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Joanne Tubb Foundation
Joanne Tubb Foundation
Story
Hi there!
I’m making a real difference and running for a cause that's close to my heart.
The Joanne Tubb Foundation is a not for profit organisation that consists of voluntary members. It was founded in inspiration of the wonderful Joanne Tubb.
We believe that every child, including those with disabilities should be able to reach their full potential.
Jo touched the lives of many sick children in her role as a pediatric physiotherapist, she was devoted to her patients and believed that laughter and making treatment fun by connecting with the childrens hearts created a positive outcome both physically and mentally. She also focused on supporting the parents giving them a short repree and an opportunity to laugh during her sessions.
She inspired those around her to live their potential, and to give and support those that were less fortunate than herself. The Joanne Tubb foundation honours Jo's legacy and inspiration by:
Helping kids with disabilities move from surviving to thriving, through working with other organisations.
We do this by seeking out and create cutting edge programs whose primary focus is aligned with enabling kids with disabilities to meet their full potential. We look for entrepreneurs and leaders with the aim of supporting them to create sustainable programs with purpose.
We make a difference...
We've created this Melbourne Marathon 2017 fundraising page because we want to make a real difference to childrens lives. Please help us by giving whatever you can using the 'Give Now' button. The more people that know about our efforts in the Melbourne Marathon 2017, the greater the impact, so please also spread the word by sharing our page with your friends and family.
Thank you in advance for your generosity and support - it means a lot!
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Mission Massimo Foundation
The Mission Massimo Foundation is a non-profit organisation that promotes the prevention, diagnosis and treatment of childhood Leukodystrophies. These are a group of life-threatening genetic conditions that affect the formation of myelin, a complex fatty substance that acts as an insulator around nerve fibres in the brain much like electrical wiring. Unfortunately, more then 50% of childhood Leukodystrophies remain genetically unclassified offering families little hope of treatment and a usually tragic outcome. Whilst individually rare, these disorders are not altogether uncommon. In fact they may affect up to 1 in 3,000 births yet their existence remains almost unknown. Our mission is to accelerate the discovery of genetic variations responsible for these disorders and to translate these finding into clinical treatments.
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