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Adoption and seizures,

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This was a very interesting discussion. I was adopted as a small child, so I remember nothing about my days before the adoption. I do know that I was abused during the first few years of my life (having received a letter from a biological sister). I don't believe that adoption and ptsd necessarily go hand in hand. I was just diagnosed with PTSD w/seizures. I started having them about 13 years ago, when I was going through other difficulties in my life. It took quite a long time for the doctors to come to a consensus. I would have preferred the diagnosis of epilepsy over "it's all in your head" or my favorite (told to my husband) "she's crazy and doing this for attention" Do not be ashamed of your past or your diagnosis. You probably had trauma in your life that is still suppressed. I agree with others, that you need to find a trusted psychologist to help you through these issues, but if the anti seizure medicine helps you (it didn't help me because it wasn't epilepsy) then what harm is there in taking something that might improve your life? I am not a fan of medicine, but sometimes it does work :) I hope that you can find comfort and peace in your life.
 
@heylena

I have suffered from memory lapses...missing time. Feel like I was fainting or waking up. Last week had a seizure (first time I remember...but probably because it was outside grocery store and people were standing all around me staring...and someone providing first aid told me.) Then told next day I had 2 more seizures once an ambulance took me to a hospital. I was only in hospital 2 days...yet I thought I had been there at least 5-7 days. First time staying in a hospital.

Hospital couldn't find any physical reason - they did EKG, brain scans & various blood test.. Doctor's were surprised how quickly I recovered since they said I was so "bad off" when I got there.

I don't have answers to your questions. I just send you "support" and a "hug."

I will tell you I was put on an anticonvulsant - Lorazepam (Ativan) for a couple weeks. It has helped with other problems (or related) such as shaking and gagging when I brush teeth or chew gum. But I know it's not for long term use.... But no seizures since taking it.

At same time I'm with you - I don't trust doctors or medicine.

Side note: My childhood is better off not remembering. Therapist says I was terrorized (constant fear of fear of dying from a parent...)
 
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First, I want to thank you for all the support, understanding, thoughts as well as discussion! Three years later from my 'diagnosis' (which I initially rejected) and one year later after my original post on this website, I wanted to provide an update to my situation.

I wanted to respond to this particular question: 'why can't I simply have a seizure? Why can't I simply accept that?' Three years ago, I was half-diagnosed with epilepsy / confirmation that I'm not crazy and that I do have seizures, but I rejected the prescribed anti-seizure medication from the neurologist because; to be honest, I didn't want to believe it. I was in "denial" because I wanted to be a normal human being. Point blank, if you tell someone that you have epilepsy, they will - in their mind - label you. Granted, I didn't introduce myself as: "Hi, my name is ____. I have seizures / I have epilepsy!" In any case, I was in denial and I was trying to 'down play' the attacks. After I was diagnosed, each new doctor would ask of any medical history, and I remember with one particular doctor that I said: "No. Well - I might have epilepsy." She was confused: "What - what do you mean? You 'might' have epilepsy?!" More confusing that I don't accept it; therefore, don't take the prescribed anti-seizure medication...thus: I continue to have seizures. In which, I am knowingly harming myself.

Three days ago, I had an "attack" which kind of awakened me - if you can call it that. In the past, I've had myoclonic and atonic seizures, which are just jerks or twitches and/or "drop attacks", but I've always been conscious and known that I was falling. While I couldn't; per say, stop the seizure, I was conscious and so, could stop my fall by putting my hands up so that I don't injure my head or forehead. Well, three days ago, I can't say that I had a "drop attack" - the closest I can describe it to is that I fainted. I say this because I don't actually remember falling or what even happened, which might be evidence that the seizures might be escalating without anti-seizure medication. In more detail, what happened was that I had two small myoclonic seizures at my desk at work (mini-jerks or bodily twitches; to the normal person, this is the state when they are going to sleep and their body 'convulses'). A trigger might have been that I had drank three beers last night (I only weight 130lbs - am a lightweight), but in the morning, I didn't have a headache/hangover so I didn't think anything of it. When these convulses happened, I decided to go to a nearby Café for something to eat as to "balance out my body" - on the way there, I had two atonic seizures, in which I fell and my phone flew across the floor. These were normal though, so I didn't think anything of it except that I was annoyed that I had four seizures repeatedly after the other (this should have been a sign). After purchasing a box of berries, the last thing that I remember is walking to the elevators.

