Cognitive problems symptoms and conditions

In 1988 I had some complications with my pregnancy. I went into premature labor on June 5th. My due date was August 17th. My son was born premature on July 19th, with a good birth weight of 7.11 pounds. I received Yutopar drip while I was in the hospital for 5 days beginning on June 5th. When I returned home I continued Yutopar medication in a pill form up to July 19th when my son was born. Other than jaundice, he had no other apparent problems. While in pre-school at the age of 4 years, his teacher noticed he was having several problems. One of which was staring spells. We took him to a pediatric neurology clinic. His eeg was normal, but the doctor did notice he had problems with cognitive delays. Our next step was to take him for a neuropsychological evaluation. He was diagnosed with sensory motor integration deficits. From there we did everything that was offered to help him, including occupational therapy. Also, we thought he was born with lazy eye. It turned out to be exotropia. We took him to eye therapy to avoid surgery, but it did not help. At the age of 6 he had eye surgery to tighten his eye muscles. From the age of 4 to 6 years old, our son went through a lot with all the testings, therapies and surgery. He continued to struggle with some learning problems and low self-esteem throughout his school years. Currently, at the age of 21 he still has some small cognitive problems. In April, at the age of 17, his hair stated falling out in hugh clumps. He hid this from us by wearing a hat all the time. In June, he was diagnosed with an autoimmune disease called alopecia areata. By the time his senior year of high school started, he had lost 45% of his hair in patchy baldness. With the help of steroid injections into his scalp his hair came back into growth. He came out of remission at the age of 18 and 19 and is currently in remission. To make things even worse, he started feeling like something was wrong with his heart. This was during the time his hair was falling out when he was 17 and 18, and he was receiving treatment for his hair loss. He also hid this from us. It was October by the time he told me and I brushed it off as stress. He finally told me again in December. He said he felt like he was going to die and his heart didn't beat all the time. I took him to the doctor. He was tested and 2 days after Christmas the doctor called and told us to take him to the hospital asap! His heart was pausing anywhere from 2 to 7 seconds. He was transferred out of the area to a pediatric icu. He was diagnosed with Ventricular Fibrillation and received a pace maker at the age of 18 years old. His pace maker currently does 40% of the work to help his heart beat. There was a team of doctors trying to figure out why this has happened to his heart, but couldn't come up with specific answers. They did every test they could think of. I asked them about Yutopar and they say no. I asked them about the short term amount of steriod injections he had to make his hair grow back and they say no. They say his heart may have had a virus or he may have been born with the defect. He had already started having behavioral problems when he was 15 right after his Dad and I split up. His problems became much worse after his heart and hair problems. We have done and still do try everything possible to try to help him, but our hands are tied because he is 21 years old. His self help is marajuana and doctor prescribed street drugs. He has what I would call severe anger problems, very low self-esteem and a very bad temper. His behavioral problems and mental status can't get any worse than it is right now. As far as a mental illness diagnosis, we don't have one. I know he has one though. I'm always left to wonder if the drug Yutopar I took while I was pregnant had anything to do with all of his many problems throughout the years; especially with his sensory motor integration disorder, ventricular fibrillation heart defect and autoimmune disease.

I am a female in my mid-to-late 30's. I was on Topamax for about a year. The memory, vocabulary, concentration, focus, loss of words and 'confusion' got so bad it became a real problem at work and the rest of my life. When I started forgetting how to get home, the neuro doctor took me off of it. Those problems decreased a bit, but never entirely disappeared. After weening off the medicine, the full-blown headaches/migraines returned (Topamax only moderately relieved pain). So now in addition to the pain in my head, I have the lingering sides-effects to deal with. It cost me my job. I've been off Topamax for over a year and still have not regained control of my own thought processes. Among other things, it's embarrassing because I feel stupid. I no longer understand about half of what I read, have trouble following (and remembering) conversations, habitually forget what I'm supposed to do/have done/am doing. Forget being able to follow a series of directions. I am afraid Topamax has caused permanent damage to my cognitive brain functions and I have no idea what to do about it. Has anyone else experienced this problem?

My fibromyalgia has totally flared since I had Mirena put in about 2 months ago. The fibro always was better when I was pregnant and since Mirena has increased progesterone (like pregnancy) that it wouldn't make it worse - maybe even better like pregnancy. But it's definitely worse and I'm really thinking it's because of the difference in hormones. When you are pregnant - estrogen is increased as well so maybe that difference is to blame. Who knows. I have also had more breakouts. No hair loss yet but major fibro problems (aches and pains, memory/cognitive problems, sensation of swelling/stiffness etc...). I am hoping if I have it out the flare will subside a bit. If I am still majorly flaring in a few weeks - I think I will have it out.

am a 61 year old male and after a heart attack 7 years ago they put me on Lisinopril. I gained 20 pounds and look pregnant with 8 months of starting it. My stomach looks like I am pregnant.

My mother called the other night and said she had symptoms of a stroke.
I took her to the emergency room and the doctor looked over her medications and immediately diagnosed Lisinopril as the culprit and it was not a stroke. She stopped taking Lisinopril and immediately the symptoms disappeared and her stomach bloating disappeared.

