Memory symptoms and conditions

Dizziness, back ache, severe hip and shoulder pain, transient global amnesia, after discontinued taking of Lipitor, speech problems, loss of words.

Gabapentin caused me to feel wonderful at first! Then my libido hit the roof and beyond. I would get bloated in the belly and urinate more frequent. I never slept. My hair thinned.I developed a bladder infection and hyponatremia and went off of the drug. At first it helped my pain, my social phobia, anxiety, better memory, i was no longer depressed and saw life through rose colored glasses. I was loosing weight on it. How I miss it.

I'm a 41 year old female in very good health- other than the obvious migraine problem that I have. I have been on topamax for 3 months and am now tapering off of it. I have had all of the side effects that others have experienced to the point that I can't continue taking the medication. My memory is horrible. I can't remember simple things, which is really causing problems at work. My mood is dull and lifeless, and all I want to do is, well, nothing. I'm not a big soda fan anyway, but now it tastes really awful. I noticed that almost immediately. And once in awhile I crave a coke, but can't drink one because it is nasty!!!
I have lost about five pounds, but I don't think I will lose any more since my appetite has returned. That's o.k., because that wasn't my goal anyway. The tingling in the hands, feet and face happens almost daily and feels like little tiny needles being stuck in me. It's actually quite painful sometimes. And, I have noticed blurriness in one of my eyes. This drug has not helped my migraines. We're trying something else. But either way, I would get off of this drug. It's not worth it to me. If you are considering it, I would think twice.

Oh I forgot.. Same as "Blackbolt" said, I feel like I've gotten "dumber" also.
My memory has gotten so bad now. I forget everything.
And I still feel kind of "foggy" sometimes, although I think it might be getting a little better finally. I hope!

Been on Topamax for almost a year. My dose was 150mg once a day for alternative treatment for chronic depression. I am also on Effexor and Lamictal. The tingling in the toes has lessened but not gone away. I have severe thirst all the time. My body seems to overheat easily. I lost 20 lbs but i was doing weight watchers and had just had a baby so its hard to give all the credit to Topamax. I definitely feel dumb. Words come and simply float away out of sight. My memory is extremely affected. I can fight with my husband and by the end have no idea what I had just said. Feel quite foolish. I am now titrating down and off by 50mg every 4 days. I am down to 50mg and have not had a good night's sleep since reducing my doses. My brain just turns on in the middle of the night. I am also pretty nauseated at this lowest titration. I just gained back 6 lbs but eating chocolate doesn't help either. I seemed to be able to keep my weight at 140 lbs no matter what i would eat. Not so anymore. Always trying to find the faster, easier way toward staying thin but it always comes back to that same bottom line. I have to discipline myself boooo.

ok, so I am 28yrs old just had my lap for endo on October 1 and my doctor has recommended lupron, and am going to be getting the med in a week to 2weeks,but after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do,and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? did any one have a baby after doing this. my bigs thing is being able to have a baby. Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

I am a generally active and fairly healthy 77 yr old who had been taking 10 mg of Lipitor for over 12 years with no obvious adverse effects. Recently I started having pain in my right leg, severe enough to wake me at night. This was followed by a significant weakness in both legs, and for a while, accompanied by a lightheartedness. The doctor had me take a series of lumbar and leg x-rays which didn't show much of significance. He wrote a prescription for physical therapy, which I did not follow.
I did internet research on my own which made me aware that Lipitor could be the cause, in spite of the fact that I had tolerating the drug for so many years. I told the Doctor of my suspicions and we agree to stop the Lipitor for at least 6 weeks to see. A few days later, all my symptoms were gone. So be cautious, adverse effects from Lipitor can occur anytime.

I'm 41 and have been on BCPs since I was 17. Been on Yaz about 2 years, the best thing I can say about it is nothing. I'm dropping it immediately. My attitude is crappy, No memory, Joint pain,especially in fingers, zero sex drive. Now mostly I've just thought this was my age, but 3 months ago I had to have my gall bladder removed! I've never been unhealthy in my life, so what gives? The more I read on-line the more I see a connection to Yaz and these symptoms. There lots of lawsuits being gathered about yaz. Be careful ladies, the juries still out on this one, literally.

Been on warfarin for three months for DVT left calf. I got to this site looking up fatigue associated with the rat poison. I've also experienced increased sensitivity to sunlight both directly on my face and extreme sweating from doing lite work. I also have a constant ringing in my ears and memory seems to be worse. My dad also takes this medication and doesn't have any of the same symptoms. I will deal with it for the time being rather than have my calf swell up like a cantaloupe.

