Bones and joints symptoms and conditions

I had the mirena placed in in May of 2008 due to losing to much blood during my period. I had become anemic. my Dr. gave me two options...Mirena or hysterectomy. i had gone through iron treatments that didn't work and i was miserable. Of course, with three kids, i chose the mirena. my doc didn't give me any schpill on the effects of mirena and also said that it would be a little prick at the time of insertion...WRONG! I screamed when she inserted into my uterus and since then i have suffered these side effects:
1. 20 pound plus weight gain (on a 1500 caloried Weight Watchers diet for 8 months and steady exercise program). Have taken two rounds of prescribed appetite supressent - gained weight!

2. gone up a full cup size in bra

3. ache all over in my bones and joints.

4. sharp pain in back that will NOT cease or go away. It is like a pulled muscle. I have had this pain for close to a year.

5 headaches

6. breast tenderness

7. nausea all of the time

8. cramps out of the blue that make my knees buckle

9. and very strong desire to eat sweets...which i can't because of my type 2 diabetes!

I am having the devise removed on Tuesday and I absolutely can not wait! I have discussed all of this with my husband and he is just stunned at the effects that i have had. I think that i would rather be anemic that to feel this bad! I sympathize with all of you! This is ridiculous and should be forwarned by your Doctor prior to insertion! Any doctor who says that you should watch what you eat after gaining all of this weight due to the mirena needs to have their head checked! i should be a size 0 right now with as little as i have eaten in the past year. I am as heavy as i was when i was pregnant and my boobs bigger than they have ever been!

I am being treated for ulcertive colitis. I have been on prednisone since Sept of 08. I started out on 40 mg. In late Oct. my doctor started tapering me off 5mg per month. Each month following the tapering date, I would get sick. As I look back, all the signs of withdrawal were there. This Jan. I tapered once again, but the window was only 3 weeks. I hit rock bottom. If there was a symptom, I have it. Nausea, burning in my digestive tract, diarrhea every time I eat, muscle ache, numbness in my legs, swollen feet, sore bones and joints. ( The worst was in my feet. I ended up seeing a podiatrist. He thought plantar faciaitis until I told him about being on prednisone. The small bones in my foot were swelling, The muscles in my calf were buning they were so sore. That was last week. Today my other foot started. I can hardly walk. In addition to that, I am lightheaded, have elevated blood pressure, and fatigue. I also had some vision problems that sent me to the doctor. I went through a ton of testing which all were negative. It seems that pseudotumor is another symptom of withdrawal. I have a history of that. It would have been nice to know that. As I look back each month, I had different muscle and joint pain that lasted about a week. I was put on an acid reducer in Dec. to help my stomach, but in all of this time, I was not told that these all may be withdrawal symptoms. I have been off work for two weeks now in addition to the days I missed each month. My physician is now controlling the tapering procedure. They up the dose to 10 mg again. They plan on weaning me by 1mg doses. This has been a terrible experience for me. I have only been severely sick one other time in my life. This pain is awful. It is chronic. This drug may be beneficial, but it is like poison too. Anyone who takes this should really ask a lot of questions, and be careful..

I have taken 4 doses of Fosomax-1x a week - and have noticed weight gain, nausea and lethargy. After the first three doses noticed a mild headache, which I blamed on my sinuses. After this last dose ( taken 6 days ago), I have had an excruciating headache, and facial pain. I have a constant burning feeling in my stomach. I will not take another dose. I saw that someone had previously mentioned taking Bone Up, and had good results. Has anyone else tried this? As a breast cancer survivor with borderline osteoporosis I am looking for a good alternative.

My symptoms are the same as all (anxiety, mood swings, low sex drive) and I plan to have this thing taken out ASAP. It has been so bad lately that I cannot function. I've had more panic attacks than I can count in the last couple of weeks. What I want to know is how people fare on the other side of things. I would imagine it takes a while for your body to regulate after removal, but how long. And to echo- no more artificial things in my body.
Side note- has anyone tried cold shower therapy, apple cider vinegar or lemon balm for the anxiety? (******)

I have just tried Advair, and after 4 days, joints all over my body started to ache. My eyes hurt alot and my vision got blurry. Lastly, I just have a general feeling of unease. I quit the advair and was much better within 3 more days.
All pain is gone and eyes feel normal again, although my eye sight seems diminished. I took no other drugs and felt fine before taking the Advair.

I am 44 and suffer from mild copd. I can get by with Albuteral, and will do
so from now on. I know that one is safe.

