Tendonitis symptoms and conditions

I had a severe reaction in 2006 (posted with you in 2007. My question now: is there a class action suite or are lawyers just looking into the possibility of a class action suite

I've been searching for answers on LONG TERM side effects of Lupron hoping that it could give me answers as to what's going on in my body now!
23 yrs ago my fertility dr. gave me Lupron to inject MYSELF EVERY DAY (experimental back then). I had SEVERE endo since the age of 16 and was fighting that as well as trying to get pregnant thru invetro. I was 26. At 29 I had an emergency hysto. Now at 48plus I have chronic tendonitis where the tendons will shred off of the joints. I have been diagnosed with C spine and T spine disease, osteoarthritis and a mystery that I'm going to have to go to the Mayo to figure out (hopefully). I have tumors that are growing in my lower back...growing around nerves, tendons and bone, They aren't sure why they are there, why they are growing, or even what they are. Surgery removed 2 of them...but pathology shows foreign matter other than tissue/bone. All they DO know is that it is not cancer. One year ago I started losing weight (25 pds) for no reason. I'm now holding my own at 112 and hoping to figure all of this out. I can't help but wonder if Lupron or any other experimental drugs I was on has something to do with this. Is there anyone out there that used this drug so long ago??

My girlfriend is 36 she had a kidney infection and got Levaquin IV in the hospital. Her legs were going numb and she could hardly get up to go to the bathroom in the hospital. She thought it was her infection. They sent her home two days later with 5 pill containers. One of them was Levaquin. She called me today and said she is having terrible pains in her hands, wrists, hips, and knees. She says she cant make a fist or hold a bag of groceries and her hands have swollen up so that she cant get her rings off. I told her I would do a search on the net to see if it might be one of the drugs she was taking. Slowly but surely I made it to the Levaquin. The drug maker fairly non chalantly refers to tendon rupture as a side effect effecting mostly people over 60 years old. I dug a little further and found this web site and was amazed at how many people are being poisoned by this drug. I am praying if she stops taking it the pain and debilitating effects will go away quickly. She has two disabled boys she has to take care of, including lifting them into wheel chairs and into beds. This is no joke! I am so angry at this drug maker and these doctors who often times do more harm than good.

Ironically, when I was in high school, I was sick for 2 years; I had migraines so bad I couldn't read, write or even watch TV. I was nauseated every day.. felt a bit better in the evenings. But my eyes were so sensitive to movement, if i was to move my eyeballs just to look at something move on the TV screen, I would be in agony. At the time, my mother was so worried about me, she took me to see every specialist there was in the city (Winnipeg), I missed 2 years of high school. After seeing about 50 doctors, finally one asked me if I was on the birth control ill and told me to get off it. 3 months later I was completely cured! Since then, i have been so afraid about birth control. i have used nothing but condoms.. until my son was born, my maternity doctor recommended the Mirena. I was skeptical because it had hormones in it, but she assured me they were different hormones then what were in the BC pill, and she said the risks were so low. I thought I would try it, and be on the look-out for the same symptoms I had with the pill. But I didn't have any. No visual problems, no nausea, no headaches... so I thought it was the greatest thing on the planet. Meanwhile, I was miserable, angry at my husband all the time, had no interest in sex whatsoever, was not sleeping.. I thought it was post-partum hormones. We decided our son needed a sibling so i had Mirena removed to get pregnant, and after our daughter was born in Dec '07, i had it put back in... again, thinking I had post-partum depression or something. Even 6 months later after I quit breast-feeding, I still couldn't lose the weight. I was eating chocolate and peanut butter by the cup every single day, crying all the time, had no energy to look after my kids and wanted to nap all the time, and cried when I couldn't! Then a few months later all of a sudden my joints started hurting. My wrists, elbows (like tendinitis), then a couple of days later I was limping because my hip or my knees hurt or my ankles felt swollen and weak. I felt like a hypochondriac because I was always complaining of something. Did I mention the hair loss?
So, sorry for the long story. But most of my symptoms have disappeared since removal if the Mirena this past Valentine's day 2009. However, as I was forewarned, I have recurrent symptoms every month while PMSing. I have never suffered from PMS in my life, until I had Mirena removed. I get depressed, eat more, and my joints hurt so bad, and sex repulses me. My poor husband; A couple of weeks ago I got so grossed out during sex that I made him feel like a creep.
These last 2 weeks, I wasn't supposed to have joint pain, because i wasn't PMSing anymore. But it has gotten worse. That's when I put up my post asking if anyone else has this pain. I was beginning to think I had Fibromyalgia. I also have very dry burning eyes, which is also a symptom on Fibromyalgia. I saw my doctor twice last week, and she thinks I may have it too. Is anyone out there in a similar boat?