I really wish I would have found this site before making the decision to have Mirena inserted. I had it put in yesterday, September 24,2009. It was the most painful things I have experienced. My Gyn had told me that I would have "period type camps" for a couple of hours after insertion. Well I spent my entire day on the couch with a heating pad on high and 800MG of Motrin. None of this touched the pain. I ended up having to take a sleeping aid so that I could go to sleep and hoped I would wake up the next morning feeling much better. Well I woke up this morning and the cramping was not as bad, but still more than "period type cramps". I also noticed that I was having very bad lower back pain. I was cleaning my house and every time I moved the pain would be stabbing. I have not spotted at all yet, but I know it has only been a day. Today I was working and noticed that my right arm went numb from the elbow to my finger tips and my eyes seem very tired.
I am a little upset because the Mirena booklet did not discuss any of these side effects. And also my Gyn had made it sound really promising because I cannot take regular birth control pills. I think I will be calling them on Monday and asking to have it removed. I really wish I would have done more research before having this done.

After several attempts to lower my cholesterol, my doctor has settled on 40 mg of Lipitor, but, after reading these comments, I'm going to self-medicate and work my way off the drug completely. My main complaint is the fatigue and brain fog others have experienced. I do have a shoulder that has developed pain and weakness, and my legs don't seem to be as strong as they used to be, but it's the fatigue and memory/cognitive slowness that concern me the most. Also, like others, I assumed it was normal aging (I'm 58 and have been on statins for about eight years). I'll report my results after getting this stuff out of my system. Good luck to everyone going through this...we're not crazy after all, huh?

Like many of you in this forum, I'm experiencing the pins and needles feelings all over my body, especially on my arms and face. I have weird lapses in memory. I attributed the joint pain I've been feeling this past year to being a 45-year old runner. However, upon reading so many comments regarding joint pain, I can only ascertain this isn't just something caused by age and running. Is anyone of you men experiencing erectile problems? Since starting Lisinopril a year ago I've noticed performance difficulties. My doctor said that can be expected with high blood pressure and prescribed me Cialis. Good Lord is that drug awful! I'm going to flush my bottle of Lisinopril right now and call my doctor tomorrow and discuss a safer alternative to this medicine.

I've been on Yasmin for about a year and a half now... This is my first time really using birth control. I tried BC in my teens but hated the side effects so I got off them right away. Now that I am in a serious relationship and we're both in agreement we don't want to get pregnant until after we're married, I decided to start BC. I've had a few side effects but didn't really think much about them until I went for my annual pap last week. My doctor asked how the Yasmin was going. I told him that I've noticed I have little to no sex drive. He basically said that's not typical for Yasmin. I decided to get online and research side effects, that's when I came across this website. After reading several of the responses, something just clicked... I have many of the same symptoms!

I have never in my life experienced migraines until I started Yasmin. Fortunately I've only had a few since I started but nevertheless, not fun. I do however get frequent headaches. While I'm on the subject of my head, my memory seems to have slightly diminished. I often have a hard time remembering the simplest of words, causing me to misspeak often. I even have a difficult time remembering what I did a few days before! I've always had a very good memory! Has anyone else experienced difficulty with your memory??

About 4 mos after being on Yasmin I had a really weird uncomfortable pain just above my inside ankle. A few days later that pain had traveled up to the inside middle portion of my calf. At this point the spot where the pain resided was now discolored, looked almost like a bruise. Within a few hours the pain had moved up my leg just below my knee, still on the inside of my leg, again discolored. To make a long story short I went to my doctors office and he said I had a blood clot in my leg. He told me to keep my leg elevated and apply heat that it should be okay. I haven't had any bad cases like this again but I do occasionally get a similar pain in my leg but the pain seems to subide after a day or so. Ladies, if you experience similar pains and/or discoloring on the back of your leg(s) make sure you see your Dr. This can be deep vein thrombosis which are dangerous blood clots, they can cause pulmonary embolism's- blood clots in the lungs.

In addition I've had many other side effects including: little to no sex drive, severe dryness down below (kind of causes problems in the bedroom...), slight vision problems (I usually have near perfect vision, now I often feel like my vision is blurry), odd colored periods (brownish colored), sticky mucusy periods, a very sharp yet dull and uncomfortable pain in my right breast (at least once a month), frequent Urinary Tract Infections, mood swings (had a bad one this morning, threw a fit because my hair took forever to dry- so trivial, right?), severe melasma (hyperpigmentation) on my upper forehead and the top of both cheekbones, and last but certainly not least very low energy.

