In 2014, Megan Bugg was diagnosed with stage 4 Alveolar Rhabdomyosarcoma (ARMS), the most aggressive form of Rhabdomyosarcoma, affecting the soft tissue most commonly in children,
Be part of our team, uncovering how childhood cancers work – and helping find the treatments that could go to clinical trials to improve outcomes.
My name is Michele and I am a scientist, a cc-TDI Board member and Shane’s Mom. Shane is my third child and our family’s connection
In 2017 David Sullivan never imagined he would ever run a marathon. He was significantly overweight, out of shape and watching as his niece Kiley
In August 2019, Gabby Sariñana was a happy, active 2-year-old. Her family and friends describe Gabby as fearless, gregarious, determined and zealous. One day her
As we come to the close of a tumultuous year, probably the last thing anyone wants to hear more about is politics, but nonetheless we
(This blog acknowledges the incredible dedication, skill and value our volunteers bring to our efforts to advance therapies for childhood cancers with unmet needs) Early
“We noticed the lump in Shane’s groin when he was 8 months old. We thought it was a hernia. Our paediatrician did too, so we
We would need to master nuclear fusion to reach the stars, but with an incredible grant of $160,000 ($320,000 over two years) from The Vince
OK – due to coronavirus the full Nanocourse (described on our specialized website http://nanocourse.org/) will be be postponed until August 2021 … HOWEVER, we will
In 2014, Megan Bugg was diagnosed with stage 4 Alveolar Rhabdomyosarcoma (ARMS), the most aggressive form of Rhabdomyosarcoma, affecting the soft tissue most commonly in children,
Be part of our team, uncovering how childhood cancers work – and helping find the treatments that could go to clinical trials to improve outcomes.
My name is Michele and I am a scientist, a cc-TDI Board member and Shane’s Mom. Shane is my third child and our family’s connection
In 2017 David Sullivan never imagined he would ever run a marathon. He was significantly overweight, out of shape and watching as his niece Kiley
In August 2019, Gabby Sariñana was a happy, active 2-year-old. Her family and friends describe Gabby as fearless, gregarious, determined and zealous. One day her
As we come to the close of a tumultuous year, probably the last thing anyone wants to hear more about is politics, but nonetheless we
(This blog acknowledges the incredible dedication, skill and value our volunteers bring to our efforts to advance therapies for childhood cancers with unmet needs) Early
“We noticed the lump in Shane’s groin when he was 8 months old. We thought it was a hernia. Our paediatrician did too, so we
We would need to master nuclear fusion to reach the stars, but with an incredible grant of $160,000 ($320,000 over two years) from The Vince
OK – due to coronavirus the full Nanocourse (described on our specialized website http://nanocourse.org/) will be be postponed until August 2021 … HOWEVER, we will
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