I have a history of sinus infections. After two rounds of Augmentin did not clear up my latest one, my doctor finally gave me the steroid pack and Avelox. He had tried to avoid the steroids. I have had them so many times. I finished my steroids 5 days ago and my Avelox yesterday. I read the side effects and did as it suggested. Since it mentions low potassium would not be good I ate a banana every day and had some orange juice to keep my potassium levels up. The drug warms against taking any pain killers such as Aleve, Advil, etc. One earlier reviewer admitted taking Aleve and had a bad reaction... well.... bad move.... I have had no real side effects that I can say for sure are Avelox related. I did feel a little less focused at times, but was not obviously groggy or woosey. I did have a little abdominal discomfort that I usually do not have with drugs, but it was short-lived and only occurred 3 of the 10 days. Many people have bad effects because they do not follow the warnings against anti-acids, pain killers, low potassium, etc. Some people are more likely to react to any medicine, while others like me rarely have a side effect. My tendons did not hurt... nothing.... People who are out of shape, have a poor physical life style, etc. sometimes help contribute to the drugs reactions by being in basically poor physical health to begin with. America is one of the fattest, out of shape nations out there due to our abundance of everything. The majority of persons can take Avelox with no real issues. I will take it again. I truly feel concern for those who had problems, but sometimes we are partly guilty by how we don't take care of ourselves when we are well...... As with any drug, some persons will react no matter what... It's often just a matter of inherited genetics...... Be safe everyone, and take time to evaluate how you take care of your body and really decide to do better. For the record I am almost 58, 5-9 158 pounds and work out semi-regularly.... Take care of that temple God gave you. Its the only one we get on this Earth,,,,,,

It has been almost two years since I took one tablet of 500 mg levaquin for a throat infection. I immediately felt lightheaded, then came the hot prickly skin, rapid heartbeat, insomnia and just a feeling of doom. I did not take another pill. Right after this my ankles started to hurt and podiatrist said had a torn posterier tibial tendon. To this day, I cannot walk without a limp, and can only wear athletic shoes with orthotics. If I stand for or walk for a small period of time I am in a lot of pain and have to sit. I was diagnosed with rheumatoid arthritis from the inflammatory markers in blood tests and rf factor, even though mri of my hands and wrists are normal. My right shoulder and arm hurt, my wrists and fingers hurt, my knees, neck. It is better, but I will never be the same as I was - no more running, walking my dog, going camping with my daughters girl scout troop - can't go hiking. I am 50 and I feel like I am 90. Would like to sue someone.

The doctor prescribed Levaquin for an infection that I had. After taking one pill I awoke with a heaviness on my chest, shortness of breath and tingling down my left arm. I have never had any of these things happen to me before so I suspected a reaction to the Levaquin, but the doctor told me to go to ER, from there they admitted me to the hospital but found nothing wrong with my heart or lungs....I continued with the Levaquin and after 6 days I had a pain just behind my left knee. On the 7th day it went to pain behind my right knee. I could not straighten out my leg without having pain. It was like the tendon was very tight and hurt....tendinitis???? On the 8th day we discovered Levaquin could cause tendinitis so stopped taking it. That has been over a week ago and I can hardly walk and if I straighten out my leg it produces excruciating pain. It has effected my shoulder and wrist also....Also found out that this tendinitis can come back in the future just from this medication. Is there a suit going on about this? Please reply if anyone knows of one. I think we need to take action with all the problems this drug is causing.

