Pain management symptoms and conditions

I started taking 20mg of Simvastatin on 10/17 due to high cholesterol. Five days later I came home from work feeling very tired and fell asleep. I woke up feeling severe flu like aches and pains in places I didn't know could hurt and then got the chills. I stayed home from work the next day and it's a good thing I did. I awoke with a severe cramp in my upper right thigh. I have always been prone to calf cramps so wasn't too concerned. However I stopped the meds on 10/22. This continued on a daily basis and I went to the dr on 10/27. I had an x-ray done which showed a bulging disc and some uncushioned discs. She put me back on the meds BUT with a COq10 am and pm and cut the pill in half. Do you think she knew it could be from the med? I foolishly restarted and by 11/4 took myself back off, had an MRI and such severe nerve pain in my right leg that I thought I would die. It was a bolt of lightening starting at my upper thigh and coming out the bottom of my foot. It felt like a hot poker running down my leg. The episodes were on a daily basis, would come every two hours, and could last as long as 45 minutes with no relief. I am now going for pain management and had an epidural a week ago which got rid of the nerve pain but I am still numb down my right leg to my right ankle. I have been healthy for years and feel that this was all brought on by Simvastatin. Any idiot can figure out that your nerves are running through your muscles. I am angry to think that this could have caused me permanent damage.

i have been on 30 mg of abilify for about 3 years.obviously, i slowly titrated up to that. for the first month, the doctor gave me another drug to go with it-carbidopa/levadopa to keep me from having tardive dyskinesia. after the first month, i came off that med and stayed on abilify, and increased the dosage.the first few weeks were tough,as with any drugs like this, but i knew to expect it and just hold on for the ride...my dr is using it off label,for pain management of "rebound pain"-which is pain that doesn't know when to tell your brain to quit,basically. it has been wonderful for this,and i'm calmer now in other aspects of my life. i was already on an antidepressant,and it compliments it well. i hopes it works as well for everyone, and i hope the doctors understand to give something for the first month to cut down the twitches!

I had mirena put in 2 weeks ago and i can't stand it, i have my period and it's not normal it smells really bad and the blood is dark major camping no time for any pain management. i have headaches all the time. i'm always crabby i'm more depressed then i am now.. it needs to get the hell out of my body. i hate having my period and i just feel bloated and lazy,i think i have cysts on my ovarys it hurt on one side then in the middle like a cramp im only 21 with two kids and i'm healthy but i can't understand these side effects their just not right,i think it shouldn't be on the market at all...

I have had a total of 5 kenalog injections in my back for no disk left between two vertebrae, doc says fused naturally and no movement. I still have pain. I am scheduled to have yet another shot in the neck area, 5 bulging disks causing pain around the shoulder blade. I have less sciatic pain, but I have HEADACHES for the 3 months since the first shot, they don't go away. No OTC pain relief works for these headaches. The doc says the kenalog does NOT cause headaches, I know these guys lie or don't care about the FDA list of side effects. I am hesitant about getting another shot. He wanted me to have this one done under sedation, I declined, since I had the others without. He said more sensitive area and don't want you to flinch. I also get, I assume kenalog injections in both feet for morton's neuroma. Left foot shot worked. Right foot 3 shots and still hurts and numb, they can't seem to get it right. I am tired of getting the shots, and today I went to that pain management doctor and forgot to ask him how long can I expect the shots to help the pain, years? months? or weeks. I barely do anything anymore, afraid to bend, or even move. I had to go to ER first time for my back on 2/14/09 and sent to different docs and finally pain management. For those of you whose docs don't order an MRI for you, I wouldn't have the shot. I had and MRI of the back and neck and this doctor gives the shots while I lay on a fluoroscope table, I can see on the screen in front of me where the doctor is injecting. Hit and miss without an MRI is just not medically correct. Good luck to all and gonna think about whether to get another shot next Thurs.

