Lamictal and seizure

Gran-Mal Seizures and myoclonic jerks for over 30 years as a result of being struck by lightning while serving in the Marine Corp. Have tried "all" of the medications and most made it difficult to do my civilian job. (School Administrator) The best advice I every received was to keep a diary and record everything I could remember happening to me before a seizure. By doing this I have been able to develop a warning system of oncoming seizures. (Same think as most people saying they can feel a headache coming on,) I can live with the myoclonic jerks as they only occur once or twice per day. The seizures while at work or driving are a different matter. (I have warning signs for seizures on the average of once or twice per week, and around one per month goes into a seizure.) Most of the medications other than Lamictal cover up my warning signs and I simply refuse to take them. I work very close with my family Dr. who understands my case better then most Neurologist I have ever had. Neurologist want to give any drug at a strength that will stop all seizures and that can and often does result in side effects that prevent normal live. Lamictal in low dosage, 25mg twice per day may make my seizures less sevier. Any higher dosages causes many of the side effects others have described on this site, but for me the biggest problem is that it blocks my warning signs of oncoming seizure. I get 20 to 30 minutes warning of oncoming seizures and many times can avoid a seizure by just stop doing what I am working on and taking a break and resting. If that does not work, I take two 10 Mg Valium and find a soft place to lay down, the valium will stop or lessen my seizure and I will sleep for one or two hours, and wake up. Sometimes I will have a seizure after taking the valium, but I am in bed or resting and usually under observation. My key has been to learning the warning signs of an oncoming seizure in time to get to a safe place and by always having the valium with me. We are all different individuals and our medical problems are different. Share everything you can remember with a Dr. you trust and attempt to develop warning signs of an oncoming seizure is the best advice I can give after over 30 years of living with a seizure disorder.

I am trying to find out if anyone has experienced 5 minute delayed reaction from Lamictal. My 18 year old son has been on Lamictal for over 3 years. He started out at 200 mg, had a breakthrough seizure after 1 1/2 years and is now on 600 mg. Since they increased him, he has episodes about every two weeks where he feels really dizzy and then forgets what just happened five minutes before. His short term memory is getting progressively worse. You wouldn't know anything is wrong if you were talking to him, but since he has had four grand mal seizures, he knows something is up. Any ideas would be greatly appreciated.

I started taking Lamictal for a seizure disorder a little under 1 year ago. It was difficult to tell how it effected me because I was going through xanax withdrawal at the same time, which I am sure is the reason I had the seizure to begin with. I did not realize this was the case at the time and so i cannot really tell you what my initial reaction to Lamictal was. Now I am noticing some side effects. Difficult to fall asleep (but that's always been the case.) Nightmares (they have gotten less intense, though). Occasional nausea, although never to the point of vomiting. I recently cut my super-long hair b/c it was falling out a bit. It' not as bad now that I got some of the weight off of my hair. I definitely have trouble finding words and often find myself feeling embarrassed when I'm in a social or professional situation and I'm not able to contribute as much to a discussion. I will probably stay on the med til I have been seizure free for a couple of years. I only had the one grand mal seizure. I am 31 and trying to decide if I want a child within the next couple of years, but have to consider the risks associated with the Lamictal. Good luck to everyone. Just do your best to be healthy and take care of your body.

Hi, I have been reading all the postings and my heart goes out to everyone. I been there, done that. Myself, I have a seizure disorder and been on Lamictal since 2003 (I can't recall/remember) - I had tried 5 other seizure meds that didn't work for me. For quite a while now I take 600mg a day and Keppra 250mg to control my seizures. I lost my driver's license twice so far (I know that is the rule in CA) , and once not long ago (I got my license back) I got totally lost in my town, which I used to know like the back of my hand. I thought I had lost my mind. I asked my doc if I was getting demenia and he said oh no you are too young (53). I have also learned doctor's (for the most part) are idiots too. They don't think outside the box for us. I can't spell anymore, get depressed easily. I really want to work, but I can't. I have tried time and time again, but (yesterday) it just about did me in...people explained to me how to do things on the job many many times but I couldn't retain any thing. People just looked at me as if to say what planet did you come from. I cried on the job so hard I wanted to disappear. I am so sick of my family saying "I know you can't - don't remember this or that..... I can hardly bare that. Now I have a potential kidney problem. Suppose it is from these meds? I am really scared.

