Nerve blocks symptoms and conditions

I have been taking perocect 10's for the last 1yr or so and it is very bad when I don't have them I feel like crap. When taking just one it is like taking 3more 10 min later cause it does not work as well from when I first started taking them. When I run out I am looking for them everywhere and taking other pain meds to cover the withdrawals. Man it is so bad feeling like that the runny noise,sweating,being angry,shaking, throwing up,shiting my guts out etc. I have a chronic back problem and I'm only 24yrs old. I have a very supporting husband who is there for me when I'm withdrawing all the time and I love him for that cause if it was any other man they would of left me hanging. I advice anyone who starts this pain killer to only take it when needed cause the chemical in the pill will mess your who life up and you will have some serious problems for realist is true but how I'm going to stop I will take a week out of my life to go to the hospital for help. Also there is so many other medication that can make you sleep.(PEROCECT'S WILL MESS UP YOUR LIFE SO DON'T GO DOWN THAT ROAD, PLEASE TAKE THIS MESSAGE SERIOUS THEY ARE VERY BAD, DON'T COVER UP THE PAIN GET IT TAKING CARE OF AND IF THE DOCTOR GIVES THE PEROCECT'S TO YOU DON'T TAKE IT CAUSE THEY DON'T CARE IT IS NOT THEM PLEASE DON'T).

IT'S OUT!!!!!!!!!!! What a mess I went through. For those who missed my prior posts, I got my Mirena in June 2008 after I got married. Even though I'm 29, I'm a medical student and not ready for a baby.. Within weeks I had oily skin, oily hair, hair loss, sore breasts, and no sex drive at all. But I never had a single period after the second month, so I was happy!

By August or September I was gaining a lot of weight (20lbs) and started feeling "brain fog" and fatigue. By December and January I was seeing neurologists for SEVERE migraines and dizziness. In April I developed symptoms like MS such as tingling/numbness in my head, face, and one foot... profound fatigue, and incapacitating dizziness.I've had every test done from thyroid workups to MRIs/MRAs and nerve conduction studies. I was on 3 different migraine prescriptions and was even getting nerve blocks in my neck for them.

In May I became withdrawn, irritable, depressed, and had anxiety attacks. I'm not ever a moody person, and never had PMS. But here I am, crying for no reason, yelling at my husband, snapping at my mother, and SO FREAKING EXHAUSTED that going to work is impossible, driving the car seems dangerous (severe brain fog.... like I'm drugged), and even just doing the dishes or feeding the pets takes all my effort (with tears) to complete. I don't feel like myself at all.

I found this website and thought perhaps all these symptoms were from the Mirena. So I found a new OBGYN who was awesome and said he'd take it out. I went to have it removed but the first a$$hole who put it in for me cut the strings too short so they could not be grabbed. The new doc tried to reach them but couldn't. I ended up having to have THE MOST PAINFUL PROCEDURE OF MY LIFE.... I had to take cervical dilation pills and then get a hysteroscopy which is where they shove a camera into your uterus to look around and find the little sucker. The cramps were unbelievable.... 10 times worse that getting it placed. (Mind you I've never had children so it was really bad). After he found the strings, he grabbed them and pulled. I thought I was going to die.... my poor cervix had a scope in it, an instrument holding it still, a dilator in place, a speculum in the hole, and then an instrument went in along side the scope and pulled the little bugger out. AHHHHHHHHHHHHHHHHHHH! I was in a hot sweat worse than menopause I bet!

So here I am, home, bleeding, only minor cramps. But now I wonder... how long will it be until the depression and brain fog go away? I want to be myself again. I want to be happy. I want to laugh instead of cry. I WANT TO HAVE ENERGY. My greatest fear is that I went through all the pain of putting it in, taking it out, and the cost, and the depression, fatigue, and brain fog won't go away, meaning it wasn't the Mirena to begin with. (If that was the case, I could have dealt with the weight gain, oily hair, and migraines as long as I had the nerve blocks). But I find it hard to believe that the Mirena is not the cause since so many of you women say the same thing. BUT.............. most of you had the Mirena placed after having a baby, so it's possible it was PPD?

THIS IS MY QUESTION TO ALL OF YOU OUT THERE.... did any of you WHO HAVE NEVER HAD CHILDREN have these things after getting the Mirena? Also, isn't it weird that the severe fatigue, depression, and really bad brain fog started after 9-10 months of having it and not sooner? I was on OCPs before the Mirena and did fine.... but this time I am so depressed and irritable, dizzy, and FREAKING TIRED TIRED TIRED.

:( How long until I feel better if it was the Mirena?

