Meningioma: Anyone else? I'm frightened

Posted by pixie49247 @pixie49247, May 12, 2023

I just found out I have a Meningioma tumor from a MRI I had for something else. Doctor said they are almost always benign and am going to get an appointment with a neurologist. Anyone else have one of these. I’m getting very frightened now.

Interested in more discussions like this? Go to the Brain Tumor Support Group.

Have you asked about Gamma Knife Ray Surgery? That was one of the options I was given. It is non invasive but has to be done by a neurosurgeon trained in it. Just an idea.
Good luck

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I was diagnosed with meningioma in 2022 and it was scary to hear brain tumor. My neurosurgeon suggested we monitor with annual MRI and if no growth we can just leave it alone. In May 2024 the MRI showed that it was growing, now I'm doing a lot of research to determine best type of treatment. My current neurosurgeon wants to do a craniotomy. It's a scary thought but this support group is helpful. Good luck in your journey.

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Elisabeth, I had a craniotomy/brain surgery 7 months ago to remove a 2.7 centimeter meningioma. It was not as bad as I had imagined it to be. I left the operating room on prescription pain meds of some sort, but after that I was just on tylenol every 8 hours while in the hospital for 2 days. Once at home, I didn't take tylenol at all. The worst part was the stress I endured worrying about it before the surgery.

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i have a meningoma that was found on an MRI about 8 years ago. i have had at most minor symptoms eg mild to moderate headaches

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i have had a meningoma for almost a decade that apparently has recently changed. i’m seeing a neurosurgeon next week. please share what it’s like to have a meningoma biopsied and surgically removed

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Profile picture for Maryann @mkoch

Is Gamma Knife the one where they have to mold a mask to your face?

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Yes gamma knife is the one they mold a mask to your face. I’ve had repeated meningiomas and gamma knife over the past 5 years. It stops the growth and I do receive MRI’s every 6 months so all are monitored for any signs of regrowth. Stay positive it’s the best way to heal and keep moving forward, my very best to you.

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Profile picture for elisabeth007 @elisabeth007

i have had a meningoma for 5-6 years that has been monitored by my neuro-oprhamologist. On May 7, 2024, i had another scan and was told by my neuro-opthamologist that the meningoma had enlarged. He immediately referred me to an oncology neuro-surgeon he highly trusts for an evaluation. Presumably, the two will develop a treatment plan. I would think among the first things the neurosurgeon will want to do is get a biopsy

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Well I’ve yet to meet with neuro surgeons but shall update. All the best to everyone & thankyou for replies.

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Profile picture for jmb73 @jmb73

No, the one I had wasn't a mold. They put a helmet on me and gave me lidocaine and then screwed it on. The lidocaine stung but I only felt pressure with the screws. It really wasn't bad or painful.

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Thank you so much. I have 2 meningiomas that are being watched and was told I may need to have gamma knife. It must be cyber knife that a mask mold is made and I am claustrophobic and could not tolerate that.

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Profile picture for Maryann @mkoch

Is Gamma Knife the one where they have to mold a mask to your face?

Jump to this post

No, the one I had wasn't a mold. They put a helmet on me and gave me lidocaine and then screwed it on. The lidocaine stung but I only felt pressure with the screws. It really wasn't bad or painful.

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Profile picture for ella62 @ella62

I was diagnosed with a meningioma in 2011 and have only had it monitored in all these years. Met with the neurologist after another brain scan to find it’s grown a lot. It’s now 24mm & is of the fossa posterior. I’ve been referred to neurosurgeons now but for radiation therapy. If anyone has had such therapy could you kindly tell me the process. Thanks & good luck

Jump to this post

i have had a meningoma for 5-6 years that has been monitored by my neuro-oprhamologist. On May 7, 2024, i had another scan and was told by my neuro-opthamologist that the meningoma had enlarged. He immediately referred me to an oncology neuro-surgeon he highly trusts for an evaluation. Presumably, the two will develop a treatment plan. I would think among the first things the neurosurgeon will want to do is get a biopsy

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