Thanks for your comments G.R.
I'm actually in Namibia and saw a South African neurologist in Cape Town. I
had an MRI last month which was clear but the EEG was the clincher. I've
never lost consciousness - just the well-known aura of smells and deja-vu.
I'm on Epanutin or Phenotoin as the generic drug. Seems to be controlling it
well as I've been ok since Easter.
No major illnesses but I worked in a low-grade uranium mine for several
years. Haven't heard of any connection there either although quite a few
ex-colleagues were diagonosed with brain tumours - some fatal. My scans have
shown nothing in that respect.
The neulrologist did harp on about my supposed heavy drinking but assured
him that my intake on a Friday night only, was very moderate.
The only common factor was that the symptoms started when I began intensive
computer CAD work. I was spending 6-10 hours every day working on the PC.
Whether this is pure coincidence or not, I couldn't say but I think it may
well have triggered something.
cheers
Mike
> Did the Dr. in Zaire? run either an Electroencephalogram (EEG) or a
> Magnetic Resonance Image (MRI) to see if there was any Internal damage that
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> cheers (sadly, without a beer!!! :-))
> Mike
Some people 'around here' have varying levels of Photosensitive Triggers, a
few with older screens with lower Refresh rates, that sometimes the (hard to
see) Flicker was enough to set them off.
I don't know how you'd check the Refresh rate or if it could be altered
by software control. One woman (~1998) had to use a Liquid Crystal screen
to prevent her type of szrs... She had had them since Childhood, and I
don't think they were CPS (Complex Partial Seizures) like yours? and mine.
If you go to Julie's site or Howdy Dave's (if they're still listed in a
message that's up), they have links to Ep. Foundation of America (efa.org).
You likely know if you're doing any searches for that or Temporal Lobe
seizures, that the Deja Vu is usually a sign the seizure focus is in the
Right Temporal Lobe. Other parts of the aura might include sour Lemon Odour
or taste. I used to get a Reverse effect, where Lemon cleaners would
trigger an aura when I had been 'normal' before that. I also avoid lemon
drinks or foods now for the same reason-- since I'm controlled with meds.
there's no use throwing that away.
Since you don't lose Consciousness, you might be classed now within
Simple Partial Seizures, OR the medications you're using are preventing the
szr. from Generalizing into a Full C.P. seizure. G.R.
> Thanks for your comments G.R.
> I'm actually in Namibia and saw a South African neurologist in Cape Town. I
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> > Did the Dr. in Zaire? run either an Electroencephalogram (EEG) or a
> > Magnetic Resonance Image (MRI) to see if there was any Internal damage
that
> > might explain where the Complex Partial Seizures would come from?
> >
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> >
> > Then too, you're getting pretty old! ( :-> ) I'm 57 and my szrs.
started
> > when I was 48, from Encephalitis I had when I was 35. You'll probably
see
> > people here from Low 20s up to 60s or above, whose szrs. started from
either
> > accidents, infections, unknown, and sometimes a malformation that was
never
> > detected years ago when Medical Science wasn't as advanced as now. That
> > dang 'unknown' can cover a lot of things that haven't been identified yet.
> >
> > Depending on which medications you use, Beer (within reason) might
still
> > be allowed. There ARE Anti Ep. Drugs (AEDs) that might be compromised or
> > effectiveness reduced by alcohol, and by other Over the Counter
Medications.
> > If you haven't been Prescribed anything, yet, above doesn't apply.
> > *IF* however you think you might be having either Absences (where you
> > drift away for a few minutes then come back --> **i.e. others would have
to
> > witness those, *you won't realize you did it usually), or Still have C.P.
> > seizures (where you lose consciousness), then I'd speak to the Pharmacist
> > who Fills any prescriptions. They often have more of the Medication
> > Literature than most of the Doctors might have time to read.
> > If you look through the efa site you'll find some information on
Complex
> > Partial Seizures. The Olde Name (used from ~1930? to 1960 or so) that
some
> > Other sites you might find might still use, was Temporal Lobe Epilepsy
> > (since many of the C.P. seizures might start in one of the 2 Temporal
Lobes
> > of the Brain). If you do any searches and come across the Olde name, it's
> > likely worth reading those too, to see if any of the Symptoms or
Treatments
> > might apply or describe any symptoms you have. G.R.
> > P.S. If you describe any Symptoms or what happens when you have any
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> > I still have them and wondered..............................has anyone
> > considered what effects the mercury amalgam from the fillings might have
on
> > the brain?????
> > Could there be a connection between Hg and CPS?????
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> > cheers (sadly, without a beer!!! :-))
> > Mike