hi there
just wanted to let you know that all of my recent testing is because of this problem too...
i felt great for 2 months after surgery. no pac's or anything. i was on the road to getting back to 100%. then in late july/august, i started to notice i was getting what i thought was dizzy. i kept called it dizzy but i have now learned its not really dizzy, it is lightheaded. i don't feel as the the room is spinning, i just feel not 100% there, i feel like i could faint at anytime and i am off balance and driving is difficult. it was also around this time that i started to notice SLIGHT pac's. now obviously the pac's and lightheadness have gotten worse and do not go away at all. i wake up with it, it gets worse as the day goes on. night time being the worst.
i don't trust myself to drive my babies anywhere other then my town. i feel weird. it's hard to explain it to people who don't have the problem. this is where i think my family doesn't believe me or that it is all in my head.
so finally after almost two months of not being able to deal with it, in september i went to my local cardiologist. he said there is nothing wrong with me. and gave no answer for being lightheaded. he told me to see my primary care doctor.
so i went to see my primary care doctor.
she ran all possible blood work and it came out normal. she didn't have any answers for me except to go see an Ear Nose Throat doctor and a Neurologist.
so i saw the ENT first. he did a hearing test among other tests at first he said it could be meineres but then after my results he said no i dont believe it's your ear, see the neurologist. but he called me a week later to see if i had been to the neurologist yet and told me if they don't find anything to come back and see him.
so then i went to the neurologist. she did an mri, hearing test, dizzy battery test and everything once again came out fine. at first she thought i could be having vestibular migraines. but after my results she said nothing was found that could be causing this problem.
so i decided to go downtown to my cardiologist there. and this is what my most recent posts have been about. (she did the echo, holter monitor) so as you know she said the pac's were benign, more of a nuisance and wouldn't be causing my lightheadedness. she saw my echo results but wanted to see the physical cd so i am still waiting to hear back to her from the echo CD copy i sent her earlier in the week.
nobody has answers. nobody seems to understand. my family probably thinks i am just complaining or trying to find something wrong. i just want an answer or solution. it's driving me crazy. i have 1 million things i would love to do today but can't leave the house with my kids for too long. it is really hindering my life here. i feel like if someone told me i would be like this the rest of my life i would go crazy. it's not a nice way to live, since i am not 100% all there. it's like a fog. sometimes i feel like i am watching a movie of myself. weird way to explain it i know.
so are you truly dizzy, (room spinning) or are you lightheaded? this makes a difference to the doctors i have learned. like i dont feel like i am spinning around, i just feel like i am floating around and that my head is not connected to my body. my vision is different and like i said this all makes it difficult to drive. i feel off balance.
also about 7 times now, i have gotten sudden vision problems for about 1 minute. it's always in my left eye and its like my eyes are crossing or something strange. this is what scares me the most. thank god it has not happened while i am driving. one of the doctors thought it could be TIA's. so of course i read about those, and it says you are more likely to have a full blown stroke within 90 days of having a TIA. great. but once again, they showed no concern or gave me anything to help with those.
so i am truly with you on this. you are not alone and it's making my life miserable. everyone said i would feel better after this surgery. funny thing is, i felt fine before my surgery, i only got the surgery because of my aneurysm which didn't produce any symptoms. i feel like i ruined my life by getting the surgery. i know this is a negative way to look at the surgery when so many have had their lives saved by it. but for me, it's taken me backwards.