I am a 41 year old woman who had an epidural injection using Kenalog in my lower back (for stenosis, disc herniation, degenerative disc disease, etc.). My first injection was on 4/1/09. About two weeks after the injection, my period started a week early. I had light to moderate spotting, not quite like my normal period. I also noticed that I broke out with major acne, had bad mood swings, constant urination and increased hunger. I had a second injection in my back on 429/09. I told my pain management Dr. what I had been experiencing, and he said that it was the side affect of the drug, Kenalog.

I just saw my GYN for my yearly pap smear and told him what I had been experiencing. He said he had never hear of anything like what I was going through as it related to an epidural injection, though he also admitted it wasn't his area of expertise. Due to my age, my GYN commented that the spotting I was having could be due to my body changing and getting ready for menopause. He said that spotting was very common in women my age. He gave me a prescription for Progesterone 100mg to start taking for 15 days to see if that stopped my spotting (and hopefully return my cycle back to normal). He also did a uterine biopsy to rule out any other causes. My uterine biopsy came back normal. I'm currently taking the progesterone and my period seems to be tapering off, but it still hasn't stopped. It went from spotting to more heavy bleeding to spotting again. I'm due to stop the progesterone on Tuesday 5/26/09 so we'll see what happens there. It's officially been six weeks of having a period.

I'm very frustrated that I've had a menstrual cycle this long. I canceled my other future epidural injections as right now, by back in doing much better (the injections did help, though the side affects are the pitts!). If my back flares up, I will seek other solutions as I will NEVER have any Kenalog again.

For those women who've had the same issue with their menstrual cycle, did your cycle ever return to normal? If so, when???

I was diagnosed with Rheumatoid arthritis at the end of 2007 and have been on prednisone since then. I started on about 105mg a week and am currently trying to reduce it but it is really hard as the moment the dosage goes down I lose all mobility and cannot even get out of bed. I am only 23 years old and really feeling the disease to the extent that I cannot even cope with my life. The prednisone has really taken its toll on me and the side effects are crazy! I just want to go back to my old self as I am finding it sooo hard to get through a single day. My side effects include:

Insomnia, tooth sensitivity, depression, anxiety, mood swings, moon face (my face is so swollen that I cant stand looking in the mirror anymore, dizziness, temper, feelings of uselessness, nightmares, night sweats, water retention, and to top it all off the arthritis is getting worse and I am in constant pain. Is there anything anyone can suggest then please help me!

I am a 38 year old male suffering from a combination of occipital neuralgia and migraines. For 20 years, until a year ago, i would endure pain that was only manageable with narcotic pain relievers (imagine all the gamut of such kind). I would have neck and head aches typically 3-4 times a week, accompanied by vomiting, dizziness which would put me to bed for the entire day. Work and family suffered in magnitude comparable to my own suffering. So then I finally saw my GP for that. The pain meds went up the roof, imitrex, maxalt was added to the equation with only marginal side effect. I saw a neurologist. He had me do an MRI and put me on Topamax starting from 25 mg, which I upped to 200 mg within 6 weeks. Past the initial side effects, the headaches subsided, the frequency reduced and i was able to enjoy weeks at a time with no episodes. Stayed at 200 mg for 5 months. In the meantime, the MRI came back positive for some brain inflammation. False positive they said, does not fit the clinical picture. Second MRI, same positive, this time proceeded with LP, which was negative. Third, MRI still positive; making the neurologist uncomfortable. While dealing with MRI results, the topomax had yielded positive results as far as pain management was concerned. But little by little I noticed that I was becoming more irritable, more impatient and more forgetful. Someone would have to remind me of something several times before it would even register in my mind. I empathize will all the posts that mention feeling like having Alzheimer's. I didn't care in the meantime. As long as I didn't have to deal with the pain it was ok with me. But the situation became worst and worst. I couldn't concentrate on anything, the mere task of remembering to do something was insurmountable. I would wake in the middle of the night and find myself staring at the bathroom mirror for no reason. I would have terrible panic attacks which i control with valium. But yet i continued on with topamax convincing myself and being convinced by other people around me that i just had a "personality disorder". Finally, work begun to suffer. I was loosing track of meetings, deadlines and when this happens someone knocks on your door (boss) telling you that something just doesn't click, something just doesn't feel like a personality quirk. Other people playing doctor would slap on my face that i just had ADD, that I should take something for that and get on with my life. But something was wrong. Pain or dizziness or lack of concentration etc are all electrochemical processes in your brain. It turns out that topamax was helping my headaches but it was not slowly deteriorating other cognitive abilities. Finally, the neurologist decided I should wean of the topamax, stepping down from 200 - 150 and then we go to 100 and so on. I dread the re-occurrence of the headaches. I am waiting for them to happen again at some point as I drop the dosage. But in the end of the day, I'd rather be in pain and in control of my life rather pain free and absent minded.