OMG...I want to thank everyone for their comments, as I thought I was just crazy, I have not been able to walk more than 25 steps in three years because of this stupid Lisinopril. I could honestly just cry. Three years have been just taken. My daughter was 8 and now she is 11. We have not been able to go to the mall one time because mommy's muscle pain and weakness is so bad and it is just embarrassing to try to walk around a mall or the airport. I am only 39 there is no reason my primary Dr. should not have caught this. I have been referred for and had multiple MRI's, cortisone injections, nerve testing and nerve blocks, taken Tramadol until I can not take it anymore. Thank you all of you. Thank you. God Bless you, in Jesus name, Amen.

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 thirteen and a female. I had throat inflammation, swelling of my sinuses, and an ear infection. The doctor gave me a cortozone shot and recommended a z-pack. About 2 hours after i took the first dose i got severe stomach cramps, nausea, dizziness and loss of hearing. I keep having to run to the bathroom because i feel like im going to puke. I keep sweating too and i feel hot and sticky. I hope the side effects wear off soon but after reading these comments i don't think i'll be that lucky. I don't plan on taking this again. The side effects are worse than actually being sick.

Please, is the anyone who knows of a way to treat the dibilating muscle/joint pain experienced as a result of taking the antibiotic, levaquin?

I WAS TOLD TO TRY NERVE BLOCKS AS AN ALTERNATIVE TO SURGERY. I HAVE A RUPTURED LEAKING DISC AS THE RESULT OF A CAR ACCIDENT AT L4,L5, I HAD THREE INJECTIONS, I WAS NOT EVEN TOLD THEY WERE USING A STEROID. WHEN I STARTED HAVING NIGHT SWEATS, IRRITABILITY AND EXTREME FACIAL HAIR MY GYNO SAID IT WAS THE NERVE BLOCKS. THE NP AT THE PAIN TREATMENT CENTER SAID IN TEN YEARS SHE HAD NEVER HEARD OF IT. THE DEPO SHOT I WAS GETTING WAS NEGATED SO I GOT MY TUBES TIED. I HAVE AN APPT WITH AN ENDOCRINOLOGIST IN JUNE, I GOT IT IN NOV, MY HUSBAND SAYS WE WILL HAVE A CIVIL UNION BY THEN!! THE PAIN RELIEF LASTED 19 DAYS, THE HAIR 2 MONTHS AND COUNTING. THE SURGEON TOLD ME BEFORE HE PUT ME UNDER HE DIDN'T THINK IT WAS GOING TO WORK. I WISH I KNEW ABOUT THE SIDE EFFECTS. NOT HAPPY AT ALL. TREATMENT CENTER SAID BECAUSE OF SIDE EFFECTS I WAS NO LONGER ELIGIBLE FOR NERVE BLOCKS AND CLOSED MY CASE AS A PATIENT. I ALSO HAVE 2 BULGING DISCS IN MY NECK AND CHI FROM THE ACCIDENT. I GUESS I MAY HAVE TO HAVE SURGERY. THIS HAS NOT BEEN A GOOD EXPERIENCE.

I had RSD (Reflex Sympathetic Dystropy in my (R) ankle which was only relieve by 5 nerve blocks. Does taking Prednisone bring back this condition?
I am on Prednisone for a month and have started to experience some sharp pains in my (R) ankle moving from inner aspect to middle then back to inner aspect.

I am a paraplegic and have experienced severe nerve pain in my legs and feet since my spinal cord was severed in 2002. After going through a stringent pain management program,(two months of evaluation, psychological testing, spinal cord stimulation, nerve blocks, etc), my Pain MGT Physician at UT Southwestern Medical School in Dallas, began prescribing me Lyrica. Lyrica was just beginning to be prescribed by physicians. We gradually ramped my dosage to achieve the most pain relief for me. After experiencing excruciating nerve pain for three years, Lyrica was a miracle working medication to me. Finally, finally, I had found some relief in the burning, squeezing, and exploding shocks in my legs and feet. I take 600mg, 5 times a day. After every four hours, I can feel it wearing off and the same screaming pain comes racing back. Nerve pain is so difficult to control. I can't say that I am completely pain free, but at least it is a manageable animal.

Hi..I just went off Yaz last week after being on it for 18 mos for severe periods. I've had nausea,diarrhea, gained 20 lbs, sore and aching legs, and the worst lower back pain. I've been go a gastrointestinal specialist for a endoscopy and colonoscopy and everything came back normal. I've also had a CT, MRI and nerve blocks for my back but nothing helped. My daughter had a really bad reaction to the Mirena IUD and a light bulb went off that maybe the Yaz was responsible. I'm 46 and I feel like I'm 86. I literally manage to go to work (most days) and then am too sore and exhausted to do anything else except lay on my couch. It's been a week since my last pill and I have to say I feel worse today than ever. If it's the Pill, how long would it take to start feeling better? I had really hoped that this would be the answer. I used to be very fit and active and I can't believe that I might feel like this forever.