Daily headaches symptoms and conditions

I've been on Topamax for about a month now for daily headaches/migraines with 50mg/day and will be moving up to 100mg/day in the next few weeks. So far I have noticed the tingly hands and the nausea but the worst is the dry lips and how every beverage tastes either flat or odd. The only thing that tastes good is water and I can't get enough of it because I am always thirsty. My urine has turned a bright yellow, which I noticed no one else has reported so I'm a little concerned about that. However the headaches and migraines due seem to be improving so I'm keeping my fingers crossed!

I have had my Mirena out for almost three months now and couldn't be happier with the results that I have had. I do not get the horrible daily headaches anymore and my skin has cleared up. I was having gallbladder attacks due to the rapid weight gain that I had with stained. Now that I have started to lose the weight, I no longer have issues with my gallbladder. The weight is coming off really fast, I have lost 20 pounds in two months. Finally, I feel that I am returning to my old self. I am much happier and know for a fact that it has to do with having the Mirena taken out. I think that if anyone is suffering with any side effects from the Mirena, they should have it removed.

Like almost everyone else on here, I seem to be having a really bad reaction to this birth control pill! I started taking it shortly after I gave birth to my third baby because there is absolutely no way I can handle any more kids right now! Soon after I started taking it I noticed a lot of weird things going on with my body. Just walking up the stairs gets me out of breath and causes my heart to beat rapidly. Sometimes it starts to beat like this just from driving! I am also constantly nauseous (like morning sickness nauseous), have daily headaches, have no sex drive, and have acne! Up until I started taking Yasmin my skin was like porcelain and I could literally count the number of zits I got on one hand. Now my face looks like a freakin pizza!

I also go through phases of being really depressed and really angry. These mood swings are even worse than the ones I had during pregnancy! I have 3 healthy kids, a beautiful home, an amazing husband, wonderful friends...but I still cry all the time and want to die. I know that I am extremely blessed so there is absolutely no excuse for me to be feeling this way!

At the time I had passed all these things off as my hormones trying to adjust after being pregnant, even though I have never had any of these problems before when I had my other two babies. I also noticed that this was the first pregnancy where I wasn't able to shed any of my baby weight. It seemed no amount of diet or exercise could get it off, whereas with my 2 other pregnancies all I had to do was eat healthy and use the treadmill everyday and was back to my normal size before I knew it!

Now I realize that none of these things are due to having my baby at all but due to Yasmin! However, I have never used birth control pills before so this is my first experience with them. Is it possible that this is just a brand that reacts badly with me, or do all brands have side effects like this? I'm trying to decide if I should switch to a different pill or just stop taking any all together and just be extra careful with my husband! Regardless, I will definitely no longer be taking Yasmin!

I have great experience with this pill unlike others. Just like with any pill you can get melasma which is dark spots on your skin. I got few but from my previous pill witch was Yaz (it was terrible; daily headaches, no periods which is normal but kept buying pregnancy tests because of it, terrible breast soreness, vaginal dryness, zero sex drive). With this pill, at the beginning of taking this pill, first few days I felt little nauseous but nothing that bothered me. First month I had some breakthrough bleeding but that was gone after a month. No headaches, slight breast increase which I am not complaining about (it can happen in pills with higher estrogen). No breast soreness, no weight gain, no darkening of the skin so far, sex drive is normal. The only negative, this pill costs $75.

I have been on NuvaRing for a little over a month now and I'm going to take it out probably today. I have been extremely nausea. I feel like I did when I was pregnant with my daughter. It's horrible. I kept taking pregnancy test because I really thought I was pregnant. Thankfully I'm not but this is a horrible side effect from the NuvaRing. I'm also experiencing daily headaches and occasional migraines. I have been very tired and have no energy or sex drive. I would never recommend this to anyone

I am finally getting mine out on Tuesday and I can honestly say I've not been this excited for ages!! I have suffered nausea, extreme emotional outbursts, terrible, daily headaches, increased appetite and weight gain, the list is endless. I have come close to losing my relationship too Enough is enough, just so relieved I'm not alone, thought I was going mad! Good luck to all fellow sufferers M.

Hi I posted this on the Coumadin site when I should have been here,

I am a 66 year old female and up to a year ago I felt 20 years younger now I feel 20 years older.

I fell and broke my hip June '08. Had a hip replacement and developed a blood clot (DVT) in my left leg.

They put me on Coumadin and when that didn’t do the job they added Lovanox (another blood thinner requiring shots in the stomach).