This isn't a new side affect but I didn't have a good time with Femcon at all. I only took it for about 2 months and I bled for 2 almost 3 weeks. I was depressed and I know now that I gained 10 pounds while on it. I would never recommend anyone to take this. I am not taking anything now and I don't play on taking anything. I am going to talk to my Gyn. about pain management until I decide to get pregnant again. I just don't understand why doctors seem to think that birth control is a one size fits all drug and it isn't. But I don't know much about nothing so who knows.

I read with interest several of the posts here. I have been on Lipitor for about 5 years. I have been experiencing leg pain, back pain, neck, and hand pain for likely 4 of the last 5 years. I have arthritis, I thought. Two weeks ago I ran out of Lipitor. I read several other forums where Vitamin C and Omega 3 were suggested as a possibles to replacing the Lipitor along with generous amounts of water. I said, What the hell, I will give that a try. Within days of stopping the Lipitor, most all the pain has subsided to the extent that I have not had to take any other Pain management medications at all. I was prescribed Perocet for the pain I have been experiencing. Two weeks ago, I had a tough time opening a bottle of soda, or even a relish or pickle jar. Today I can! Coincidence, I think not!!

Hello, I have been on Lamictal 25 mg 2 times per day for mood stabilizing since Sept 2008. For the past five months I have had extreme lower back and hip and leg pain. I have been being treated for the pain and so far no one has been able to find the cause. I am currently going to pain management because I am in drug and alcohol recovery, pain meds are not and option for me and just had my 2nd epidural spine injection with no relief. I am so GRATEFUL I found this site. God works in his own way. I am calling my doctors now. Thank you all and God Bless.

PS I have never even looked up my drug side effectives before let alone post on a site.

I am a 36 year old woman living in hell for 3 months now.

In early October of last year I was admitted to the Hospital with diagnosed bronchitis a possible pneumonia. I was given Avelox which is a member of the Fluoroquinolone drug family. At the time I was in sever distress, could not breath, and was extremely weak from the infection. I stayed in the hospital for 6 days while they gave me Avelox along with various other meds to treat my symptoms and was released after finally getting a clear chest x-ray. The drug had done its job. But it was a week later that hell started. I was re-admitted to the same hospital with sever abdominal pain. They told me that I had hepatitis due to a reaction from the Avelox. My Dr. Also suspected I could have Wilsons Disease so he prescribed a liver biopsy, to say the very least this was a painful procedure. The biopsy came back negative and the liver function began to return to normal just as the pain everywhere else began.

joint and muscle pain
headaches
insomnia
uncontrollable twitching
arm and leg numbness
neck pain/spasms
a mass on my left breast (further diagnosed after mammogram, CT and Biopsy as a side effect to the Avelox)

My internist, Rheumatologist and the liver specialist all suspect “Post infection pain syndrom”.

