Migraine sufferer symptoms and conditions

I was prescribed 25 mg Metoprolol-XL for irregular rapid HR episodes and slightly increased BP (after all the tests to rule out heart disease). It did the job, but I began to suffer with insomnia (a common side effect). So for the last month and a half, I've been only taking half the dose (I made sure that it was the type of tablet that was ok to break...it is, but they do caution you not to chew or crush it). No more insomnia, and the irregular HR has not returned, BP remains normal.
I figured out that the cause of the palpitations etc. was delayed anxiety attacks from a recurring family situation (the delay made it hard to link the cause and effect until I started journaling). Knowing that was the beginning of being able to better cope with the situation, so I thought I would be weaning myself off the medicine. However, I also am a migraine-sufferer and realized that I have not had to take an Imitrex since starting the metoprolol (3 months!). I used to get 4-5 migraines a month...now I may get none, one, or two and none so bad that one Ibuporfen can't handle it. Not so sure I want to stop taking it now.
New problem: Since cutting the dose, I find that any exposure to warm environment or to mild exercise, where I would normally only sweat mildly, if at all, now my scalp sweats profoundly, so much so that sweat runs rivers down my back, my chest, into my eyes and ears. The rest of me only sweats like I normally ever did. Is this because I decreased my dose...will it last forever? I did read that one should not go off this stuff cold turkey and that one of the things that would happen if you did could be excessive sweating. All I did was go from 25mg to 12.5 mg! What if I go off it completely...what am I in for??

I thought I researched this product thoroughly, I even worked with a lady who had one inserted and she said she was just fine. My specialist said it was "new improved technology, the best on the market". So I had it inserted which apart from being poked and prodded which is never nice, and him pinching my skin, was reasonably ok.

I was fine for a long time, but after a year or so I found that my quality of life was very low. I am 40 years old so put some of it down to that, I have a one year old so put some of the tiredness down to that, but whatever I did I never felt better. The iron levels in my blood are high and all other checks, i.e. thyroid, are fine so why was I suffering from:

Nausea and Weight Loss (the weight loss is the only good part)
Extreme Tiredness
Thrush
Dry Itchy Skin
Dizziness and Vertigo
Facial and Scalp Breakouts
Greasy Hair
Depression
Anxiety
Headaches and Migraines (I am a migraine sufferer anyway)
Sore Itchy Eyes
Spotting for Two Weeks (6 months of the year!).

I didn't have any problems with my periods before, I had just decided to have the Mirena inserted to avoid further pregnancies.

I hadn't been on any type of contraceptive pill since I was 22 years old and I now remember why I stopped taking the pill in the first place.

Some days I felt great, but would then feel like I'd hit a brick wall about 4pm so would have a very strong coffee to get me through the evening. I'd then sleep like a log and wake up feeling hungover even if I hadn't drank any alcohol the night before (I may as well have and I probably would have felt better).

I then decided to google 'Mirena Side Effects' and found this webpage. I discovered that thousands of women around the world are having the same problem. I got on the phone instantly and made an appointment with my Doctor to have it removed.

I had the Mirena removed last Tuesday, and within a day I wasn't so tired, I didn't need a coffee to get me through the day, or a nap, and my eyes felt better. It's now been five days and I feel much calmer (no anxiety). I'm still tired from running around after my daughter but not like before the removal. I have been having crazy dreams but I assume that is just my body adjusting.

It appears that the Mirena device works for some people, but just not me.

If you feel this way, then have it removed - your quality of life with worth so much more.

Oh, and I can drink wine now and not get migraines - yay!

I was given a 2 Kenalog shots in my lower back to treat a pain in my sacroiliac joint, which refers to the front of my leg/groin area. My doctor barely examined me, I was sent for no scans or other diagnostics. He said that the shots should bring down the swelling. They didn't work at all and yesterday, a couple of months later I felt a significant indentation on my back - precisely at the injection site (just where my lower back meets the top of my buttock). I have also suffered seven weeks with no period, coupled with nausea (thanks for the pregnancy scare!) then very heavy periods. I am a migraine sufferer and my migraines have increased in intensity. I also have constant, painful eczema, where before it was sporadic and light.

