Glioblastoma aka GBM Amber Barbach

Join us for the Season 3 premiere of The Glioblastoma AKA GBM Podcast, where we delve into the heart and mind of multi-platinum singer-songwriter Mike Posner. In this deeply personal episode, Mike shares his journey through the harrowing landscape of glioblastoma as he witnessed his father’s battle with this aggressive form of brain cancer. As we explore the layers of grief and healing, Mike opens up about how this experience has reshaped his creative process and his outlook on life.

In this conversation, we cover:

The profound impact of his father’s glioblastoma diagnosis and the family’s journey through treatment and loss.

How grief has influenced Mike’s music and artistic expression.

Cherished advice from his dad that continues to guide him.

Mike's vision for living a meaningful life in the wake of personal tragedy.


Mike Posner, known for his hit songs and remarkable resilience, brings a unique perspective on dealing with loss, channeling creativity, and finding purpose amidst pain. This episode is a touching reflection on love, loss, and legacy.

Trigger Warnings: This episode contains discussions on medical conditions, cancer diagnosis, and end-of-life themes.

For more insights and to support the Glioblastoma Research Organization, please visit GBMResearch.org.

Disclaimer: The content shared on The Glioblastoma AKA GBM Podcast represents personal stories and is intended for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult your healthcare provider with any questions regarding a medical condition.

In this episode of the Glioblastoma AKA GBM Mini Series, Amber gives a recap on the inaugural Padel for Brain Cancer event, goes through life hacks as a caregiver, touches on hospice & palliative care, and unboxes her dads things from storage.

Topics covered in this episode include:

Hospice care & palliative care

Staying organized as a caregiver

End of life & food

Sleep & sleep therapy

Unboxing your loved ones items


Thank you to our partners at xCures for supporting the Mini-Series season. To learn more, visit their website at https://xcures.com/.

Learn more about Earos here: https://earos.com/
Learn more about Certifyde here: https://certifyde.com/

"Glioblastoma AKA GBM" is more than a podcast; it's a lifeline for those touched by glioblastoma.
Stay connected with "Glioblastoma AKA GBM" and the Glioblastoma Research Organization on social media for updates, resources, and to join the community:
Instagram: @glioblastomaresearch @glioblastomaakagbm
Twitter: @glioblastomaorg
Facebook: https://www.facebook.com/glioblastomaresearch
Website: https://www.gbmresearch.org/
Subscribe now to be part of this transformative journey and contribute to raising awareness for glioblastoma research.
#GBMPodcast #Glioblastoma #HopeForTheHolidays

**As always, the information that is discussed in Glioblastoma AKA GBM is not meant to treat, diagnose, or prevent any disease. What we and our guests share are personal stories of what has worked for the individuals in question, and should not be taken as medical advice or opinion, and is not a substitute for medical advice. If you have any questions about your own situation, always consult with your medical provider and healthcare team.

In this episode of the Glioblastoma AKA GBM Mini Series, we delve into our 2024 plans, dating, and a holiday debrief.

Thank you to our partners at xCures for supporting the Mini-Series season. To learn more, visit their website at https://xcures.com/.

Merch of the week: https://www.gbmresearch.org/shop/p/for-a-cure-20

"Glioblastoma AKA GBM" is more than a podcast; it's a lifeline for those touched by glioblastoma.
Stay connected with "Glioblastoma AKA GBM" and the Glioblastoma Research Organization on social media for updates, resources, and to join the community:
Instagram: @glioblastomaresearch @glioblastomaakagbm
Twitter: @glioblastomaorg
Facebook: https://www.facebook.com/glioblastomaresearch
Website: https://www.gbmresearch.org/
Subscribe now to be part of this transformative journey and contribute to raising awareness for glioblastoma research.
#GBMPodcast #Glioblastoma #HopeForTheHolidays

**As always, the information that is discussed in Glioblastoma AKA GBM is not meant to treat, diagnose, or prevent any disease. What we and our guests share are personal stories of what has worked for the individuals in question, and should not be taken as medical advice or opinion, and is not a substitute for medical advice. If you have any questions about your own situation, always consult with your medical provider and healthcare team.

