Hours of sleep symptoms and conditions

My daughter was being treated for headache pain and eye pain. She was put on prednisone z-pack which did nothing. The pain got worse so she spent 2 weeks in the hospital where they were giving her 1000 mg bags of prednisone in her IV. She finally came home and nothing was found. They did numerous MRI's catscans, you name it. A week after she was home she developed severe pain in both legs we believe is from coming off of prednisone. Does anyone know how longs this lasts, and what can be done about it. She averages 1-2 hours of sleep. She is on every kind of pain medication known to man but nothing helps. Please help!!

I'm 48 and got a Mirena put in last January at the suggestion of my doctor. I'd been having menstrual migraines and we thought that a steady dose of hormones might help with the dips and prevent my headaches. Well, it has helped some, as the headaches don't come every month anymore, however, I do still get them, so it hasn't really done what we hoped. Add to that my (growing!) list of symptoms and something has to be done. I am very active. I do Taekwondo 4x a week and was working out 5x a week this summer in preparation for my black belt test. You would think that I'd lose weight with the workouts I've done for the past 10 months, but no, my weight has increased over 10lbs! And it's not muscle, either: My breasts, waist, hips and thighs have all increased. I feel bloated, tired to the point of exhaustion even after 8 hours of sleep, and all of my joints are achy. The brain-fog has gotten so bad that I've had to go back on ADD meds to try to maintain my focus at work. I'd been doing my workouts for 3 years prior to getting the Mirena, and I never felt tired the way I feel it now! I'm seeing my doctor next month and this thing is out of here!

I think that I finally figured out why I am so physically and mentally sick. I received the mirena almost 2 years ago and I was a true advocate of the product...I love it!! About 6 months ago I started to have panic attacks and anxiety (i have never experienced this before) it was so bad that I barely made it to work everyday and could no longer handle being out in public. My PCP placed me on different types of anti-depressants (which made me depressed). Currently I take Budeprion which has decreased my anxiety but I do not feel like myself. The past month and a half I wake up with the feeling of morning sickness (the numerous pregnancy test say that I am not), have headaches, low energy levels and little motivation. I was pretty sure that my hormones levels must be "off" but my PCP and OB insisted that there is no way that my symptoms have anything to do with my hormones because my child is almost 2 and I am 29 years old. I have gone through numerous tests, scans etc.to find the cause of why I feel so awful and all tests came back Fine. After reading the stories on this website I now know that I do not need anti-depressants and I am not going crazy...I just need to get the Mirena removed.

I have been on Yaz for over a year now and it's been less than pleasant. First the mood swings which I attributed in the beginning to lots of stress (I started taking Yaz about a month before my wedding). The mood swings continued. My anger has been uncontrollable at times and I get upset for nothing. I have always been a reasonable person but Yaz has taken all that from me. After giving it more than enough time for my body to adjust to this pill I have finally decided to get off Yaz next week and talk to my doctor about an alternative option. Apart from mood swing I've experienced severe fatigue no matter how many hours of sleep I get. I can't stop eating, have severe problems with heartburn and constipation. My sex drive is pretty much gone and I am negative about pretty much everything. I really hope that I will get back to my old self once I get off this pill. To everyone out there with similar experiences, I feel for you.

I am taking the Metoprolol generic and have mixed reviews, although I don't think that any of my side effects are life treating. My greatest complaint is insomnia. Most nights I get 4-5 hours of sleep. I also have the itching(hives), and sometimes numbness in my arms. I do feel much better since starting on this med in May, and my blood pressure is normal after being sky high. I can live with the hives, the insomnia is irritating, and my menstrual cycle was horrid before, and is now worse, 8 days out of every 27. Hopefully menopause is coming soon. I am taking 1 25mg tablet twice daily. My BP was out of control before starting any meds, so I will live with the side effects. I haven't noticed any weight gain, actually lost 14 pounds since starting it, but that could be the results of a low fat, low cholesterol diet too.