I went to my doctor today and insisted he take me off this poison . Over the last 7 years I have gained over 40 pounds, all in my stomach.
I am hoping this does me good.

I am a 25 year old graduate student that began taking Topamax for migraines after I was involved in a bad car accident. I started taking Topamax in April of 2008 and by July I could barely formulate sentences, couldn't remember simple things like where I parked by car (in front of my apartment) and my family member's names, simple math was impossible, I was always tired but could never go to sleep, had numbness in hands and feet, and was very moody with suicidal ideations. I was then referred to a neuropsychologist to assess any possible brain damage from the accident since I was now having cognitive problems. They tested me for brain damage where I was diagnosed with Severe Brain Damage, I was reading on a 8th grade level, did math on a 4th grade level, needed to begin speech therapy immediately and my doctor felt I needed direct supervision at all times. I was initially told by my neurologist that the medicine would help with the migraines but would "make my thinking slow". That was a huge understatement. I was a 4.0 graduate student in the middle of my program and I suddenly couldn't perform basic daily activities. I have been doing much better since coming off the medication. I have the migraines less frequently but they are still pretty bad. I have regained most of memory, reading, and math skills back the rest is attributed to the car accident. I wouldn't recommend this medication to anyone and I think it should be taken off the market because it almost destroyed my life and had me and my family worried to death about a condition which symptoms were clearly being exacerbated by Topamax.

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.

I have been taking Lamictal for 8 years for the clinical diagnosis 'double depression.' I now have no depression so for me this medication as been a miracle.

I take 100 mg at bedtime. I have very vivid dreams every night which I do remember upon waking. Whatever I am thinking about or watching on TV seems to be the theme of my dreams so I have stopped watching frightening movies or television.

I also experience balance problems, I have difficulty reading out loud, and thinking of words when I am having a conversation. My cognitive problems are not with thinking but rather verbal expression. I have a lot of problems with three dimensional thinking, as in reading blueprints.

I suppose as my doctor suggested you have to decide if the quality of life is improved weighed against the side effects. As my doctor said "you'll have to decide whether you want to be depressed or clumsy." This is a no brainer for me after many years of depression.

I've been taking Topamax now for about 6 weeks, and my headaches are still just as bad as ever, except now I have headaches with the thrill of numb fingers, confusion, weight loss, memory loss, an absolute horrid taste in my mouth, and now the latest.... my hands feel dirty all the time. Has anyone experienced this?? I just feel like my hands are dirty. I wash them, and a half hour later, it almost feels like there's a film on them, and I have to wash them again. Almost ocd-ish. So 6 weeks in.... Anyone have any advise on how much longer I should give this topamax before I give up on it & try something else? My doc said it should have worked by now if it was gonna - but I have read on here, that it sometimes can take months...? I just don't know if I can take these side effects, AND the headaches for much longer without going NUTS! {grin}
Any advise?

I have been on lipitor for a little over two years now. I experience extreme joint and muscle discomfort. I am also picking up weight at an alarming rate. No matter what I do to lose the weight, it's not working. I've had several blood tests, but all come back fine..but I know I don't feel well and I'm having trouble remembering things....

My mother has been taking Lipitor for four or five years. We moved and the new doctor increased her to 80 mg. He also put her on Zetia. Mother is 86 and weighs barely 100 pounds. This past year her short term memory started getting worse,more so than normal for her age, according to doctors. I was also noticing cognitive problems. She went through a battery of tests. She did not have alzeimers and nothing could be pinpointed other than she was worse than normal for her age as I already stated. Then this last week of the year, her muscles all over her body started hurted and feeling very sore. Then she started have lots of trouble walking, getting in her car, etc. It was so bad so quickly that I became extremely alarmed. My sister mentioned Lipitor and I started the research. I talked to two pharmacists, since we could not reach the doctor. They were both alarmed at the symtoms I described. We stopped both medications three days ago and she is already improving. I now believe that even the memory problems and other things that were gradual were because of the Lipitor. (the pharmacists did tell us it would be okay to stop both for the time being.) I was ready to take mother to the emergency room. That is how bad she had gotten is such a short time. I watched her and talked with her. She was very discouraged at the rate of decline in her walking. It was as if paralysis was setting in. I believe she would have been in a wheelchair soon had we not stopped the Lipitor. We are going to try some natural things to keep her cholesterol down. The quality of life is important too. This has been very scary for us but we are hopeful as she is already experiencing some improvement. We do understand that it can take time to get back and at her age that is expected. Being an elderly person though does not justify that all of these symtoms were 'just' her age. She has always been very active and alert and could outdo me (and my sisters) on most days! I will check this site often for comments and stories of others on this drug. Thank you for the help to those of you that I read your stories and good luck to you that are having difficulties.

I had a kenalog shot about a year ago for allergies. A nurse gave it to me, not my doctor. A few days later I felt as if I had no muscle tone. Major loss of "meat" especially around my joints. Went for months looking for an answer. Always suspected the shot, but really do after finding this site. Yesterday, neuro found inflammation on my brain. Could this be associated? Having many cognitive problems, including typing this message even though I've been typing for 32 years! Does anyone know if the fat ever readjusts and comes back as it should? I'm worried this gave me scleroderma and this might be what's on my brain? Thank you for any help.