I was diagnosed with peti-mal epilepsy aprox 17 years ago. I tried many different anti epileptic drugs and had many negative side effects from teeth problems to depression and none of which controlled my seizures. 12 years ago I went on lamictal (600 mg a day) and I haven't looked back, I feel I have my miracle. So far I have no side effects, am completely seizure free and I have a life. BEFORE lamictal some side effects were poor concentration ( when reading a book I could not remember what was written on the top of the page by the time I got to the bottom), little co-ordination with sports (most times I could not catch a ball when thrown to me, this caused a lot of social problems), forgetfulness and I was quite clumsy. I hope you all can one day find a medication that works just as well for you or even better a cure. My heart goes out to you all.

I am on this medication for seizures. Besides all the other side effects being posted (typing, speech, spelling, forgetfulness, etc), I have EXTREME daytime sleepiness. To the point that I will not/cannot drive and have to stay where I'm at until I "wake up". I have been off work for 5 months, but had to go back for financial reasons. I work partial days and go home and take a nap, which the neurologist prefers I don't. Anyone experiencing daytime sleepiness (disorders)??? Thanks

Thanks, everyone! My (brand new) doctor had convinced me that I was simply experiencing anxiety to explain my side effects. After being off Lamictal and all medications for several months, and then restarting on Lamictal only, I noticed all the following side effects, some of which I've had before, and some completely new. Also, the ones I'd had before came back at a level of severity which I had never experienced.

One familiar side effect was hand tremors and general shakiness which sometimes also affected my speech. Even strangers would notice and ask me if I was ok. Luckily, this was during this past winter, so I would basically lie and just say I was cold and a bit shivery. Another familiar side effect that a lot of others are mentioning are cognitive issues and short term memory loss. Sometimes I felt like my tongue was lazy or I felt tongue-tied, and I couldn't get it to work right to say the words I was thinking. Sometimes, I just plain lost my train of thought or couldn't think of the words to express what I was thinking. I'd all my life been prone to mishaps of speech like occasional spoonerisms and such, but on Lamictal it was happening probably daily, and I'd even started stuttering. Teaching and explaining often difficult concepts and public speaking is part of my job, so this was causing me a lot of anxiety. I, too, completely blanked on spelling out words when friends and colleagues relied on my spelling abilities more than their computer's spellcheck. I also thought I was having sudden leaps in experiencing getting older (early 30's) because of my memory, I typically have an almost photographic memory and can picture where I saw my keys last or what have you, but all of the sudden I couldn't even piece the photo together anymore or it was foggy in my memory.

The newest side effect also experienced by others was clumsiness not only of my own body but of my surroundings. I suddenly noticed that I was doing things way more often like tripping, falling, stubbing a toe, nicking a finger, dropping things, etc. Where I was an excellent parallel parker before, I'd get out of my car and realize I'd parked 2 feet from the curb and crooked.

I decided to look up Lamictal's side effects after discussing this with my excellent talk therapist because I was extremely frustrated with my new doctor telling me I was just anxious and there was really nothing he could do for my (imagined) "side effects." And here everyone is experiencing the same thing. I don't think I should be made to feel like I don't know any better and that I should suffer the REAL side effects of this drug. I didn't study medicine, but I still have a degree in biology so I'm not so stupid that I'll believe anything any doctor tells me.

I think I would almost rather suffer a mild mood swing than suffer these side effects. I'm going to try to look for something else.

45 years old, female, diagnosed bipolar II in 2006. On Lamictal for 2 years. Initially, very positive effects of Lamictal - felt "normal" and stable for the first time in years. Didn't notice any side effects. Gradually increased from 200 to 400 mg per day 6 months ago as I still experienced mood swings with a tendency towards depression. I have been on 400 mg/day since August 2008. It is difficult to say what are the side effects of the medication, and what are "natural causes". Since doubling the dosage, I experience memory loss and increasing cognitive problems (slow thought process, difficulty putting together coherent sentences in discussions, fumbling for words. I have spent more than one hour on this posting!). I sometimes wake up during the night drenched in sweat. It could be that I'm menopausal, but I find it unlikely. Mood swings have perhaps become less pronounced, but I would like to regain my mental capacity. I plan to cut back to 200 mg of Lamictal - and perhaps some day learn to live with bilpolar II without medication and a lot of help from my friends and loved ones.