I actually have a follow-up appt this afternoon with my Dr. I am going to ask him about other options for birth control. Thank you to all of you for writing about your symptoms! Your comments have really helped! Good luck to all of you!

As I read these posts I want to S C R E A M! This drug is like a slow death from Arsenic. If your Memory is impaired, it should be. It's listed as one of the side affects right inside the pamphlet that the Pharmacist gets. I have a Pharmacist friend and she read me, muscle pain, joint pain, muscle twitching and on and on. It's poison for sure and anyone on it should get off it ASAP. My husband's been off for one year next week and he still experiences mental sluggishness and cognitive deficits. So much so, he's retired because he could no longer do his job. It creeps in on you slowly, and insidious. When you start to notice, you're scared to say anything or you don't associate it with this drug. Guess what, the only drug he's ever taken. And, oh yeah, lead to depression. This is a centrally active Ace Inhibitor that cross the blood brain barrier and is literally poisoning you. Actually, there is a derivative from a Brazilian Pit Viper. Synthetic or not, it's poison. Get off people, get off. It will eventually affect your memory more and more until you resemble some form of dementia. Maybe that's why so many people are sitting in Nursing Homes with full blow dementia. The disease that caused it are the DRUGS you're taking.
Get off.

Wow, I was amazed to find this site! and glad I did. I went to my doctor about 3 months ago, and I had some reflux coming up and he prescribed me the omeprazole. I didn't do any research on the drug and thought it was just a stronger version of tums or rolaids because I've never had to deal with this before. Well, I started on the Omeprazole and I felt like I was in another world. After I started taking it, I honestly feel many other things have happened, such as after I would eat, I couldn't breathe! It's not that I felt the food was getting stuck, but was moving slower or something and I couldn't take air through my nose or mouth...not once did I blame it on this meds...anyhow, My neck started hurting VERY bad! I thought it was just stress....next, my memory feels like it's really slacking and I'm only 38. I can't concentrate. So, I ended up in the ER and was having very bad chest pains...thought it was a heart attack, but everything turned out to be ok and they said I had GERD. They prescribed me Nexium. That's when the true hell began. The first day wasn't bad,but a lot of gas and chest pain, along with the shortness of breath continuing. By day 2 on nexium, I was having severe, and I mean severe anxiety and panic attacks...I ended back up at the ER, again, they said everything was ok and they gave me ranitidine to take too. If I'm not mistaken, nexium and prilosec are almost the same thing? Tonight was the worst of my life.....my panic attacks were horrible, felt like something was stuck in my throat, my neck hurts so bad and my mouth was so dry I couldn't even spit, I was so dizzy I couldn't walk, my ears were cramping from the anxiety and my eyes were blurry...I honestly feel crazy. I have taken prilosec on and off for 3 months, and now I know why my anxiety was so bad for so long, but the nexium topped it off. I heard that 40 mg of prilosec is actually 20 mg of nexium....this drug is BAD and I will never take it again. I will try the apple cider vinegar method w/ some honey. My grandparents swore by it and just start watching what Im eating. I heard its 72 hours before this crap gets out of your system..I can't wait!

I've been taking Lisinopril now for almost 7 yrs yrs. Over those 7 yr's, I've became a totally different person, & almost lost my family because of it. I became angry, more depressed over physical pain I've had since the age of 11, when I had a disease that totally messed up my body, having both legs amputated. "How do I know it was this drug?" Someone might be asking... Because finally, after arguing, trying to convince my doctor, "Lisinopril is causing all my personality changes", & getting put on other anti-depressants (which is a whole different CessPool for a later time), making me suicidal.. well, I've had enough, so I went off Lisinopril.. and GUESS WHAT? I was right! Its the third day without it, & I'm my old self again. Some people might not be happy, but TOO Damn bad for them!

Along with the personality changes, I could hardly move from my office chair, when I got to it. I had no motivation, no strength, & OH yeah.. I lost the ability to have bowl movements. let me rephrase that.. I lost the ability to push.. I hope everyone gets what I mean. BM discussions don't go over well here in America. That ability came back on the second day without lisinopril. My memory was totally trashed. Its slowly getting better. The left side of my face has been swollen for some time now, & my doctor says, "doesn't know why.".. I do.. that seems to be getting better too. ITS AMAZING what the FDA lets drug companies do to us!