I was given the drug Levaquin 2 times in Nov 26, 2008 and 3 times in one day on Nov. 30, 2008. Now I have Tendinitis and Left Frozen Shoulder. I have to get Surgery in 1 week and numerous Physical therapy. I also have it in my knees, I complaint about these things while I was in the hospital and they never wrote it down. I have Severe Knees pain, left shoulder pain, severe migraines, blurred vision, right wrist paint.

Currently on month three of side effects. LIghtheadedness, head pressure and tingling, feeling like I am going to pass out, awful Castro pain, gas, belching, chest pain. Tendinitis in both knees and left wrist with swelling. Weak, tired, sick 80% of the time. I have been scoped, had mid section ultrasound, heart stress test, numerous EKGs, blood workups, all within range except for low potassium. This is poison and it just goes on and on. Most Doctors are skeptical although I have found two that believe this is a result of Levaquin, after seeing a half dozen including my internist, Gastro Doctor, urgent care Doctor, ER Doctors, cardiologist, etc. I would think the insurance companies would want this off the market. My medical bills are out of sight and my deductible which is rather large was met two months ago.

It's been almost 1 1/2 years since I have taken Levaquin for Bronchitis. I took it for only 3 days, after that I couldn't stand the pain and that was the only thing different so I knew it must have been the Levaquin. I suffered major, severe joint and muscle pain. I couldn't even walk down the stairs to the living room. As for lasting side effects, I am dealing with arthritis in my knees...which I never had before and I am only 40. I have severe tendinitis in my elbow which may require to correct. I know I am getting older but jeez....I am unsure if the arthritis and tendinitis is completely related to my reaction to the Levaquin, but what else could it be. I am not that old nor am I that out of shape. My only hope to spread the word about this evil toxic poison before someone else gets hurt.

I took Levaquin 3 times for 10 days each time over 2 or 3 years. I am not exactly sure as I'd have to backtrack my records. It was for a stubborn sinus infection. (BTW, it didn't help) Is it possible that now, 2 years after taking it, that my tendons are 'tight' and sore from the drug? I have been complaining that they feel like tight springs for months, totally inflexible. I didn't know about this, so I decided to really stretch them. I did 4 squats and the next day, my R knee was blown up. I got an MRI which showed a torn meniscus from doing the squats. Since then, I've discovered what Levaquin does. Could it be that my tendons were so tight, that they didn't give, but the pressure from them being so tight could have put so much pressure on the meniscus, that it tore?

I was “poisoned” by Levaquin -- resulting in acute tendinitis in both Achilles tendons.

Background:
I am a healthy, athletic male in his mid-50s who has never had an Achilles tendon problem. In early July 2008, my doctor (general practitioner) prescribed Levaquin for an infection. I took the medication for 14 days, as prescribed.
Sudden onset of acute tendinitis in my Achilles tendons occurred near the end of the medication period. The tendinitis occurred in both Achilles tendons simultaneously. Nothing related to my lifestyle would have caused the tendinitis.

Symptoms:
Symptoms included the following at one time or another:
1. aching
2. sharp pain
3. feeling of heat/burning
4. tightness
5. pins and needles in small areas (micro tears?)
6. weakness at rear/base of each heal.
7. When I woke-up each morning my tendons and the back of my heal pads felt sore, weak and tight.
At the height of the problems, I had extreme difficultly walking and negotiating stairs, and I thought there was a risk that my tendons would detach from my heal bone.

Doctors’ Advice:

My general practitioner’s and my podiatrist’s advice was to: (a) not run, cycle, hike or otherwise exercise my legs in any manner other than easy walking and swimming, (b) gently stretch, (c) take ibuprofen, (d) ice regularly, and (e) use heal lift shoe inserts made by my podiatrist. Their advice was based on the view that the damage that was done is more like damage cause by an injury than damage caused by an insidious drug. My readings on the subject indicate that little is known about the mechanisms behind this fluoroquinolone-specific toxicity. It is believed that the tendon’s collagen fibers become disorganized and infiltrated with small blood vessels -- resulting in weakness. And there are no specific treatment plans for this problem.

