Meningioma: Anyone else? I'm frightened
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.
It’s such a comfort to know someone has already gone through this and knows the outcome . It’s hard not to be afraid . It’s a 6hour surgery . Thank you for responding to my message. I’m sure you’ll hear from me again thank you.
Hi @mkoch, what was the size of your meningioma when it was removed in 2023? How much did it grow from 2017, 2.7 cm? Regards.
That breaks my heart for you. It makes me sad that doctors seem to rely on imaging when the patient is sitting right in front of them telling them something is wrong. I asked the neurosurgeon where to turn or what to do and wasn't given any direction. I'm sad that there are symptoms with no solution. I sure pray you get the right treatment and that everything is successful.
Thank you. It is frustrating and sad especially since I (we) go through so many other unnecessary appts and other diagnostics (they were testing me for myasthenia gravis) ptosis surgery which was not successful since there's an underlying cause (CS meningioma) and going on since 2019. Im thankful as I remind myself it could be worse. I pray you also get the treatment necessary and wish you so much as I do with all off us going through this, all the best and for positive outcomes. Hugs
I'm so happy to hear they figured it all out for you. How had your recovery been? Did your vision /droop get better?
I am actually waiting on an appt for a 2nd opinion and my initial team seems to be more on top of the situation (up coming appts) with the 2nd finding.
Thank you so much!
ninha06: In a five year period my sphenoid meningioma grew from 1.7 to 2.7 centimeters. So, about a two millimeter growth per year. As I've mentioned before, I was told by a neuro-radiation doctor that they don't like to use stereotactic radiation on tumors larger than 3 cm.
@mkoch Thank you.
Hi! I had my first MRI last Tuesday and my results came back showing a 1.9cm high right parasagittal convexity extra-axial mass most compatible with a meningioma. My family doctor has referred me to neuro and I am waiting for my appointment. My MRI was ordered due to dizziness, inflammation of the left eye and blurry vision of the left eye. I am also in perimenopause and states that hormones like birth control or replacement therapy should not be taken and could increase meningioma growth. My hormones are off balance and causing major issues (hot flashes, night sweats, exc) and I am not sure what to do. Anyone have this issue? If so, what did your doctor recommend to keep you balanced until you reached menopause?
A neuro doctor who specializes in radiation for meningiomas told me that there is a
POSSIBLE link between estrogen and the development of meningiomas. So I would keep on your hormones until you consult with the neuro doctor and get his opinion. As one who has been down this road before, (perimenopause) your quality of everyday life is worth something, too. Secondly, you need a really good gynecologist who can direct you. My opinion is that an OB/GYN has only so much time to keep updated on current research and I chose to see a GYN. who wasn't delivering babies but was reading medical journals more focused towards women at a different phase of their lives.