<div>Hello and thank you for taking the time to read about our fundraising event.
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<div>In August 2024, a team of family (Including Amarli's father and brother), relatives and close friends of Amarli’s, aim to trek up and down the Snowdonia Mountain Range six times continuously (roughly 60 miles) in the hope of completing the trek in the space of 30 hours.
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<div>We have chosen Snowdonia as it signifies Amarli’s ups and downs that she has been through during these first six years of her precious life.
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<div>On August 3rd &amp; 4th 2024, Amarli's family &amp; friends have organised a walk from Sydney Kids Hospital at Randwick to Wollongong Hospital. This walk with the "Amarli Army" will co-incide with the Snowdonia Trek in the UK.
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<div>Family will walk from Randwick Kids Hospital and meet up with friends and supporters at Stanwell Park to continue the coastal walk through to Wollongong Hospital.
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<div><strong>Amarli's story, so far……...</strong>
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<div>Amarli Broome lives in Wollongong NSW Australia with her Mum Jade, her Dad Lee and her two brothers Bohdi and Jordi. Amarli will celebrate her sixth birthday in April this year (2024). Amarli has spent most of her young life in hospital due to her rare and complex medical condition.
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<div>This is Amarli's story as told by her mother Jade…
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<div>As I sit down to recount the journey of our precious daughter Amarli, I'm filled with a whirlwind of emotions—love, gratitude, fear, and hope in my heart. It's a journey that began with the joyous anticipation of welcoming another member into our family, yet quickly transformed into a rollercoaster ride of medical challenges and unexpected twists.
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<div>Amarli was diagnosed with a rare genetic disorder at just 8 months of age, called GRIK 2. This rare condition has resulted in Amarli being developmentally delayed. She regularly experiences epilepsy, her fine and gross motor skills are affected. Her ability to walk, speak &amp; eat along with severe breathing difficulties requires 24/7 care.
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<div>Amarli is so strong and brave though and continues to prove this every day. She has learnt how to sit in the past 6 months and has achieved so much, after we were told this would likely be impossible.
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<div>Amarli's birth, on the 27th of April in 2018, was a moment of sheer joy and relief. Holding her tiny 2.4kg of pink perfection in my arms, I felt an overwhelming sense of love wash over me. At that time it all seemed normal and we had no concerns and we were just so thrilled to finally have our baby girl in our arms safe and sound.
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<div>Little did we know, our lives were about to take an unexpected turn.
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<div>The initial shock came with the news of Amarli's failed hearing test, just days after her arrival. Amarli was diagnosed with Bilateral Auditory Neuropathy Syndrome. I vividly remember that day and as a mother, the thought of my precious daughter never hearing my voice or the sound of music was a blow beyond measure. It felt as though the dreams I held for her were slipping through my fingers.
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<div>But that was just the beginning......
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<div>Amarli had an MRI at 4 months of age which showed Delayed Myelination. At that point we were told by her Neurologist that she would be developmentally delayed, but to what degree, he was unsure. We were basically told to take her home, love her and wait and see.
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<div>At just 8 months of age Amarli gave us the fright of our lives. She had an unresponsive episode and stopped breathing, I commenced CPR and Amarli was rushed to hospital via ambulance.
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<div>Amarli continued to have these severe breath-holding events nightly for weeks and spent the next four months in hospital. We were absolutely terrified at this point and I still remember we were only coming to terms with her disability and now not knowing what was happening to her was something no parent should have to endure.
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<div>As the days turned into weeks, and the weeks into months, we were confronted with more challenges than we ever could have imagined. Seizures, respiratory concerns, feeding difficulties—each hurdle seemed to test us in ways we never thought possible.
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<div>The diagnosis of GRIK 2, a rare genetic disorder, shook us to the core. At the time there was only 3 other children known in medical literature. With little information available and no clear path forward, we felt as though we were navigating uncharted waters, grasping for answers that remained just out of reach.
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<div>Yet, amidst the uncertainty and fear, there was one constant—the unwavering strength and resilience of our little girl. Despite the countless ambulance trips, hospitalisations, procedures, needles, x-rays and medications, Amarli's spirit remained unbroken. Her smile, held a brightness that lit up even the darkest of days.
