Mayo Clinic Connect
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?
Liked by Scott, Volunteer Mentor, EES1, gloriajean
hello – five yrs ago on Oct
17/2013, I had a seizure (my one & only). And that's when a grade 1 benign mengioma – 3 cm was discovered. That was on a Friday evening – I had sold my house & HAD to move on the following Monday. They wanted to operate o that same day!!! No warning, no family, no social work or help with an horribe decision to be made – never been ill or in hospital. Terrified beyond belief – even now – what I went thru was awful beyond belief. BUT I checked myself out of hospital and got on with my life. If it was to be short, so be it.
And I was in OK shape – tumour was not growing, in fact reduced in size/shape.
Underlying all of this was my treme dous fear of someone, allbeit a top neurosurgeon, was going to open my brain. I just couldnt cope with that and so, took my chances.
But in May 207, my cognitive abilities went downhill and I had to make THE decision to have the craniotomy. I still to this day, don't know how I managed to walk thru the doors of the hospital!!!
As 70 yr old single woman, I enjoyed four pretty good years of life, all the while knowing I jad something inside of my head, pressing down on my beloved brain.
Somehow I overcame my tremendous fea of the surgery, and the tumour was completely removed.
I do not regret waiting all those years – perhaps I was lucky.
It is NOT an easy decision to reach ( LO) but I truly wish you well as you travel along this new path in your life.
Please free to "chat" with me as you need.
Peace & Happiness!
Liked by Colleen Young, Connect Director, Teresa, Volunteer Mentor, Lisa Lucier
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Gloria Jean how is your recovery going? You are such a brave person!
Liked by Teresa, Volunteer Mentor, Lisa Lucier
Kind words but I was truly so scared that really I was "choosing" to have the tumour tale me away rather than to have my brain cut open!!!! That is not bei brave.
Liked by Teresa, Volunteer Mentor
What now keeps me somewhat on track is that I was only on the operating table for 1.5 hrs..- incision closed with 34 staples – main chewing muscles on the left side of my face – oh, I can go on and on. I was not informed about so many elements of my "short" brain surgery! My balance is ruined BUT then my cogntive abilities are very good and getti g back to where I was before I had the deadly seizure.
I have been grieving about the tumour and now I am in the angry phase of this process.
And I have not even touched upon the severe depression I endured for several months fter having my brain opened up.
Hard, hard decision to be reached without family or support.
Gloria Jean my story is similar to yours in the beginning. The ER admitted me after finding a mass in my brain after a ct scan. I felt like they were pushing me toward brain surgery the second morning after admission so I checked myself out with a possible diagnosis of acoustic Neuroma 3.3 cm
I needed more insurance and to do my research. I am 68 years old and have had a # of surgeries and hospitalizations. I knew i might be facing a serious surgery and wanted a very experienced surgeon to drill into my head. I called Mayo Clinic at the advice of a doctor friend of mine. My husband drove me the 7 hours to meet with surgeons. I believe i had the 2 best in the west. A few weeks later I went for surgery armed with a lot a research and additional insurance. The surgery lasted 8 hours and all four of my adult children were there along with my dear husband of 42 years. It was so sad to learn that you went through surgery all alone. After 5 days in the hospital i went to rehab for 8 days. I am now in the 3rd week of home health care and think i am progressing well. I am hoping to be able to drive again but my balance needs more work. I have to fight feelings of self pity and some anger at times but I turn to doing things that cheer me up and press on.
Liked by Teresa, Volunteer Mentor, Lindajean, Lisa Lucier
Goodness, 8 hrs of surgery! Ad you were pleased with the surgeons' abilities. And you have your husband and your children. What a team you have!. There is the good side of an earth-shattering point in your life.
have your dpctors addressed the balance provlem that so many of us who have had brai n surgery endure
Weren't you afraid going into the hospital? I didn't even want to undress – the nirse wouldn't give me the pill promised by the neurosurgeon "as soon as I walked thru the front door of the hospital".
I behaved worse than a child until I got sedated.
What are you now finding the most difficult ?
Peace & Happiness
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.
Hi I've been recently diagnosed with a 2cm meningioma in the Falx and parasagittal regions. Neurosurgeon wants to wait and watch. I was seeing a Dr for newly acquired migraines. This was a new Dr and decided an MRI but not expecting anything. Neurosurgeon says he doesn't think the meniginoma is causing my migraines. I'm just at a loss!
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,
Have you had any paresis or symptoms other than the migraines?
Liked by Lisa Lucier
Welcome to Connect, @twomama. I'm sorry to hear about your diagnosis, and so glad that you've joined this group. While we wait for others to join in, here's some information from Mayo Clinic which you might wish to read: https://www.mayoclinic.org/diseases-conditions/meningioma/symptoms-causes/syc-20355643
@twomama, would you be able to share a few more details? How did the concussion occur?
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.
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'm terribly sorry to hear you fell again, @twomama. Please do consider contacting your doctor with the concussion symptoms.
Please take care of yourself, @twomama . As Lisa said, I hope you contact your doctor soon.
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.
Hi, @kkenn, and welcome to Mayo Clinic Connect.
You may be interested in this Mayo Clinic information on meningioma: https://www.mayoclinic.org/diseases-conditions/meningioma/symptoms-causes/syc-20355643.
You mentioned that after sending you for an MRI, the doctor you saw about newly acquired migraines did not think your migraines were caused by the meningioma in the falx and parasagittal regions with which you were recently diagnosed. Hoping that some of the other members in this discussion might have some thoughts about the migraines and also may have some insights for you as someone who is newly diagnosed with a meningioma. Please meet @robinem @cindyt63 @sandra511@wendyah @wkindel and others.
Did your doctor talk about what might be causing the migraines, @kkenn?
The neurosurgeon didn't take the time to talk about them. So I will be heading to my PCP to talk more about things.
Liked by Colleen Young, Connect Director
I've had some ringing in my left ear recently.
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