My 17 year old son has been taking Lamictal for seizures for 2 1/2 years. He started out at 300 mg a day and was seizure free for a 1 1/2 years until November 2007. Since then his physician slowly increased his dosage to 500 mg a day. and he hasn't had another seizure . Unfortunately, Since the increase he has acne on his jawline and back. We are trying to find a way to get rid of the acne, but have been unsuccessful so far--decreasing his dosage is not an option as he has grand mal seizures. Also, he has these tiny red bumps all over his arms. His dermatologist say's they are a hair follicle problem, but I think it's quite a coincidence that they started when he began the Lamictal. If anyone has any suggestions, we would greatly appreciate them.

I take Lamictal for seizures for 3 years. I had my first unexplained seizure at 25 and another 6 moths later. Both times I had drank heavily two nights in a row. After the second seizure I was put on the Lamictal. I was slowly ramped up to 100mg in the morning and 200mg at night. On occasion, I get horrible "poop pains" as I call them. It feels like my insides are being ripped apart. I can sit on the toilet and poop incredibly runny stool, then I have to wait up to 15 minutes for the second batch. The pain doesn't subside until the second batch but it is immediately gone. It usually only happens when I wake up in the middle of the night. I have tried to correlate it to foods that I have eaten and can't match anything up. I also have horrible short term memory. I sometimes tell the same person the same story twice and they will be like "you just told me that." Also, golfing is the best example. I have a hard time remembering my strokes. My long term memory is fine. As fair as hair loss, I was already on track to lose my hair before I was on the meds so I don't know if they made it any worse or if this is a natural progression. It seems somewhat rapid but I never loose it in quantities or clumps. I just notice it in my hats and beanies every once in a while. I also have a hard time falling asleep on occasion and if I wake up in the middle of the night I have troubles falling back asleep as well. The bottom line is that this drug WORKS. I can live with the side affects cause they are random and not that often. I am a volunteer Fireman and cannot risk loosing that again so I am too hestitant to change meds as the doctor said Lamictal has the least side affects of the seizure drugs.

I have to comment on some of the Lamictal "new comers". I've taken Lamictal for 1 1/2 years. For the first 6 months, this was the miracle drug. As months went by, I began all of the same symptoms: fogginess, weight gain, short-term memory loss, NO libido, headaches, and nausea, to name a few. As of this moment, I am weaning off of the Lamictal. HARD to do. This is not a drug that can be "stopped" immediately. On my fifth day of weaning off, I am dizzy, tired, weak, irritable, and have vomitted. Only about 3 days left. I am starting Topomax after. I'm anxious to see if there is any difference. Especially the weight gain part. I went from 120 to 135 in one year. (I run and eat healthy meals.) I will continue to take Effexor, which, in 2 years, has had little or no side effects. My advice to anyone just starting to take Lamictal is to GO SLOWLY. My doctor had my doses increase so rapidly that I didn't really see if the lower doses would have worked. (I take 200mg.) The bottom line is to do what feels right for YOUR body, rather than a specified dosage. Best wishes to you fellow BP-ers!

I am 32 years old, and still have acne. I have been taking it for almost 14 years now. I know that Lamictal causes skin rashes. I asked my neurologist if Lamictal causes acne. He said no. I will never be able to get rid of acne, as long as I keep taking it. I have been seizure-free for over 2.5 years now. Dad won't let me get off of it, and be on primidone only. It's more important to keep driving seizure-free, than to have clear skin.