i had twins this march, 2009, and i had to weight about 2 months to get my mirena put in. i was consistently losing weight before hand.. it was great i wasn't hungry i had energy to exercise, but i also couldn't weight to get it put in, the thought of getting pregnant anytime soon scared me so i chose mirena at first it was great.. no refilling no periods just some cramping ... but then i started feeling tired alllll the time.. i mean all teh time.. before i could stay up easily with my new born twins , could go a whole day with only a couple hours of sleep.. now im exhausted.. its strange.. and i eat like im pregnant again. i hate it.. i cant wait to get it out. im going to get back on the pill.. i had energy when i was on the pill i might have been hungry but i had energy to work out.. i need this out so i can be myself again.. anyone else
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I'm at the end of a 10-day cycle of doxycycline (100mg 2xday). Worst side effects: insomnia and restless leg syndrome. I think I'm averaging about 3 hours of sleep a night. Stomach pain, occasional cramps, severe loss of appetite. I've also experienced some of the stranger side effects others have mentioned: mood swings, depression, suicidal thoughts, feeling like I'm in a dream, mental problems (after I write something I realize I've spelled half the words wrong).
Next time my doctor mentions this drug, I'm going to say no way and see if I can get a sulfate based antibiotic or maybe good old amoxicillin.

I have had 6 kenalog shots in both my upper theighs fot bursitis and although I am long past menstrual periods I too have experienced some harsh symptoms. Before the doctor only did one theigh per appointment but this time she did both. I have had sever flushing, night sweats (thought I was over them) and after reading some of the others wonder if the weight lose I've experienced is due to the kenalog. Insomnia has been a problem with these injections too and am lucky to get 4 to 5 hours of sleep. I was only told any symptoms could possibly be soreness at sight, bruising and bleeding at sight....why oh why...are we all given such a small amount of information on these drugs and what is the long term effect going to be?

This post is for the ladies who wonder will they feel better or notice any change after having the mirena removed. This is my own personal experience . I've had it out for about 2 weeks now after having it in for 3 1/2 years. I feel Great! I couldn't have a panic attack if I wanted to. I have had more energy, haven't had a headache. I have a returned sex drive. Sadly my hair is still very thin and patchy. The big kicker is I've lost 4 lbs as of today. My stomach now looks like I'm 3 months pregnant as opposed to 5 months. The big difference is noticed in my face and waistline. I don't feel so hungry all the time now and feel motivated to keep this going. I haven't had one heart palpitation since either. Yes I still yell sometimes, but not out of anger or rage. It's now to be heard over the yelling and screaming of my happy kids who used to cower because of my yelling that was so mean spirited and full of frustration from being so tired and feeling ill most all the time. I just worked last night 13 hrs got 5 hours of sleep today picked the kids up from school, played with them and cooked dinner to boot. I would have been in bed 2 weeks ago waiting for my husband to come home and rescue me. This has been my experience thus far and I keep posting to give those ladies hope that they can feel better once they get mirena removed. I hope others will have a positive experience with removal like I have had. Good Luck and Happy Recovery.

I have been on lamictal for about 7 months. I was not happy with the side effects I was experiencing (no sleep, bad motor skills, brain working slow) plus I was still having fits of rage and suicidal thoughts. I finally had enough and last week told my doctor that I wanted to get off to see if I felt any difference, because I pretty much felt the same on the 200mg than before I started. I'm slowly being weened off and now I am down to 100mg. So far I have not been getting up in the middle of the night as much and actually slept a total of 7 hours and only woke up once in the middle of the night for like 2 minutes versus the waking up every 1 to 2 hours and sometimes not being able to go back to sleep at all. My conversation ability has been returning and I'm not so nervous to talk and lose my train of thought or try to search for the right word. I've been dealing with a difficult situation in my life and I actually feel like I'm handling it better now than when I was on the full dosage . The only downside so far which is probably withdrawal is that I'm extra sleepy and I've been having to take 2 hour naps during the but I have a feeling that will go away. Besides my body might be making up for lost time from the 3-4 hours of sleep I was getting. I'm looking forward to being off of it soon.

