🧡🧡 UPDATE ON AVARNI-MAE 🧡🧡

Avarni-Mae’s Journey 🎀

It’s been a really rough night for our little girl. Throughout the night, Avarni-Mae has been up quite a few times being sick, and unfortunately today she has woken up really flat and just doesn’t look herself at all. 💔😢

This morning her temperature was 38.1°C, and not even 4 hours later it had risen again to 39°C. She is really not looking well today, and it’s horrible seeing her so poorly, especially after everything she has already been through.

Her CRP has also gone back up to 39, which is obviously concerning and something they are keeping an eye on.

We’re taking things hour by hour and just hoping we can get her feeling a little more like herself soon. 🧡

I’ll update you all with any further updates if and when needed. Thank you, as always, for all your love, support and messages for our girl. 🧡

🧡🎗️SEPTEMBER IS CHILDHOOD CANCER AWARENESS MONTH🎗️🧡September will always hold a very different meaning for our family.Be...
01/09/2026

🧡🎗️SEPTEMBER IS CHILDHOOD CANCER AWARENESS MONTH🎗️🧡

September will always hold a very different meaning for our family.

Before cancer, Avarni-Mae was just our happy, beautiful little girl — full of personality, laughter, mischief and so much life. 💕 She was making memories, growing, learning and simply being a child. We never imagined that our lives were about to change so completely.

Then came the signs that something wasn’t right.

What started as changes that we never could have imagined would be connected to cancer eventually led us to the devastating diagnosis no parent ever wants to hear: our child has cancer. 💔🎗️

From that moment, Avarni-Mae’s world changed.

Hospital appointments became our normal. Tests, scans, procedures, treatments, long hospital stays and endless uncertainty replaced so many of the ordinary things childhood should be filled with. There are days of fear, tears and exhaustion, but there are also moments of incredible strength, courage, laughter and love.

We watch our little girl face things no child should ever have to face.

Cancer hasn’t just affected Avarni-Mae — it’s changed our whole family. It’s changed the way we see time, the things we worry about, and what we consider important. It’s made us realise just how precious the simplest moments really are.

🎗️ Childhood cancer doesn’t stop because September ends.

Behind every statistic is a child.
Behind every diagnosis is a family.
Behind every hospital bed is a childhood that has been interrupted.

This month and every day, week & month onwards we will carry on sharing Avarni-Mae’s story not for sympathy, but for awareness, understanding and hope.

We want people to know the little girl behind the diagnosis. To remember who she was before cancer, to see the strength she has shown throughout her journey so far, and to understand just how much childhood cancer can change a life.

Avarni-Mae is so much more than her cancer diagnosis. She is our girl. Our fighter. Our reason to keep going. 💗

So this September, please help us shine a light on childhood cancer. 🎗️

Talk about it. Share awareness. Support families. Listen to the stories. Remember the children.

And most importantly, never take the ordinary days for granted. 💛

For Avarni-Mae, and for every child fighting cancer — we see you, we love you, and we will keep fighting alongside you. 🎗️💗

30/08/2026

🧡🧡 absolutely amazing what Echoes Events have done for Avarni-Mae… Thankyou to every single person involved. Use have done absolutely amazing 🧡🧡

🧡UPDATE ON AVARNI-MAE DAY +3 🧡3 days past transplant and our amazing girl is still doing absolutely fantastic! 🥹🧡Avarni-...
30/08/2026

🧡UPDATE ON AVARNI-MAE DAY +3 🧡

3 days past transplant and our amazing girl is still doing absolutely fantastic! 🥹🧡

Avarni-Mae continues to amaze us every single day. She is in such great spirits, still smiling, playing and keeping everyone around her on their toes! ✨ Seeing her so happy and active at this stage means the absolute world to us.

Yesterday, her platelets were a little too low, so she needed a platelet transfusion. This is something we know can happen as her body goes through the transplant process, and thankfully she took them really well.

