In this deeply personal episode, Julia opens up about her father’s diagnosis with astrocytoma, a type of brain tumour, and how it reshaped her family and her understanding of invisible disabilities.
Julia shares the emotional rollercoaster of discovering her dad’s condition—initially hidden until chemotherapy made it undeniable. She reflects on how the diagnosis affected their family dynamics, especially communication and emotional expression. Julia also explores how her relationship with both her parents evolved, the impact of her father's permanent brain damage, and her journey through counseling and journaling to process grief and uncertainty.
This conversation sheds light on the importance of empathy, creating safe emotional spaces, and the need for greater awareness around the often unseen struggles people with brain tumours face.
🎧 Topics Covered:
Coping with a parent’s cancer diagnosis
The silence and stigma surrounding illness in families
The power of journaling and therapy in emotional healing
How invisible disabilities affect daily life and relationships
The emotional burden of caregiving and overprotection
🧠 Key Takeaway:
Every family copes differently, but open communication, emotional support, and awareness of invisible disabilities can change everything.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
In this powerful episode, Victoria shares her deeply personal journey of being diagnosed with a meningioma brain tumour in June 2017. What began as a few "funny five minutes" quickly escalated into a life-alteringdiagnosis. She opens up about the emotional and physical challenges she faced, including a moment when she couldn't recall her own daughter's name.
Through resilience, the support of her loved ones, and her discovery of mindfulness and hypnotherapy, Victoria found a path to healing. Now a certified hypnotist, she uses her experience to help others find calm and clarity, teaching techniques like breathwork and guided relaxation. This episode is a heartfelt testament to the strength of the human spirit, the power of community, and the transformative nature of self-care.
🌐Victoria's site: https://naturallycalmtherapy.co.uk/brainset/
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
Sarah’s life changed in an instant when she experienced a grand mal seizure. The cause? An oligodendroglioma grade two brain tumour. Facing the unknown, she underwent awake brain surgery, remaining calm in a situation that would shake most.
Post-surgery, she found healing through positivity, spirituality, and self-education, even watching brain surgeries to understand her journey. A quote that resonated with her:
"When you change the way you look at things, the things you look at change." – Wayne Dyer
Hear Sarah’s incredible story of strength and perspective in the latest episode of Aunty M Brain Tumours Talk Show Podcast!
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
In this episode, Michelle shares her journey with oligodendroglioma grade 2, a brain tumour she was diagnosed with in 2010 following a grand mal seizure. Despite the challenges, she gave birth to a healthy daughter and found strength in her community. Michelle opens up about her experiences with surgery, radiation, and the lasting effects of an acquired brain injury. She discusses the importance of support networks, the anxiety of MRI results, and her advocacy for increased funding for brain cancer support services. Her story is one of resilience, hope, and the power of community.DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
In this episode of Aunty M Brain Tumours Talk Show Podcast, Madi shares her powerful journey with an oligodendroglioma grade two brain tumour. Her story begins with unexpected seizures that led to a life-changing MRI. Initially told her tumour was slow-growing and not a major concern, Madi's move to a new province meant navigating a complex healthcare system and seeking new specialists.
She opens up about the challenges of getting clear answers, the difficult decision to undergo a biopsy, and the unexpected complications that followed—including issues with her vision. Through research, support groups, and personal resilience, Madi found strength in understanding her diagnosis and redefining her future.
Her journey is a reminder that a diagnosis isn’t an expiration date—it’s a new path to navigate.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
In this episode, Christine shares her journey with angiomatous microcystic meningioma, a diagnosis that profoundly impacted her daily life. She opens up about the significant symptoms she faced, the emotional toll of waiting for surgery, and the relief of finally receiving treatment. Christine describes how surgery brought noticeable improvements but also introduced unexpected complications during recovery.
Despite the challenges of pain management and emotional fluctuations, she found strength in the support of her family and friends. Christine reflects on her experience, emphasizing that brain surgery was less daunting than she had feared. With no further treatment required, she expresses gratitude for skilled medical care and the importance of clear communication throughout the process.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
In this powerful episode, Imogen shares her journey of love, loss, and resilience after her husband, Wayne, passed away from glioblastoma in May 2024.