Ok I Would Like to ask for anyones thoughts on this...and please don't feel like I am attacking anyone but tell me the truth...I am 23 years old I wasn't looking at having children however my beautiful daughter is 7 weeks old and like all of you I had the Mirena inserted last week. I am 5'5 and before I became pregnant I was 113 give or take at the end of my pregnancy I was 155, when I went in to have the mirena placed I was down to 118 and starting to fit in my old jeans again...again I said a week ago. Now like many of you I too have always had problems with my weight I have since my previous marriage I will not go too much into detail but it ended because I was 120. Now I watch my weight VERY closely and when I gain 3 pounds I am spun into a depressed state. When I first had her I was perfect even with 2 hours of sleep a night and a stomach that looked like a big floppy pancake I felt great I loved my motherly body I was not depressed what so ever. Now im not blaming the mirena yet but after reading these post im honestly scared. Before I was pregnant I was on a low hormone pill and I would get horrible migraines to the point where I would faint out of the blue they would strike and down id go Anyway...and please be honest...do you think that people who are prone to these symptoms they are simply intensified not that thats any better but is there anyway to live with them? In my past I sought out therapy and even medical treatment. I ask because My sister has the mirena and so does my neighbor...no weight gain no depression no anger no side effects what so ever. Me I already feel the weight coming on I am no longer anywhere near fitting into my jeans and I haven't eating anything for 3 days I know thats unhealthy but I need to know if this is really the cause...those of you that have had the mirena removed do you honestly feel a big improvement?

I never had anxiety or depression before and consider myself quite happy and well balanced. A unique life event all of a sudden through my head on a tail spin. I became very worried, had panic attacks, became depressed, emotional and lost a lot of weight. My doctor prescribed Paxil (20 mg). He told me that it could take up to a month for the drug to be effective. At first I was miserable. The stress and the Paxil taken before bed, gave me insomnia for almost a month (I never had sleeping problems in the past and used to brag about my solid daily 8 hours of sleep). After 3 or 4 weeks on Paxil, I became a new person. I do not feel depressed, anxious, and I am now able to sleep without taking medicine. The issue that triggered my depression is still present but somehow it does not seem that threatening as before.
I did however started having night sweats. At first I was very worried as night sweats can be related to some kind of infection, but having no fever was reassuring. I was at peace when I found out that Paxil can indeed cause the night sweats. I intend to wean off Paxil in a few months, once my issue is put to rest and will do so with the help of my physician, but for now I must say that I highly recommend its help.

I can't believe that after months of searching for an answer to my daughter's health problems I may have found it! My daughter was a healthy, active happy child until recently. She is 17 and started experiencing joint, bone and muscle pain and swelling, unexplained rashes, migraines, tingling in her hands and feet and was diagnosed with neurocardiogenic synchrony (heart rate and bp out of synch) shortly after her first shot (she was 14).

We have been to a rheumatologist for the joint pains, they did blood work and there is a marker for some sort of auto immune disorder, but nothing specific.

I never connected the dots to the shots. In January of this year she started having severe diarrhea, stomach and intestinal pains. She has no energy, the most basic activities wear her out. We ended up at a gastroenterologist looking for a diagnosis (they thought it was Crohn's or lupus). All the tests have come back negative, they said she had gastritis and blew us off. She is on medicine for the intestinal pain, a prescription for an antacid for gastritis and an anti-inflammatory for the joint and bone pain.

She was a straight "A" student up to January and has had to finish her junior year at home. It has been a very stressful experience for all of us.

