Cavernous Sinus Meningioma

[Ashers12]

My husband has been diagnosed with now :cm Cavernous Sinus Meningioma. It was 2cm and slow growing so wait and see was the plan. The tumour is now 3cm and Surgery is now the only option as the doctors lost his scans (which had to be repeated) and in a more dangerous position .Not given time to ask questions as we were in shock but are now on a waiting list and haven’t heard anything and are worried about everything including how big it will have grown to.

Has anyone had similar experience?

[Shannon_TBTC Partner]

This must be a really worrying time for you Ashers12, you may find the following document helpful. This is our step by step guide which includes information on surgery, actions to take and questions to ask. Our support team are also here should you have any questions and can be contacted on 0808 800 0004 or by emailing [e-mail]. thebraintumourcharity.org/b...