After 2 months of living with these symptoms, I decided to change course.

My Approach to Healing:

Because I never believed my pain was the result of inflammation, I stopped icing and taking ibuprofen. Because stretching seemed to further weaken the tendon and set me back, I stopped stretching. Because I believe that the body heals itself best when used, I started cycling at an easy pace. I then worked-my-way-up to cycling more aggressively, and to walking in the neighborhood. That’s where I am today. Two days ago I had my first day without discomfort in 3 months. Yet, I have a long way to go. I am not yet hiking or running. It’s a slow healing process with occasional setbacks when I push my tendons a bit harder than I should, Given the progress I have made, I am hopeful for a full or nearly-full recovery in another few months.

Other things I have done in the past month:

1. Taken L-Lysine (1000mg daily), which is believed to aid collagen formation.

2. Taken Magnesium (250mg daily), which some believe may help leech the fluoroquinolone molecules from the tissues because of the affinity of these antibiotics for minerals.

3. Taken Fish oil pills (3000mg daily), which improves circulation

4. Used a heating pad, which improves circulation

5. Started regular Acupuncture (first time for me), which improves circulation

What you can do:

1, Be easy on your tendons until you get a handle on the problem. Don’t over-use tendons when they are in a weakened state.

2. “Listen” to your body and take steps you think best to help the healing process.

3. Tell your friends to beware of potential side effects from fluoroquinolones.

4. File a MedWatch report with the FDA at fda.gov.

5. Share your findings/advice on this forum.

Good Luck

I HATE MIRENA!!!!! I had it put in last December after the birth of my fourth child. In May, I developed intense ankle pain and was diagnosed with tendinitis. Never once did it occur to me that my IUD could be the culprit. I went for an MRI which was negative. The pain did not improve - it spread to my knee and then my lower back. After a back MRI, which was also clear, it occurred to me to start researching mirena side effects. I discovered that tendinitis was a rare side effect (though my ob claims it is not possible). When I went to have the thing removed, the doctor discovered it was embedded in my uterus. Had a procedure done to remove it yesterday and I am already feeling less pain than I have had in months. How insane for something to cause me so much pain and send me to so many doctors. I urge anyone on mirena with any bizarre symptoms to have the thing removed!!!!!

To the best of my knowledge I never had any of the 'immediate' symptoms.
My problems are probably due to the fact that I was prescribed Cipro 3 possibly 4 times from Aug 06 - Dec 07 and then finished up Dec 07 with a round of Levaquin. My father is over 60 and was recently given Levaquin and had immediate and serious problems. He is seeing a doctor recommended by the CDC today. Yes, he is even working with the CDC on
this one. Due to all he is being told he is convinced that the medication is behind my medical decline as well. Since taking these medications (symptoms started slowly in 07), but after taking the Levaquin at Christmas time I never got up from the couch. My thyroid gland has quit working, my adrenals are shot, I have been diagnosed with fibromyalgia, chronic fatigue, blew out 3 disks in my back, vision is deteriorating rapidly, and really so many things I can't list them all. I had a complete physical
in Oct 05 and was given a perfect bill of health. Through Aug 06 I was riding my bicycle 33 miles per week. I'm still trying to figure out what hit me??
What my father has been told is that in some individuals Levaquin will attack the glands (like the thyroid) and will compromise the immune system. This damage appears to be permanent. All I know is that I went from being extremely healthy to terribly sick. If in a day's time I have enough energy to load and unload the dishwasher it is a banner day. I can
not work and seem to get worse instead of better as each day passes.