Today, she needs a little magnesium correction as her levels have dropped, so the team are topping her back up and keeping a close eye on everything. 💕 These are all little bumps along the road that we expected, and we are so grateful that, despite them, Avarni-Mae is still up, playing and being her amazing little self.

It honestly blows our minds how strong she is. 💪🏼Her body has been through so much already, yet here she is, three days post-transplant, smiling, playing and showing us just how much of a little fighter she really is. 🥹🧡

We’re taking every day as it comes, celebrating the good moments and getting through the little hurdles together.

Day +3 and you’re absolutely smashing it, our beautiful girl. 🌈🧡

Keep fighting, Avarni-Mae. One day at a time. 🦋✨

27/08/2026
27/08/2026

The Thursday Night Club with Harvey Whiteley is live from 6.00pm 📻

Coming up tonight, we have lots of great music to kick start your bank holiday weekend, just that little bit early. 🎵

Harvey is also joined by the lads from Echoes Events, Adam Harris, Marc Taylor and North East Rave legend Mark Banks as they, look ahead to their massive and important fundraising event in aid of Avarni-Mae’s Journey's this Friday night at The Middlesbrough Empire

Make sure you tune in! 🫵

📻 Listen Live:
104.5 FM | DAB | Smart Speakers | Mobile App
Online: www.cvfm.org.uk

Download the FREE CVFM Radio App – just search “CVFM Radio” on your app store!

📱 Get in Touch:
SMS & WhatsApp: 01642 688104

27/08/2026

🧡 TODAYS TRANSPLANT UPDATE 🧡

A Little Update on Our Girl 🧡🎗️

Our brave little Avarni-Mae has now officially had her Stem Cell Transplant (bone marrow transplant) — and it’s completed. 🥹🧡

After everything she has been through to get to this point, it feels almost surreal to be able to say that the transplant is DONE. 🎗️

Now comes the hardest part for us… the waiting. Waiting for those precious new stem cells to settle in, grow, and start doing what they need to do. 🤞🏼🩷

There is still a long road ahead, and we know there may be difficult days along the way, but today we are choosing to celebrate this huge milestone. 🌸

Avarni-Mae, you are the strongest little girl we know. We are so incredibly proud of you and everything you have fought through. 💗

Thank you to every single person who has continued to follow her journey, check in, send love, prayers and messages, and stand beside our family. It means more than we could ever put into words. 🫶🏼

The transplant is done. Now we wait.
One day at a time, one milestone at a time. 🧡🎗️

🧡

🧡 UPDATE ON AVARNI-MAE 🧡Today has been another big day for our brave girl. Avarni-Mae has needed her first blood transfu...
26/08/2026

🧡 UPDATE ON AVARNI-MAE 🧡

Today has been another big day for our brave girl. Avarni-Mae has needed her first blood transfusion since coming onto Ward 3 and starting her prep for the transplant because her haemoglobin is low. It’s been another reminder of just how much her little body is going through, but as always, she is taking everything in her stride. ❤️

And tomorrow… tomorrow is THE DAY. 🥹🩷

Tomorrow is the day of Avarni-Mae’s bone marrow transplant. We’re not sure yet what time her stem cells will be put up, so we’re waiting patiently to find out. We are so incredibly excited and hopeful for this next step, but if we’re being honest, we’re also feeling so nervous. There are so many emotions all at once.

For Avarni-Mae, though? She is completely unfazed by it all. 🥰 She continues to amaze us with her strength, her bravery and her beautiful little spirit. Nothing seems to faze our girl, and we couldn’t be prouder of her.

Tomorrow marks such a huge milestone in her journey, and we are praying with all our hearts that these precious stem cells do exactly what they need to do. 🙏🧡

Come on Avarni-Mae, you’ve got this! 💪🏼🎀

Please keep our girl in your thoughts and prayers as we take this next, incredibly important step with her. 🧡

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