I got all those problems but the higher the dosage the more attacks i had.Another neurologist think that i just have pseudoseizures-paranoia attacks.Anyways the doctor screwed me up,he gave me 5 years ago something different and my seizures started daily than switched me to lamictal.I must say that sometimes i have or HAD electricity in my left hand all the time and once a women touched me and got stunned lol.anyways lamictal is bad,i didn't have any side effects like loosing hair but i did have A LOT of head hecks.I must share something with you,when i read epilepsy.com it seems that my seizures called myclonics in the end they are not but they similar in effects.Myclonics its seizures that happens only in the morning.Heres the catch for me,i figured out that if i won't close my eyes the first hour after i got up and went to the sun outside than i didn't have seizures.Its not a real solution so i decided to raise the lamictal from 175 which was ok for me to 200-250 like the good doctor said,just made me worse.Now i started dropping it by 25 mill each week and i must say i feel better only a little tired after 5 years that my body got used to it.Anyway if any of you have myclonics than don't close your eyes.BTW i have AURA-feeling before the seizure but luckily for me after a second if i open my eyes nothing will happen although i don't always take notice of it.In midway it would happen if i seat in front of computer and will lose attention if someone will call me or whatever but its a mill-sec seizure,barely noticible if at all and i never get "disconnected" from reality!!!
the ONLY thing which is bad for me is that except that im sick now my blood pressure is huge-140/82 and pulse 106 which is being like that for couple of days but i will get trough that.Since i lowered my dosage my midway seizures stopped,now im on 100.

P.S=Check yourself with the neurologist with a different one preheps.IF you can describe the whole seizure it means you don't dispatch from earth which mean it might be psydo seizures which are psychotic and not epileptic,the most important thing is that if someone takes lamictal or any anti apileptic drug even tho he doesn't have real seizures the medicine can do this.I got screwed and now i try to get over it,the doctor trowed me on woods with tablets after having a first seizure WHICH IS WRONG because you sepused to get tablets only after 3 attacks and after describing seizures and doing eeg tests to make sure that you DO have the problem.

Anyways remember what i said about the closing eyes in the morning part,if you close your eyes and feel weird keep them open at least those that have them after they wake up,that was a solution for me and it can help you to...MY doctor said everyone like me but i think he is laying,the other neurologist said my doctor was wrong probably about the seizures,i think i have both but i do know that believing and saying that you don't have anything WILL help you and lower your seizures,after speaking with the doctor i actually started to believe i don't have anything and walla i have almost NADA,today i had zero!!!! :D

OF course don't lower dosage without first consulting with someone expert,but since i know i can control basically every seizure i have and i know what to do to avoid it i let my self start dropping dozes!!!

GOOD LUCK my friends believe in yourself and if you want some personal info leave your msn i will add you and try to answer you the best i could,i was researching my self trying to figure out the core of the problem for 5 years but after 6 months knocking my head in the pipe when i washed my face i learned what i should avoid to minimize the chance!!!Try that

I would like to let people who are new to the Lamictal "experience" that it was VERY uncomfortable for me during the first few months also. In fact even at the very low introductory doses, I did not think that I could ever function in society.

The extreme confusion, the memory problems, the spaceyness, the feeling of detachment from everything that surrounded me... at the time I felt that I would never be able to function as a worker, a friend, or as a social being.

As time went on though, things did clear up for me. It took a few months, but I'm guessing that my brain function/chemistry finally somehow regulated itself, and my side effects did clear up. I am at a dosage of 600mg per day now, and yes, I do sometimes feel detached, but I certainly can function. My memory has also improved. It sometimes takes me a second or two to find the "right word" during my conversations, but a simple, light hearted mention of the problem resolves the issue for the person that I am speaking to.

If you are just getting on Lamictal, try to be patient. I have found that in time, it has helped me much more than the side effects hurt me. It did take a few months to get used to, and I did have to explain to others at work that I may be acting strangely for a couple weeks because of it... but the overall effect is quite nice now.

Lamictal now helps control my seizure problems almost completely, and has the added benefit of making me feel much more confident, and balanced.

