Watching a Meningioma Brain Tumor

Robin, very sorry to hear of your situation. In May 2018, at age 67, after having 3 seizures during the preceding 6 months, I was diagnosed with a 6 cm meningioma in my right forehead area. It was described as being the size of a tangerine! I was immediately referred to a neurosurgeon and not offered the “wait and see” option. I was very fortunate to not have had other symptoms, which I was told could be significant and some could be possibly be irreversible. Surgery was scheduled for and occurred in August 2018 at Oregon Health Sciences University (OHSU) in Portland, OR. While everyone is different, based on my experience, I would not dread the craniotomy surgery if I had to do it again. I had an excellent surgical team, an experienced neurosurgeon, and terrific post surgery care, things I would research a lot if I had to do it again. I should think that the Mayo Clinic would be a great choice, as was OHSU for me. Having the surgery was helpful to me to get that thing out of my head and not have to worry about it anymore, although unfortunately, a small part that was closely associated with my right optical nerve, was left in place so as to not compromise vision in that eye, a decision by the surgical team for which I am grateful. That has placed me into a “wait and see” situation to see if the remnant stars growing again. Successive MRI’s since surgery have shown it to be stable, which is great. My thought for you is, if the surgery becomes recommended, be strong, do your research in choosing your surgeon and hospital facility, and get it done. I understand the fears you face, as I faced them, too, but it could be worse by not doing anything when/if your doctors recommend removal. I wish you the very best.

How are you feeling lately @bobhills?

I was diagnosed with this tumor in January. It's being monitored as of now. Has anyone been diagnosed with one maybe similar to this..I'll just write my docs notes and should I be worried...because it seems not to be a big deal...a watch and wait thing..here's what was found..meningioma of the sphenoid alley in front of the optic chiasm on the right under frontal lobe.. has fairly large vessels in the tumor itself. It measures 2.5 x 2.0 x 1.6 cm. It does not appear to be compressing..there is contact of the. Optic chiasm but does not appear to be compressing it. It may be growing down and around the optic strut and optic foramen.. ok..so what do I do with that. I'm told not to worry but that's messing with my vision.

I was diagnosed with this tumor in January. It's being monitored as of now. Has anyone been diagnosed with one maybe similar to this..I'll just write my docs notes and should I be worried...because it seems not to be a big deal...a watch and wait thing..here's what was found..meningioma of the sphenoid alley in front of the optic chiasm on the right under frontal lobe.. has fairly large vessels in the tumor itself. It measures 2.5 x 2.0 x 1.6 cm. It does not appear to be compressing..there is contact of the. Optic chiasm but does not appear to be compressing it. It may be growing down and around the optic strut and optic foramen.. ok..so what do I do with that. I'm told not to worry but that's messing with my vision.

I was diagnosed with this tumor in January. It's being monitored as of now. Has anyone been diagnosed with one maybe similar to this..I'll just write my docs notes and should I be worried...because it seems not to be a big deal...a watch and wait thing..here's what was found..meningioma of the sphenoid alley in front of the optic chiasm on the right under frontal lobe.. has fairly large vessels in the tumor itself. It measures 2.5 x 2.0 x 1.6 cm. It does not appear to be compressing..there is contact of the. Optic chiasm but does not appear to be compressing it. It may be growing down and around the optic strut and optic foramen.. ok..so what do I do with that. I'm told not to worry but that's messing with my vision.

Hi @dusktodawnisparkle, I'd like to add my welcome. You'll notice that I moved your message to this existing discussion about Watching a Meningioma Brain Tumor. Click VIEW & REPLY to read through past posts.

You might also be interested in reading the posts of members like @robinem @ees1 @cnesselroad and more in these related discussions:
- Meningioma and Cavernoma: Stressed Waiting and Watching https://connect.mayoclinic.org/discussion/meningioma-and-cavernoma/
- Meningioma - I'm scared to watch and wait https://connect.mayoclinic.org/discussion/have-had-a-mri-that-revealed-a-large-structure-that-is-presumed/

Being told that watchful waiting is your treatment option can be stressful. In actual fact, your medical team is not inactive, but rather actively monitoring you. This is likely because the risk of treatment is more dangerous than the possible benefits. I prefer the term “active surveillance” rather than “no effort”.

I'm unclear about one thing in your post. Are you currently experiencing vision issues?