My husband also had pneumonia at Christmas and took Levaquin but does not seem to have had an problems. I suspect it was possibly the cumulative effect of having basically 4-5 rounds of the antibiotic in a years time. According to the people at the CDC that have spoken to my father the symptoms that I have can all be traced back to the medication. One never knows what effect a medication will have. Just please be careful when taking this medication, and limit how many times you take it.

I was prescribed the 4mg methylprednisolone pack along with 50 mg tramadol for acute tendinitis in my wrist. I took the first 3 days of the prednisone and only 2 doses of the tramadol over the three days. For a total of 60 mg of prednisone.

The first day I had hot flashes and insomnia but attributed it to the tramadol because I had never taken it before and had taken the prednisone several years ago for poison ivy with no adverse reactions. I didn't take the tramadol the second night and then took it again last night along with my daily dose of prednisone. I had extreme difficulty falling asleep, heart burn, hot flashes; and tossed and turned all night trying to fall asleep. At around 2am, I began to have difficulty breathing, tightening in my chest, confusion, and racing thoughts. It felt as though my throat was closing up on me. My anxiety progressed to the point that I was pacing back and forth. I woke my husband up and told him to prepare to take me to the ER. After calling my insurance's 24 hour help line, it was recommended that I go to the ER. I had an x-ray, blood work, urine drug screen, and echocardiogram. Luckily, everything was negative. The ER doctor told me that I likely had a reaction to the prednisone and commented that some people will experience these symptoms when taking it. He stated that he had a similar reaction when he took it and it felt like he was climbing the walls, which is an accurate description of my experience that night. He recommended that I either stop taking it altogether or call my primary care provider and cut it down. He prescribed me xanax and administered some to me at the ER which greatly helped. The next day I stopped taking the pred but am still having dizziness, chest tightness, hot flashes, and mental dullness. I have decided to never take this medication again. Fortunately, I don't have any of the physical sx that some have experienced, and my heart goes out to you. I think the mental symptoms were traumatic enough for me and can't imagine having both as I would be a basket case. I have mood swings, some melancholia, and am very fatigued.

I think it is imperative to research any medication that is prescribed to you before you take it. Many providers will say that side effects are rare, but my experience is that side effects are more common than rare. My prayers go out to those of you who are going through what I am going through. I hope that it clears our systems quickly because this is no way to live. I'd rather put up with the pain of tendinitis or carpel tunnel than to have these symptoms.

I was prescribed an 11 day supply of Levaquin - 500 mg. I'm on day 7 and struggling to make it 4 more days. The first day I took the tablet around 5 pm. I was up all night. Since taking in the morning, I've been fine. Now, I'm suffering from very sore biceps, heels and stiff knees. The fatigue is overwhelming. I also experience extreme dizziness as well. I may call the doctor tomorrow to see if I can stop this. I've taken various antibiotics throughout my lifetime and never have experienced the side effects such as this one.

My 80 year old mom is going through Chemo for Bladder Cancer. She is also diabetic. Bacteria was found in her urine so the doctor gave her 4 tablets of Levaquin. Saturday night of Labor day weekend mom took the first pill. Sunday she woke up almost BLIND! She panicked and, thinking it was her diabetes causing the problem, took her blood sugar numbers. (She was so scared that she can't recall what the numbers were, just that they were 250+). She started taking her fast acting insulin. She couldn't get the blood sugar numbers to come down after numerous injections. She called me so confused and not knowing what to do. Thank God I wasn't gone that weekend. I rushed 18 miles into town. I calmed her down. We just kept watching the numbers and she kept taking her injections. About 6 hours later the numbers were down to normal for her. We narrowed the cause down to either the Levaquin or the infusion of platletts she had on Friday. We called the pharmacist and he said that Levaquin could cause blurriness of vision. She didn't take any more Levaquin.
It had been 10 days since she took that one pill and her eye sight is still messed up. When she tries to read the newspaper the letters jump around. She has a hard time reading the dosage numbers on her syringes now. She is so scared that her eyes won't get better and she will have to be dependent on someone.