And I saw a post someone here, that was asking, "Why the FDA lets drug companies kill us off, one by one." (I did a little editing of the quote, but its close). They get away with, knocking us off, for a very simple reason. Because they grease the palms of our elected officials with piles of $$$$$$ throughout the year, so they (Elected officials) will let them (Drug Companies) have free rein to do what the heck they want, & put out the garbage they do.. & not be prosecuted by our laws. They also pay them (elected ones) to keep them (Drug pigs) king of the hill, & not let companies selling Natural herbs, & others like them, from marketing their products in competition with the drug kings here in the USA. They're nothing more then a Mafia.. if that word's to harsh for anyone, then try Kingpins of low life SOB's. Does that work?

wow- glad I found you guys! I'm female, 54, thin, healthy, have always exercised and watched my diet. cholesterol went up to 280 a couple of yrs ago- tried more diet/exercise but it only came down to 250, so since then have tried 4 low-dose (40 mg) statins (crestor, lipitor, zocor, and now pravastatin), all of which after 2-6 months made me feel like I was jumping out of my skin and caused chest pain and palpitations that stopped almost immediately when I discontinued them. Also, I've always fallen asleep quickly and now take an hour or more, and recently my fingers have started falling asleep/tingling. I'm stopping the pravastatin today! Maybe 250 isn't so bad, if this is the alternative. Does anyone have any remedies to suggest besides low fat/low sugar diet? I just read that we should avoid reduced-fat milks (I drink 1%) because they contain oxydized cholesterol, which irritates the artery wall.

I've been taking Lisinopril for about three months and wonder if this could be causing my anger. Before this medication I was definitely not a angry person but lately even the smallest things set me off. Has anyone else experienced this type of side effect from this medication? It has definitely regulated my blood pressure maintaining at 120/80

Thanks,
M.

I have been taking Ambien CR for 2 months - almost nightly. I think it does help me sleep. Or at least if I don't sleep, I don't remember not sleeping. I do wake up the morning after with headaches. I have a lot of headaches anyway... so that is not that bothersome to me, unless they get to the migraine point. I feel like it affects my memory the next day. Also for about 2-3 hours after taking it, my husband and son say that I am very talkative (which I don't remember) I have had 15 min conversations with my son and not remember. I have sent text messages and not remember. I have not been told that I have done anything else. But that is concerning to me. If I didn't have any other options for sleep meds, I probably would stick to it, but I am going to try something else that has less side effects.

**I found something that helps the foggy head, forgetfulness, short term memory, and sleepiness that comes with taking Lamictal!!**

I want to pass this along , because it has helped me SO much. I was diagnosed bipolar II recently and was put on Lamictal. I'm a writer, so my biggest concern was being able to find the words I need and having the concentration for my work, but suddenly I lost my ability to string words together when speaking OR writing. The words weren't even close to coming to me. I felt like I was sleepwalking half the time, along with other symptoms, but the bouts of spacehead were hardest to take. I felt pretty desperate and kept researching until I came across a post on a message board that claimed to have the answer.

If you can manage, do not take Lamictal at night. The following is so simple that it might seem strange that it works (it did to me):

All you have to do is set your alarm for a half hour to an hour before you would normally get up. Then take your Lamictal and go back to sleep for a half hour to an hour (it takes a little practice to get used to this morning routine at first, but it's totally worth it). For some reason, it's ESSENTIAL that you do go back to sleep for that short period and do not just rest with your eyes closed until it's time to get up.

I tried this, not really expecting anything from it, but on the very first day it seemed that at least 85 percent of the foggy-head was gone. Just gone. It has continued to work every day that I have managed to do it, and when I don't do it, the foggyhead is back again with a vengeance. I finally feel great, as if the medicine is doing exactly what it's supposed to.

Taking Lamictal at night (like doctors often recommend) can make the fogginess worse than any other time. The person who posted about this originally said he told his psychiatrist about his experience, and the psychiatrist told his other patients on Lamictal to try it. It worked for them too.

I hope this is helpful to others as much as it is to me, though I know everyone's body and brain are different, so it's possible that it won't work for everyone. I do hope if it works for you that you'll spread the word, because this is such a debilitating side effect.

Best wishes to you all.

