Our Why: Conquering Rare Childhood Cancers for Michele
Every day at cc-TDI we press forward to develop less toxic, more effective treatments for rare childhood cancers like rhabdomyosarcoma driven by the deeply personal
Every day at cc-TDI we press forward to develop less toxic, more effective treatments for rare childhood cancers like rhabdomyosarcoma driven by the deeply personal
The Hundt Strong golf outing began in 2017 as a way to support Billy Hundt during his extensive treatment for rhabdomyosarcoma (RMS). From that very
As we make our final approach to the new year, we want to share a story that embodies the #givingbackchildhood spirit of cc-TDI’s mission. Meet
In August 2023, the cc-TDI team was introduced to the Bliss family, a vibrant and loving family who wanted to make a difference in the
In fond remembrance of Ally Anderson, we joyfully celebrate a life that, despite the challenges of pediatric cancer, radiated hope, love, and an unwavering spirit.
[Press Release] The Silicon Forest in Hillsboro, OR, October 3, 2023 – The Children’s Cancer Therapy Development Institute was recently awarded $70,000 in continued support
The Megan’s Mission Foundation Awards $100,000 in Rhabdomyosarcoma Research Funding The Children’s Cancer Therapy Development Institute (cc-TDI) was generously awarded $100,000 in support of two
The Children’s Cancer Therapy Development Institute (cc-TDI) was awarded $100,000 in support of Diffuse Intrinsic Pontine Glioma (DIPG) research by The Lyla Nsouli Foundation for
After my brother Shane passed in 2015, I asked my parents if we could hold a lemonade stand down by the shore in honor of
Ron’s daughter Ashley was a fun, snarky kid who just wanted to have a good time. She loved spending time with her friends telling jokes,
From the time she was little, Pheonix Spangler was an active, vibrant child with a passion for giving back to her community. Pheonix had an
Mia’s cancer diagnosis changed our lives forever. Those in the childhood cancer community see this phrase often. But it really is true. We can’t un-see
Alexa was your typical carefree 15-year-old teenager. She enjoyed school, spending time with her friends and being active. In late 2017 Alexa developed shoulder pain, unusual due to her
This is the story of our beautiful, firstborn daughter Zoe. The first 6 months of my pregnancy were completely uneventful. Yes, I had odd cravings,
To honor cancer siblings and their experiences on National Sibling Day, we partnered with some of our bravest supporters, willing to share their stories in
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,
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
“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
Every day at cc-TDI we press forward to develop less toxic, more effective treatments for rare childhood cancers like rhabdomyosarcoma driven by the deeply personal
The Hundt Strong golf outing began in 2017 as a way to support Billy Hundt during his extensive treatment for rhabdomyosarcoma (RMS). From that very
As we make our final approach to the new year, we want to share a story that embodies the #givingbackchildhood spirit of cc-TDI’s mission. Meet
In August 2023, the cc-TDI team was introduced to the Bliss family, a vibrant and loving family who wanted to make a difference in the
In fond remembrance of Ally Anderson, we joyfully celebrate a life that, despite the challenges of pediatric cancer, radiated hope, love, and an unwavering spirit.
[Press Release] The Silicon Forest in Hillsboro, OR, October 3, 2023 – The Children’s Cancer Therapy Development Institute was recently awarded $70,000 in continued support
The Megan’s Mission Foundation Awards $100,000 in Rhabdomyosarcoma Research Funding The Children’s Cancer Therapy Development Institute (cc-TDI) was generously awarded $100,000 in support of two
The Children’s Cancer Therapy Development Institute (cc-TDI) was awarded $100,000 in support of Diffuse Intrinsic Pontine Glioma (DIPG) research by The Lyla Nsouli Foundation for
After my brother Shane passed in 2015, I asked my parents if we could hold a lemonade stand down by the shore in honor of
Ron’s daughter Ashley was a fun, snarky kid who just wanted to have a good time. She loved spending time with her friends telling jokes,
From the time she was little, Pheonix Spangler was an active, vibrant child with a passion for giving back to her community. Pheonix had an
Mia’s cancer diagnosis changed our lives forever. Those in the childhood cancer community see this phrase often. But it really is true. We can’t un-see
Alexa was your typical carefree 15-year-old teenager. She enjoyed school, spending time with her friends and being active. In late 2017 Alexa developed shoulder pain, unusual due to her
This is the story of our beautiful, firstborn daughter Zoe. The first 6 months of my pregnancy were completely uneventful. Yes, I had odd cravings,
To honor cancer siblings and their experiences on National Sibling Day, we partnered with some of our bravest supporters, willing to share their stories in
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,
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
“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
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