Living with Scanxiety is a podcast dedicated to discussing the difficulties families face when their child is diagnosed with cancer.
Your host is a cancer mom that has completed her journey; she touches on topics you need to know.
04/29/2022
Newest Episode
Season 5 Episode 4 Join me at the mic with Meg Gallagher, who discusses everything from friendship and the end of treatment. What she says about childhood cancer and aya cancer might surprise you. She gives a fresh perspective on life with and aft...
04/19/2022
Come Join Us Tomorrow: on the clubhouse app at 10:15 am EST
Tuesday, April 19 at 9:15am CDT with Adriana Lewin, Rosaria Kozar. Come join the WEEKLY discussion around mental health and childhood/AYA cancer with 2 mental health professionals who have lived it. Find support, be support, and find community.
Season 4 Episode 5: Sit with me as I chat with a Stupid Cancer board member David Richman. We touch on AYA cancer, Stupid Cancer, the non-profit, his experiences with oncology, and his work as a humanitarian. For all the details of this episode, t...
11/28/2021
Welcome to the Scanxiety Shop:
11/03/2021
Check out the newest episode where we talk about childhood cancer and how it affects mental health. This is part 1 of a 2 part series.
If you want to participate in ‘Go Gold’ this September (childhood cancer awareness), take a pic tag Scanxiety If 50+ participate across my socials, I will be donating to a non-profit…just wear gold/yellow (childhood cancer color), the color used to represent childhood cancer…it free.
You can just respond here too. You can be creative, ribbons in hair, shoelaces, makeup, clothing. By providing a photo, you are allowing me to use it on social media-a collage of the participants
Who will get the donation? A non-profit that helps childhood children in the now, TBA.
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This podcast is dedicated to discussing the difficulties families face when their child is diagnosed with cancer. Each topic is hand picked by me, a cancer mom, that has finished my journey.
My name is Rosaria Kozar, and my son, Brody, was diagnosed with Rhabdomyosarcoma when he was only 23 months old. He suffered through numerous scans, infusions, and more before he lost his battle at the age of 3 in 2015. During his fight, I felt lost and had difficulty connecting to therapists who did not fully understand my situation.
That’s why I created this Podcast, so you can connect with people who understand you — people who understand the anxiety and heartache.
I also welcome and encourage listeners who want to understand or are just curious to tune in.
You can expect to hear from guests ranging from bereaved parents or family members, parents or family members of survivors, survivors, doctors, and social workers.
Here is my family; Brody’s brother, my husband and I as of 2019: