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10-20-2007, 10:13 PM | #1 | ||
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I used to post on this web site for my sister who had a brain cyst. Now I am posting for me... I had an MRI monday, my ENT wanted to see what might be causing my dizzy spells and ringing in ears. He said he didnt find what he was looking for but saw that i have a annie about the size of a piece of unpopped popcorn. He referred me to a nerologist, who i see if five weeks. My ENT wasnt that concerned and the nero wasnt that concerned. They said it was small, (advice: just dont do any contact sports or lift anything heavy.) I am freaking out. I am a VERY healthy 46 year old woman. What is any of your takes on this. Should I freak or not....??? I would have never known i had this if it wasnt for the MRI no symtoms at all, other than I feel dizzy but that has been going for much of my life. I have allergies so I think a lot of it now is just congestion in my head. but, now I am having panic attacks!!
I am leaving to go out of town for a week tomorrow. They said it was OK to travel. Thanks for any of your thoughts Suzi |
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10-22-2007, 06:37 AM | #2 | |||
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Hi Suzi
I dont know anything about aneurysm so can offer info, but I did just want to give encouragement that if your doc and the neuro arent alarmed then hopefully this is not serious . I hope others who know more on this will be along shortly to give you their input Cheri
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~Chemar~ * . * . These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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10-23-2007, 01:38 AM | #3 | ||
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I would try to get an appointment with the best neurosurgeon in your area.
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10-27-2007, 10:32 PM | #4 | ||
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Hi,
I have one aneursym that was clipped in March and have another one that is currently untreated. It is such a shock when you first find out. I was afraid to sneeze. I'll send you a private messag and you can contact me with any questions at all. I'll try to help you out. Sarah Last edited by sarahin; 10-27-2007 at 11:17 PM. |
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11-05-2007, 01:35 PM | #5 | |||
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I feel for you Suzi. Even after I went through 3 separate procedures and being told everything now looks fine, I still wonder if it could change or even rerupture again.
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Ruptured Left PCom 5mm aneurysm and coil occlusion Feb/06, follow-up Angio July/06 revealed coil compaction with increase size at the base. Stent placed Sept/06. Second coil occlusion of PCom Jan/07, successful MRA May/07. Angio pending. |
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12-13-2007, 11:00 AM | #6 | |||
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Hi Debbie! If it were me, I would go get another opinion immediately with the very best neuro you can find...it's your brain, your life...irreplaceable and priceless. I wish you the very best! Huggs! CRITTER =^..^=
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"To know whatcha know... and to know whatcha don't know... is to know, Grasshopper!" . |
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01-07-2009, 03:43 PM | #7 | ||
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Quote:
I've dealt with the same type of fear. We all know our bodies, especially after going thru a traumatic event. I had a cranial anuerysm of the left corotid artery between my brain and eye a few years back. Had the artery coiled and things were fine after a long recovery. But i have had strange pains in and around my eye and face and neck on the right side now for about a year. Been to several Doctors and had MRI's and ultra sounds done and everyone says I am fine. So my point is, if they say you shouldnt worry about it but you still feel scared and need verification, get a second opinion. It may help put those anxious feelings at ease.. After my surgery I was all kinds of nervous and paranoid.. It's natural.. |
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01-27-2009, 07:31 AM | #8 | |||
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Hi Suzi
My aneurysm was discovered as an incidental finding. I had a routine MRI (I have MS), and they did an MRA as well (which looks at the circulatory system in the brain). My neurologist didn't tell me about it for more than six months, when I went back for my next routine exam he told me about it, told me not to worry about it and that we would monitor it. My best friends are nurses, and they freaked out and said 'no way - get a referral to a neurosurgeon these are too nasty to muck around with'. So, I got a referral and off I went. The NS looked at my films and told me that I should get it clipped. It ended up being 13 months from discovery to treatment, but after it was done the NS said the walls were very thin and it would have only been a matter of time until my kids found me dead on the floor. I have a photo that was taken during surgery and you could clearly see what he meant. My point - and sorry for the long story about me, is please make sure that you see a Neurosurgeon or Cranio Vascular Surgeon. If you decide to monitor it fine, lots of people do, but find out all of your options. Cheers Lyn Last edited by Lynn; 01-27-2009 at 07:35 AM. Reason: typo |
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01-27-2009, 09:59 AM | #9 | |||
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I have a dear friend who had her annie clipped last August. She has been doing well, but recently was in the hospital 5 days. Back on anti-seisure, and blood thinner meds again and has had mini TIA's. Last spring she had neck fusion after a severe impact car crash.
Please send your prayers and positive thoughts her way, she always thinks about others....even when she is having her own struggles. She is a new memeber here, and I am glad this forum has this available to her. If you would want to send her a private message...her member name is Ouch. thanks
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. "MY LIFE IS BRILLIANT, MY LOVE IS PURE, I SAW AN ANGEL....OF THAT IM SURE"james blunt |
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02-07-2008, 12:13 AM | #10 | ||
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Suzi, By now you have had your specialist visit, and should know more. I can share this, I had an aneurysm detected by CT scan in Feb 07, had the surgery to clip it in Oct 07. Mine was 7mm on the AcoA. Chance of rupture 1%/year. So waiting was not all that risky. Many reasons for the wait but nonetheless I did wait. I suspect yours being the size you described the risk of rupture is even less (mine was described to the the size of a pea - obviously larger than a piece of unpopped popcorn). Still I fully understand the feeling of having a ticking timebomb in your head, I did until I finally was able to see a neurosurgeon. Let us know what your doctor tells you and what you plan to do. |
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"Thanks for this!" says: | Beth1957 (09-21-2008) |
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