Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Wow Delores, that's quite the adventure you've been on ! I'm sorry things have been so bad for you. Neurology in general seems to be a very poorly understood specialty. The brain is just too complex. I hope they get it all figured out for you. bug Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Bug, I had a 30-minute seizure the day after my J-tube surgery, but it was most likely set off by caloric deprivation, as they withdrew my TPN immediately and I couldn't tolerate much through the J-tube for quite a while due to pain. I figure I was getting about 600 calories per 24 hours. Not enough! Follow-up EEGs have been read as normal. I know there are other adults in this group who do have seizures. Hope you can sort out what's going on. Barbara > Are there any Mito adults out that have been dx'ed with a seizure > disorder ? I recently had a standard EEG and a sleep-deprived EEG, > both of which were abnormal. The doc hasn't called back to give me > her official interpretation, but the copy of the results states : > > " Several moderate amplitute isolated left temporal sharp waves were > seen. This increases the risk of focal seizures arising from this > region. There was very frequent intermittent left temporal > slowing. Temporal intermittent rythmic delta activity (TIRDA) was > also seen. Some studies have shown ann increased risk of seizures > associated with TIRDA " . > > All I can say is that I'm glad I was persistent about the resident > ordering the follow up sleep-deprived test. He told me my first EEG > was fine, despite the fact that the Neuro lab stated the results wre > abnormal and recommended they order the sleep-deprived study. Why > does life have to be so darn difficult sometimes ? That resident is > an idiot and unfortunately, I've had to see him a few times. He > seems to be bouncing around between the neuromuscular clinic and the > general neuro clinic....maybe he should get a job in the custodial > dept cleaning toilets...although, he might not be qualified ! My > neuromuscular doc agreed with me that the test should be > done...thank God. > > bug Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Thanks Laurie. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 I had a few grand mal seizures (possibly due to Carnitor), but now have only " absence seizures " (sort of loss of consciousness without falling down). My EEG shows " slow waves " which indicate sleep-like patterns while awake. But I haven't been told I have epilepsy, just " absence seizures " or " seizure-like episodes " . From what I've heard, some stroke-like episodes are pretty close to seizure-like episodes, so without an EEG or MRI at the time, it's anyones guess. But I've never had a sleep-deprived EEG, just regular and 48-hour video EEG's, the latter which showed slow waves, absence seizure episodes without abnormal EEG activity, and episodes of slow heart rate (under 50 bpm at one point). Take care, RH > Are there any Mito adults out that have been dx'ed with a seizure > disorder ? I recently had a standard EEG and a sleep-deprived EEG, > both of which were abnormal. The doc hasn't called back to give me > her official interpretation, but the copy of the results states : > > " Several moderate amplitute isolated left temporal sharp waves were > seen. This increases the risk of focal seizures arising from this > region. There was very frequent intermittent left temporal > slowing. Temporal intermittent rythmic delta activity (TIRDA) was > also seen. Some studies have shown ann increased risk of seizures > associated with TIRDA " . > > All I can say is that I'm glad I was persistent about the resident > ordering the follow up sleep-deprived test. He told me my first EEG > was fine, despite the fact that the Neuro lab stated the results wre > abnormal and recommended they order the sleep-deprived study. Why > does life have to be so darn difficult sometimes ? That resident is > an idiot and unfortunately, I've had to see him a few times. He > seems to be bouncing around between the neuromuscular clinic and the > general neuro clinic....maybe he should get a job in the custodial > dept cleaning toilets...although, he might not be qualified ! My > neuromuscular doc agreed with me that the test should be > done...thank God. > > bug Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 My seizures that I considered " grand mal " were teeth clenching, fall on the floor seizures. I and my husband have older (in their 40's now) cousins who have " epilepsy " (or whatever the name is now), so the " old " terminology sticks with me. But I know there are several types of seizures that go beyond the original petit mal or grand mal categories... The doctors I go to say things like " we need to see if your seizures are from epilepsy or not " which I guess means if they are due to misfirings in my brain or metabolic reasons. The only real seizure specialists I've seen were at Columbia- Presbyterian. Both there and during a neuropsych eval I had medical professional witness the seizures, and both said " absence seizures " . I understand there may be a few more types? Take care, RH > > > Are there any Mito adults out that have been dx'ed with a seizure > > > disorder ? I recently had a standard EEG and a sleep-deprived EEG, > > > both of which were abnormal. The doc hasn't called back to give me > > > her official interpretation, but the copy of the results states : > > > > > > " Several moderate amplitute isolated left temporal sharp waves were > > > seen. This increases the risk of focal seizures arising from this > > > region. There was very frequent intermittent left temporal > > > slowing. Temporal intermittent rythmic delta activity (TIRDA) was > > > also seen. Some studies have shown ann increased risk of seizures > > > associated with TIRDA " . > > > > > > All I can say is that I'm glad I was persistent about the resident > > > ordering the follow up sleep-deprived test. He told me my first > > EEG > > > was fine, despite the fact that the Neuro lab stated the results > > wre > > > abnormal and recommended they order the sleep-deprived study. Why > > > does life have to be so darn difficult sometimes ? That resident > > is > > > an idiot and unfortunately, I've had to see him a few times. He > > > seems to be bouncing around between the neuromuscular clinic and > > the > > > general neuro clinic....maybe he should get a job in the custodial > > > dept cleaning toilets...although, he might not be qualified ! My > > > neuromuscular doc agreed with me that the test should be > > > done...thank God. > > > > > > bug > > > > > > > > > > > > Medical advice, information, opinions, data and statements contained herein are not necessarily those of the list moderators. The author of this e mail is entirely responsible for its content. List members are reminded of their responsibility to evaluate the content of the postings and consult with their physicians regarding changes in their own treatment. > > > > Personal attacks are not permitted on the list and anyone who sends one is automatically moderated or removed depending on the severity of the attack. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Interesting RH, thanks for the info. bug Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 I think any normal person would have seizures with so few calories ! You wonder how the thought that was good for you. bug Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Sounds scary to say the least. At least for the observer. bug Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Janet, I appreciate you sharing your story. I never considered MELAS for some reason. Makes sense. Sorry to hear about your family. Hope you have better success with your health. bug Quote Link to comment Share on other sites More sharing options...
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