Hear the Rare

Hear the Rare

Podcast by Rachna Prasad

Listen to families, patients, physicians, researchers, foundations, and others speak about their experience with DIPG. We aim to raise awareness by sharing different perspectives of a similar story and foster a sense of hope for this community. Whether you are someone who is new to DIPG and wants to know more, or someone who is already a part of this community, we hope these stories provide you with more insight. As always, we are stronger together!

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13 episodes
episode Episode 12: Interview with Dr. Nick Vitanza artwork
Episode 12: Interview with Dr. Nick Vitanza

Episode 12 features Dr. Nick Vitanza who was part of the first interview that I hosted with Jace Ward. He was Mithil's first doctor and now serves on the Board of the Mithil Prasad Foundation and is a close friend to our family. Dr. Nicholas Vitanza is a pediatric neuro-oncologist at Seattle Children’s Hospital and laboratory researcher at the Fred Hutchinson Cancer Research Center. In clinic, he cares for children with central nervous system tumors and, in the lab, he focuses on understanding the epigenetic aberrations of diffuse intrinsic pontine glioma (DIPG) and its molecular vulnerabilities with the hope of improving outcomes for affected children. He also assists in the development of immunotherapy clinical trials for children with brain and spinal tumors.

19. okt. 2021 - 32 min
episode Episode 6: Interview with Jill Morin artwork
Episode 6: Interview with Jill Morin

Episode 6 features Jill Morin, mother of DIPG warrior Luke Morin. She is the founder of Luke’s Posse [https://www.facebook.com/DIPGendsnow/] which raises funds for DIPG research at Children’s Hospital Colorado. In this episode, listen to Jill talk about Luke’s story, the beginning of Luke’s Posse, and hear her share some advice for families dealing with a new DIPG diagnosis.

04. okt. 2021 - 28 min
episode Episode 11: How I Dealt with Grief artwork
Episode 11: How I Dealt with Grief

Unfortunately, an important part of the DIPG/ DMG journey is grief. Many families have faced it, many will but hopefully one day it will no longer be a part of these children’s DIPG story. However, until that day comes, I think it is very important to talk about grief openly and honestly. Episode 11 serves as a tribute to Jace Ward, the inspiration behind this podcast series, a dear friend, courageous DIPG warrior, and outstanding human being, who passed on July 3rd, 2021. This podcast cherishes the unique friendship I had while having an open and honest conversation about grief

04. okt. 2021 - 17 min
episode Episode 10: Interview with Mithil's Best Friends artwork
Episode 10: Interview with Mithil's Best Friends

Episode 10 features Yury and Nethan who were my brother’s best friends. They had been friends since they were all very young and never left Mithil’s side through his battle with DIPG. In episode 10, we hear Nathan and Yury talk about their fond memories of Mithil and the lasting impact of Mithil’s passing.

29. mar. 2021 - 20 min
episode Episode 9: Interview with Dr. Jessica Foster artwork
Episode 9: Interview with Dr. Jessica Foster

Episode 9 features Dr. Jessica Foster from Children’s Hospital of Philadelphia. Dr. Foster’s current research focuses on immunotherapy for pediatric solid and brain tumors. Specifically she is investigating chimeric antigen receptor (CAR) T cell therapy. The goals of her research are to develop pre-clinical CAR T cells for translation into clinical trials to help these devastating tumors.

28. feb. 2021 - 17 min
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