Watching a Meningioma Brain Tumor
I've just been diagnosed with a 2cm meningioma tumor on the right front of my head. I am 59 years old and the surgeon has told me I will need to "do something" with my tumor someday since I am younger. What is the benefit of waiting?
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@lisalucier @hopeful33250
I went to the doctor today and was diagnosed with a concussion. The headaches continue so I’m supposed to limit my activity for a few days. I know this is very minuscule in comparison to what many of you are facing. I simply wanted to let you know that I did go to the doctor.
I've had some ringing in my left ear recently.
The neurosurgeon didn't take the time to talk about them. So I will be heading to my PCP to talk more about things.
I had a 9cm brain tumor removed 6 weeks ago. It is wrapped around my carotid artery and optic nerve on my left side. The neurosurgeon could only remove 85% of the tumor. I have lost vision in my left eye due to the tumor. My jaw is still really bothering me where they had to cut and remove tumor. I can't open my mouth wide and having a hard time eating. I have a lot of pain when I eat. Is this normal and just part of healing? It hurts in my tmj area temple area. I am good to a neuro-opthamologist October 15th to see what else to except with my eye. The neurosurgeon said I will eventually go completely blind in left eye so I hope to learn more on October 15th of what to expect.
Please take care of yourself, @twomama . As Lisa said, I hope you contact your doctor soon.
I'm terribly sorry to hear you fell again, @twomama. Please do consider contacting your doctor with the concussion symptoms.
I tripped and fell again today, another accidental fall. I’m experiencing some mild concussion symptoms again (headache, dizziness) but haven’t called my doctor. It does make me think about the meningioma again.
I fell while at work. It was an accident and not at all related to any other problems. I hit my head pretty hard when I fell resulting in a concussion. I had headaches and dizziness for several weeks following that and it was during an MRI for that when the meningioma was discovered.
I hate to admit that I still haynot gone in for the follow-up to look more closely at the meningioma. I know it’s something I should do. I just keep thinking that it’s probably nothing. I know that’s probably not the best decision.
Hello @kkenn
I would like to add my welcome, along with Lisa's, @lisalucier, to Mayo Connect. I looked at the National Institute of Health website that discusses this type of surgery. Here is the link to the article,
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831269/
Have you had any paresis or symptoms other than the migraines?
Gloria Jean
The hardest thing for me is not being able to drive. I can't go see my kids or grandkids. I have to wait for my hubby who still works or to take me or for them to come to see me.