Next thing I know, I'm in a 'dream state'. It's hard to explain because I had no memory of falling, but I had apparently fallen and somehow had gotten all the berries (strawberries, blueberries) on my blue jeans. The berries was all over my jeans, which makes me think I might have had a grand mal seizure because I had somehow gotten the berries on the front and back of my jeans - I don't know how I managed that. The important thing that I want to emphasis is that I did not remember falling, having an attack, and was extremely confused when I opened my eyes. I felt like I was dreaming so I was confused as to why I was on the floor of an office building with paramedics all around me, and the Administrative Manager and Foreclosure Manager of my work nearby as well (imagine opening your eyes and seeing your boss kneeling in front of you - and just staring at him). It took a few minutes to get 'conscious' and aware of my surroundings; I have a feeling that I fell asleep because I was disorientated of how I got here and why everyone was huddled around me. When I first saw my jeans, I thought my face was bloodied, but the Paramedic immediately explained that it was berries and not blood (I think she explained this to me two times because it took a bit to 'come to reality').

The effect of this felt like a bad case of excessive drinking (not remembering that I fell, where I felt, and being completely disorientated by time, placement, what happened). Which makes me question: has anyone else had seizures due to excessive drinking? Three drinks is nothing, but in the past, I have connected my seizures partially with excessive drinking as a way of my body "cleansing" myself and not knowing how to process the alcoholic poison; in which, the myoclonic seizures and I have to lay in bed all day in order to not induce any injuries. Am I an alcoholic? This worries me.

In any case, this has 'woken me up' in order to follow up with the original neurologist and my hope is that anti-seizure medication will work and I'll realize my stupidity and unhealthy manner of dealing with my epilepsy symptoms. There are articles that attempt to persuade people to confront their seizures because there is an argument that if you don't try to 'stop' your seizures, that your the seizures will create a pattern in your brain if they occur more often without any attempt of prevention. So, of course, that is what I am worried here, that by not actively preventing these attacks, that the seizures are escalating. A different way in which my body & mind is screaming: "Yo, take care of us!"

On a side note, if the anti-seizure medication does not work, I will be speaking to a psychotherapist/psychologist if these attacks are purely psychological, but I don't believe this will be the case because the EEGs have 'spikes' in which the neurologist has strong suspicions that I have epilepsy.

I need to take better care of myself. And not actively ignore that I need this body & mind.
 
Yes, drinking can indeed cause seizures. I suggest quitting drinking and taking medication. (The med label will strongly advise against drinking anyway).
 
But but but but---beer!
But but but -- your brain! :p

Seriously, though - your brain.

I wasn't thrilled when I had to give up drinking because of medications. Well - actually, at first I was relieved, because I had been self-medicating with alcohol and it was a real problem. But, I also was frustrated that I had to give up every kind of social drinking.

Once I got used to my meds, and I was comfortable chancing it, I had a small amount of alcohol one night. And the hangover of my life the next day. I was sick as a dog.

So, I just don't drink. And I've gotten over it. I would rather have at least a semi-functional mind and no more guinness.

I'm really glad you are taking the seizures more seriously. Psychogenic seizures, the kind that are non-epileptic, will show no electrical spikes in the brain. If you are showing that kind of activity, then you are having seizures. It doesn't necessarily mean that epilepsy is your diagnosis - and I can only imagine how frightening that diagnosis would be, I really take your words to heart about that. But getting into the process where you can medicate in order to manage the seizures better will very likely improve your quality of life. And it will ultimately be better to know, than not to know.

I will be speaking to a psychotherapist/psychologist if these attacks are purely psychological
Have you thought about going into therapy, regardless? Whether there's unresolved trauma for you to work out, or whether you have a medical diagnosis to adjust to - either way, someone to talk with could be very useful.
 