I've been on Lamictal for 3 years, and it's started to fail. I was on a generally small dose for epilepsy, 100mg twice a day. Well, I started having these twitches that caused a car incident, so I had to go to the doctor to get the dosage increased. Well, I did that, slowly, and I was twitch free. I thought that this was great, I can finally rest easy. Also, for some reason after I increased the dose I was oversleeping. No severe side effects though. But then, just yesterday, I had what we believe to be a full fledged seizure during a shower. I missed my dose by 2 hours the night before, and luckily I was having trouble falling asleep (or perhaps unlucky), and I probably got 5-6 hours that night, which lack of sleep is always a bad thing with epilepsy. So, during my shower I started twitching, bad. I turn the shower off. Then the next thing I'm on the shower floor, and I see blood on the wall, though too dazed to make anything of it. My family hears the bang and comes down and tells me to open the door, but I yell out to wait until I'm dressed. Then I felt horrible. So obviously the dose increase didn't help, and the Emergency room doctor put me on Depakote plus the lamictal until I see a neurologist next week.

I have been on Lamictal and Topamax for approximately 4-5 years now. I also take effexor. I have a seizure disorder. At first everything was alright, however now I have been having double vision, staggering, memory loss that has occurred slowly within the last two years or so, and of course as with most meds the usual diarrhea or constipation. I wonder how long does it take being on medication for these side effects to kick in? I read all literature whenever I start a new medication even if it is a OTC drug. (over the counter). I just got out of the hospital and am being sent from one doc to another. I feel like a guinea pig in a lab! Please help!

I have been on it for about 7 weeks now, I have the best Dr.I dont know what I would do with out her..I am transitioning from the Dilantin, been on that 25 years, now have ostiop........... ( Used to be a really good speller, maybe thats a forties thing!) in my hips and back. I started feeling really good, now having huge lapses of depression, Lonliness, eye sight which I hear very common, spotting different times of month, headache, dont know if its a side effect but each time I up my dosage things I think are becoming clearer, and cry a couple days, like to much information is flooding my mind. I Have bad dreams the kind that you can obviously analize, but wake up crying. Its a very lonely place to be, people think you will have a seizure thats why they avoid me ( I have been told) which I dont understand because Im taking more medicine and feeling better!

I was on Lamictal for 4 years and after the first year I suddenly started having all kinds of teeth and gum problems for no discernible reason. But since Lamictal has the possible side effect of "sores or blisters on the inside of the mouth" I wondered if it could be related.

I did a Google search and am coming up with no experts yet, but lots and lots of posts connecting anticonvulsant meds, particularly Lamictal, Topamax, Neurontin, and Depakote, with dental problems. Dilantin is well known for causing gum disease and breaking down tooth enamel, loosening of teeth, and even breaking down of jawbone tissue.

I don't think the experts have connected the dots yet, but is anyone else having this problem?

lamictal controls seizures if you take it at the right time. i am on 200 at night and 200 in the morning plus epilim. sometimes i just sit and cry wen im trying to concentrate on reading books i have to study or trying to remember work i learnt at school which has left my brain. im failing school not matter how hard i try, i study all the time then the next day i have forgotten it. im so young and i havnt even started my future yet and i may have screwed it already. failing exams because i forgot wat i learnt the night before hurts so bad. its hard to say "hey everyone the reason i failed is because lamictal screws my memory" i know thats what it is. i was extremely intelligent before i started taking it, but now im a failure. i guess deep inside i know really im not a failure, but lamictal makes me one. : ( p.s add a constant hand tremor and sudden jerking movements every now and then.

I started taking Lamictal about six weeks ago for epilepsy. Now keep in mind, I was on Dilantin which worked great for 17 years and then suddenly stopped working. I have been in medication hell since then. First Topamax made me dumb as a rock. I would space out all the time. Worst drug ever. Then Keppra which was better in that my memory/ability to speak came back but I had these intense ups and down. I had rages constantly. Now I'm on Lamictal. So far, it's better than the Topamax and the Keppra, however the dreams are very intense as are the night sweats. I'm also experiencing much hair loss. Fortunately I have a full head of hair but I'm afraid I will eventually lose it all.

Hello! I've been taking Lamictal for about 6 years now. I'm diagnosed as BP II and have the most difficulty with depression. I currently take 500 mg-- 400 mg at night and 100 mg in the morning. I have to say that Lamictal has been very good to me for the most part. As long as I don't put myself into extremely stressful positions-- such as my last job-- I do quite well. I also take a combination of supplements with Lamictal which seem to give the extra push that I needed to completely get out of my last depression. I take 1000 mg EPA (fish oil), B-100 Complex, Folic Acid, Cal-Mag, multivitamin (high quality, organic), Vitamin D (at least 1000 mg) and a few others.