I am not sure how many side effects can be attributed to the injection - but the indentation at least is a definite. I live in the UK - I wondered if there are any other Brits here who have had the injection, or anyone generally who had it in the same place as me - I'm worried about what happens from hereon in. Can it affect my mobility? The original problem (still undiagnosed, but after a year of begging I am being sent to a hospital next week - to a Rheumatologist - is that even the correct field of expertise?) causes me huge amounts of pain anyway.

I also have a great number of the conditions the doctor is supposed to make sure that you don't have - why did he just "do it anyway?" In the UK it is difficult to bring any kind of action against a doctor >:-(

I'm relieved to find this board - best wishes to you all :-)

I am a 41 year old female in DENIAL about my high blood pressure as I don't drink, smoke and I am a fitness instructor. My BP averaged 145-95 daily. The DR explained TOPROL was designed for someone like me. The med will not be fighting my life style, just the blood pressure. There are no life style changes I can make, it's my dads fault! It's my 4th day, the first being the worst. I had a terrible headache and was wiped out. I am a bit tired today, but not too bad. Better today than yesterday! My BP is 114-71 on average. I have been a migraine sufferer my whole life, the last 3 years being the worst. I'm looking for brighter days! Hang in there. More women die from Heart disease than breast cancer.

I have been on Loestrin 24 for 2 years!! And I am finally getting off... and so happy to find this site! I have had to be put on Topamax because my migraines became so bad, which helped my weight gain (that I attributed to my own depression that I thought was my own fault!) I didn't even realize bc could cause depression but it all makes sense! I came on here to find out if Loestrin has been the cause of my SEVERE HAIR LOSS over the past year and a half! When I started taking it, I was also going through a stressful situation and thought that was the cause, but have now realized that my life is back to normal that something else must be causing it. I tried to get my Dr. to take me off of Loestrin about a year ago due to the EXTREME nausea, dizziness, headaches and fatigue that it was causing and he decided that I should just be put on Topamax because I was just a Migraine sufferer! What a nightmare. I can't wait to switch tomorrow!!

I am 30 years old and have been put on Depo Lupron after a laproscopy to help with endometriosis. I am 2 months into a 6 month course (one shot every 3 months) of Depo Lupron and my life has drastically changed. I started feeling life altering hot flashes and night sweats two days after the first shot and nearly drown myself in sweat 24 hours a day. I experienced a little postpardum depression after giving birth 6 years ago but have found myself sunk into a sinking hole of depression and anger like I've never felt before. I bawl at McDonald's commercials and become enraged if the dishwasher isn't loaded properly! I am ecstatic one minute and severely depressed the next. I have even had thought of suicide since being on this shot. I am normally a very outgoing, athletic, cheerful, happy person - but since taking this shot, I have become a stanger in my own head. I tell my family all the time that I need to "go stick my head in the freezer" to cool off because of the horrific hot flashes. I have to carry a handheld fan with me 24 hours a day and sleep with ice packs to keep cool. Since the shot started 2 months ago, I have lost all sexual drive, am thoroughly exhausted by 9am and find myself crying at my desk at work by late afternoon because I am so tired. My family thinks I am going crazy and I've never fought more with my husband. My daughter has gone to grandma's for awhile because I'm just so tired and irritable that I feel like an awful mother. Migraines have also come full circle since the onset of the shot as well as blurred vision and shaky hands. I'm a little achy throughout the as well. I know that everyone responds to medication differently, but I'm finding a lot of people with the same side effects as myself and have to wonder why the doctors don't warn patients about these types of problems before prescribing medications such as Depo Lupron. I don't think I'll be going back for the second shot. Could it get any worse?

I was given Metoprolol, a generic for Toprol-XL several months ago, for high blood pressure. It was prescribed after I was determined to be allergic to Lisinopril. ( It caused a cough that lasted 3 months; I sounded like a TB patient.) Anyway, I have been taking Effexor for years, for anxiety attacks. Now that I take Metoprolol along with the Effexor, I am so tired and drained all the time, that I am contemplating quiting work. I go to the grocery, come home and lie down. I can't seem to have energy to breath correctly. My Dr. won't believe that this has anything to do with meds. I have now developed blood and mucous in my stools, diarrhea, and very urgent BMs. This all started after taking these two meds in combination for about 4 months.

