Arachnoid Cyst
Hi there, I am living in Ontario, Canada (although my profile lists an american state. There was no option for me to select a canadian province) and I am a 39 yr old woman. I have been diagnosed with an arachnoid cyst of the right posterior fossa which measures 2.1x1.6x1.6 cm.
The diagnosis came from an MRI after I started experiencing tingling and numbing sensations in my hands and feet. Well, later to follow was extreme fatigue, extreme burning pain in the base of my head and neck, behind my left ear, dizziness, light headedness, feeling like air is trapped inside my head, ears popping and buzzing, mood swings and i have had two episodes where I have almost fainted holding my baby.
I have seen one neurologist here in Ontario who tried to tell me i was pre-menopausal or depressed, neither of which is true. It seems like the medical profession here in canada do not recognize these tyes of cysts as being symptomatic, yet i have found thousands of people all over the world with the same cysts causing the same symptoms. It is so frustrating being told that my symptoms are "not likely" caused by this cyst, yet there has been no other medical reason found. The symptoms have progressivly gotten worse since I had my son, who is 20 mths old now. I am no longer working becuase the headaches and fatigue have become dibilitating. I want my life back!! I sleep endlessly during the day and night and feel as though my body just doesn't have enough energy to work for me. I am losing out on precious moments with my children and no one will help me.
If anyone out there has experienced teh same thing or help me in any way please contact me. i desperately need help.
I understand from my enormous research that I have done that these cysts are often triggered to be symptomatic after a c-section child birth (which is when this all happened for me) because of the epidural or spinal that has tapped into my spine because the cyst is near the top of my spinal cord and cerebellum. I also understand that neurosurgeons in other parts of the world are doing great things with these cysts.
thanks in advance to anyone that can help me.
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Hi,
Thank you for sharing. That explanation doesn't mean much to a non-specialist, except to say that my cyst was also intraventricular. Not the lateral one, I think.
How are you feeling? This all really leaves you feeling a bit dumbfounded, doesn't it?
If I can give you any encouragement, my recovery was rapid and I was up and about pretty quickly.
I really feel for you!
Thanks for the encouragement Kyoto much appreciated. It has been a tough couple days... physically and emotionally. On the positive side, I just got a call for my specialized MRI for Monday 9pm. I also asked for a referral to another specialist in Toronto who did brain surgery on a colleague from work, will see where that takes me...
Hi @gingerbread14 I am curious how or what has happened with your cyst? My son was receny diagnosed and has had a similar experience to yours
My son also has mass effect and same thing so much confusion and lack of help with all of this. We had internal medicine tell us mass effect indeed is having an impact on my son and symptoms. Yet we see neuroligist and they say no ...they say it's pushing on his brain but not iratating it...how can that be?? If something's pushing the. Brain and you know that and have symptoms how can it be said it's not iratating ????
I too have many of the same debilitating side effects that were brought on after epidural that was supposed to help relieve pain. I am at my wits and the pain is constant 24/7. Is there any help that can be had? I am certainly willing to do just about anything but I will not do cervical spine surgery that will be more debilitating. Because I am already a quadriplegic and all I have is above the shoulders. Please recommend help Help!
Where did you get surgical support? I will most likely be needing surgery so please recommend a surgeon for me , an where in the country is it located ? Thank you, Dave
There has been some development since I last posted, I had my second MRI with dye, and I have been referred to a neurosurgeon in Montreal and will have my initial consultation on Monday.
I have been having some additional symptoms as well, tingling of the scalp pretty much all the time now, occasional localized burning sensation of the scalp, intermittent internal vibrations and the palpitations every time I change position.
I have been using Doterra essential oils to help with my various symptoms, as I am not a big fan of pills and it does help tremendously. My sister is a Doterra rep, so I am a good candidate for testing her products too! I was told yesterday to not take any medication between now and then, so hoping it is a good sign that I may have surgery sooner rather then later. In the meantime, keeping the faith!
Hello @kyoto,
It has been a while since you last posted. Are you continuing to feel the benefits of the surgery you had a couple of years ago? I look forward to hearing from you.
Can I ask what happened after surgery? Did you have problems did you have seizures? My cyst has been with me for my life I just turned 26. Surgeon is worried about what it how brain will react or if it will move as it's been use to this thing pushing on it for so long
Hi, I am really well. The symptoms are almost gone. The specific problem of working memory disruption is completely under control with the anti-convulsant medication, which I take twice a day. It is odd to describe yourself as having to take "anti-convulsants", but the alternative of having these silent epileptic seizures is much worse. The cyst is gone, and apparently there is no reason to worry that it may return, according to the doctor. Occasionally, I get severe headaches that do not respond well to regular painkillers, and at those times, I begin to worry a bit, but they go away again. Functionally, which is the important thing, I am absolutely fine.
How are you?