Ryan O’Shea Story
Name: Ryan O’Shea.
Tumour type: Grade 1 Diffuse Astrocytoma.
- Headaches/migraines for over 6 to 8 months.
- Progressively worsened 6 weeks leading up to diagnosis.
- Days leading up to diagnosis my speaking started to stutter and my memory also started to decline.
20/04/2022 – CT Scan.
21/04/2022 – Emergency MRI Scan (AM).
21/04/2022 – Urgent meeting with Dr Gibson (PM).
23/04/2022 – Flown over and admitted to National Neurology and Neurosurgery London.
29/04/2022 – Biopsy of left frontal tumor and insert EVD (external drain) – Surgery by Mr Kitchen.
05/05/2022 – Removal of EVD and insert Ventriculoperitoneal Shunt (Internal drain).
11/05/2022 – Discharged.
22/06/2022 – Molecular Analysis results came back and confirmed tumour and type.
Support from Charity:
- Counselling post surgery and continued support while returning to normal life and work.
- I have been given the option to join the buddy meetings.
How did it feel emotionally at the point of diagnosis:
Due to the fast pace of everything I didn’t really have much time to think, I was basically in auto pilot. I did get upset but it was more for other people than myself. I live by the saying ‘It is, what it is’ as I couldn’t control the situation I just had to agree to whatever the surgeons recommended was best for me. I would say though, having to; sign my will, the surgery paper work and having it confirmed as a tumour were hard to deal with emotionally.
I was unable to drive from the day of surgery until Thursday 3rd November 2022.
I returned to work on the 11th October 2022 on reduced hours and planning on returning to full hours by end of March 2023.
I have to under go MRI scans every 6 months for the near future and possibly the rest of my life.
The current plan is to review the scans and see if there are any changes, I was made that my type of tumor is typically found in people 55-65 so to have it at my age is rarely seen.
I believe this situation has made me look at life differently and has changed my priorities.