My story about the Mirena started from 2002. I had my seconnd Mirena placed 2 years ago. Having them put in and taken out are extremely painful you need way more then advil I had to take painkillers given to me by my doctor. I never knew about all the side effects I was never told and now know that everything that has happened to me is because of the mirena thanks to your blogs and my doctor. The first problem was serious stomach issues so bad that they had to remove my galbladder. Well that didn't work so I have had 2 upper g-i's and 5 colonoscopies the last one they found colitis which they could not explain why I had it. I still have stomach issues so bad that I run to the bathroom after eating. With all that being said you think I would lose weight well no I have gained 15 pounds since the last one was placed. My heart I have had an extremely fast heart beat since having the mirena so fast that I have passed out numerous times; the cardiologist said its definitely hormonal but would never tell it was from the mirena. I went through 22 different tests for my heart, evern wore a monitor for an entire month. Sex drive is not there, I never am in the mood. Exhausted I am constantly tired I have to fight laying in bed, but at night I can not fall asleep even on prescribed pills only get about 4 hours of sleep; before the mirena I could sleep 10 hours with no problem. Last but not least is the headaches and neck pain they have been so bad I have had 5 nerve blocks since having the mirena. I have gone into the hospital 3 times since 2002 for severe headaches which they have run every test known to man on me and can not tell me what I have. I have had to recieve iv therapy for the migraines that you can only receive in the hospital with a nurse watching you for 48 hours since you have to receive 3 doses of it. I could not walk, talk, or even look at light. My stays at the hospital have ranged from 3 to 7 days. I have gone to specialist after specialist and no one would tell me the truth or knew what to tell me. Finally 3 weeks ago I went to the neurologist and he told me straight out after looking over my medical history and speaking with me that without a doubt it was from the Mirena. After 7 years,11 specialists, my galbladder being removed, numerous hospital visits, and endless procedures I finally know the truth. I hope people read my story and think twice about using mirena; you could end up like me. I am only 28 years old, married with twin daughters. I have had to live like this for 7 years; I will never get that time back but once I have this removed I know I will have my life back.

I am so happy that I found this thread! I had the Mirena put in last May and I am about ready to get it taken out. I am not one to sleep in all day, but since I have had the mirena I feel like I sleep in so late. I can't get to sleep and then when I do it doesn't matter if I have 1 hour, 6, 8, 10 or 12 hours of sleep, it still feels like I haven't slept at all. I have no energy for my 11 month old. I had wanted children for so long and not having the energy to dedicate to her is beginning to depress me. I had a lot of hair loss on my head and a huge increase of hair on my jaw line. I have a sharp pain in stomach that rarely seems to go away - I have just grown accustomed to it. I pretty much have a headache all the time. I bleed for 3 weeks, have 1 week of not bleeding, then the cycle starts again. My sex life has become just about nil due to my decreased sex drive and constant bleeding. Since I am now uninsured I just have to find an affordable place to get the removal done (which is easier said than done, some of the quotes I have received have been amazingly high). Thank you to everyone for sharing their experiences.

I received my first Gardasil shot back in September '08, and my second shot December '08. I was supposed to go back the 1st of this month to get the third but decided not to go. After the first shot my whole arm was so sore I could barely move it for about a week. I became extremely tired and run down, and began getting symptoms like I had the flu. These symptoms lasted for about two weeks after the shot, them seemed to somewhat go away. I figured my body was just not used to the medication so I went ahead with the second shot. This time the symptoms were worse. Again my arm was sore to the point of not being able to use it, and I was extremely tired. I remember going home from work that day and immediately going to bed at 5, no waking up until almost noon the next day. for the next couple of days i slept almost non stop until Monday when i had to get up for class. Since my second shot I have not had nearly as much energy as I used to, I am always tired and feeling like I need to take a nap even if I got over 8 hours of sleep. I feel like I am not all there, or as smart as I used to be for some reason. I'm not the same person I used to be. I wish I had never gotten the shots to begin with, I want all of my energy and my old life back.