I notice that when I take it at night if I don't go to sleep right away, my mouth and tongue will tingle. Sometimes when I take it in the morning, I feel foggy and dizzy and sometimes get vertigo. Every now and then the side effects seem to get worse, which I am not sure about. I started searching on the internet because I've been noticing that the "tip of the tongue" problem has been occurring more and more often. I often cannot think of the word I want, simple things even. As others have mentioned, I also have difficulty with memory. I am still very successful, currently pursuing a 2nd Master's Degree, but have noticed that achieving the same level of quality of work takes a lot more effort than during my previous degrees.

I do have some periods of anger/irritability and have recently been sleeping a lot, though it probably has a lot more to do with the time of year-- winter with less light-- than anything else.

I am particularly worried about my memory loss and inability to sound "well-spoken" in a setting which demands that of me. It is frustrating! I don't want to do any lasting harm on my brain. After increasing to 500 mg from 400 mg, I have noticed more of these brain issues, but I'm also doing so much better mood wise!

I'm 25 and have never had great skin, but I've found that minocycline will clear up my acne right away. That is, it used to, until I started with lamictal. Even with the minocycline plus tazorac and an antibiotic cream, my skin is breaking out on my face, especially at the jawline and outside of my face. But the really weird thing is that my back and chest are breaking out. That has NEVER happened before and it's not the infamous rash.

Other things I've noticed: sensitivity to computer screens and TVs, probably because my vision is getting worse, but so I get headaches; brutal periods with extreme breast tenderness; slurred speech and short-term memory loss at first, but not any more; occasional feelings of just being "out of it;" a bit of weight gain and I've always been superthin, but even with diet and exercise am having trouble maintaining my weight. Oh, also the nausea mentioned above, in the mornings; it was so bad I thought I was pregnant.

I'm only on 75mg/day at night for mood stabilization, but mostly because I take wellbutrin and had a seizure on it last year, though I'm not epileptic. I've always been sensitive to medications, and I have to say I've felt extremely "stable" on lamictal, but almost too stable. It's been a bit disorienting and I've felt my creativity diminish (I'm a writer). When I first started the lamictal I had also started a new job. This was a really bad idea as I couldn't remember any of the things my boss was telling me and my speech was messed up; I even stuttered a bit, which was scary.

My 14 year old son began Lamictal 2 weeks ago for absent seizures, starting at 12.5 mg at night for one week, then 25 mg for one week and then will increase by adding a morning dose at this rate; ultimately to titrate up to 100 mg at night and 100 mg in the morning. The slow increase in dosing is supposed to avoid the life-threatening Stevens-Johnson syndrome (indicated initially by a rash).

I have noticed he is moody, angry and tearful now. I find this concerning since it is also prescribed for mood stabilization. He complains of body aches and especially leg pains/soreness. I think his short-term memory difficulties are worsened. He has made comments that he doesn't care if he lives or dies.

I noticed that his lymph nodes in his neck and just below his skull are a little enlarged, though he saw his pediatrician yesterday and they are not big enough to be considered outside normal range.

I am a nurse, and drew blood work at home today to rule out infection and look at liver function. There are no tests which quantify a therapeutic range for lamictal--it's very individualized.

I want to take him off of the lamictal and am looking for alternative ways to minimize seizures, such as exercise, diet, vitamin supplements, omega oils, perhaps neurofeedback, massage therapy, music therapy--any and all things which may help.

I feel like my child is sliping away from me with this personality change; I want to find out why he is having seizures rather than just treat symptoms which are the siezures. I'm reading--night and day and will not give up until I am convinced there are no natural approaches which are better than drugs. It's exhaustive to put the work into it, but I think it is necessary.

It is recommended that Lamictal be tapered off over about 2 weeks, to prevent siezures--whether you are taking it for this or not. I don't know how his neurologist will respond to this request to take him off. I think it's important to have a good working relationship with your doc. However, in my view a good doc is open to individualized concerns and alternative treatments.

