MamaDuck4
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My name is Amanda (prefer Mandy). Im currently living in TN and I have 4 wonderful children and a pretty great fiancée. I'm a nursing student on my way to becoming a midwife (CNM) or was at least. I had seizure activity suspected in 2005 but normal eeg. I never followed up.
On mother's day of this year I experienced my first grand mal seizure. My fiancée was driving me to the ER when I had another one. He stopped at an ambulance station and had them take me. I had so much trouble talking and just wanted to sleep. The ER visit was. 6 hour blur. I was given IV keppra and ativan and sent home. The following Wednesday I was scheduled to have surgery. Dr went ahead with it and I had a seizure coming out of anesthesia. Dr admitted me overnight for observation and had a neurologist cone see me.
Released from hospital Thursday and suffered 3 back to back seizures and was taken by ambulance to er once again IV Keppra and ativan. I slept the whole 6 hours. The only tests ran were blood and urinalysis.
Following day I go to see neurologist who orders an MRI and EEG.
Meanwhile I'm battling PPD pretty bad and needed to be hospitalized for severe anxiety.
Fast forward to June 6th... I was shown my eeg results and all the weird blips and spikes. I asked what it meant. My Dr informed me I have epilepsy and a pretty severe case but is hoping keppra will keep it under control. So far.... not so much.
I can't drive (nightmare with 4 kids!) I cannot be alone with my 2 younger children yet. (He wants it managed first) I was already fighting depression with all I had and this has turned my whole world upside down. I'm ready to have normal again but not sure if and when that will happen. I'm trying to adjust to my new normal and not handling it so well.
I have 3-4 grand mal a week, many many many absence seizures, and the odd sensation ones. Not sure what they're called. I'm sporting some wicked fraction burns and bruises from my grand mals. I sleep constantly. I use a bus to go to my several Dr/therapy appointments a week.
Oh And the myoclonic jerks are the most annoying part of my day. They're happening every 2 minutes. Sometimes they scare me.
So that sums my epilepsy up.... I know very very little about epilepsy and am trying to learn more so I can cope easier.... if that's possible.
Any questions feel free to ask. I'll answer what I can.
On mother's day of this year I experienced my first grand mal seizure. My fiancée was driving me to the ER when I had another one. He stopped at an ambulance station and had them take me. I had so much trouble talking and just wanted to sleep. The ER visit was. 6 hour blur. I was given IV keppra and ativan and sent home. The following Wednesday I was scheduled to have surgery. Dr went ahead with it and I had a seizure coming out of anesthesia. Dr admitted me overnight for observation and had a neurologist cone see me.
Released from hospital Thursday and suffered 3 back to back seizures and was taken by ambulance to er once again IV Keppra and ativan. I slept the whole 6 hours. The only tests ran were blood and urinalysis.
Following day I go to see neurologist who orders an MRI and EEG.
Meanwhile I'm battling PPD pretty bad and needed to be hospitalized for severe anxiety.
Fast forward to June 6th... I was shown my eeg results and all the weird blips and spikes. I asked what it meant. My Dr informed me I have epilepsy and a pretty severe case but is hoping keppra will keep it under control. So far.... not so much.
I can't drive (nightmare with 4 kids!) I cannot be alone with my 2 younger children yet. (He wants it managed first) I was already fighting depression with all I had and this has turned my whole world upside down. I'm ready to have normal again but not sure if and when that will happen. I'm trying to adjust to my new normal and not handling it so well.
I have 3-4 grand mal a week, many many many absence seizures, and the odd sensation ones. Not sure what they're called. I'm sporting some wicked fraction burns and bruises from my grand mals. I sleep constantly. I use a bus to go to my several Dr/therapy appointments a week.
Oh And the myoclonic jerks are the most annoying part of my day. They're happening every 2 minutes. Sometimes they scare me.
So that sums my epilepsy up.... I know very very little about epilepsy and am trying to learn more so I can cope easier.... if that's possible.
Any questions feel free to ask. I'll answer what I can.