Addison Kemp’s Aplastic Anaemia Page

Addison Kemp’s Aplastic Anaemia Page Meet Addison Kemp who is currently battling a rare fatal bone marrow disease - Aplastic Anaemia As it stands Addison body does not produce enough blood cells.

Meet 5-year-old Addison who is in urgent need of a Bone Marrow transplant. Despite hopes that her sister Crimson would be a match, we have just received the devastating news that she is not

As we wait for results from the global donors list, the ongoing costs to Addison's family are growing. She does not produce enough platelets, so can bleed out if she has a cut and no neutrophils, so no product

ion against virus, bacteria and fungus. As Addison embarks on her Aplastic Anaemia/BMT journey this will leave only one working parent at home with her little sister Crimson and another at the hospital with Addison. This will be a long journey, should everything go well of 2 years and possibly more. We are also reaching out to friends and family members to consider being tested and joining the register. Donors must be between the ages of 18 and 35

If you are interested in becoming a donor or registering, you can find more information at the following link:
wmda.info/become-a-donor

For those of you in the UK, you can also use this link:
www.anthonynolan.org

And for anyone living in the UK who is over the age of 35, you can still register to become a donor through the DKMS Foundation here:
www.dkms.org.uk

Please share and spread the word to help find a match for Addison ❤️

18/02/2025

16/02/2025

Without learning ladders Addison would be so behind. They just make everything fun and educational!

15/02/2025

Learning Ladders Capalaba has been a part of Addisons amazing team while she recovers.

Before Addisons diagnosis, Addison had quite a few learning a speech delays. Now with treatment taking Addison out of society and definitely school, naturally we were worried if she would become further delayed.

Kerri and the team have made a real difference. Picking up from the QCH hospital school left. Working with Addison to get her ready for the return to school. Then continuing support along side.

When your child is screaming at you, "I want to go Learning Ladders". You know you're onto a good thing!

Keep following for more videos and see the growth in Addison in her learning, speech and enjoyment!

13/02/2025

Recap of her morning 💖

13/02/2025

So this happened today. Weekly catch ups with her class!

04/02/2025

A BIG thank you to the Nurse Station Cafe in the owner donated complimentary coffee to all oncology caregivers at the Queensland Children’s Hospital.

✨The most recommended coffee spot by the staff! Yes it’s that good!!!✨

Julie, thank you so much! I can say the it was very much appreciated and the nurses were very jealous! lol ☕️

Children's Health Queensland

Today we lost one of our oncology family members.💔💛Such a beautiful soul, only 2 years old and yet he touched the hearts...
01/02/2025

Today we lost one of our oncology family members.💔💛

Such a beautiful soul, only 2 years old and yet he touched the hearts of so many.

Remembering him, for us will be whenever you mentioned his name to another oncology family, staff member, charity member, they would smile. You instantly saw the lasting memory he had on them. The instant memory of his cute little face, his beautiful personality and his loving, amazing family.

Below is his favourite character.

Whenever we see Bluey, we will remember you Raffa! Sweet dreams beautiful boy 💙💛

01/02/2025

💖Clarification, regarding last nights post.💖

I will let the video do the talking. X

Sadly some people are very aware of Addison Kemp’s Aplastic Anaemia and what it means to have a child to be constantly i...
31/01/2025

Sadly some people are very aware of Addison Kemp’s Aplastic Anaemia and what it means to have a child to be constantly in hospital, keeping her from dying!

They still try and name me as something evil.

When all I’m doing is looking after my sick child and trying ways to find the pilling up of bills whilst having a family on a single income in a cost of living crisis!

I should never of posted yesterday! Addison has severe pain in her tummy and head. Panadol and Oxi wasn’t working, so as...
28/01/2025

I should never of posted yesterday!

Addison has severe pain in her tummy and head. Panadol and Oxi wasn’t working, so asked by the BMT team to present to ED.

As we’re about to leave the house, she tells me, “mummy I can’t see”! The exact start to her seizure last time. We had 2 amazing ambulance crews turn up and bring us in to the QCH.

Just waiting on the oncology team to organise the next step.

Fingers crossed we’re in and we’re out! 🤞🏼

27/01/2025

Loving life back at home 🏡 Jumpflex Trampolines

17/01/2025

Today I was interviewed about what’s going on with this specific case. You can watch it below;

Remember, what’s important now is the law does it’s thing, her child recovers and those families/children who really are dealing with awful life’s in the hospital system can heal, move on with respect and not through this awful acts eyes!

I can say this has really affected the oncology families at the QCH. As a parent who has basically lived there since Mar...
16/01/2025

I can say this has really affected the oncology families at the QCH.

As a parent who has basically lived there since March, we would never dream on our worst enemy for their children to go through this.

The actual emotional, physically and financial burden it takes on us!

This has made a mockery of everything we and our children go through.

Her poor daughter has been tortured and for no reason!!! A constant conversation within the families is “how we will help our children deal with the mental affects of treatment once cured”.

This woman put her child in harms way with no other reason but to earn money, get TikTok likes and make herself famous.

She is obviously not well! May she find the help she needs.

Most importantly, may her daughter recover and grow to be healthy, beautiful girl that she is.

14/01/2025

💖Happy 6th Birthday!!!💖There’s no reason for her diagnosis. Just on Monday the 25th March the marrow biopsy results said less than 5% bone marrow. It’s all her body had. Strange you think we live till 80+. But Addisons body was only give her 5. Forever grateful to the team at the Queensland children’s hospital. Forever grateful to all the blood and bone marrow donors globally! You are all a part of Addisons story, Addisons new life, a part of our family!!!Addison, you are 6!!! And we can’t wait for the other 74+ birthdays to come! 🎂 #6 Children's Health Queensland Children's Hospital Foundation Addison Kemp’s Aplastic Anaemia Page Starlight Children's Foundation Australia Bianca Kemp Daniel Kemp A Current Affair

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Cleveland, QLD
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