My heart goes out to all of you who are struggling with your own problems and suffering side effects. I wish I could do something to help you. In my journey to learn, I will post any things which I discover to be helpful to my son, though they may not pertain to your particular problems, they may also be of help to you.

I have learned that seizures cause oxidative stress to tissues, just like an apple browns once you have bitten into it--it does so due to oxidation. Vitamins C, E and selenium may help, since they are antioxitants. Siezures disrupt the metabolism of essential fatty acids, so supplementing with omega 3 and 6 oil may be helpful--these oils also stabilize cellular membranes, because cell membranes are constructed of phospholipids derived from these essential oils. At minimum, I would do these things.

Exercise may help, and also a modified Atkins diet. I have always struggled with depression, and nothing helps me other than exercise and eating a diet restricted in simple carbs and sugars. I think this is important for everyone, as this is the way to prevent and sometimes also reverse type 2 diabetes. Everyone should eat like this and exercise--this is the best mood stabilizer of which I know.

I think that most illnesses are related to metabolism, and in this day, we are exposed to unhealthy foods continuously and our lifestyles/jobs make it difficult to get physical activity. I believe our bodies are screaming at us to make changes in this, and that is why we are having so many problems with illness in general.

I know it is hard to exercise when you are depressed, but if you can do it, you will see the changes in the quality of your lives. Be careful though, becuase the meds you all are taking may put you at unknown risks for injuries that I have no knowledge of.

I wish you all well.

Sherry

I believe that it is best to try to find natural ways to help

I have been prescribed Lamictal for seizures, and am currently taking 400mg daily, with my 300mg of Dilantin. Had horrible side effects this weekend-nightmares, exhausted, worsening depression, crying jags, difficulty swallowing. Has anyone else experienced mood changes for the worse while on this drug?

100mg 2x daily for complex partial siezures.. Initially thought this was great after dealing with dilantin and feeling like a tired zombie. The only side effect I had was a chronic runny nose. I then started having low back pain, then nearly unbearable muscle spasms down the back of my legs. It was so bad I was setting alarms so I could take ibuprophen round the clock. I began having stomach issues from the ibuprophen, so I scaled back to only taking it in the am. Muscle spasms are now tolerable, but I've developed a new issue - I'm often dizzy and have random blurred vision. I waited 6 months to get my license back (after one minor siezure). Now I don't drive because of the side effects. I don't know whether cutting back the dose of lamictal would help, but I intend to ask.

Took mostly for seizures, but have been informally diagnosed with Bipolar II.

Had tremors at night, almost immediately, marked anxiety, weight loss, strange heat flashes, severe headaches (already have a migraine problem), complete w olfactory hallucinations (could have been breakthrough simple seizures, or headache auras).

Felt detached from myself and others. But the most disturbing symptom of all was auditory hallucinations. I have no history of psychosis and this only happened after starting Lamictal. Basically I could hear a constant chirping sound, subtle, but loud enough at night to keep me from sleeping unless my radio was playing to distract me from the sound. Could it have been a new form of seizure? Maybe, but regardless, the sounds started at the time I started this drug. Plus, according to a psychiatrist, I had no signs of psychosis, just the unexplained phantom sounds. One last possibility: Maybe an inner ear problem. Still would like to look into that.

People are right when they say this is still an experimental drug. If I had known what I was getting myself into, I never would have tried this drug to begin with. If any of you have had auditory hallucinations on this drug, without a history of any sort of hallucination or psychosis, PLEASE respond here and let me know about your experience. Thanks!

I recently was given 200mg over the recommended pharmaceutical dose of Lamictal. My dr.'s partner prescribed this after a trip to the ER for a seizure to get me by until I could see my regular neurologist at the beg. of the week. The extra dose caused major blurred vision side effects, inability to walk, extreme sensitivity to light, and nausea. I am now at 400mg of Lamictal and starting Topomax with it so I hope this works. Any thoughts from anyone else taking this med combo?

