Austen was diagnosed with Neurofibromatosis Type 2 (NF2) in February 2025.
After years of worsening balance and hearing issues, he was repeatedly told nothing was wrong — until an MRI revealed multiple tumours.
At first, he was told there were four.
Then eight.
Then seven in his spine.
A total of 15 tumours.
In this honest and down-to-earth interview, Austen shares: • Being dismissed for years before finally getting answers • The shock of being diagnosed with a rare genetic condition • Finding out the full extent of his tumours in an unexpected moment • Living with hearing loss and balance issues • Starting lifelong treatment with Avastin • Making the decision not to have high-risk surgery • The uncertainty of symptoms — not knowing what is tumour-related • Fatigue and the reality of daily life with NF2 • Leaving work to prioritise his health • The mental challenge of not knowing what the future holds
Austen speaks openly about how isolating rare conditions can feel — and why connecting with others who truly understand makes such a difference.
He also shares how something as simple as getting a dog completely changed his life, giving him purpose, routine, and a reason to keep going.
His message is simple:
You can’t let it run your life. Just take it day by day.
This episode is part of a 31-day series sharing real brain tumour stories for Brain Tumour Awareness Month 2026.
If this episode resonates with you, please share it. Every story helps raise awareness.
⚠️ Content note: This episode discusses brain tumour diagnosis, chronic illness, lifelong treatment, hearing loss, fatigue, and mental health challenges.
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