Not only has they not helped but my blood clot is growing.

My symptoms:
daily headaches, debilitating leg pain (the pain is so bad that it is crippling me), fatigue (an overwhelming feeling of tiredness, I set down for a few minutes and wake up hours later.), loss my concentration (trouble doing simple crosswords), can’t study simple directions, numbness in toes and hands. I can go on.

And the doctors? “It’s all in my head. It can’t be the blood thinners.”

I am going to copy your blogs and take them to my doctor and demand something be done.

Thanks again to this site and all of you. I was beginning to think there was something wrong with my mind.

I'm not crazy!!!! Thank you..

I fell and broke my hip June '08. Had a hip replacement and developed a blood clot (DVT) in my left leg.

They put me on Coumadin and when that didn’t do the job they added Lovanox (another blood thinner requiring shots in the stomach).

Not only has they not helped but my blood clot is growing.

My symptoms:
daily headaches, debilitating leg pain (the pain is so bad that it is crippling me), fatigue (an overwhelming feeling of tiredness, I set down for a few minutes and wake up hours later.), loss my concentration (trouble doing simple crosswords), can’t study simple directions, numbness in toes and hands. I can go on.

And the doctors? “It’s all in my head. It can’t be the blood thinners.”

I am going to copy your blogs and take them to my doctor and demand something be done.

Thanks again to this site and all of you. I was beginning to think there was something wrong with my mind.

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?

Just had the mirena inserted on July 10. I have been getting daily headaches, nauseated, and extremely tender in the pelvic/ovary region, I think it has also made me seem moody. I am calling on Monday to see about taking it out.

My 11 year old son started singular in March of 2009 for exercise induced asthma. Within weeks he started having symptoms of heartburn - which he had never had before. I brought him back into the dr. mid June- they said wasn't related to singulair and actually increased his does from 5 mg to 10 mg. Since increasing his does, he started experiencing, daily headaches, stomach pain, leg cramps, night sweats w/ shaking & overall FEAR. Last night he was in tears - he kept saying there is something seriously wrong with me - I can't stand feeling this way he was afraid he was going to die and didn't want to go to sleep.

Last night I did my own research and found this board. THANK GOD!
He didn't take his singulair last night & he never will again.

I called his dr. this morning to tell them I think he is having negative side effects from singulair. They actually told he it was "HIGHLY UNLIKELY" his symptoms were related to singulair and NOT TO STOP USING IT. They instead said I should start giving him pepcid. I told them he had stopped it - for good and that we need a plan B for is exercise induced asthma. Looks like my plan B is finding a new Dr. that isn't in bed with Merck.

Has anyone had any experience with a NATURAL approch to controlling exercise induced asthma?

I was taking Topamax for about 4 years for chronic/daily migraines. It helped tremendously after I had taken almost everything else with no success. Then I had an episode where I ended up with 5 kidney stones. They passed but my neurologist wanted me off the Topamax in case that was the cause of them. I went off and my headaches came back with a vengeance. I had them daily until I begged my primary care doctor to put me back on Topamax. I honestly would rather have stones than daily headaches. I am a mother to four and have a husband and a job. I can't live with daily migraines. After being back on it for about two weeks the headaches have disappeared. I take 200 mg twice a day. I do have memory loss and loss of words big time. It is VERY frustrating. I feel stupid. But I can live with that. I have tingling cheeks , lips and hands. I'm sensitive to sun and have to wear my sunglasses a lot more now. I now talk in my sleep- a little nervous about that :) I lost weight last time around but haven't yet this time. I am very happy, not sure if that is the RX or just me reacting to not having headaches. I guess you have to weight the side effects with the benefits. The choice is ultimately up to you. Good luck everyone!

