I was just diagnosed with the same. I fell and hit my head and that is how it showed up. I went to a neurosurgeon and he said to wait a year and have another MRI - right now it is 11mm. My vision has changed in my right eye but he says that is not the reason. I read others comments about vision changes but the doctors all seem to say that is not the cause. Makes me wonder why there are many of us that are having the same issue.
Hi @gigikocmankokemoor1, I'm tagging @kkenn and @pegorr who may have experiences with meningioma involving the falx cerebri, the brain membrane that separates the left and right sides of the brain.
Gigi, has your care team suggested treatment or are you on active surveillance? How was the meningioma discovered?
Good morning,
I'm new to this chat. Happy to have discovered this support group.
Couple of weeks ago I had a routine MRI of brain after resection of a meningioma back in 2017. My last MRI in 2021 was clear and no signs of anything, but this time around, something may be growing in the anterior falx, according to MRI report. I'm very nervous and anxious as I have to wait a couple of weeks to discuss report findings and images with my Neuro. The findings say that there is a "plaque-like thickening of the anterior falx with homogenous contrast enhancement, possibly reflecting small meningioma measuring 4 x 10 mm"? Is that a concern you think?
Good morning,
I'm new to this chat. Happy to have discovered this support group.
Couple of weeks ago I had a routine MRI of brain after resection of a meningioma back in 2017. My last MRI in 2021 was clear and no signs of anything, but this time around, something may be growing in the anterior falx, according to MRI report. I'm very nervous and anxious as I have to wait a couple of weeks to discuss report findings and images with my Neuro. The findings say that there is a "plaque-like thickening of the anterior falx with homogenous contrast enhancement, possibly reflecting small meningioma measuring 4 x 10 mm"? Is that a concern you think?
rox25: I have a 6 x 3 mm. right, posterior falx meningioma. It was discovered at the same time as 2 other meningiomas when I was being screened for a stroke. (Didn't have one) The neurosurgeon did remove one of the meningiomas that was 1/16th of an inch from my optic nerve a little over a year ago. But with regard to the falx meningioma, the neurosurgeon has suggested a watch-and-wait approach. It hasn't changed/grown in a year and a half. So I am at peace with just getting MRIs once a year and monitoring its possible growth. As you probably already know, those of us diagnosed with a meningioma seem to have a tendency to develop others.
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I was just diagnosed with the same. I fell and hit my head and that is how it showed up. I went to a neurosurgeon and he said to wait a year and have another MRI - right now it is 11mm. My vision has changed in my right eye but he says that is not the reason. I read others comments about vision changes but the doctors all seem to say that is not the cause. Makes me wonder why there are many of us that are having the same issue.
Good morning,
I'm new to this chat. Happy to have discovered this support group.
Couple of weeks ago I had a routine MRI of brain after resection of a meningioma back in 2017. My last MRI in 2021 was clear and no signs of anything, but this time around, something may be growing in the anterior falx, according to MRI report. I'm very nervous and anxious as I have to wait a couple of weeks to discuss report findings and images with my Neuro. The findings say that there is a "plaque-like thickening of the anterior falx with homogenous contrast enhancement, possibly reflecting small meningioma measuring 4 x 10 mm"? Is that a concern you think?
Best,
rox25: I have a 6 x 3 mm. right, posterior falx meningioma. It was discovered at the same time as 2 other meningiomas when I was being screened for a stroke. (Didn't have one) The neurosurgeon did remove one of the meningiomas that was 1/16th of an inch from my optic nerve a little over a year ago. But with regard to the falx meningioma, the neurosurgeon has suggested a watch-and-wait approach. It hasn't changed/grown in a year and a half. So I am at peace with just getting MRIs once a year and monitoring its possible growth. As you probably already know, those of us diagnosed with a meningioma seem to have a tendency to develop others.