However, after hearing now 3 separate times from 3 seperate Dr's about the possible side effect of Avelox I did a little research and every single one of my “symptoms” are on the lists of dangerous side effects for this drug. Now none of my Dr.s can tell me if I will ever get rid of the pain I am in. None of them seem to be able to do ANYTHING but treat my symptoms. By treating the symptoms all they can do is pain management which means pain killers. I simply can not function day to day with most pain killers so I am forced to live with the pain.

More drugs than I have ever taken, Dr.s visits, time off work, stress and a standard of living that simply put is not living, not to mention the tremendous outlay of cash...to say the least I am frustrated.

I have had numerous side effects with tramadol (nausea, heart skipping beats, restless legs at night) but I was too desperate and needed something so I just started taking 2 half pills a day (total of 50 mg). Well, now I've quit after about 2 years because I have sudden onset swelling and tendinitis in both of my achilles tendons. There was absolutely no trauma involved and tramadol was my only medication. After doing research online, I found that this is a rare side effect to some other medications but it hasn't been mentioned for tramadol. I truly believe this is a side effect that just hasn't been reported yet. Also, it can lead to both tendons rupturing. I just hope I stopped the medication in time so that it doesn't lead to that. It's only been a few days and I have a lot of pain and difficulty with stairs. I think this will take a while to get over -- like all orthopedic related problems.

As a fairly healthy 34 year old male, I went to my doctor for help getting over poison ivy mid-July 2008. I received the Kenalog 40 injection without being advised on any potential side effects. Within 36 hours I started having severe anxiety attacks with spikes in my blood pressure and vision problems (spotty, increased sensitivity to light). These attacks continued for 4-8 weeks during which time I underwent an MRI (head), stress test, and blood work to make sure nothing else was causing my symptoms.....conclusion: everything normal. My doctor prescribed me Xanax to help with the out of control anxiety. Started feeling more normal 60-90 days later. I started trying to run on my treadmill to get back in shape at the 90 day mark, and once again....symptoms returned. It's been a couple of weeks and I'm getting closer to being back to "normal", but I have no idea how long it will be before the Kenalog has completely metabolized out of my system, and I can get on with life. This has been a horrible experience and I would caution anyone from receiving this drug!

Three years ago I was prescribed Levaquin for an infection. After the Levaquin I was unable to stay up in my wheelchair for more than two hours. I started taking two extra strength Tylenol and I was able to increase that to three hours. I added Naproxen 325 mg and that has decreased the pain and has also increased the time in my wheelchair by about an hour. I am also on a drug called Lyrica 150 mg which has decreased the pain further. I am a quadriplegic so I cannot feel anything below my shoulders but my body responds to pain. I can tell that my body is in constant pain but of course I cannot feel were it's coming from. Ever since the Levaquin I also have a condition called Terry's nails. I looked at this condition on the Internet and is says that Terry's nails occurs when the body is in distress usually with kidney disease or liver disease or cancer. I've had more blood tests than I can count and all of them are normal. My body's sensitivity to pain appears to be getting worse. I'm not sure what can help anymore, have any of you found anything out about pain management?

I had 2 surgeries at once last week and was prescribed Meprozine 1-2 capsules every 4-6 hours. The first 4 days I took 2 at a time and within 20 minutes my pain was gone, I felt relaxed and a little drowsy and was able to nap, which I needed for at least the first two days after my surgery. Twice in 4 days, one of my legs twitched and once my arm twitched. After the first 4 days, I would take only 1 as needed, usually in the evening after I has been up all day and was in a little pain. I had slight dizziness when I first stood up the first day only when I would get up to go to the bathroom. Other than that, I had no nausea, and I have to eat something before I take any medication, no stomach pains, no allergic reactions (I am allergic to medications with codeine in it), no depression, no emotional swings (in fact, if I wasn't sleeping, I was so relaxed that I was able communicate normally, laugh, make my normal jokes, etc.), I did not hallucinate or see things. I was also on an antibiotic, which my pharmacist said would make me very thirsty so I attributed my dry mouth to that. Last year, I was prescribed several different strong pain medications for severe chronic headaches and they did nothing. I would recommend Meprozine for short term relief for pain management. I do know someone who got addicted to Meprozine after taking it everyday for several months because a doctor kept prescribing it to her, so it is definitely only to be used for short term use. If I ever have to have surgery again, dental work, or need something for pain management, I will be asking my doctor for a one time prescription for Meprozine.

