362 avsnitt

This Podcast is going to be about Pediatric Cancer and the need to keep the awareness of this terrible disease in the public eye. My plan is to be able to interview a wide spectrum of people who all have a passion and a stake in finding a way to make the lives of these Pediatric Cancer Patients easier. I will interview oncologists, nurses, recovered patients, parents who have had to oversee their children's cancer fight, heads of Pediatric Cancer Foundations and Organizations , and others who would like to use this forum to advocate for these children.

Help and Hope Happen Here Mark Levine

    • Hälsa och motion

This Podcast is going to be about Pediatric Cancer and the need to keep the awareness of this terrible disease in the public eye. My plan is to be able to interview a wide spectrum of people who all have a passion and a stake in finding a way to make the lives of these Pediatric Cancer Patients easier. I will interview oncologists, nurses, recovered patients, parents who have had to oversee their children's cancer fight, heads of Pediatric Cancer Foundations and Organizations , and others who would like to use this forum to advocate for these children.

    Ramona Jarvis will talk about her daughter Lelia who was diagnosed with Stage 4 High Risk Neuroblastoma in the summer of 2017 when she was 19 months old, and is now 7 years past her original diagnosis and is living her best life possible.

    Ramona Jarvis will talk about her daughter Lelia who was diagnosed with Stage 4 High Risk Neuroblastoma in the summer of 2017 when she was 19 months old, and is now 7 years past her original diagnosis and is living her best life possible.

    When Ramona Jarvis's 19 month old daughter Leila was running on and off fevers, she was told by Leila's doctors that these were caused by viruses and that her fevers would go away. Unfortunately that was not the case and during that summer of 2017 , Leila was diagnosed with High Risk Stage 4 Neuroblastoma. After a harrowing regiment of treatments which included 132 days of being an inpatient, Leila was put on a DFMO Clinical Trial at the Arnold Palmer Children's Hospital in November of 2018 w...

    • 45 min
    Ashley Guthrie will talk about her son Davis who is well past his battle with Acute Lymphoblastic Leukemia and her positions as Clinical Liasion and Board Member at the Austin Hatcher Foundation for Pediatric Cancer.

    Ashley Guthrie will talk about her son Davis who is well past his battle with Acute Lymphoblastic Leukemia and her positions as Clinical Liasion and Board Member at the Austin Hatcher Foundation for Pediatric Cancer.

    Ashley Guthrie's eldest son Davis was diagnosed with Acute Lymphoblastic Leukemia when he was 6 years old and now at 16, is well into his survivorship years after his pediatric blood cancer battle. Ashley volunteered at the Children's Hospital in Chattanooga Tennessee while Davis was in treatment and is now the Clinical Liasion and Board Member of the Austin Hatcher Foundation for Pediatric Cancer. This Foundation was started by Amy Jo and Dr. James Osborn after the passing of their son Austi...

    • 56 min
    Courtney Marzilli's daughter Chloe was diagnosed with Rhabdomyosarcoma just before her 7th birthday in January of 2021. Chloe successfully completed her treatment in the fall of 2022 and now as a 10 year old, she is doing well and is leading a normal li

    Courtney Marzilli's daughter Chloe was diagnosed with Rhabdomyosarcoma just before her 7th birthday in January of 2021. Chloe successfully completed her treatment in the fall of 2022 and now as a 10 year old, she is doing well and is leading a normal li

    Just by chance on a Saturday evening in 2021, Courtney Marzilli noticed a lump on her then 6 year old daughter Chloe's thigh. This lump turned out to be a tumor and Chloe was diagnosed with Rhabdomyosarcoma just before she turned 7 years old. Chloe went through a 42 week Chemotherapy treatment protocol at the Jimmy Fund Clinic in Boston and completed her treatment in the fall of 2022. Now 10 years old, Chloe is doing well physically and thankfully is leading as good of a life as posssible.

    • 57 min
    Estella Patrick was born with Spina Bifida but after surgery to correct this Spinal Cord Disease, and 2 further surgeries she is now a 20 year old artist and illustrator, whose work has appeared in 3 books concerning Pediatric Cancer.

    Estella Patrick was born with Spina Bifida but after surgery to correct this Spinal Cord Disease, and 2 further surgeries she is now a 20 year old artist and illustrator, whose work has appeared in 3 books concerning Pediatric Cancer.

    Pain and suffering were a major part of Estella Patrick's life ever since she was born with Spina Bifida in 2004. Fortunately Estella had surgery to correct this Spinal Cord disease when she was 3 months old and now is an extremely talented and successful artist and illustrator. Her illustrations have appeared in 3 books which have been published by authors who are well known members of the Pediatric Cancer community.

    • 58 min
    Melissa Rodger will talk about her daughter Chloe who was diagnosed with Acute Myeloid Leukemia just 2 hours after going to a hospital emergency room in Melbourne, Australia in July of 2022. Chloe is now doing as well as possible healthwise.

    Melissa Rodger will talk about her daughter Chloe who was diagnosed with Acute Myeloid Leukemia just 2 hours after going to a hospital emergency room in Melbourne, Australia in July of 2022. Chloe is now doing as well as possible healthwise.

    Melissa Rodger's then 9 year old daughter Chloe had a lingering cold in July of 2022 and was told by a doctor that her cold was just a product of "back to back" viruses. Not too long after that Chloe was dehydrated and this time she was sent to a hospital emergency room where she was quickly diagnosed with Acute Myeloid Leukemia. Chloe had to undergo 2 Bone Marrow transplants with first, Melissa, and then her father Luke being her donors. Today Chloe is back in school, doing very well, ...

    • 51 min
    Anna Terrell will talk about her son Anthony who was diagnosed with Acute Lymphoblastic Leukemia in March of 2023 and has been doing so well in his treatment that his doctors have given him a 96 percent chance of survival.

    Anna Terrell will talk about her son Anthony who was diagnosed with Acute Lymphoblastic Leukemia in March of 2023 and has been doing so well in his treatment that his doctors have given him a 96 percent chance of survival.

    The discomfort that 5 year old Anthony Terrell was suffering from in late 2022 was originally thought to be simple growing pains, but by March of 2023 he was diagnosed with Acute Lymphoblastic Lymphoma which was quickly changed to a diagnosis of Acute Lymphoblastic Leukemia. Anthony is now roughly 40 percent into his Continuation Therapy protocol and he is doing so well that his doctors have put his survival rate chances at 96 percent.

    • 59 min

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