Courageous Parents Network

Arika Patneaude is a licensed clinical social worker who is the director of bioethics and pediatric palliative care at Seattle Children’s Hospital. She is also a passionate advocate for health equity and awakening to unconscious bias in medicine and the impact it has on underresourced and historically excluded populations. I experienced her passion as a Call to Action in multiple ways.

Ashley and Theron are parents of three children, including Viggo Rick, who died at 6 months of complications related to Trisomy 5p. They offer so much wisdom to other caregivers and suggestions to clinicians about what helps (and what hinders) parents of newborns born with very rare, life-limiting conditions.

Mom Amy and her daughter Lauren's palliative care doctor, Erin, talk about Erin's care of 7-year old Lauren: how she saw her as the full child that she was -- not just a cancer diagnosis -- and how she managed Lauren's 'total pain' during her 3 years of treatment for cancer, including addressing Lauren's fear of dying.

CPN's Blyth Lord talks with child and adolescent psychiatrist Elena Lister about the importance, value and life-long positive impact of talking with children honestly about illness and death. "What is mentionable is manageable." This far ranging conversation focuses especially on supporting siblings of children who are sick or who have died from illness.

Jerris advocated for his daughter Faith from her diagnosis at age 4 with osteosarcoma, through 23 major surgeries, side effects, setbacks, and complications, until her death shortly after her 18th birthday. Towards the end, they met Dr. Bob Macauley who helped get Faith home. Jerris emphasizes the need to create a space for dads as advocates and emotional caregivers.

CPN's interview with Pediatric Palliative Care NP's Luke and Sean, Valley Children's Hospital, Madera, CA

Shared Struggles: CPN's Blyth Lord talks with contributing editors parent Ann Schrooten and Dr. Barry Markovitz about their book and the collective wisdom from parents and physicians about the sacred, shared enterprise of caring for children living with serious illness and medical complexity.

CPN’s Blyth Lord talks with Michelle Moon, a bereaved mom and adult neurologist, about her decision to pursue fellowship in Hospice and Palliative Medicine: what about her experience with her daughter Julianna led to this career pivot and how is it feeling for her as she nears the end of her fellowship and considers her future as a doctor while always honoring Julianna’s life and legacy.

Dr. Wynne Morrison, director of pediatric palliative care at Children’s Hospital of Philadelphia, talks with Blyth Lord about what drove the creation of Courageous Parents Network.

CPN's conversation with mom and writer Faith Wilcox about her experience parenting her teenage daughters Elizabeth and Olivia, following Elizabeth’s diagnosis with Osteosarcoma. Elizabeth died at age 14. Faith talks about how she and Oliva grieved together and separately in the years that followed.

An audio recording of CPN's In the Zoom Room event on Tending the Adult Relationship with families and psychologist Nancy Frumer-Styron.

CPN’s Blyth Lord talks with Carla, the mother of Talia who had infantile Tay-Sachs and died shortly before her second birthday, and Robin, Carla’s mother, Talia's grandmother. Theirs is a particularly close relationship

In this episode, CPN's Jennifer Siedman talks with her son Noah about the days leading up to Noah's brother, Ben's passing. They explore grief, the pressures siblings feel and creating a new family dynamic.

In this episode, Amy and Ray Miller , parents to Dan, who had Hunter Syndrome and Hailey join CPN’s Jennifer Siedman to talk about surrounding their son Dan with love, family and friends during his final days, their identity as parents and being happy again.

CPN's interview with Dr. Kate Davidoff on her journey to becoming an attending pediatric palliative care doctor: what drew her into medicine and then working with seriously ill children and their families.

In this episode, CPN’s Jennifer Siedman talks with Chelsey Klenke Robertson about the challenges and gifts of loving Craig, her brother who had Hunter’s Syndrome(MPS II). Her mother Kris joins them to talk about Craig’s final days, the grieving process and how Craig’s legacy has impacted their careers.

In this episode, CPN’s Jennifer Siedman talks with Grey Chapin, founder of the BLAIR Connection, a digital resource to support siblings as they experience the challenges of having a terminally ill brother or sister. Jennifer is the mother to three – Noah and Isabelle, and their brother Ben, who died in 2014 from Sanfilippo Syndrome. Grey is the younger sister of Blair, who also had Sanfilippo Synd...

Patient disease advocacy organizations are united in the common goal of improving the lives of those living with the rare diseases they represent. For some in the community, the science has advanced and treatments are available. For others, a treatment is still off on the horizon. In this episode, CPN’s Jennifer Siedman talks with Leslie Urdanta, Family Support Coordinator for the National MPS Soc...

CPN's Jennifer Siedman talks with Diana Pangonis, Director of Family Services for NTSAD. For the very first time since its beginning over 60 years ago, the NTSAD community has or is anticipating early stage clinical trials for its diseases, Tay-Sachs, GM-1, Sandhoff, and Canavan. It's a new landscape for the NTSAD families. Jennifer talks with Dianoa about what supporting families through the clin...

Today the landscape for families of children diagnosed with rare and fatal conditions looks very different than it did even a decade ago. New therapies and treatments are here, including gene therapy. But what do the innovations mean for parents who may be faced with the opportunity to enroll their child in an early stage clinical trial which is, at its core, an experiment? In this episode, CPN’s...

Rebecca Kuzarski, mom to Ethan, Hannah, and Sophia, sat down recently to talk with her friends about the death of her daughter Sophia 5 years ago. Sophia was diagnosed with Leukemia at the age of 3 and unexpectedly died 7 months into her treatment. Listen as this intimate group of friends, these 5 years later, reflects upon how they came together as a community to support the Kuczarskis, the child...

Emma Artinian was diagnosed with Sand-hoff disease when she was 12 months old and she died when she was 3 and a half. Here her mother Becca and her grandmother Christine, Becca's mother, talk about what it was like to love and care for and lose Emma, together. Emma's little sister Ava was born after Emma passed away and has brought new light into their life.

Cari is the mother of Dylan and his older sister Jessie. Jessie died in December 2015, at the age of 13, from Sanfillipo Syndrome, a form of MPS. Cari and her husband Matt say that Jessie was the light of their family, always happy, and with a huge smile for everyone, especially her brother who she absolutely adored.

Sarah is the mother of Emerson. After 7 sleep-deprived but blissful months, Sarah and her husband Steve learned that Emerson had Gaucher Type 2. Gaucher Type 2 is always fatal in early childhood. Sarah shares here the vital role that Courageous Parents Network AND pediatric palliative care played in the months that followed the diagnosis and then Emerson’s death shortly after her first birthday, i...

Ben is 15 years old and lives with his mother, father and two younger sisters, McKenna and Joelle. Ben was born with Cerebral Palsy. He loves school, the Red Sox, and spending time with his sisters. Makenna and Joelle include Ben in everything they do and have become compassionate advocates for children with disabilities.