Good luck to all.

hello ladies im a 34 y/o mother of 2 a 14y/o and ten month old i had the mirena inserted in late nov and did not realize i was having any problems till bout a month ago. in the time since i had it inserted i gained twenty pounds i have had no energy i wanted to eat all day i had horrible gas pains i was bloated and felt like a 98y/o woman with osteoporosis. my bones and joints ached so bad i had kidney pains mood swings hair loss no sex drive and had no idea where this was coming from. i owe it to my daughter for seeing a commercial on t.v saying that mirena makes u gain weight i had it removed today when i went in to my dr. office and explained my symptoms he said "IT WAS HIGHLY UNLIKELY" that they were cause by the mirena. it was weird because it seem like he really didn't want to remove it and my other dr. pressured me into getting it. just be aware i DO NOT recommend it. at times i felt like i was going crazy the depression was severe and no sex drive. once again i DO NOT RECOMMEND IT. i will come back to this site and give an update as to how things are improving. best of luck and god bless. Barbie

I just got an injection yesterday in my shoulder. The injection had the following in it: 1ml of 40mg per milliliter of kenalog solution along with 1ml of 1% lidocaine solution without epinephrine and 1ml of .5% marcaine solution.

Here is what happened after the injection... Within 30 minutes I was experiencing nausea and a headache on the left side of my head, behind my eye, and to the outer side of the eye. Within an hour I had pain radiating throughout my entire body! It has not been almost 24 hours and I am still in pain. My head is splitting, I'm still experiencing nausea, and the pain is all over in my bones and joints, and my hips hurt really bad. I'm also experiencing a terrible dizziness, and light headed feeling, and confussion.

Here is the real kicker... I have severe drug and food allergies! There is virtually NOTHING I can take without having a reaction. I can only eat fish, fruits, and veggies, otherwise I get very sick, and have severe stomach cramps to a point I cannot even stand or walk! My doctor knows all of this, and he still told me this was perfectly safe, never been a reaction, and I would be okay. Only problem that may arise is infection, but that is extreamly rare!

Does anyone here have any idea what is happening to my body, and how long it might last?

I'm 23 and I was diagnosed with adenomyosis, which is internal endometriosis (in which the endometriotic tissue grows within my uterine wall) I have been on Lupron since Nov 2007. I do not recommend this treatment to anyone unless they are in dire need. Though I am supposed to be on it for 6 months, I will not be continuing Lupron due to the negative side effects I have experienced. I've been experiencing extreme mood swings, from being enraged, on edge, anxious, emotional, or very depressed. I get intense head aches, very nauseas, swelling in my stomach at times as well as stomach pain, blurry vision, achy bones and joints, confusion, hard time concentrating, forgetfulness, insomnia, cramps and pressure...and the list goes on.
Please inform yourself and do lots of research before ever thinking of taking Lupron. I would never do this again, especially after realizing the harmful effects it has had on my body physically and mentally. I've learned to trust that the best people to listen to are those that have actually experienced this drug, rather than those that are trying to promote it. Everyone that I have talked to that has either taken Lupron or knows someone that has, have had the similar experiences to mine.
I'm disappointed about my experience with Lupron, and I would never recommend this treatment to anyone.

I have been taking Yasmin for only one week, and have been sick ever since the second day. I started taking the pill last week. I had a baby in May, and the doctor decided this would be a good start for birth control. I have never taken BCP's before and if this is what they do to you, I never will take them again. I have had achy bones and joints, massive headaches, constant pain in my chest and back, and today, I broke out in a fit of acne that is obscene. I look like I have the chicken pox. I am totally disturbed by this. Has anyone had side effects like this in such a short time of taking these pills? I am stopping them today!!!

My first treatment was administered in the back of my hand. I had stiff fingers and what seemed to be an arthritis flareup in a knuckle at the base of my hand which lasted for many weeks. I had a discernable swelling, which impinged on another joint, and was painful. Also, the first time I had the treatment, about 12 hours after I had it, I felt really weak and ill, had creepy crawly skin, fatigue, and flu-ike blahs. Kept waking myself up moaning from pain in all my bones and joints. This lasted about 24 hours. After that, though, I felt pretty good, and a pain I had had in my hip before treatment was gone. The next time it was much less of a response. The third time not much at all, just a little tired. However, since beginning treatment I have had stiff hands.(I now insist on getting the infusion in my arm, which helps some) I also got tendonitis in two tendons in one hand,after the first treatment, and bursitis developed after my third treatment in one shoulder. I feel as though the treatment kicks up an arthritis response with me. I am wondering if it is building up bone in joint areas, which, if they already have arthritic invlvement, further restricts the space for tendons to function in. The change in my hands is my most enduring symptom. I have to really work to get all my joints in my hands working every morning. My middle joints are most affected in my fingers, and have been a little stiff ssince treatments began. I never had this before. I figure it's worth it, but....