After reading these posts I am more confused than before, because my experience is so far very different. I was diagnosed with DVT about two weeks ago and now take Coumadin daily; the Lovenox injections have been discontinued. The reason I'm so confused is I now feel the best I have in 5 (five) years.

Before being placed on the anti-coagulants I had memory and concentration issues that were progressively getting worse and greatly affecting my job, and had daily headaches. I had joint pain that made it difficult to get up after sitting for awhile; they felt constantly inflamed. I felt fatigued all the time and my muscles hurt like I had really pushed them; I just didn't have any strength, and had muscle cramps. I was constantly yawning and found my jaws hurt from clinching my teeth, subconsciously trying not to yawn. I was extremely sensitive to physical touch, even hugs hurt. I also felt extremely depressed and cried almost daily. My lips and left cheek tingled, as well as other parts of my body. Plus I would get the feeling of sudden pressure in my head (different from a headache) like it was going to pop off, and I my eyes didn't seem to track what I looking at and had difficulty in remembering or comprehending what I just read.

About 6 (six) days after starting treatment it completely changed and these symptoms are essentially gone. I have talked with my doctor and pharmacist and they are baffled. I am concerned this change, while welcomed, may indicate an underlying condition that is not yet diagnosed. Has anyone ever heard of such an impact from starting Coumadin treatment?

I have been on Diovan for 11 years. Most of those years, I believe the dosage was 80 mg. About 2 years ago my doctor increased my dosage to 160 and again up to 320. I am also on medication for Diabetes and High Cholesterol. I believe my doctor was over medicating me because I started to experience many different side effects. As a result, I never ended up taking the full dosage of Diovan until October 2008. He also had me on two other medications for High Blood Pressure. Within two days, I felt like I was so fatigued I couldn't move. And my blood pressure wasn't all that low either. My wife and I looked at the side effects accompanying the medications and we concluded I should stop taking one of the medications. A few months later, my doctor added another med to the list. I didn't mind this one and the dosage was low.

In any case, between the 320 mg of Diovan and 80 mg of Atenol I was feeling constantly tired. Getting up in the morning, I felt like someone had given me a heavy tranquilizer. Now I have complained about that feeling for a few years now but never thought it was medicine related until the effects worsened. Then, once I was up, I used to feel good all day long but now I was feeling drugged all day long. Driving the car, I felt tired and questioned if I should even be driving a car. But I had to drive to work. At work, I had trouble concentrating, I was so tired.

My memory was gone. It was like I had a full blown case of Autheimers which came on in a period of about 3 months. I couldn't think straight or remember anything.

Finally, the effects got really scary. My wife and I both have a tendency to snore at times. Since we are getting older, we are developing allergies which makes us snore at night. For my wife, her problems are when she wakes up in the middle of the night and I am snoring so bad she can not fall back to sleep. For me, her snoring is a problem when I first go to bed. In the past, I would try shaking the bed hoping she would stir just enough to move and stop snoring. I really didn't want to wake her up fully to get her to stop. This routine of shaking the bed would go on for about 20 minutes or so. Well, on this one particular night, after about 2 minutes, I got this urge or desire to put both of my hands on her back push with Superman strength so she would fly out of the bed and on to the floor. This bothered me because I do not normally think this way or get this violent.

The next day, I was in a meeting at work. I am not sure what happened but I could tell my mind was going some where scary. I was convinced that I was becoming psychotic! That night, I layed in bed deciding that I was going to stop the medications since I believed they were causing these psychotic thoughts. But I also made up my mind, if the thoughts continued, I was going to have myself committed rather than wait until I hurt someone. Stopping the medication meant gradually cutting back on the dosage that I was taking. I cut the Atenol in half and only took half and it worked. The next day I felt better. But gradually the fatigue would come back, just not the psychotic thoughts. To make a long story short, I kept reducing my meds until I was only taking about 80 mg of the Diovan.

There has been concern that I am heading for Kidney failure so I was sent to a Urologist. He is concerned over my high blood pressure and decided to put me on Diovan HCT 320/45 mg. I figured he didn't grasp my concern about that being too much medication. Oh, the HCT I was on then taken off and now put on because I have been experiencing significant swelling of the ankles, feet and legs.