I had the Mirena IUD inserted on April 7th after 13 yrs of being on the pill, the last 3 of which was continuous use and only 4 periods a year. I had been dealing with chronic daily headaches since Aug 2007 and had finally found a wonderful headache specialist that of instead of prescribing more and ore meds and upping doses did lots of bloodwork and tests and found that my hormone levels were messed up, specifically I had nonexistent testosterone levels caused by all the estrogen in my pill. So he took me off the bcp and I choose the IUD thinking that that would be the best birth control since I am married with 2 kids, but sure that my family is not done yet, but not ready for that 3rd child just yet.I wanted the paraguard because I was hesitant of the progestin in the Mirena, as it is the same in the Levlite bcp and had caused me to have severe anger mood swings about 9 yrs and I had to go off of it, but the gyn that I had been seeing had gone on a leave of absence so I consulted with her partner and was told that yes, this would be the best IUD for me because of my history of anemia and that side effects of the Mirena would be localized and I would not experience any mood swings or headaches. So against my better judgement I went with it.
The insertion went fine, had some bad cramping for about 4 hrs later, spotted about 3 days. Then cramped on and off for about 2 weeks. During this time frame I was actually HEADACHE FREE!!! For the 1st time in almost 2 years. Going off the bcp had worked, you cannot imagine my excitement and my whole families, they thought I was going to be me again! Then I started getting mood swings, yelling at them for no reason, getting angry and knowing that what I was doing was wrong and way out in left field but I couldn't stop---- it was reminiscent of my Levlite experience and my hubby freaked out. Said it had to be the IUD. I wasn't sure, but thought maybe so. Then I started getting acne on my chin and jaw and had never in my life, even as a teenager had acne. I also gained 6 lbs. I then started my period, VERY light spotting that lasted 20 days and with came a migraine!! A migraine that won't go away. It started April 26th and I still have it today! I knew then that it was the Mirena. By that time I had found my old gyn-instead of going on leave of absence as they had told her patients, she had actually left to start her own practice, but of course confidentiality agreements wouldn't let her say anything. Luckily I work in a hospital and ran into her in labor in delivery, so I made an appt with her on May 11th for my pap and to have my iud checked and while I was there I told her every side effect I was having and she totally agreed that it was the Mirena and she said that in more than half of women the Mirena hormone is localized, but the rest it causes a full body systemic reaction and I was one of the lucky ones!! She said with my history of migraines and my history with the Levlite that I should have have NEVER, EVER have been advised to get the Mirena. She said to go ahead and do the pap and then reschedule to have it removed since she was busy that day and needed to get to the hospital. So I rescheduled and had it removed on May 20th- 6 weeks, 1 day after having it put in. I am so glad it is gone. The cramping is gone, I am not having mood swings, no new acne flare-ups just trying to deal with getting rid of the ones I had! The headache I still have, but I think it is because my period started 2 days after removal....28 day cycle like clockwork! Maybe when my period ends, the headache will go away. Unless I just have to wait for the Mirena to completely clear out of my system?? Anybody know how long that can take??? Those 2 weeks that were headache free were a godsend and I can't wait till it happens again! In my opinion the Mirena is HELL! For those of you that have gone through similar issues I am sorry and glad that you can understand what I have gone through. For those of you who have one and have had no side effects, you have no idea how lucky you are!!!

I was recently switched from a combo pill (that I have been taking for 12 years) to Nora-BE due to migraines with aura. Since the headaches increase my risk of stroke, as do combo pills - they were required by law to switch me.

Unfortunately, since about two days after switching, I have been having eye twitching, severe headaches, vision loss, cramping etc. The eye/headache problems only start about 1 hour after taking the pill.

I went back to the doctor, who will not switch me back, and suggested going to a neurologist (hard since I just lost my job and insurance), and that I was basically out of luck. She also tried to blame it on pretty much everything other than the pill (allergies, caffeine, stress etc.). Apparently it is better for them for me to have increased risk of stroke from daily headaches (and liver/stomach issues due to heavy intake of pain killers now) than one from combo pills that never caused me any issues. I even offered to sign a waiver, but that did not make them budge a bit.

I understand their liability in the issue, but it is extremely frustrating to have headaches this badly daily, as well as having issues seeing (badly enough I cannot read highway signs). It is to the point where I may have to forgo any sex life with my fiance in order to get off these pills - which won't make him very happy :p. That, or go to another clinic, and go through the whole PAP again, as well as the bill, bleh..

Been taking Topamax since August 2008 for migraines . in November 2008 my doctor upped the dose from 50 mg to 100 mg because I began having daily headaches , even though these weren't migraines . This headache has been CONSTANT for 3 months, right behind my eyes , is with me morning . noon and night along with blurry vision . I have been taking hydrocodone for the pain while I went on a round of doctors visits and tests ...blood work - normal , ct scans -normal . Interestingly , along the way , my OB found an ovarian tumor that was 12cm and made with thyroid tissue of all things so I had surgery to remove my ovary ...but still the headache remains and the awful eye pressure . Also , word recall and math skills have become laughable ...doctor kept saying .you are 43 . maybe you are just getting older . after reading these posts I say I believe that my eye pain and my headache and my sudden stupidness and maybe possibly even the tumor can be attributed to the Topamax ...tonight I start titrating down from 100 mg back to 75 then 50 then OFF because I am not brave enough to go cold turkey ..I am already not sleeping at all since I gave up the ambien last week ( I have decided less pills may equal more health ) but the topamax seems to make me anxious NOT sleepy like it does some people , so I will also start splitting the dose am and pm to see it that helps . I will write back in a week or so with an update . How simple it will be if 30 doctors visits ( at 20.00 each ) plus a cancer specialist for the tumor ..weeks in waiting rooms and hundreds of hours on the internet wondering what was wrong with me could all boil down to ....one little pill. For me , I will go back to working with my migraines if this is the case .......