I took levaquin for 2 weeks to treat a infection, i am 26 years old and have never had muscle pain for longer than a couple days after working out...now i have moderate pain in my rib area and muscles near the groin area and even upper leg, and have done hardly any physical activity while being treated...i have seen no improvement for a few weeks now, but think my infection is gone... going back to my doctor tomorrow...need help

I was prescribed Levaquin for a bout of diverticulitis six weeks ago. About a half hour after taking it each morning, I felt completely unwell--dizziness, fatigue, overall weakness, odd sensations of pressure in my head, chest, and bladder, weird bouts of sudden joint pain. The worst side effect was terrible insomnia. I'd go to sleep OK, but wake up after 3 hours and not be able to get back to sleep, sometimes for the rest of the night. Instead of getting the rest I needed to get better, I was getting more and more exhausted. Now, a month after stopping the medication, my sleep hasn't returned to normal. I'm still awake in the middle of the night for two or more hours. Is this a residual side effect from Levaquin? Has anyone else experienced it? When can I expect my sleep to improve? Is there a way to detoxify from this drug?

My pain started within a few days of a switch from Fosamax to a generic form. I had been on the med for about ten months and hadn't had anything significant as far as side effects are concerned. First my shoulder blew up with very painful tendinitis and bursitis - doctors said it was likely a strain. Then I had jaw pain a few weeks later and that was supposed to be because of a crown I had done. The latest and worst has been my right hip and right leg to the knee - very sharp and burning pain - really made it impossible to walk. The doctors did not make the connection to fosamax and I think they probably still think I am crazy - but I KNOW that it where it is coming from. I am being treated for the pain with the usual stuff - it has been about two weeks. I think I have a long haul ahead before I feel really great again. The biggest problem with these drugs is that the side effects can present so long after you start the drug that most people don't make the connection. I figure people have been living with osteoporosis forever - so I will risk my osteopenie without any more of this toxic stuff. How many people are out there suffering without a notion that this is the cause - still taking that magic pill once a week?

Well, it's been almost 3 days since I have had the Mirena removed. What a relief! I suddenly felt a sense of release when it came out-almost like I had lost 10 lbs from my uterus. I have not had a hot flash in 2days and have a wonderful sense of well being. Yesterday, I carried my full laundry basket up the stairs with out any help from anyone. I was unable to walk up the stairs without holding onto the railing and pull myself up before. My feet still hurt, knees are a little better and still experiencing back pain. By the way, I have only lost 1lb. BUT lost 11/2 inches on my waist. GOOD BYE BLOAT! I know recovery will be long BUT at least I feel like I can face it now. I feel so much Clearer now.
Can anyone tell me how long before the joint pain goes away and if it even does completely?
thanks

Ok ladies...day two since removal. Still no major relief of symptoms...but I did start a period...pretty moderate flow. I'm exhausted and my emotions are all over the place. (I have cried about 4 different times today...and yes I've been at work for most of it. Nice.)

I found a posting on here earlier...can't remember whose it was (Sorry!) about checking out a site from "nerdnuggets" where it posted a product monograph which is the informative packet released by Bayer Corp. in Canada. If you can find that posting, do it! Pull it up and print it out...it's a 46 page description of the medication. Page 10 specifies all of these side effects...even the tendinitis I've been treated for! Page 33 lists the absorption and distribution of the medicine into our bodies and specifically discusses how the medicine becomes systemic in our bloodstream within 15 minutes of insertion! So what I did was printed out several copies, attached letters, and sent it out to all my doctors and specialists, including my EX-gynecologist asking him to use the information to educate not only himself, but his staff as well so they do not grossly discount another patient's side-effects they way they did mine. Keep in mind that this information is not readily available to us here in the US...this is a Canadian report.

Hence my other phone call made today to attorney Justin Wikin (out of Florida I believe...thank you, Amayaa, for this info) at 850-916-7450 regarding a possible class action suit. They took my story down and recorded names of all my physicians and told me I should hear back from them within 7-10 days.

