Lamictal and headache

I have been taking Lamictal for months (not really sure due to the memory loss from taking this drug).
I can't seem to remember ANYTHING. My spelling has been reduced to a 4th grade level and trying to find the correct words in a conversation is horrible. The lack of coordination is only a slight problem, mostly at night. I started on 25mg nightly and currently taking 400mg. Nausea, vomiting, depression, feeling guilty about everything I have everdone or said, headache.
I am going to tell my doctor about these symptoms and hopefully he will reduce my dosage. I didn't have all theses problems on lower dose.

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!

My chronic pain has really increased since being on Lamictal for 15 months for bipolar. I have had fibromyalgia for years. The bipolar developed after that. Since starting Lamictal, I have developed headaches so severe that I have been off work 3 times in the past 7 months, inc. 5 weeks recently. I've always had headaches, but these new, more severe headaches are non-stop. I have to take 3 time-release 100 mg codeine tablets every day, plus Gravol to keep the headaches bearable. Even then, many days I end up bed-ridden. I've also developed chronic, very bad plantar facsiitis in my left foot since starting Lamictal. I did weeks of intensive physio, plus swimming therapy to no avail. Finally had to get a cortisone injection in my foot.

I hate being like this; I like my job and was used to leading a very active life, despite the fibromyalgia, before I went on Lamictal. I briefly tried Lithium recently, but it had a whole other set of side effects, so I am really frustrated.

Has anybody else had increased or new pain since being on Lamictal?

Rosslyn

I have been taking Lamictal for a few months now. I have horrible pains, tingles in my feet and legs. At times I feel like I am getting electric shocks in my feet. I started at low dosage of 25mg and now up to 175mg. I am taking this medication with Lexapro 10mg for depression and bipolar. I am also diabetic and thought maybe these pains are from neuropathy. I got tested for neuropathy and it was negative. I am not weening myself off of Lamictal and my leg pains are subsiding a bit. I now have a bad headache. My nose has been running to and I have bad waives of nausea throughout the whole time I am on this medication. I hope when I am fully weened off that this side effects will go away.

I haven't taken this drug yet I am about to go get it from the store and I do not know when to take this medication. Morning or night? I already have racing thoughts at night so I do not want to be more awake at night than I already am. I also suffer from a weight issue, is this medication going to help me loose or gain weight? I cant afford to gain a few, I can afford to loose a few. I also suffer from back pain now so I do not want that to increase. Anyone have any helpful tips for me?

I have been experiencing a flu like symptom for over a year now. They started about 2 months after I began taking 350mg of lamictal a day. Symptoms include exhaustion, headache, soar/achy throat, post-nasal drip, TONS of nausea, lack of digestion & regurgitation of food. I am tired and feel warn out all the time... I have had everything checked by doctors and they've found no health reasons to explain these symptom's.

HAS ANYONE ELSE EXPERIENCED THIS????

I'm having serious side effects currently. The onset of the side effects began after taking Lamictal for over 2 months. I started slowly on 25 mg and gradually increased to 200. I felt a great improvement in Bipolar disorder-mood swings- at 100mg but was told that is not the theraputic dose, so we increased to 200mg.

I had no side effects until the rash began to appear. At first only on legs, then arms, then neck, then face...and surprisingly in private areas. Unbearable itching. Rash continued to rage even after a pack of steroids. Swelling became apparrent in face and entire body. Slight difficulty breathing. Went to the ER and received another dose of steroids intravenously. The rash continues to improve but is still extremely itch. The swelling improved for a couple of days but is back. Had one day of severe headache. It has been 14 days and today I am experiencing blurred vision in the left eye, and new swelling in the tongue.
I sit at home with an Epi Pen next to me waiting to hear back from the doctor.

All of this is so unfortunate because I felt more stable than I have in years while on the medication. I'm feeling very concerned about my continuing side effects. Don't know what to expect.

Light Rash, dizziness, BAD blurred vision making it hard to drive, BAD heavy bleeding(changes in menstrual cycle lasting three weeks with spotting then heavy bleeding) easy bruising sometimes black and blue ...headache,cant think, kidney pain I have (VUR) and am not sure if i should have been givin Lamictal.... I just stopped taking it went from 200mg to 100mg for a week now not taking any its been two days. and im hoping I start to feel better soon.

I am on 300mg for bipolar. I am having trouble concentrating, remembering (i forget what i'm doing while i am doing it!), I often worry about driving-just don't feel like i can focus well enough-riding down the road thinking "hope i know what i'm doing". It is like i daydream constantly with periods of not daydreaming. I feel pretty cheerful and not having any real emotional problems, but the physical problems are a mess. I am so tired that i feel like every single day is a "well i'm sick today, i'll give myself a break, maybe i'll feel better tomorrow". i do have better days sometimes, but for the most part, i feel kind of useless-not "useless" like i'm depressed-i mean "useless" like i get nothing done and it takes me two hours to get some lunch for myself and my three-yr-old child, and i mostly sit around because i'm "taking a break" and my legs are so sore or i have a headache or i feel shaky, or nauseated - each day, i feel so sleepy i am desperate for my husband to get home to care for my daughter (and me)-it feels like i took NyQuil or Benadryl or something! So, i am literally pretty useless. It's such a shame. I can't find a medicine to help me cope, it is always a trade-off...and going on and off them to try another is a nightmare. At least, right now, it is just a daydream...

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?

When I do sleep, which is not very much, I have the strangest dreams, waking with punching my husband or screaming, any one else have this? Other than that I have a headache every afternnon but only for a little while and they go away on their own

Began taking Lamictal 6 days ago. Blisters and severe headache developed yesterday and medication was discontinued. Blister are continuing to spread throughout my mouth--onto tongue and gums. Quite painful and great discomfort.

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