Don't think there is anywhere else to put this. Please someone else tell me you know what I am talking about and that I am not crazy! After two years of doctors treating me for muscle issues in my left neck/shoulder area someone finally realized I MRI images were not clear and ordered another. I have Mild Degenerative Disc Disease and three bulgin/herniated discs. C-6, C-7 and T1 (I believe). Anyway, prescribed Predisone and immediately had severe lower back pain. It was almost like back labor or the worst menstrual cycle ever. I stopped taking it for two days, lower back pain went away. I tried taking it again and the same thing happened si I stopped again. Theb I received a total of seven trigger point injections. All but one caused the same awful lower back pain, but went away after a day. I just had my second cervical epidural injection. The first one had the same painful side effects, but again went away after a day. The second one whick I had Monday, September 9, 2008 was the worst yet! Not only did I have excruciating lower back pain but it also moved around to my lower abdomen. Oh gosh labor all over again, but without being pregnant. I have three children so I know what it feels like. I have tried everything including: Ibuprofen, Naproxen, Acetametifen, heat, moist heat, ice packs, hot baths. Pain Specialist doesn't prescribe enough pain meds to make the pan tolerable. So I end up running out 2-3 days early so I can't ask for more. has anyone ever has this side effect form steroids? I so, do you have any other suggestions. Please help, one more injection to go and can't take the pain anymore. My kids need me!

I have been taking simvastatin since June 28, 2008. I am 44 years old and have always been majorly active with my 17 year old daughter. Recently I have become chronically fatigued so much as to want to go back to bed within 2-3 hours after I get up in the morning, (definitely not me). I have felt spaced out,depressed to the point of wanting to cry all the time, have severe back, hip, knee, leg, and hand pain. I go to pain management for my back and hip problems (past surgery), but the usual pain has been intensified over the last 2 months and I wasn't sure why, until i decided to check out the Simvastatin to see if it has made me put on a few pounds, and boy have my eyes been opened!!!!!!!!! I AM STOPPING THE MEDICATION IMMEDIATELY!!!!!!!!!!!! Thanks to all who have spoken up, I wish I would of checked on this sooner!!!!! I'm calling my Dr. first thing in the morning!!!!!!!!!!!

By exhausted in Canton

I was taking mobic 15mg for 2 weeks for arthritis and shoulder impingement. After 5 days I began to have hot flashes and developed a heat rash on the back of my legs from the heat built up from sitting in a chair. I called the doctor and I was advised the mobic was not causing the problems and to continue taking it. Near the end of the second week of taking mobic, my skin was noticeably hot all the time (I was not running a fever). I could not sit or lay down for more than 10 minutes without the heat buildup getting to hot to bear. The last night I spent standing up under a ceiling fan to keep from getting uncomfortably hot. I stopped taking the mobic and symptoms began going away within 24 hours. The mobic worked much better than the naproxen for pain management, but the side-affects were not tolerable.

I've been taking Osteo Bi-flex with MSM Advanced for about a month and the only significant and serious problem is that I bleed deep red blood from the slightest injury and have a hard time getting the bleeding to stop. I have never had an issue of this type before and cannot afford blood loss because I get radio frequency treatments in my back and bleeding is the most serious issue of the treatment. I am due for one now but I would be terrified at this point nor would my Pain management doctor touch me under the circumstances. Has anyone else out there ever experienced a bleeding problem while taking Osteo Bi-flex with MSM Advanced?
by MSB