I am 43 , I have been taking TOPAMAX for 3 yrs for migraines 50mg for 1 1/2yrs and then increased to 100mg. It helped for the first 2yrs but, not now... The side effect have took over my life!! All the routine S/E I have heard you all talk about plus, eye pain and more headaches!! Not migraines but, bad headaches! I thought I was having sinus pain...BUT, it never stopped and was daily for a yr. I could barely work! I am a R.N. and I have researched this drug and, talked to many different doctors...unless, it is for seizures I would NOT take it again!! If it seems to help your migraines, be sure you understand there is a trade off!...and it is NOT good in the long run! I felt like I was going crazy..and started feeling so "old"?
I went cold turkey 4 days ago...eye pain/daily headaches GONE!! I do have a nervous feeling, and do not feel hungry and ...I am sure withdrawal s/s.
I hope the "stupid" feeling will go away soon...feeling more energy already :)
I use to love this med...now I hope I do not have any long term memory effect ect... sorry if I misspelled any words ....the TOPAMAX you know!!LOL!!
Good Luck to you all!

Well how stupid I feel right now! I have only had mirena for a week and already hate it. Although my doctor did warn me on the day I went in that some people spot for a while, I did not know about the tiredness and cramping I would feel. I have had both of those as well as bad pain after intercourse with my husband. I think I will also get this removed. Never again will I get something done to my body that I do not thoroughly research first...at least more than just the official Mirena website. I have also been extremely tired but I guess I didn't even think about this being an effect from the IUD. I am anxious to hear from someone who has already had it removed to see if symptoms went away.

I started at 20mg and it was great, but then doctor said to try 40mg to see if even better, but it wasn't, so back to 20mg. It has been a couple years now. I had to start taking it at night, because I was getting too sleepy while driving to work and back. That made it better. Definitely has helped with emotions, pain in my arm, and small daily headaches. I have gained weight, and can not sit still long-or I get sleepy. I didn't know blurred vision and concentration were side effects, until reading this. I think I may try to go to 10mg. Really, never want to get off of it, because I have lived with IBS my whole life, which is very painful, and makes me have to get to a bathroom quick. Celexa has changed my life in this regard. Now have daily movements that are healthy. No more pain. It has to be the Celexa, because it happened at the same time I started taking it. The doctor says he has had others say it, and it is probably because it calms you down.
Good luck to all of you!

I have taken Advair 250/50 for approximately 7 years. It was a life saver for me. My asthma was out of control. I slept with my albuterol inhaler in my hand at night. Advair was the wonder drug. It worked when nothing else did. I had bouts of depression and weight gain over the years, but nothing really major. I ran out of Advair a few days ago and just hadn't had the chance to get a refill.I had been experiencing daily headaches, and an inability to sleep at night. I felt lethargic and beginning to feel a little depressed. I contributed it to the lack of sleep, but wasn't really sure why I wasn't sleeping. Today while sitting in class (I am a Nursing Student & will graduate in December 2009), I got a horrible cramp in my left leg, then my left arm went numb. I got a little light-headed and my head was busting! My heart rate felt fast, so I had my instructor take my Blood Pressure. It was 164/105. Now my B/P has NEVER been anywhere near this. I went to the ER, had labs done (all normal) and an EKG (perfect). After about 4 hours my B/P went back to 117/78, normal for me. The Dr. had no explanation for what happened or why. My husband came home, got online and found several forums addressing these same symptoms. I have made a decision to talk with my doctor about alternative treatment.

I have had pressure in my ears and daily headaches for about three months now. I was prescribed Singulair by my dr. i took my first dose of this medication yesterday. 23 hours later i had a panic attack. I called the pharmacy about this issue and they told me that it was not likely that this drug caused my panic attack. After reading others experiences i will not be taking Singulair again.

