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#1
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Hi, I'm new.I've learned so much from this site already. Do you guys think it might be just a D/phosphorous level? Sleep deprevation? I really hope I don't need meds.... |
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#2
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| Hi Jimboslice, welcome! If you have a low seizure threshold (say, from head injuries or concussions), then you can be more sensitive to secondary triggers (like alcohol, dehydration, or nutritional imbalances). So it's hard to say for sure if changing your behavior or taking supplements can help, but being proactive about your health certainly can't hurt. There's a lot of good info here to get you started: Proactive Prescription for Epilepsy I haven't heard of a connection between low phosphorus and seizures (which doesn't mean there isn't one!), but here's one some possible links between low vitamin D and seizures: http://www.ncbi.nlm.nih.gov/pubmed/21333455 Best, Nakamova |
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#3
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| Hi Jimboslice Welcome im sure you will find a lot of answers here,i know i have Neil |
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#4
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| Hi, Jim, Welcome! Vitamin D deficiencies are common among people with epilepsy. Take a look at this thread: News Article Seizures and Vitamin D Deficiency Don't know what your calcium levels are, but a low level often comes with a low level of D. If your calcium was low, take a look at this: Quote :
Hypocalcemia = low calcium Quote :
Quote :
On phosphorus, Quote :
Last edited by Endless; 03-28-2011 at 07:40 PM. Reason: added one more link |
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#5
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| Since my first post I've had an EEG, MRI, and a sleep study to see if I'm having nocturnal seizures. I'm a bit nervous, my neurologist called today and left a voicemail saying they need to see me. I was originaly scheduled for a follow up on April 5th. I won't know any of the results until then... |
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#6
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| Jim, It can be scary when the doc calls you in. Don't worry before you have to. It could be something, or nothing. Mine called me in to give me my test results so I wouldn't worry. Hang in there. |
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#7
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| I know that it's scary when the doc calls you in before your scheduled appt, but look at it this way - if there's something wrong it can be fixed faster. I know that if I'm having problems and the neurologist wants to see me sooner then he wants to try to fix what's wrong and actually SEE me so we can talk in person about what's happening to me instead of trying to do it over the phone. |
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#8
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| They scheduled a sleep deprived EEG for this Thursday at 730 am. |
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#9
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| I took my sleep deprived EEG. From what the nurse was telling me, and how I was feeling I thought I was in the clear. My neurologist called at 8pm last night and sent me off to the pharmascist right away to get my prescription of Keppra. He said I had seizure activity during the breathing excersizes and also during the light show. Both for a couple seconds each and from both sides of my brain. He says any longer and i'd go into a gram al. I'm on keppra for the next 2 years. |
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#10
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| Jimbo, I'm sorry about the brainwaves, but glad they found the problem in time. The quicker they get it stopped, the better the chance you have of being seizure-free someday. How are you getting along on the Keppra? |
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#11
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| I cannot comment on the keppra much as of yet. I'm on my second pill. Next week I start 2 pills a night before bed. Right now there are no Ill side effects. I just feel like I'm finally getting a good nights sleep. |
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#12
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| Sorry to hear about the diagnosis. I know when I had my first EEG, the neurologist said "oh yeah, you definitely had seizure patterns, especially when you fell asleep," and I was stunned because I though I had been awake through the entire EEG. Yay for the good night's sleep! That's a positive sign. |
| The Following User Says Thank You to Nakamova For This Useful Post: | ||
Jimboslice (04-03-2011) | ||