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Little Ts Rhabdomyosarcoma journey

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Little Ts big journey

My nephew little T an energetic, adventurous, happy go lucky blonde haired little boy  , late last year (2019) a  small lump appeared on His  cheek ,it rapidly doubled in size and was clearly noticeable. After many  Tests, x-rays and scans where taken ,Tyson was diagnosed rhabdomyosarcomas on his 4th birthday.

Rhabdomyosarcoma also known as rms is aggressive and highly malignant form of cancer that develops from skeletal (striated) muscle cells that have failed to fully differentiated. Rms treatment will include chemotherapy, radiotherapy and surgery.

T has already started his first round of chemotherapy at Westmead children's hospital. It’s Going to be a long  road ahead his body will undergo changes during treatment. I’m sure it’s going to be taxing on the little guy as well my brother and Ts mum. My brother has quite his job and is looking after T full time . for those who would like to support financially – no matter how big or small – to help ease some of the financial burden of this unexpected diagnosis.

Any contributions will help with the costs associated with additional medical, daily and living expenses, bills, and anything else they may need while they take time out from work to care for Little T.

Whether or not you’re able to help financially at this time, we would also appreciate it if you could share this campaign for Tyson and our family . we are praying for a full and fast recovery.






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    Organizer

    Pete Meers
    Organizer
    Asquith, NSW

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