Hey how are you doing? Thank you for responding. And yes I was a little unlear about the vision. They had told me nothing to worry at that very moment. I was like well...that's my vision your actively monitoring...like dont mess around. I want to always be able to see my beautiful daughter. But the answer to your question is yes...some...on some days my right eye will go blurry...I mainly notice when I'm up and around..just messing around online in the morning..my opthamalogist says the tumor is making contact with the optic chiasm..let's come back in 3 months...well it's been right at 3 months. My left eye is clear when I cover my right eye. When I switch totally blurry...if I had to rely on that eye to read it wouldn't happen..I noticed today my reading glasses didnt really help either. It did 3 months ago..the neurologist says could be an age thing ..could be the tumor...if one more person. Tells me anything with this tumor could be agreed related instead I'll cry. I turned 51 today. I have trouble concentrating really bad the last 2 years. What brought me to get the MRI IS HEADACHES...bad...I hit my head 2 years ago....so hard..on my shed wall coming off of a step and lost balance. Messed my neck up real good...I was shimmy feeling for 3 days...didnt go to hospital...kept on truckin... probably not a good thing to have done..anyhow...I'll let ya catch up..but from that I have a reverse curve in neck going on ...ddd..neuropathy...raynauds ..fibromyalgia. ddd in lower lumbar with compression fractures..oh and carpal tunnel syndrome. I probably forgot something. Lol..but all these things have came about it seems since I hit my head. I know some is age related of course. My Pcp says I just rushed things along when I hit my head. I drives me nuts to sit stand lay down..I'm just all over some days..filled for disability..denied 3 times..just got denied by appeals council. My lawyer was worthless. They didnt know about the tumor. Been seeing docs for 2 years trying to find out what is causing headaches...then they found tumor right after my hearing...

Hello @dusktodawnisparkle, I'm sorry to hear about your diagnosis. A brain tumor is never good news. I myself have a Glioblastoma diagnosed in the fall of 2018 located behind the optic chiasm. It is an aggressive tumor with a diagnosis of impending death. I tell you this because, despite what the doctors say, I am still alive (very much alive) and to this day, I have not lost any cognitive function or vision problem. (After my chemotherapy treatments, I happened to have a few short episodes of visual epilepsy. It lasted a few minutes (10 minutes). It doesn't hurt. It's just strange because part of the vision changes during the seizure but then returns to normal.
I like to think positively, (it helps me get through the disease) so, with each visual epileptic attack, I told myself that it was a sign, a good sign that my chemotherapy was working. I have learned in recent months that current medicine does not know much about brain tumors, so be skeptical, especially about the bad news. Your body is resourceful and it wants to heal. I don't know much about meningiomas, but I do the ketogenic diet, and I take certain dietary supplements (ask a certified naturopath) that control tumor growth. I now live with this tumor as if it was of a chronic disease and I try to do everything not to feed it (a bit like a plant that we do not water so that it does not grow). It seems to work pretty well. For the moment, my tumor remains quiet and does not grow.
Hope this can help you, good luck and most of all, keep your spirits up because it helps you and your brain fight this meningioma.

Hey how are you doing? Thank you for responding. And yes I was a little unlear about the vision. They had told me nothing to worry at that very moment. I was like well...that's my vision your actively monitoring...like dont mess around. I want to always be able to see my beautiful daughter. But the answer to your question is yes...some...on some days my right eye will go blurry...I mainly notice when I'm up and around..just messing around online in the morning..my opthamalogist says the tumor is making contact with the optic chiasm..let's come back in 3 months...well it's been right at 3 months. My left eye is clear when I cover my right eye. When I switch totally blurry...if I had to rely on that eye to read it wouldn't happen..I noticed today my reading glasses didnt really help either. It did 3 months ago..the neurologist says could be an age thing ..could be the tumor...if one more person. Tells me anything with this tumor could be agreed related instead I'll cry. I turned 51 today. I have trouble concentrating really bad the last 2 years. What brought me to get the MRI IS HEADACHES...bad...I hit my head 2 years ago....so hard..on my shed wall coming off of a step and lost balance. Messed my neck up real good...I was shimmy feeling for 3 days...didnt go to hospital...kept on truckin... probably not a good thing to have done..anyhow...I'll let ya catch up..but from that I have a reverse curve in neck going on ...ddd..neuropathy...raynauds ..fibromyalgia. ddd in lower lumbar with compression fractures..oh and carpal tunnel syndrome. I probably forgot something. Lol..but all these things have came about it seems since I hit my head. I know some is age related of course. My Pcp says I just rushed things along when I hit my head. I drives me nuts to sit stand lay down..I'm just all over some days..filled for disability..denied 3 times..just got denied by appeals council. My lawyer was worthless. They didnt know about the tumor. Been seeing docs for 2 years trying to find out what is causing headaches...then they found tumor right after my hearing...