In the report, I also found how it is excreted form your body once removed. It has a half life of about 20 hours. Layman's terms: After 20 hours, or approximately one day, only about 50% remains in your body. The next day, 50% of that is removed, leaving about 25% in your system. (So: Day 3, you should only have about 12% left, Day 4 = 6%, Day 5 = 3%, Day 6 = 1%.) Realistically, every day should get better and better...and I should start feeling some major relief when, after about 1 week, all this is out of my system.

Good luck to us all and for those of you who are having the same problems with their doctors as I have been...print out that report! (Plus, it's fun to see the look on their faces when you show them a medical report that they cannot dispute!)

I'm a 46 years old male normally good shape,I was put on Lipitor due to high cholesterol and family history of heart problems.I've been on lipitor for four years , 2years on 10mg, 1 years on 40mg and 1 year on 80 mg.
The last 6 months I have been experiencing severe archiles tendonitis to the point where I can hardly walk. I am extremely disatisfied with this drug and have read a lot of complaints regarding this drug.

Has anyone else experienced this side effect?

Please reply to this post.

Thank You

I am a 36 year-old female, and in very good physical condition. I have been a runner for 15 years. I was prescribed levaquin for a recurrent sinus infection, 500mg x 7 days. On the second day I developed severe carpal tunnel syndrome (tendonitis of the forearms & hands); I could barely hold a pen in my hand, much less write. I refused to take the 3rd dose. On the 5th day (even though I am not taking it anymore) I woke up with severe hip pain (both hips). I can barely walk, much less run. I am a full-time physician and have a small child. I am not sure what will happen to my favorite hobby, running. This drug is extremely dangerous, and I will never prescribe it to anyone. It should be removed from the market!!

My Mirena Removal....
So i posted here a few weeks ago after I found this site. I had EVERY side effect listed and was so freaked out that i immediately made an appointment for removal.
For those of you reading and wondering what the removal is like..
Well, NOTHING like the insertion. I was so so nervous and it was over before we actually started. The DR was surprised that i was back in his office to have this removed. He then proceeded to do an ultrasound to be sure it was placed properly before removal. And yes, all was OK on the position of it. I explained to him my reasons and he looked at me like he had never heard this before. I honestly can not imagine with all the women he sees that NONE of them have complained. But...as I was getting dressed afterwards, I took a good look in his office. There was Mirena literature ALL over the place. In fact, that was the ONLY thing he was advertising. Not to mention...they made me pay up front with the insertion back in Nivember...billed my insurance and I still have yet to receive my reimbursement. Oh yeah, and that...they charge more than the actual Mirena costs, then they bill your insurance for the price they know they will pay and the DR then makes about $150 profit. Nice.
Ok, back to my side effects post Mirena. The removal was not painful at all. I did spot for about a week- nothing too heavy but it was clotty and def there.
A couple of days after the removal it felt like I was coming out of my skin something terrible. I figured this was my body adjusting to the lack of hormones. I also had some headaches.
It has now been 2 weeks and the spotting has disappeared. I also can see the bloating of my stomach is starting to go away. It looked like I was about 4 mos preggo while I was on it. I also have an increased sex drive. And sleep-- well let me tell you, I have not slept this good in a very long time. I am actually sleeping more than 6 hours now and the night sweats have also discontinued.
I can't believe EVERY time I come to this site and look up Mirena ALL the people that have posted their experience as being negative. Yet, the DR looks at me like I am crazy! I have been seeing him for years and I have never complained about something like this. I really am so happy that I have it out and wish I would have done my research on this prior to insertion (which was one of the most painful things ever!)
So..for those of you out there that are either contemplating having it inserted...I say NO WAY. And for those of you out there that are nervous about the removal or not sure..I SAY YES, DO IT! For our bodies to be reacting this way, it is clear to me that it should not be inside of us. Listen to your bodies...they really do speak to you and let you know when something is not right. Forget about the DR saying it is safe or he has not heard of any of these side effects...YOU be the judge.
Good luck! And I promise it gets better once you get that lil' demon out!
Mona