I've been on Lamictal for 3 years after a brain tumor removal. I was intially on Dilantin but the side effects made me crazy. My face constantly tingled and was numb, I couldn't speak well and the dizziness was debilitating. My neuro put me on Lamictal. I started off at 100mg, once in the morning and once at night, and had another seizure. I finally figured out I was having my seizures in the late afternoon and deduced the drug was wearing off around that time. My neuro put me on 150mg 2x a day and 100mg at lunch time. I've had no seizures for 2 years and 3 months so I think we have the dosage problem licked. However, I am really dizzy in the late afternoon and if I get excited like when I'm at a party. Shopping makes it much worse and I think that is due to moving my eyes around so much. Grocery shopping can be a tough task. I don't slur my words but I frequently cannot 'find' the right word. I'm slower in everything. I cannot take a walk looking at the horizon because I lose my balance and get dizzy again. Sometimes my head tingles. Heat makes it worse and when I get hot flashes (yes, I'm over 50) makes the dizzy much worse. Sometimes my fingers don't automatically go to the home key on the computer keyboard. I have to really concentrate on things that used to be automatic, like knowing a stop light is red. I used to be able to 'see' that and react appropriately. Now I have to concentrate on those red lights so it is irritating. I feel like I'm getting old. However, I will stay on this medication. It works and though the side effects are tough to live with, I'd rather stay on a med that I know works, rather than try one that might work. I lose my driver's license every time I have a seizure. I guess that is the worst side effect :-( I'm hunting for something to combat the dizziness and am using mybraintrainer.com to see if brain training exercises will help me become faster again. It can't hurt and so far I've had a little bit of success. I'll just keep going.

double vision, twitches of large muscles to point of near seizure eventually then walked like I had parkinson's - could not lift my feet when walking so had to shuffle.
My primary care MD and my prescibing psychiatrist didn't either one believe these things were not symtoms of lamectal
toxicity "cause they never read about them: infact psych. suggested I probably wasn't BP after all and just needed counseling - and she was the one that gave me that diagnosis/label about 6 yrs ago ! Primary went along with her.
Don't deny counseling would help, but very angry when they said "behaviors" couldn't be due to lam. cause level too low.

I started Lamicatal May 19th, 2005. I was warned by my doctor of dangerous rash and itching. If so, stop taking medication, call him if not too bad that I need to call 911 to go to the hospital. On my print out from the CVS pharmacy is clearly stated: Serious (sometimes fatal) skin rashes have occured while using this medicine. Immediately notify your doctor if you develop any type of rash. If this medicine is the cause of the rash, the medicine must be stopped. Even after stopping this medicine. It is still possible for the rash to cause permanent or life-threatening scarring along with other problems.

Possible Side Effects:
drowsiness, trouble sleeping, dizziness, nausea, vomiting, loss of appetite, muscle aches, double vision, blurred vision, fatigue, weakness, headache, shakiness, or clumsiness.

Symptoms of an Allergic Reaction include:
rash, itching, hives, fever, swollen glands, swelling of the lips or tongue, painful sores in the mouth or around the eyes, severe dizziness, or trouble breathing.

Symptoms of Overdose:
may include unusual dizziness, serve headache, unusual sleepiness, involuntary eye movements, and loss of consciousness.

I starting itching really bad the second day on the medication. To the point I had huge bruises allover me. I got a spurt of energy that I have not had in several years the second night but not since then. I can't go to sleep at night. Even taking 6 Tylenol PM and a Klonapin I don't get sleepy until around 9 to 100am in the morning and then I sleep all day long. I have started to have frequent headaches, suspious bumps around my mouth area. My muscles ache, too. It is Memorial day weekend so I can't call my doctor but I am going to on Tuesday. I have (MDD) Major Depression Disorder, Manic Depression, (TRD) Treatment Resistent Disorder. Nothing I have taken thus far has helped me with my depression.

Does anyone have first hand knowledge on ECT treatment? I am seriouly considering this procedure. I am desperate but I have no insurance or money because I haven't be able to work for 9 years now. This is the only thing that has kept me from getting the ECT treatments, is money! I have contacted every Talk show, hospital, clinical trials and no luck in finding free help with ECT.

Any ideas, guidance or suggestions would be most appreciated, I am dire to get help soon or I won't make it.
Sincerely,
Lost Hope