My doctor visit was June 2, 2009 and today is July17, 2009. I have been experiencing many moments of extreme dizziness. My wife and I were in a store when I bent over to pick something up and near fell. I stood up and a few minutes later, I was conscious of myself staggering from dizziness. Last weekend, we went to a store and I didn't feel right as we head inside. We got in and the store got very bright, colors seemed to lighten and it felt like I was passing out. It was like I was standing on a cliff waiting to fall off. The brightness did not go away but I also never passed out. Also, I had been having lots of headaches since going back to this heavy amount of Diovan. Currently, the last couple of days, I am having trouble focusing. It is as if my eyes are good but my head is somehow effecting my eyesight. Yesterday, I kept having these moments where it was like I was being hit in the head. I kept seeing stars. Oh, did I mention I am only 52 years old? Too young in my opinion to be chalking this up to old age.

My next appointment is August 24th. I am hoping I can make it to that appointment. I think this is too much medication and I am afraid if I don't get it cut back soon, it will kill me.

I am not against Diovan but I do think there is a point where one can be prescribed too high a dosage. And I am at that point. Oh and my blood pressure in my opinion isn't that great for all of this medication. I am concerned that something is causing the high blood pressure and rather than OD'ing me on medications, the doctors should be helping me determine why my blood pressure is so high. Also, I am now on this kick to see whether I can lower my blood pressure through certain foods and diet. Where is doctor Oz when you need him?

I was placed on Topamax, off label, for suspected bipolar illness (now disproven). My cognition, word finding abilities, memory has been so adversely affected that I am now on disability. I had 5 kidney stones due to the development of Renal Tubular Acidosis, nearing renal failure (a side effect doctors don't warn patients about). This in turn led to osteomalacia, softening of the bones, only discovered after I broke all three major bones in my leg and snapped off my foot stepping off the lowest seat of a bleecher. I've suffered tingling in arms, hands, legs & feet (nerve damage), lesions in the brain, muscle spasms, heat & cold intolerance, insomnia etc... Although I lost weight, I gained it back (then some) as soon as I reduced the dosage of 800 mgs. Upon stopping the drug to save my kidneys, thus my life, my kidney function returned to almost normal within a few months, although there is residual damage. All other side affects remain two years later. Losing weight is not worth dying! Beware of this drug being used off label! I would never trust this drug!

after taking ambien CR for a few months with no real side effects all of a sudden I started doing bizarre things with very little memory of doing them, I walked around the house in the middle of the night in a blackout I cleaned things, ate things, made phone calls to friends and they couldn't understand me because I was slurring my words, My family said I was acting very drunk swaying back and forth and not making any sense. I"ve driven places and don't remember driving and that is enough to make you say o.k. something is wrong with this medication

Ladies,

I hope you don’t mind a male posting on this forum but I do have a reason for doing so. I am a Coroner’s Officer in England. I will not at this time disclose whereexactly I am based as I need to protect the identity of the family. I would however like to use you as a sounding board in the hope that you can help me, help the family and perhaps, just perhaps, I can help you.

Sadly I am dealing with a suicide. The lady in question, who has taken her own life is in her 40’s, married and has children (all over 11 years). The lady has no history what so ever of any form of depression during her life.

The lady has described her life as being perfect with a family that loves her and who she loves in return and as the Investigator I believe she is truthful in that comment. She states she has been extremely happy until last week. She makes comments of - I am just very ill, cannot sleep, feel dizzy, cannot concentrate, sometimes lose my vision, feel sick all the time and sweat at night. She cannot understand, but it makes her feel bad. I am not myself, something has made me ill which means I can’t be my normal positive, active busy self. I can’t bring myself to do anything that I normally love, like gardening, cooking etc. I am losing my memory badly going fuzzy in the head.

Her final comment, which is the one that has prompted me to post on this forum (with the permission of the family) is ‘I just don’t understand this – I’m so sorry . I can’t understand myself or what is wrong with me or what I’m doing so sorry. Just remember I’m not myself somebody else has taken over – I don’t know if it is all the anti-histamine pills that has mixed up my chemical balance along with the Mirena coil or is it just me’.

The mention of the Mirena coil has therefore prompted me to investigate it. I am not, by any means suggesting that this is responsible but it would be wrong of me to discount it after having read the posts on this forum and other places on the Internet.

The lady in question had the coil inserted in 2004/5 and it would appear that there were no problems or side effects reported.

I am therefore looking for some help from you. Some comments on what I have posted etc. Some advice on where to obtain expert advice (although I am trying some avenues of my own).

I may also ask, depending on what help you can give me if you would be willing to identify yourself to me.

Thank you

P.