We would like to raise money for our brave little girl.

Brooke is 4 years old and is currently going through chemo, she got diagnosed in November 2025.

Brooke has a Low grade Glioma.

Low-grade gliomas (LGGs) are considered uncommon in the general population, representing roughly 10% of all primary brain tumors. While rare in adults, they are the most common brain tumor in children, accounting for 40% of childhood brain and spinal cord tumors. They are typically slow-growing and occur most frequently in young adults (ages 20–40)

This all started from having her annual eye test that then led to numerous appointment's.

The eye specialist firstly suggested glasses and an eyepatch to be worn for a couple of hours spaced out through out the day, within 12 weeks the eye specialist Suggested the eyepatch stays on all day every day along with always wearing her glasses.

3rd time seeing the eye specialist Brooke’s eye had deteriorated even more.

Following all this Brooke had a MRI at the Royal Surrey with a minor sedation as they can not give general anaesthetic for the MRI at this hospital.

Brookes minor sedation didn’t quite work and for that reason Brooke was quite fidgety during her MRI, We where told that there may be a possibility that we would have to go to St George’s hospital for Brooke to be put on GA to be able to get a more accurate result.

luckily the Royal Marsden said the results from the Royal Surrey was clear enough, following this we received another call from the Royal Marsden with an appointment with the consultant.

The consultant then explained to us about the low-grade glioma, this is when our Hearts dropped!

We were speechless and in tears not knowing what to do.

Our little four-year-old daughter having to go through all this, at the time Brooke was only 3.

from there we got told Brooke will have to have a port fitted within 8 weeks weeks but we received a call within a day stating that they had a cancellation the next day.

following this we then started arranging Brooke to have chemo at our local hospital and bloods to be done weekly at our house.

Brooke has to have her bloods every Wednesdays and chemo every Friday.

Brooke is such an inspiration and no matter what she is going through she still fights to be the best she can. Chemo tends to make Brooke very tired, pale and fatigue, the chemo also makes her immune system very low limiting to what we can and can’t do.

in March, ( 3 and a bit months later after firstly getting diagnosed )

Brooke had another MRI but this one was after her receiving treatment, they stated that it has not shrunk but had also not grown.

Brooke has to have chemo and bloods for 70 weeks.

After her 70 weeks,

( when her chemo is meant to finish ) Brookes low grade glioma can grow again and we would have to try another method.

With a broken heart and this kills us to say this, but they cannot remove the cancer due to where it is, we are just taking every day as it comes.

We would love to do something magical and special for Brooke with what she has and is currently going through.

unfortunately, money is very tight for us at the moment due to reduced work hours along with one of us being Brookes full-time carer.

We would love to make her dreams come true.

Thank you for taking your time to read about our brave little soldier.