I had the Mirena put in six weeks after having our daughter, on June 30th, 2006. I never was able to loose weight, and felt very bloated, moody, with pains in my sides (ovary level), and then in the Fall of 2007, I noticed a significant loss of vision in my left eye. I went through $40,000 worth of hospital visits, and one 8-day stay, to figure out that the Mirena had caused a rather large blood clot to form on the outside of my brain in the main vein that crosses over the top outside brain. I have suffered from multiple ER visits with migraines lasting up to 72 hours, even after shots and meds. I have been going to the University of Colorado Hospital for treatment and it has taken over six months to get me on a medication regiment that will hopefully alleviate my debilitating headaches and now am living with the possibility that my vision may never get better in my left eye. The Dr.'s I have seen: an eye surgeon, a Neurologist, a Neuro-ophthalmologist, a Retinal Specialist, and the multiple local MD's. The tests run on my body and head have been very extensive, including blood tests, multiple MRI's and the final MRVenagram that tests the flow and drainage of and around my brain that found the blood clot and have ruled out everything from MS, to Pseudotumor Cerebri (which is a lifelong disease offering only pain management for the most part), as well as a macular deterioration related with people over fifty, not 24, they have also ruled out any pre-existing tendency for being prone to blood clots . This has been the scariest thing of my life and so consuming and debilitating, that I would never recommend the Mirena to anyone. I have missed so much work and the traveling to doctors have been a drain on our financial situation. This kind of information needs to get out there because Dr's are denying any relation to the Mirena. My Dr's have definitely diagnosed my problem as the Mirena. The swelling of spinal fluid was my body trying to protect itself and that swelling caused such great pressure on my optic nerve that my macula, where a person has central and fine detail and focusing, wrinkled in a layer of my eye that cannot be operated on. I can no longer read out of my left eye and the stress that created for my right eye is a contributor to the migraines. I also see double at night, when lights or signs are illuminated by the headlights of my car. I am seeing two images! This is very hard to accept and not being able to read for very long also upsets me. The likelihood of my vision repairing on its own is slim to none. Thanks Mirena. SO please, please help the word get out!!!! Also caution anyone you know who is planning on getting the Mirena, or who has one in to be aware of any changes. My experience has been very extreme but maybe women out there are going through the same things I have been and no one will recognize the relation to the Mirena. I am only glad my Dr. was willing to admit the Mirena was the cause.

Hello: Posting about simvastatin. I have been off of the medication for about six weeks. Initially the symptoms led me to hop on an ambulance gurney and visit my local ER due to dizziness, lots of palpitations, and the feeling that I was going to drop on the sidewalk. I followed the ER with two days on the heart unit, and have pretty much have had just about every test but a brain scan (or at least it has seemed that way).

My symptoms progressed to intense burning in my torso, pronounced in the shoulder blade areas, upper chest, and into my forearms. A week after stopping the statin much of the intense burning was gone.

I still have pain and discomfort, but I have not been "white knuckling" to get through the nights like I had been, which is a relief. I read somewhere that someone described the muscle pain as feeling like he had been repeatedly punched with a bag of oranges. I can relate to that feeling, and recently I have felt the symptoms in my thighs as well.

Pain management takes up my days (although I have continued to work). I have begun massage therapy, and I am going to attempt acupuncture next week. I am trying to sort out what supplements may be the best and which ones won't interact with each other or other medications that I take. I am taking CoQ10, Omega 3 capsules, a multivitamin, and a B complex.

Anyone with similar symptoms or comments, please jump in. We are in similar boats, as they say. I have gotten the impression that some people out there (not on this site) don't see this as real. For those people, unless someone is bleeding profusely from an artery, they remain non-supportive or non-believers....