I was prescribed Z-Pak on Dec 31 2008 and it did help my bronchitis and pneumonia, however the side effects are horrible.....I still have a nagging cough but my breathing is better. I had to take gravol for three nights with this med as I was so nauseated and dizzy. Worse, I have agitated sleep and needing 10 to 12 hours of sleep because of awful sleep I am getting. I stared with diarrhea and hemorrhoids, and vaginal yeast infection. Losing urine with coughing which is due to my age and past pregnancies (53 years old), sore breasts and very sore nipples. Heavy period started 3 days ago.....which has shaken me...... as I went through menopause 11 years ago, yes 11 years ago! I had ringing in my right ear (never before) for 24 hours this week and have altered and less hearing in ear now). This is my 53rd birthday and I will call doctor Monday and see her asap. I am freaked out! Is this all from that med or do I have uterine cancer???

I am brand new to this sight and have been on the generic for Yasmin-Ocella for almost 2 years and have about had it. I have chest tightness and am so moody sometimes that I start screaming at the kids for no reason and then break down in tears because of the way I have treated them. I am exhausted all of the time, I do have 2 small kids (5 & 2 1/2) but even when I do get 8-10 hours of sleep I feel drained. Like a depression. As I type this I am having the chest tightness. Only happens during the first week of a new pack. My OBGYN is having me skip the last week of the pack-which is when I feel like 100% my old self-no exhaustion, no moodiness etc &the only week that I have ANY sex drive too-because she thinks I have a torsion ovary. I will see what she says on the 29th but I want off of these pills... What is the point if you feel like crap, can't breathe and have NO drive what so ever!

Well, let's see, I am 37, I just had my third child a year ago. When I had my first child at 19, I entered the world of Rhumatoid Arthritis, I did not take anything for it, it just seemed to go away by itself. After the second child it flared up but not long enough or hard enough to remember. After the third child at 36, wow did it get bad, so bad i couldn't get her out of her crib. That was the day I started 10mg of pred a day,,it made all the symptoms of the RA almost disappear...almost...which was a miracle,,,but it made all the side effects of the med start,,,,weight gain BIG TIME, bad moods, maybe 2 hours of sleep @ night,,,hair loss which scares me the most, blurred vision, buffalo hump looks like I'm looking for something on the floor all the time,,a wonderful neck that looks like i swallowed a couple bananas whole,,hmmmm,,,,let's seeeeee,,what else, easy bruising thankfully I like the color purple, oh, and me and mr. potty have become well friends. At first, the doc thought it was hypothyroidism because I also had 2 periods a month, but a blood test told threw that theory out. I just want to say,,,,I like that my RA is better because of it,,,but I am as of yesterday taking myself off of good ol prednisone, and sticking to a high dose of IB or Tylenol. It's just not worth it.

I have been taking Lotrel for about 3 years and I have a tingling and burning sensation in my hands and fingers, especially when lying down at night. When this occurs I usually wake up after 2 or 3 hours of sleep. I also experience pain in both shoulders.

When I was using Singulair I had trouble sleeping, then I had trouble waking, even after 10 hours of sleep! I had racing heart rates, headaches often, my blood pressure was high, which it never was before, gained weight, felt like I was often on the verge of tears, mean aggressive and plain old nasty which in unlike me. Would have the craziest dreams or nightmares I ever had. I've been off for several months (10) I've been like the old me for quite awhile now. I had surgery in 2006 and had the usual testing done everything was normal. I am getting ready to have some surgery so my dr. ordered some test, an ekg which came back abnormal, it was explained to me that it was like my heartbeats didn't have a strong beat, maybe a heart attack or something. I never felt or knew anything about this. I am wondering if the singulair did something to my heart. I was on singulair for about 18 months. If it weren't for the ekg I would have never known this problem exsisted. I have no symptoms of any heart problems. I am a 52 year old woman who eats great and exercises daily (since I was in my 20's) . Anybody else have any similar reactions?

