thanks for the invite and i will have a look at that site.no she not had second opinion when i asked the dr if this is why libby has gone into puberty cos the cyst he said he does not know if they are 2 different things or connected.i dont know about you but i find it very hard to get info out of the drs.
I have a lot of the same symptoms as sistam does, and my neuro wanted another MRI done in 3 months (this would be in October, for me)...which is interesting, because I had read that 6 months is the standard for "monitoring" these cysts. He told me I have migraines that turned into daily headaches, and put me on a low dose of Topamax to prevent these. I still get headaches/head pain every day, coupled with some intracranial pressure and dizziness (maybe the increased dizziness is from Topamax now, too), so I don't know where the migraines diagnosis came from. Perhaps I need a higher dose of Topamax to control my headaches, but I don't know if I could handle that.....I already feel pretty stupid on 25mg of Topamax and I'm an engineering graduate student. I don't think I can afford to get any stupider!!!
Hi my name is kim and i am finding all your info really helpful to me. i have suffered from intense headaches/migraines for the past 15 years and have been on the preventive meds nothing ever worked, i take migraine meds when they start most time to no effect. I have suffered from numbness in my arm, blurred vision, dizzy spells,earaches, and many more signs. In June i woke up with what i thought to be a crick in my neck, it got worse over the week, began to think i had pulled a muscle or something, when i awoke on sat. morning i thought i was having a stroke, my neck was pulled down to my left shoulder with intense pain throughout shoulder, neck, and left side of head. Had xrays done and showed nothing wrong with my neck. After about 3 wks of walking around with my neck drawed to one side it got a little better, but the headache only got worse. At 1st i think the dr. thought i just wanted the pain meds, ha they didn't help alot, so after about 6 wks of a headache that wouldn't ease they sent me for mri on neck and brain, where they found i have the pineal gland cyst. i am now going to have a mri with contrast to make sure it is a cyst and not tumor. What questions should i be asking about this? And is there something they can give to relieve the pain? Thank you for sharing your comments on here it is very helpful and relieving to be able to discuss this with people that are going through the same thing. My husband doesn't seem to understand how much this affects everything i do. I have extremely no energy and my headache will not completely go away.
Hi Kim, welcome to the club! I'm glad to hear you pressured your doctors into figuring out what the problem was...if you know something is wrong, you should never let them get away with marginalizing how you feel.
Get a copy of both MRIs--as a patient, you have a right to this, and no one should ask any questions. Tell them you want to hold onto a copy for personal records and for getting a second opinion, and that's all they need to know.
As for questions you can ask, here are a few I can think of off the top of my head:
How large is the pineal cyst (if they do find it is a cyst)?
Is the pineal cyst simple and non-enhancing, or does it exhibit any other characteristics (this will be seen on the MRI with contrast)--like enhancement or septation?
If they tell you it is a pineal cyst, ask them if they can be 100% sure of this--and since they really cannot (it's incredibly difficult and almost impossible, some would argue, to tell the different between some pineal neoplasms, like a pineal cyst and a pineocytoma; the latter is also benign but more aggressive than the former), ask them how they plan to follow-up with their diagnosis to ensure that it is a pineal cyst.
Are any of my (your) symptoms being caused by this pineal cyst? If their answer is no, you can ask why. If their answer is yes, you can ask them to explain how--depending on which symptoms they think are a result of the cyst.
What follow-up treatment or procedures will be done to ensure the pineal cyst doesn't begin causing any symptoms in the future (if they feel that none of your symptoms are being caused by the pineal cyst)?
What symptoms, if any, should I be concerned about as potential indicators that this pineal cyst is becoming intrusive and causing problems?
What are the treatment options, and what are the risks associate with each treatment option (if they believe your symptoms are associated with the pineal cyst)?
If I think of any other good ones, I'll let you know. For the pain, I would recommend an NSAID to reduce inflammation and then a painkiller, as you were already prescribed. How large did they measure your pineal cyst to be from the first MRI? The headaches likely won't go away until the cyst is removed, if, indeed, it is the cause of them (and it probably is). The lack of energy could be due to some interference with your sleep/wakefulness cycle, as the pineal gland regulates the secretion of melatonin, which controls your circadian rhythm. Like you, I also feel exhausted and energy-less rather frequently...and have weird sleep patterns, to boot. Research hasn't been able to link pineal cysts with disruption of melatonin secretion, from what I've read, so doctors aren't quick to link pineal cysts to sleeping disorders (I have sleep apnea).
Though, interestingly enough, a study recently came out that linked an increased formation of cysts and other tumors of the brain with children who used cell phones frequently, beginning when they were young, as compared to children who didn't use cell phones continuously from an early age. This included the formation of pineal cysts, and other tumors of the pineal region.
Good luck with the MRI and let us know how everything goes!
Thank you for your info. Yes i had another Mri done last week one with and one without contrast. They just called a few mins ago to tell me they were referring me to a neurosurgeon. That the cyst was fluid filled and pressing on some other place in my brain. It measured 1.2 cm x 8 mm. x 1.2 cm on my first Mri. They didn't tell me if it had changed this time or not. My physician says she is pretty sure that is what is causing my headaches to be so intense and my blood pressure to be out of wack, along with the other symptoms. But i am just going to stay on them until they fix something, life is miserable this way, and i have 4 kids that depend on me everyday. I will let you know what is said after i see the neurosurgeon. Thanks again for the info.
Ok i got my results back from the 2nd Mri with and without contrast. I am a bit confused. The report says that the cyst was now 1.3cm x 8 mm x 1.3cm which is bigger than it was the month before but on the papers he sent to my doctor it said no change in size. but obviously it is growing. Now i am having black out spells with my eyes and also when ever i move a certain way or walk i have something that feels like an electrical shock running through my body. What is going on? They are sending me to a neurosurgeon but i can't get in till Nov. 21. Does anyone have any details or suggestions? I am at a loss. This is really affecting my everyday life.
Thanks for any input anyone might have.
kim