I can't believe all of these posts, wow. I was starting to feel as though I was alone with all of the symptoms I was experiencing. I started this drug 2 1/2 weeks ago at 25mg am/pm and am currently up to 75mg am/am. I have really bad chest pain/tightness and mild shortness of breath. As someone else had mentioned, pop is enhanced not dulled, seems as though its like pins on my tongue. I have been forgetting words but not too bad, just for a couple of seconds. The anxiety is the worst, sometimes I lay in bed and the chest pain will increase and I get so axious it feels as though I'm going to die. I went to the ER last night but they did an EKG and told me my heart was fine that the chest pain most likely was not related to my heart. (I'm a 22 year old male and have never had problems with my heart) These chest pains only started after starting this drug. I'm ready to try something else. This was the first drug I was put on for my seizures, my doctor said it could possibly help the seizures/headaches/weight. These side effects are just too much.

I started taking 100 mg. per day of Topamax a month ago and have ok results, I still have a dull headache everyday but it doesn't turn to a migraine but I have no desire for food and carbonated drinks taste flat and it has changed my mood also. I would like to stop taking it.

I have been a migraine sufferer for over 13 years and have run the gammut of medications to prevent and deal with them. My mother took Topamax a couple of years ago with disastrous results. I didn't realize, but I guess she was so loopy and forgetful that it was enough to cause my grandmother and stepfather to perfom an "intervention" to get her off of it. So, here I am a couple years later starting it myself, wondering if the side effects are worth the trade off. I'll be honest and say that I love Coke. I mean, loved. Carbonated drinks of all ethnicities taste like slimy metal now. How disappointing. And considering that if I went a day without drinking a Coke, I would get a wicked migraine, I've resorted to putting Crystal Light Energy (Wild Strawberry) in my water to give me the needed caffeine.

I've also noted tingling in my face, kinda like numbness. Nothing that is earth-shattering, but noticeable. I get dizzy a lot. I've also lost about 5 lbs since starting the medicine. And today, I could not find the word "prescription" in my mental warehouse. Not a difficult word on a normal day. I've only been on Topamax for a week though. I'm going to give it a good month to see if the side effects dissipate. But if I get any stupider, I'm going to have to go another route.

I've been on Topamax (for seizures) for almost 2 years now, gradually increasing my dosage from 150 mg/day to 400 mg/day when I learned that 150mg is a migraine sufferer's dosage and not a Epilepsy dosage. I mention that because at 150mg, the side effects were present, but tolerable. I had the tingling fingers, eye twitching that was only behind my right eye (seems everyone only has it behind their right eye...why is that?), I can't find the right words in conversation, memory loss , constant sleepiness, backaches, depression, etc. At 400mg, I was an emotional wreck...I could not handle my emotions anymore. I would cry hysterically when talking for no reason, I couldn't concentrate on my work as an analyst, I had to read and re-read instructions in order to understand them, and sometimes read them out loud....and this is the kicker...sometimes when I'm buying something and at the check-out, it'll take forever to do something as simple to count out change. I have given the wrong change to cashiers a few times and then told them something to cover up my embarrassment like "Oh, I thought I gave you a quarter!", when in all actuality, I thought I gave them the correct change.
I feel like a moron pretty much all of the time. I used to pride myself on my intelligence and speaking ability but on Topamax, that is seriously diminished.
I don't know if this is related, but because of my inability to concentrate, I lost my job in Nov. '06. I thought I lost my insurance too, so I made the decision to stop my seizure meds, thinking that I was "cured". Well, I had another seizure in Jan '07 and am back on Topamax...depressed, twitching eye, the whole gamut. But you know what? The entire month of January, before my seizure...before Topamax...was the happiest I've been in sooo long. It's not worth losing a few pounds for.

I have been on imitrex and atenolol for a week. It has caused pain in the right side of my neck that runs through my right arm.I'm trying to stop my headaches, not cause more pain. Ithink the medication is unsafe if you have to use a low dose blood preasure medicine with it. Imitrex, and it's counterparts shuold be pulled from the market! It all stems from doctors trying not to prescribe narcotic type medication for headaches.