Together since their teens, Imogen and Wayne built a life filled with music, family, and dreams for the future. But in early 2022, their world changed when Wayne began experiencing unexplained symptoms. What followed was a heartbreaking battle with brain cancer—marked by treatments, clinical trials, and unwavering hope.
Through it all, Wayne remained the incredible husband and father he always was, facing his diagnosis with strength and love. His story is a reminder of the urgent need for brain tumour awareness and research.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
At just 20, Steph Still’s life changed forever. Unusual symptoms led to a devastating diagnosis— Ependymoma. Surgery was her only option, followed byRadiotherapy, but it came with a heavy price. She had to relearn how to move, how to speak… how to live. The battle didn’t end in the operating room. With a paralyzed vocal fold and a long road to recovery, Steph faced unimaginable challenges. But she wasn’t alone. Hermother—a former ICU Senior Sister—stood by her side. Community support and exercise became her lifeline, proving that movement is healing.
Determined not to let cancer define her, Steph went back to studying and is now a Cancer Rehab Specialist and fitness instructor helping others find strength in their own recovery. She knows firsthand the importance of mental well-being, communication, and the right support.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
Claire Harris shares her emotional journey on the podcast, recalling the terrifying moment her son Jake was diagnosed with a brain tumour at just four years old. Initially misdiagnosed, it was a persistent health visitor who helped fast-track the MRI that changed everything. From major brain surgery to a surprisingly quick recovery, Claire reflects on the resilience of children, the overwhelming fear as a parent, and how she became overprotective in the years that followed. She also highlights the crucial need for awareness—educating parents and doctors about early symptoms can save lives.
Her message?
Stay informed, stay hopeful, and trust your instincts.
💙🎧 Listen now! #BrainTumourAwareness #ChildhoodIllness #Parenting #Podcast
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
Israr Jan-Parker shares her journey of being diagnosed with a brain tumour, the emotional and physical challenges she faces, and her determination to raise awareness and funds for Brain Tumour Research and The Brain Tumour Charity. She discusses the various challenges she undertakes to support the charities and her hope for future advancements in treatment.
Israr was diagnosed with a petroclival tumour in 2022. She was told she had seven months to live due to the location of her tumour. Despite setbacks, she is determined to raise awareness for brain tumours.
She is participating in a number of challenges to raisefunds for Brain Tumour Research and The Brain Tumour Charity. Including theuniversity where she teaches in Chichester. They have been taking part in thismonth.
Find Out More About Israr's Fundraising Campaign on Givewheel.com here: https://gvwhl.com/AEKOP
DISCLAIMER Any of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
In 2017, Vicki was diagnosed with an astrocytoma after battling severe migraines and vision issues. She faced surgery, complications, and an awake craniotomy with remarkable resilience. Despite the tumour growing to Grade 3, she endured chemotherapy, radiotherapy, and seizures—all while holding onto hope for her daughter. Now, her tumour is shrinking, and her story is a powerful reminder that strength and belief can defy the odds.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
Maria Peta was diagnosed with a meningioma on New Year’s Eve 2009 after her initial symptoms were misdiagnosed as migraines. A second opinion revealed a golf ball-sized tumour, changing the course of her life. As she navigated the fears and uncertainties leading up to surgery, she used humour to cope.The operation marked the beginning of a long recovery, where Maria struggled with her identity and emotional well-being. Counselling played a vital role in helping her process her experiences. Over time, she connected with others affected by brain tumours, finding purpose in advocacy and support work with Brain Tumour Research.Now, 15 years later, Maria reflects on her resilience, the lessons learned, and how time has shaped her journey from diagnosis to self-acceptance.DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
In this inspiring episode, Kiera Mitchell shares herpowerful story of resilience after being diagnosed with a Medulloblastoma brain tumour at just 19, and left her with mobility issues. She talks about her challenges of rehabilitation and how fitness became a crucial part of her recovery. From struggling with mobility to regaining independence, Kiera’s journey highlights the importance of perseverance, strength training, andmental resilience. Now living life on her terms, she encourages others tokeep pushing forward, no matter the obstacles. Tune in to hear Kiera’s messageof hope and determination.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
Katie Smith shares her journey of being diagnosed with an oligoastrocytoma, the challenges she faced with treatment and recurrence, and her ongoing battle with uncertainty and grief. She discusses her advocacy for brain tumour research and the impact of her experiences on her family. Katie emphasizes the need for awareness and the emotional complexities of living with a brain tumour while also highlighting her determination to make a difference for others in similar situations.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
Madi Ruby, has been living with a brain tumourfor more than half of her life. First diagnosed at 23 in 1995 with a 6cmmeningioma, she underwent surgery and built a successful career in TV sales andIT, all while raising her son with her husband, Neil. But in 2013, her tumourreturned—this time with multiple growths.