Hello: Posting about simvastatin. I have been off of the medication for about six weeks. Initially the symptoms led me to hop on an ambulance gurney and visit my local ER due to dizziness, lots of palpitations, and the feeling that I was going to drop on the sidewalk. I followed the ER with two days on the heart unit, and have pretty much have had just about every test but a brain scan (or at least it has seemed that way). My symptoms progressed to intense burning in my torso, pronounced in the shoulder blade areas, upper chest, and into my forearms. A week after stopping the statin much of the intense burning was gone. I still have pain and discomfort, but I have not been "white knuckling" to get through the nights like I had been, which is a relief. I read somewhere that someone described the muscle pain as feeling like he had been repeatedly punched with a bag of oranges. I can relate to that feeling, and recently I have felt the symptoms in my thighs as well.

Pain management takes up my days (although I have continued to work). I have begun massage therapy, and I am going to attempt acupuncture next week. I am trying to sort out what supplements may be the best and which ones won't interact with each other or other medications that I take. I am taking CoQ10, Omega 3 capsules, a multivitamin, and a B complex.

Anyone with similar symptoms or comments, please jump in. We are in similar boats, as they say. I have gotten the impression that some people out there (not on this site) don't see this as real. For those people, unless someone is bleeding profusely from an artery, they remain non-supportive or non-believers....

I've had my Mirena for about 15 and a half months and I am having it removed today at 2 o'clock. At first I had sharp pains when I would sit down and I felt like the cords were poking me and irritating me. My OB/GYN requires patients to come back one month after having it put in so he can check it and make sure it is still in place. At this visit he also trimmed the cords although he acted like he didn't believe me when I told him that I could feel them poking me when I sat down and that it hurt. At first I didn't notice any bad side effects, but I did have one good one: my periods stopped, but I still had occasional and sporadic spotting. I didn't think to look for any bad side effects because I got the device under the impression that it had no bad side effects. I thought it only had a rare complication of perforating the uterus, but since mine was in place at the one month check, I didn't think about anymore until I started thinking about having another baby recently. I went online to see if I had to have a doctor remove the Mirena or if I could do it myself, and I found out that it's best done by a professional because bad things can happen and then you'd have to go to the doctor anyway. Plus, I didn't want to hurt my chances of having another baby. While online I discovered this whole world of message boards where women were having a lot of the same problems I'd been having in recent months and they all blamed their Mirenas. Some claimed that their problems had gone away since having it removed. I never thought to link my circumstances to the Mirena, but when I saw how many women are having the exact same problems as me I knew that I needed to go ahead and get mine out ASAP. Here is a list of my side effects, and I've found other women have had them as well with Mirena: weight gain, bloated stomach, depression, short temper with husband and daughter, acne, low sex drive, spotting, cramps, constipation, and back pain. There may be more, but I can't remember them all right now. Some of them may not even be related to the device, but I've read of so many women with Mirena who are having or have had the same issues, so I suspect a link between my problems and Mirena. I hope this helps someone out there looking for answers. God Bless!

I have been taking Levoxyl for 1 1/2 yrs, I had my thyroid removed due to severe hyperthyroid. In the past year, I have been getting pains and weakness in my hands. It is so bad now, I can't open a jar or lift a frying pan. It hurts sooo bad. My legs hurt and my knees have real bad joint pain.
The funny thing is, it's not every day and not always both knees. It is however all the time in my hands. Last week I went to an Arthritis specialist in San Antonio. He ran every blood test avail. Tested for Rhum. arthritis, Lyme disease, AA, and all kinds of stuff. He x-rayed my knees and injected cortisone in my knees and hands. - that hurt -
He found nothing wrong!
I searched on line tonight for "Levoxyl and joint pain" and this site came up. Boy am I glad I am not the only one who is questioning this horribly possible side effect. Oh, I also have memory loss. I feel like I am 80 yrs old. Just to make sure you know what type of person I am, here goes: I am fit, active, 37 yrs old and 115 lbs, I eat well and take vitamins, non smoker, non drinker.
On Monday, I am calling my doctor. I am printing this web site and all of the postings like mine. There must be something I can be put on that will fix this. Can anyone tell me if they have no Thyroid and have gotten off this stuff; does the hand pain stop? Does it get better or is this permanent damage?

Kerrville TX