← Return to Meningioma discovered: Mirrored symptoms of my multiple sclerosis (MS)

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@jhbl

Hi @candersen3 My my don’t we have a lot in common! My tumour isn’t in the same location as yours but I also have MS. In 2021, I was having what I thought was an MS exacerbation + daily headaches so I saw my Mayo neurologist and had an MRI. My MS was stable with no active lesions but I had a 9x9x2mm L occipital tentorial meningioma. My (ex) neurologist felt that my symptoms were not related to the tumour but rather to my grief. I had lost my mom 8 months prior. Really??? Needless to say I went to a neurosurgeon. Already long story shorter…I’m an RN and I didn’t want to “watch and wait” because mine was impeding on a critical area so I had the craniotomy.
In the beginning of my whole fiasco, the symptoms I was experiencing were similar to my MS symptoms but were somehow different. I had slightly new and different symptoms along with the usual MS symptoms. I also had daily headaches and new dizziness/balance issues. My vision was “weird.”
There’s no way anyone can answer your question of whether or not a craniotomy would improve your life. The outcome can be different from person to person. I’ve talked with many people who have had great results along with some people who had a far different story. I’m one of the latter unfortunately. My best advice would be to get a 2nd, 3rd or more opinion and make sure that your surgeon is experienced with your type of tumour. Also, find others like you/us! to talk to. I found an amazing support group on Facebook. There are people with many different experiences and outcomes and plans. You can learn a lot from others. The group I found is Brain Tumor Companion. I hope your journey is far more successful than mine!
- Jan

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Replies to "Hi @candersen3 My my don’t we have a lot in common! My tumour isn’t in the..."

How long ago was your surgery, have the symptoms retracted? How was your recovery, please share as much as you feel comfortable with