Despite setbacks, Madi refused to let herdiagnosis define her. She retrained as a counsellor, earned a PhD,
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
Through the eyes of her parents, we witness Amani’s heartbreaking yet powerful journey with Glioblastoma Multiforme Amani's strength never wavered from the first symptoms to the desperate fight for treatment. She dreamed of making a difference, and she did that —her #WalkofHope and #Chat2Amani were just the beginning.
Even after her passing, Amani’s parents continue her mission, turning pain into purpose. They’ve built a primary school in Malawi, fundraised for a community centre in Uganda, and fiercely advocated for brain tumour awareness and research.
Amani’s story is more than tragedy—it’s a testament to faith, resilience, and the impact one life can have. "Don’t forget our daughter". Brain tumours don’t discriminate. Let’s keep fighting.
Steve Blake was diagnosed with an inoperable meningioma. For 18 months, he battled misdiagnoses before finally hearing the words "You have a brain tumour." The emotional toll of brain surgery and the harsh reality of recovery tested him in ways he never imagined. Brain surgery was just the beginning—he had radiotherapy, and the challenge of rebuilding life followed. Now, Steve is turning his journey into purpose—advocating, fundraising, and sharing his story so no one else has to face this journey alone.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
Julia’s world changed with an incidental finding—a sphenoid wing meningioma that doctors said could never be fully removed. From the emotional toll of diagnosis to the complexities of brain surgery, radiotherapy, and Gamma Knife treatment, her journey has been anything but easy. Yet, through it all, she’s leaned on community, humour, and resilience to keep going. With support from Brainstrust and the kindness of her neurosurgical secretary, Julia now shares her practical tips and hard-earned wisdom for navigating life after surgery. She knows she’s one of the lucky ones—and she’s here to help others find strength in the face of uncertainty. #BrainTumourAwareness #Meningioma #BrainTumourAwarenessMonthDISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
Matthew Warne shares his journey with glioblastoma multiforme (GBM), detailing his initial diagnosis, treatment experiences, and the emotional and physical challenges he faced. He discusses the importance of mental resilience,exploring alternative treatments, and making lifestyle changes to cope with the disease. Matt emphasizes the significance of support systems and planning forthe future while navigating the complexities of medical advice and personal health management.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.
In this heartfelt interview with Sarah Long, we learn abouther son Oscar, a young boy full of life and promise. Oscar was diagnosed with Diffuse Intrinsic Pontine Glioma (DIPG), a rare and devastating brain tumour. His initial symptoms— a tilted head and memory issues—marked the beginning of afight no family should ever have to endure. Throughout his battle, the family focused on creating joyful memories, cherishing every precious moment together. But as thedays passed, palliative care became crucial, offering comfort in Oscar’s final moments. His parents channelled their grief into a mission to raise awareness, funding, and hope for future research. They organized events, rallied communities, and even placed tiles at the Brain Tumour Research "Centresof Excellence" in Oscar’s honour—symbols of love, loss, and the desire to make a difference. Their story underscores a heartbreaking reality: the severe shortfall in government funding for brain tumour research, especially for rareconditions like DIPG. In this interview, Sarah shares how Oscar’s legacy inspires action and how the family is determined to ensure that no other child faces what Oscar did without hope for a cure.
DISCLAIMERAny of the sites under Claire Bullimore or Aunty M Brain Tumours is not intended to provide and does not constitute medical, legal, or other professional advice. The content on Aunty M Brain Tumours is designed to support, not replace, medical or psychiatric treatment.