In this fourth episode of the Glioblastoma AKA GBM Mini Series, we chat about major questions and topics in relation to resources for current caregivers.

Topics covered in this episode include:

Glioblastoma nonprofits

Finding support groups

Caregiver benefits & financial aid

Books/apps to assist your journey

The most important advice as a caregiver - according to Amber

Social workers

Finding therapy and support


Thank you to our partners at xCures for supporting the Mini-Series season. To learn more, visit their website at https://xcures.com/.

"Glioblastoma AKA GBM" is more than a podcast; it's a lifeline for those touched by glioblastoma.
Stay connected with "Glioblastoma AKA GBM" and the Glioblastoma Research Organization on social media for updates, resources, and to join the community:
Instagram: @glioblastomaresearch @glioblastomaakagbm
Twitter: @glioblastomaorg
Facebook: https://www.facebook.com/glioblastomaresearch
Website: https://www.gbmresearch.org/
Subscribe now to be part of this transformative journey and contribute to raising awareness for glioblastoma research.
#GBMPodcast #Glioblastoma #HopeForTheHolidays

**As always, the information that is discussed in Glioblastoma AKA GBM is not meant to treat, diagnose, or prevent any disease. What we and our guests share are personal stories of what has worked for the individuals in question, and should not be taken as medical advice or opinion, and is not a substitute for medical advice. If you have any questions about your own situation, always consult with your medical provider and healthcare team.

In this third episode of the Glioblastoma AKA GBM Mini Series, we chat about all things ADVOCACY - on the caregiver AND patient side.

Topics covered in this episode include:

Your role as a caregiver

Asking about second opinions

Navigating clinical trials

Questions to ask your doctor

Decision making


Thank you to our partners at xCures for supporting the Mini-Series season. To learn more, visit their website at https://xcures.com/.

"Glioblastoma AKA GBM" is more than a podcast; it's a lifeline for those touched by glioblastoma.
Stay connected with "Glioblastoma AKA GBM" and the Glioblastoma Research Organization on social media for updates, resources, and to join the community:
Instagram: @glioblastomaresearch @glioblastomaakagbm
Twitter: @glioblastomaorg
Facebook: https://www.facebook.com/glioblastomaresearch
Website: https://www.gbmresearch.org/
Subscribe now to be part of this transformative journey and contribute to raising awareness for glioblastoma research.
#GBMPodcast #Glioblastoma #HopeForTheHolidays

**As always, the information that is discussed in Glioblastoma AKA GBM is not meant to treat, diagnose, or prevent any disease. What we and our guests share are personal stories of what has worked for the individuals in question, and should not be taken as medical advice or opinion, and is not a substitute for medical advice. If you have any questions about your own situation, always consult with your medical provider and healthcare team.

In this second episode of the Glioblastoma AKA GBM Mini Series, we chat about replying to the question "how are you doing?"

Questions that came in this week included:

When someone asks me how I am doing I feel like I am supposed to just smile and say “fine”. Is this ok?  

How do I really tell someone how I am doing when the answer feels so dark?

Am I bringing others down by being honest?

What would be the best way to answer this with honesty without making them regret asking?

I have no idea how to cope with all of this. What can I do?

I am really tired of people telling me to “stay positive”. How can I express that?

Does there always have to be a silver lining? Sometimes I just don’t see one.


"Glioblastoma AKA GBM" is more than a podcast; it's a lifeline for those touched by glioblastoma.
Stay connected with "Glioblastoma AKA GBM" and the Glioblastoma Research Organization on social media for updates, resources, and to join the community:
Instagram: @glioblastomaresearch @glioblastomaakagbm
Twitter: @glioblastomaorg
Facebook: https://www.facebook.com/glioblastomaresearch
Website: https://www.gbmresearch.org/
Subscribe now to be part of this transformative journey and contribute to raising awareness for glioblastoma research.
#GBMPodcast #Glioblastoma #HopeForTheHolidays

**As always, the information that is discussed in Glioblastoma AKA GBM is not meant to treat, diagnose, or prevent any disease. What we and our guests share are personal stories of what has worked for the individuals in question, and should not be taken as medical advice or opinion, and is not a substitute for medical advice. If you have any questions about your own situation, always consult with your medical provider and healthcare team.