Soon after receiving the first of three Gardasil vaccinations, my daughter started experiencing daily headaches which progressively worsened. Her doctor said that it wasn't likely to be a side effect of Gardasil. Over the next year, she was referred for vision testing and had a CT Scan and MRI to try to diagnose the chronic headaches which had become quite severe and often debilitating. No cause was found. She was given prescription after prescription which didn't help- and often generated additional side effects that made her feel worse. A year later she still has undiagnosed headaches and takes a prescription medication twice per day to lessen the severity of the headaches. Only recently did we find an article relaying the same story- linking the headaches to Gardasil vaccinations. With no health issues prior to the vaccinations, no underlying cause found following many tests, doctor referrals and medications, and the fact that this all started immediately following her first dose of Gardasil, we suspect this is what instigated the headaches.

I had my second Lupron shot this last mid October that lasts, supposedly, 3 months. So I will be 5 months in this mid December and I have to say I was one of the people who was fine with Lupron...up until now. I had and have all of the typical side effects of hot flashes, headaches, memory loss, mental fog, etc. Then I had my first ever migraine a week ago that knocked me on my butt for 2 days. My memory loss and depression are by far, by far, the worst side effect I have experienced. At this point I am concerned my memory problems and mind fog will not go back to normal, which has already adversely affected by daily life. I was one of the people who spoke positive of this injection even after reading all the horror stories but now I am beginning to wonder if they were right on some levels. When reading all the different experiences I would get confused and wouldn't know what to believe. I am not saying I would change things, the jury is still out as to whether the benefits will outweigh the difficulties, but my personal experience and symptoms have been getting worse just in the last few weeks, so that would be between month 4 and 5 on it. I could lead a pretty normal life up until recently and I'm a pretty tough person, I clean houses for a living and work hard with a packed schedule so I am not just stating little symptoms I experience but ones that actually have affected my daily life. Just being honest so you know what to possibly expect, depending on your body's reaction. That is a point to keep in mind, everyone's body reacts differently but if the majority of people are saying the SAME side effects, makes you wonder if there is a consistent pattern.

One thing I will tell you that has helped me is B vitamins regularly in your system and staying as active as possible. Write things down to remind you for the memory issues, don't over-commit to things because of the mental affects-it hits you hard when you can't follow through, and try to watch your sugar intake, which messes with your emotions. Hope this is helpful.
I would love to know from someone who has the same symptoms (which looks like almost everyone who is on it) and who is now off of Lupron for at least a few months, if the symptoms of memory loss and mind fog go away. Is my memory permanently damaged?

I started taking Advair 500/50 on September 8, 2008. I am sitting at my desk, unable to quiet my racing mind and I am jittery, agitated and angry. For the past 2 weeks, I have sobbed constantly, I've gained 10 pounds almost overnight, I have daily headaches and I constantly have thoughts of harming myself. I called my doctor to see if my dosage could be lowered or if I could stop taking it, but I haven't heard back yet. I wake up in pain almost every day, and I feel like an old woman. The first 3 days I took the medicine, I thought it was the magic answer for my asthma since my peak flow readings went drastically up, but I think it was just cooler weather. It's not worth it at all. I'd rather take nebulizer treatments all day.

I have been on Mirena since about March of 08 after I had our son. My Husband was overseas and we wanted something before he got home in June. We hate condoms and I can't ever remember to take the pill, so I decided to get this. Well since I have been on it I have been VERY moody and everyone can notice it. Hubby was the first to say it is probably the Mirena but I was like how can it give me mood swings? I still kind of don't understand how it has, but anyways, I called the doctor to get it taken out and tomorrow I am going to get this dang thing out of me. I am so tired of being moody, sweating all the time, i have cramps during my periods and I used to never have any kind of symptoms during my periods. You could never tell when I was on my period, now you do. I was having terrible back pain a few weeks ago and I never thought it could of been because of the Mirena but after reading some of the posts, a lot of other people have had back pain also.

I can't believe they will put something like this into you and advertise it as much as they do. I believe they should take it off the market. I hate being moody and tired all the time.

I AM SO HAPPY I AM GETTING MIRENA OUT OF ME TOMORROW.

OOOO and I also forgot to mention that I also have been getting headaches and I never got headaches before. I never thought it was because of it...how can this thing cause so much????

daily headaches, waking every hour till 2 am, vision, but mostly the headaches are what are bothering me the most. This is my second time on methadone. the 1st time was 8 months start to finish with 3 years clean then a relapse. I realized that both times I had headaches. Why the headaches? I feel like I am losing it. I'm trying to be a wife, mother to 3, independent rep and so on. Am i alone?