But but but -- your brain! :p

Seriously, though - your brain.

I wasn't thrilled when I had to give...

I have considered psychotherapy before and had, at one point, pursued it but then, only did one appointment. Discussion on adoption and/or epilepsy is walking on eggshells because the topic is still very new. For instance, my general doctor wasn't convinced that I had seizures; even though, I did my own research and could only pinpoint my symptoms to seizures. I don't know what frustrates me more: that in Russia, when I was an orphan, they had the same reaction, but labeled me as "retarded". Or, when a doctor with an American education has the same ignorance (the only reason I was referred to a neurologist was because I kept bringing it up and finally she was 'exasperated' and I was annoying her so she 'gave in'--I honestly hate doctors sometimes! Like, "Oh--I'm sorry for doing your medical research (on me) for you!" The fact that I am adopted and have no history and have a pattern of these 'attacks' should make a doctor be open to all options of medical possibilities and not be as close-minded as USSR doctors treating children who were found on the street / abandoned. Okay, I'm done - sorry.)

I have scheduled an appointment with a neurologist mid-next week and am hoping that anti-seizure medications will resolve the reoccurring seizures. I wish I had resolved all of this three years ago, but I wanted to convince myself that I was 'normal' (whatever that means) and to just "deal" with the small falls. On a side note, it's actually embarrassing because one time, I had one very noticeable myoclonic seizure at my desk, in which my head fell dramatically towards my monitor and I had physically moved my keyboard (conscious and aware and no physical harm was made). The girl next to me (I work at an 'open space office') thought I had "fallen asleep" and thought it was hilarious, to the point that she was crying tears! I just went along because I didn't want to tell her that I have seizures because; to be frank, I am embarrassed of this "condition". It's embarrassing because people think it is "falling asleep" and not a serious condition.

I almost think that all of this has a psychological connection, something is missing that connects why I have these atonic seizures, but I am taking one step at a time.

Thank you for make sense. The reality check is needed. :ninja:
 
I have considered psychotherapy before and had, at one point, pursued it but then, only did one appoint...
HI, Thanks for sharing your journey.
I have an adopted teen daughter, foreign adoption at 18 months. She has had non epileptic seizures and now seems to have had a couple "drop attacks". There is research out there about adoption trauma and non epileptic seizures. We are going to try psychological evaluatation. I will specifically choose someone with experience with adoption, trauma, ptsd, non-epileptic seizures.

Can you possibly get a new doctor? You have to right to be evaluated and cared for properly.
 
HI, Thanks for sharing your journey.
I have an adopted teen daughter, foreign adoption at 18 months. She has had non epileptic seizures and now seems to have had a couple "drop attacks". There is research out there about adoption trauma and non epileptic seizures. We are going to try psychological evaluatation. I will specifically choose someone with experience with adoption, trauma, ptsd, non-epileptic seizures.

Can you possibly get a new doctor? You have to right to be evaluated and cared for properly.

I have considered a psychological evaluation, but it would only reveal my social and possibly psychological imbalance due to how I was treated at the orphanage(s). Still haven't healed and whenever I think about my childhood (in the orphanage), I want to cry and sometimes I have a meltdown in private. I was adopted at the age of 8, but even then, my mind has repressed all the "trauma". So, there is no way of knowing what happened, and more importantly, why.

Nonetheless, good luck! I hope you find an answer and can proceed forward with positive vibes as your child grows up.

For me, there was strong evidence of epilepsy (sharp spikes as proof of an abnormality in my brain). I actually had a really bad drop attack in which paramedics had to be called. I advise that your child wears a helmet because "drop attacks" often cause injuries (that is, if the attacks aren't resolved by psychological evaluation as your child grows up). That said, I am now on anti-seizure medication, but I still have breakthrough seizures that are irregular and have no pattern as to what is causing them. I have an abnormal heartbeat that beats really fast and then "stops", or rests. The current neurologist that I am seeing is wanting me to follow up with a cardiologist in order to make sure that the lack of strength to my heart isn't causing the seizures.

At this point, I still don't have any answers. Do I have epilepsy or does my heart just can't do its job?
 
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