Guest guest Posted September 28, 2006 Report Share Posted September 28, 2006 Thank you ssssooooo much for the info..I will certainly look into the archives and see what I can learn..I have started a notebook tracking 's day and will use it to jot down info as well..thanks for the idea. May you have warm words on a cold evening, a full moon on a dark night, and a smooth road all the way to your door. [ ] Re: newbie - Hi , My special needs daughter had " absentee " seizures and we didn't know it until her teacher's aid mentioned it to us. We still didn't see them after she brought it to our attention so we just figured she was 'starring off into space' and who doesn't do that occasionally? Sorry to say but she did develop full blown seizures. We thought they were due to other medical problems which were not being properly addressed by the doctors. (I did not know of this site at that time or things would likely be different today). We did not medicate her as we were hoping to address those problems and solve them without the use of drugs. They wanted to drug her after her very first seizure but we refused.(age 13) She was seizure free for 3 years, three years of medication she didn't need. But unfortunately she did begin to seizure again at around 16 years. Even then we didn't resort to drugs as we were still trying to solve the other issues that we felt were 'bringing on' the seizures. None of the drug doctors had any alternatives or suggestions to try before resorting to drugs. Eventually after a " status " seizure we did start her on 100mg(x2) of Lamictal. That's when I found this site and discovered so many alternatives to at least try before resorting to drugs. you will have to go back and read past posts as there is a WEALTH of information on this site. Key supplements, Lobelia, diet changes etc etc etc etc. Especially at the " start " of seizure activity. It's all in here. I really beleive if I had known then what I know now, we would not have her on medication today. You've got your work cut out for you. Does your son get constipated? If so get that in working order. Pay attention to the foods he eats in case that's part of the patturn. Also, make sure he stays away from junk foods and neurotoxins like aspartame, MSG,splenda etc. Your computer is an invaluable tool. It's a daunting task but it's worth it. My advice would be to get yourself a little notebook and start writing down all the different things you hear or read about. GOOD LUCK. Sophie PS... don't feel guilty it's negitive energy just start researching! We also ended up taking our daughter to a Naturopath as they get the idea of addressing all issues and working towards solving them not just masking it with medication. > > We are new to the world of seizures and so am frantically trying to find any/all info I can to help. ( 14) has autism and had a petit mal seizure( absence?) last wednesday. We are thinking now that he may have had more in the past but we didnt recognize them as seizures so add a heap of guilt to a new dx and you can imagine the state we are all in...sigh....The dr scheduled an EEG but no meds till we see if he has a recurrance. No sign of anything yet except that Josh is sick of us following him around looking in his eyes all the time..LOL... > I have TONS of questions but dont want to overload everyone..lol..any sites you can recommend for a beginner? can these small seizures 'evolve " into grand mal ones? are there obvious triggers to avoid or does that vary person to person? > Thanks in advance for any help. > mary > May you have warm words on a cold evening, > a full moon on a dark night, > and a smooth road all the way to your door. > > Quote Link to comment Share on other sites More sharing options...
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