I get a very similar sensation. When it happens, I perceive everything around me as being faster, louder and more intense. I even perceive myself as moving faster, breathing faster/louder and etc, but I know I’m not. It’s just in my brain. My husband has no idea what I’m talking about even when I try to explain it to him. When I was younger (middle school and even into my teens) I would get short bursts of this. Mostly when I was concentrating on something like writing. It would almost be like I was sucked into a “super concentration” mode, but it would disappear almost as fast as it would appear. I would never get it for more than a minute. As soon as I would acknowledge it was there almost, it would be gone. I couldn’t keep it if I tried. Now snap forward a few years. I am now 25. I developed sudden onset chronic, debilitating migraines when I was 21 (which I think is a result of taking Accutane since I’d never had one before taking the drug and all of a sudden I was getting them every time I took it towards the end of my treatment… but that’s another story). So, my neurologist put me on Topamax. Ever since I’ve been on the Topamax I’ve experienced these “episodes” in more frequent spells and in longer duration. When I first started getting them and realizing that simply not concentrating on them would not make them go away, I found out that talking out loud to myself would sometimes snap me out of it. Now that won’t even do it. The only way to get out of this weird crazy world it puts me in now is to go somewhere completely quiet and void of any external stimulation (I will sometimes even put in earplugs) and just focus on being calm and still (sometimes I will try not to even breath for as long as possible to get the area as quite as I can). I find this sort of “resets” the cycle and the world feels “normal” again instead of all loud and fast and weird. I probably get them once every month or two and it usually happens at night right before I’m trying to go to sleep while lying in bed. I’m trying to switch over from Topamax to Enderol because I think the Topamax has definitely increased these and I don’t like them. The last one I had made me sort of paranoid… and I am NOT a paranoid type of person at all. Of course I told myself I was being stupid and just calm down and go relax and I was fine, but they seem to be getting worse.
However, in response it being “simple partial seizures”: They could be (description sounds plausible), but since mine actually INCREASED while taking Topamax (a seizure medication that just happens to work on migraine patients too) I thinking that would not be the case. If they were seizures, they should have decreased or at least not gotten worse while taking the Topamax.
I have had scans done on my brain, EEG and MRI. I wasnt overly worried but when I asked my doctor if he had heard of it, he sent me off for scans. He believed it to be related to seizures. The scans came back normal. But I still get it every now and again. I have noticed recently that it happens when my brain is over active, not really stressed but thinking alot. Relaxation or distraction helps it go away.
im glad theres others out there with it, when ever i tried to tell anyone they looked at me like i was crazy. im 24 now and been having them longer then i can remember, when i was younger i felt it helped to stop it if i pictured people walking in slow-mo. now i just deal with it, wait it out and see how bad it gets.
I would say that you most likely have Alice in Wonderland Syndrome (AIWS) - also known as Todd's Syndrome. http://www.aiws.info/ Do you experience migraines or have a family history of epilepsy? I would tell your neurologist about your symptoms and mention the possibility of AIWS.
I have a lot of the "faster/louder" symptoms, but I've never felt like objects changed their size or I changed my size. It's probably another version of the same thing though. I personally believe that taking Topamax (for migraine treatment) made mine worse. The only way I can now get an episode to stop is to go into a completely quite room (using earplugs if necessary & dark if possible) and close my eyes, focus on the silence (sometimes even holding my breath for periods just so it is as quiet as possible), try and relax. It's like I have to re-set my brain.... sort of sensory deprivation like.
Know that you are not the only one out there who experiences these things. But I would definitely find a neurologist to discuss your symptoms. Maybe they can help or at least monitor your situation.
Good Luck!