I hav been taking lisonopril now for four weeks. I feel very depressed--everyone keeps telling me that it is not the medicine, but nothing else has changed in my life.

Because of a couple tragedies that ocurred in my life, I was unable to sleep. Ambien was prescribed and with it, I woke up completely rested! BUT there were several dangerous events to share with you.

I drove several times & have no recollection! If it weren't for receipts, checks, etc. I wouldn't know anything about it! I'm a married woman and I took a male acquaintance to a liquor store 1/2 hour away once!
I drove to a city an hour from my home at least once!

Additionally, I've had phone conversations, conducted business meetings, taught a religion class...ALL with no knowledge or memory of these acts.

Yes, I would find dirty dishes in the sink in the morning too! I ate so much food! I didn't gain weight though...probably because the Ambien also removed ALL inhibitions in my life. My husband selfishly took complete advantage of this...if you know what I mean. This was not right! I'm still angry about this. It wasn't until he realized that I was driving in my sleep that he encouraged me not to take the Ambien anymore...I haven't taken it for two years. I do miss it because it really left me rested. Now I only take over-the-counter products and they leave me groggy.

I've been on Paxil for almost 9 years. I suppose it's a success for me because it has kept the depression away most of these past years. I'm on the maximum dose - 40 mg a day.

I've always been an over-achiever, a type A personality, friendly...with the Paxil I am lazy, no longer care about details, VERY friendly.
My home used to be pristine and comfortable....now I rarely put things away, there are stacks of books, magazines, and 'stuff' everywhere. Because of the mess, we haven't had visitors in our home for YEARS! I used to host parties on a regular basis in our home but these days I would die of embarrassment if anyone saw my home!

My memory is shot...I can't remember names, faces, details...seriously, I can watch a movie over and over again because I NEVER remember the ending!

My sleep cycle is shot as well. In years past, I only required about 5 hours of sleep. On Paxil, I don't fall asleep so I take lots of over-the-counter sleep aids to fall asleep and they knock me out...I can't wake up until almost noon!

I MUST take the Paxil at the same time each day otherwise the "zapping" starts. It isn't painful...just very annoying.

On the positive side, I have achieved many great things because I'm no longer apprehensive about public speaking. I've chaired several successful fundraisers for charities. But because the memory loss has become so profound, I'm no longer capable of chairing these types of events.

I've gained weight but it may be due to having thyroid cancer & having the entire gland removed...metabolism is shot.

I've only tried to go off the Paxil once but the depression resurfaced immediately and I cried for days on end...it was frightening! Of course I went back on it.

Speaking of crying, when on Paxil, it's almost impossible to cry! The tears just won't come.

Now for the really scary part...the effect of the Paxil on my depression is not what it used to be....but I'm on the maximum dose! I've tried several other meds but they just don't work as well. So what in the world will happen when it doesn't work for me anymore? That black hole called depression is the last place I want to be.

I am a 21 year old female and have been on Topamax since October of 2006. I am up to taking 250mgs a day having a constant headache and getting a migraine about every week. I have had such a range of side effects and symptoms that I can't tell the difference nor know where to begin. The most recent is muscle spasms in my eye lid and leg that won't go away. I have spasms infrequently all over, but these have been pretty constant. I also tire very easily though I always get 8 hours of sleep a night. Though those are not always 8 full hours of sleep, because I do have boughts of insomnia. I have also dealt with the intestinal problems to the point of thinking that I had appendicitis. I have had multiple trips to the hospital for abdominal pain and severe migraines. I have had the vision problems - blurred, dizziness, vertigo, and the weird one were my eyes jerk back and forth. I rarely have all at once and they have come and gone throughout the 2 years, but they have come back

I think the most mysterious one of all are the lypomahs - these little painful nodules under the skin that just appeared. They are mostly on my abdomen, but have found them on my chest as well. Any one else heard of this?