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Neurology (Expert Forum)
We see seizures at home,but eeg has only picked one up in two years
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We see seizures at home,but eeg has only picked one up in two years
by Wesley's Mom, Oct 04, 2003 12:00AM
Our ten year old son suffered from the California La Crosse Strain of encephalitis in Sept. of 2001. In the hospital he went through a waxing and waning,and would have febrile seizures,and would scream,and was in an altered state. Since he has come home,he has complex partial seizures,and has been on so many medications, we are currently weaning him from Trileptal 450 mgs. 2x's daily,he is also on Strattera 10 mgs.,and his neuro wants to put him on amitriptyline. His seizures have gotten progressively worse over the past two years,and he is now starting to shake, clench his fists,turns very pale,and his eyes also roll back in his head. The shaking is not hard though,but his whole body is affected and lasts only for one -three and a half minutes. Wesley also suffers from severe migraines after these seizures,and has basically been debilitated by all of this for two years. His eeg's have come back clear except for one,that is what stumps us! His neurologist thinks since Wesley's Parietal Lobe,and near his brain stem was affected by the encephalitis,that his seizures are deep in the Brain. Could this be the reason that the EEg is not picking these up,and it being hard to control these with medication??We have been on Depakote,Tegretol,Neurontin,elavil,Topomax,and so many other migraine medications. He also had chicken pox and chicken pox pneumonia , four months later so bad that the infectious disease specialist had not seen a worse case since the 1970's. Wesley has been through a lot,and We just want to help Wesley not to suffer anymore.Any suggestions?Mandy Myers
Doctor's Answer
by CCF-Neuro-M.D.-CS, Oct 05, 2003 12:00AM
If your son has a spell while an EEG is being recorded some change should be seen, but not absolute. However if the EEG's are being done when he is not having a seizure it is not uncommon for them to be normal. The EEG is used only to confirm the presence of abnormal brain activity. The best way to judge if a medication is working, is by monitoring his clinical response. Is the neurologist you are seeing an epilepsy specialist? If not it may be reasonable to see an epileptologist. Also, inpatient video/EEG monitoring is sometimes helpful to clarify the epileptic nature of these spells, and hopefully to localize where they are coming from. If you are in the area with have 4 excellent pediatric epilepsy doctors (Drs. Wyllie, Kotagal, Lachwanni, and Gupta). Lastly, if medicaitons continue to fail to control his seizures, then another option to evaluate is epilepsy surgery. Again, this could be investigated by seeing a epilepsy specialist. Good luck.
normal. My only relief was anxiety meds to control un-diag. head
spasms. My rheumatologist said it sounds like I have spiking-
spasms. He said not all eeg's will show seizures, especially if
deep. We did a trial of Clonazepam .5 twice day. Used to calm the
brain firing. Well after 2 wks. adjustment, it's been a big help.
Now I need a Neuro. that believes me to fine-tune Rx. You must be
suffering watching your baby go through this. Try this website:
"Seizures and Epilepsy: Hope Through Research" at Google. It
mentions MEG, a way of testing w/o electrodes. Maybe that would
work. I'm sure helps out there. Keep trying & good luck.
This is a link to a forum for those with E, there is also a forum within the site for child neurology and there may even be another that might interest you.
http://neuro-mancer.mgh.harvard.edu/cgi-bin/forumdisplay.cgi?action=topics&number=33&SUBMIT=Go
To others: this site has many forums within it for diverse neuro problems.
http://neuro-mancer.mgh.harvard.edu/cgi-bin/Ultimate.cgi?action=intro&BypassCookie=true
I hope this helps you.
If the seizures are deep in the brain that would be a good reason for the EEG not to pick it up.
I agree with the CCF neuro, if you're not seeing epileptologist now, then do so.