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<div>As her mother, I found myself in a role I never could have anticipated—advocate, caregiver, and fighter all rolled into one. Learning to navigate the complexities of tube feeding, administering medication, and managing Amarli's daily needs became our new reality—a reality that required every ounce of strength and determination we possessed.
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<div>Through it all, our family remained united in love and support, drawing strength from one another as we faced each new challenge head-on. Though the road ahead may be uncertain, we remain hopeful. We dream of a future where research brings answers, treatments, and ultimately, a cure for GRIK disorders.
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<div>We have spent many hours searching GRIK 2 in every corner of the internet – desperate for information or to connect with other parents alike. With a disease this rare it has been difficult.
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<div>Thankfully as the years have passed there is a foundation called Cure Grin who are committed to improving the lives of those with GRI Disorders and are hopeful of finding a cure.
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<div>Sadly, Amarli’s lung function has deteriorated over this past 12 months and she is now dependant on home Hi flow and Bi pap at night, secondary to respiratory failure. Amarli is finally home after a very long traumatic six month admission to the Randwick Children’s hospital Amarli’s Doctors have said that it is unlikely things will improve and that she will have a shortened life span.
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<div>Due to Amarlis deteriorating condition and increased needs, I have had no other choice but to take extended unpaid leave from my permanent registered nursing position to be at home with Amarli, until we obtain the appropriate in home support. This has taken an emotional and financial toll on our family.
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<div>If you are able to help to ease this burden while we navigate these murky waters we would be forever grateful. We are so hopeful that gene therapy will become available soon. I have been in regular contact with a Canadian family whose daughter (with a similar condition) has made incredible progress through gene therapy and is now able to walk, eat and talk.
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<div>We are initially looking to raise funds to assist us through these testing times and to also contribute to the Cure Grin Foundation.
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<div>Ultimately, we are aiming to raise funds for Sydney Kids hospitals at both Randwick &amp; Wollongong along with assisting other families and raising awareness of rare children’s diseases.
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<div>Amarli has touched so many lives with her sweet and beautiful smile that lights up any room, her courageous determination and gentle demeanour. Amarli's journey has taught me more than I ever thought possible— about the real meaning of life and to take each day as it comes, not sweat the small things, advocacy, love, hope, resilience and the incredible power of the human spirit.
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<div>As her mother I am beyond proud of her and all she has achieved.
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<div>Despite her hurdles she has had thrown her way, nothing will stop our little fighter. She is a warrior, the bravest and most resilient girl in the world. Our real-life hero, our guiding light in the darkest of times.
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<div>Amarli continues to show us how strong she is and proves everyone wrong with her continuous fight to be here. And as her mother, I am endlessly proud to walk this journey by her side, holding onto hope with every step we take.
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<div>Our hope Is to spread Amarli’s story and hopefully find a cure. 
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<div><strong>The Fundraiser Event</strong>
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<div>Amarli has had so many ups and downs throughout her life so far.
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<div>In August this year, we plan to climb Snowdonia, Wales, 6 times continuously, each climb (Up and Down equates to 1) representing 1 year of Amarli’s life and how she has overcome such adversity.
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<div>Please help us to make that future a bit easier and a little bit brighter by considering a donation. The family understands donating isn't always an option, however, what the family would be extremely grateful for is if you would share Amarli's story in the hope of reaching more people.
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<div>Jade, Lee, Bohdi, Amarli, Jordi and their family wish to thank everyone in advance for your kindness &amp; generosity and for the love &amp; support when in their darkest days is the thing that pulls them through.
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<div>Thank you and much love xx
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Jade Broome

Darryl Cooper

Jayden Goedde

Elaine Cowen

Dianne Mckeller

Anonymous

Ashleigh Gillroy

Thomas Walton

Mary Leslie

Tamara Pinilla

Thomas Cummings

Ian Willey

Paul Bottele

Fiona Rattigan

BaiMed on behalf of Joe Gafa

Jessica Clifton

Margaret Jessup

DERBYSHIRE AND SONS LTD DERBYSHIRE

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