Pain med symptoms and conditions

))REMOVED IN APRIL 09, STILL HAVING SYMPTOMS, ANYONE ELSE PLEASE CONTACT ME..I THINK I'M GOING CRAZY(((((

To spare everyone of a very long read of the SAME symptoms as everyone on here, I will list:
Dec08 inserted
PAIN PAIN PAIN CONSTANT PAIN
BLEEDING
Cramping so bad I had to stay in bed
Insist something is wrong
Dr. says all this is "normal"

April 09 Removed
PAIN CONTINUED CONSTANTLY
Dr. Says all this is "normal" be on you way

May 09 switched to new Gyn
US revealed retroverted uterus ( I knew previously)
Cyst on rt. ovarie
A small amount of fluid in cul de sac ( Dr. states that the mirena perforated my uterus & now the fluid is sitting there)
Given 2 antibiotics & a pain reliever (did nothing)

June 09 Went back to new Gyn
States that " I don't know what to do, I have never had a patient with these problems, you may want to get a 2nd opinion."

August 09 (now)
Continue to have same daily, continuous pain & pressure in uterus & rectum area.
Sometimes feels like a bowel issue as well?????? Some sort of connection here.
Pressure, heaviness down into my upper legs & knees feel swollen
Sharp knife like pains in breasts
Nausea that wakes me from sleep
Tearful, sad, becoming depressed, feel like Dr.'s think I'm crazy!
Spending money we do not have on$50 copays and GETTING NO CLOSER TO THE ANSWER!

WHEN WILL THIS STOP??????????????????????????????

Contacted Mirena, they just jotted down notes & said hope you feel better.
Blood work some white blood cells, but nothing major.
I eat Advil like PEZ candy, if a friend can give med a pain med I get a days relief then it's just right back the next day. I don't dare ask for meds from Dr.'s they already think I'm nuts!
I have wasted so much time with this, I am missing my infant experience life, my 4 yr old needs me as well! My husband can not take another minute watching me in pain & crabby all the time.

Seriously, enough already, I get it, I made a mistake.

Contact mee if you want to chat.... ******

Not doing well .....M.

I took 20 mgs a day for 5 days in September of 2006. I developed a terrible cough, but worse than that, severe chest pains & shortness of breath upon exertion. I still can't go up & down stairs; my pain is brutal and it's going on 3 years since it all began. Before I took the lisinopril, I hadn't been having any chest pains or trouble breathing.

Is there any hope of recovery? My doctors all say they've never heard of this kind of side effect; that lisinopril is a very common drug; it's clear that I have reduced lung function & definite pain & symptoms, but there is no way to isolate the exact thing causing it or to figure out how to make it go away; just to control the symptoms.

My theory: the lisinopril triggered an autoimmune response in which my body physically tries to reject my own lungs. Any thoughts on that one? I had been taking cozaar as an ACE inhibitor to slow the rate of my renal failure; I have type 1 diabetes and hypoparathyroidism, and while I needed meds before this episode, all I had to do then was manage my diabetes & I was able to live normally. Since this, it's been nearly impossible to do ANYthing. I am at the end of my rope & I want this to stop. But 3 years later, and while the shortness of breath is improved, the pain is actually worse now. I could sure use some advice & support. I'm on my way this week to get set up with a new dr. because we've moved, and I'm going to have to go through this whole thing again. Also - I'm trying to compile a list of other people who have had side effects with chest pain & shortness of breath. Also anxiety & panic attacks as collateral damage.

I was involved in a MVA about 4 years ago. I was prescribed oral prednisone for my back and neck pain. I took the recommended pack but about 3 days into the regimen I began having EXTREME pain in my joints- especially knees, hips, and ankles. I was not even able to walk by myself. My doctor never even suggested that it could be a side effect of the prednisone and told me that I had to finish the rx or it would be possible for me to have major reactions such as heart failure, etc. I was so scared that I finished the rx. My side effects included weight gain, mood swings, increased appetite, etc. but the worst was the joint pain. I survived the treatment and swore that I would never take the drug again. Well, never say never. My back pain continued and I went to a pain management doctor who recommended spinal injections. He said that the prednisone injections should not have the same side effects as the oral med so I received the injections. He said that he used a reduced amount of the prednisone during the procedure. I had great results with a reduction in my back pain for several months. I just this week had another injection and now I am in experiencing the same horrible pain in my joints as I had the first time with my oral rx. Is this normal? I have contacted my dr for pain med but I know that I am just covering up the side effects. Any one else have similar situation? What do you do when the treatment is worse than the ailment?

I have been on Wellbutrin XL for 2 years with no ill side effects and it has worked well. 2 1/2 months ago my script changed to the 'generic' BudeprionXL. Since this change, I have been experiencing severe muscle and joint pain, my hands go numb, my skin crawls to the point that I have scratched myself to the point of bleeding. Sleeplessness has just recently started to occur and my teeth have also become very sensitive. General irritability has also set in. I have not yet started to get the headaches most get with the Budeprion and it a good thing as I'm already taking 1600 mg a day of Advil to try and arrest the muscle and joint pain. After reading these other ill effects of this drug I'm now very scared and will be calling my doctor to get her to represcribe Wellbutrin -only- 'no generic'. It is clear to me the FDA did not do the proper research or makes me think TEVA has a friend in the FDA's office.