Bone pain symptoms and conditions

I received prednisone intravenously at the hospital to prevent a severe reaction from receiving platelet transfusion. I have a bleeding disorder and IgA deficiency. Because of my bleeding disorder I have to receive platelet transfusion before any surgical procedures. When I receive the platelet transfusion 20 mins into receiving the platelets my face feels flush and a tightness and pain in my facial bones. I get a sudden headache with severe pressure pain in my head so severe that you feel as if your head is going to explode. My doctor recommended the use of prednisone to prevent me from having this reaction. 20 minutes after receiving the prednisone intravenously I felt my face turn flush with facial bone pain and a pressure around my face and top of my head. I felt the pressure in my head, but not the pain which I would get from the platelet transfusion. That night I had dizziness,severe headache,nausea,stomach pains,severe sweating,over heated,weakness and unable to concentrate. This went on for 2 days straight. Today is the 3rd day and I still can feel a slight pressure on the top of my head. I also felt eye pressure and I still have the headaches. I am schedule to see my doctor in 3 weeks and I will tell him that I will not take Prednisone ever again. I am sure there are other medications that can be given.

I'm 24 and just recently finished my lupron treatment for endo. I'm still having some of the side effects and have yet to start my period again. I honestly would've rather had surgery again for endo than go through months of the side effects. The memory problems, overall fogginess, night sweats, insomnia, mood swings, hot flashes, and just the stress and complete crappy quality of life I've had most of this year has completely affected all aspects of my life. It's not easy at work, at home with my husband- surgery took a day or so to recovery from and this has been a nightmare for months and months. I'd really think about it and research the benefits for you vs the side effects before doing it. If there are any other options- I'd absolutely consider them.

I took Levaquin several months ago and have had on going foot pain. I was recently diagnosed with Complex Regional Pain Syndrome following a Stress Fracure in my heel. I have had muscle aches, all ove pains, bone pain, insomnia, depression, irregular heart beat, headaches. irritability, dizziness,stiffness in my joints, stomach aches. This has all been a terrible ordeal. Do you think it is related to Levaquin. I have also taken Cipro several times for UTI and Diverticulitis. Thanks for listening.

Was on Prednisone for 11 days for an injury to my neck. I knew nothing about the drug except what my doctor told me that it would reduce inflammation in my neck and help with pain.

Well, it did nothing for the injury and pain in my neck. BUT.... I had HORRIBLE menstrual cramps and got my period 8 days early. I've had my period for 9 days now AND terrible pain in my upper left leg. I thought the pain was related to my leg and as the days went by I realized it was in my left hip! It's so bad I can't lift my leg without extreme pain. I KNOW IT'S FROM this awful drug.

I've been off of it for 4 days and the pain is still with me. I called my family dr. and was told Prednisone doesn't do that. BULL!! The paperwork I got with it from the pharmacy show "Changes in menstrual periods" "muscle/joint pain" "bone pain".

I wish I knew this BEFORE I ever took it.

Does anyone know if these symptoms and problems will go away after stopping it? I called the pharmacy and was told it will take 2-3 weeks for it to get out of my system!!

Has anyone had problems that eventually went away after stopping the drug?

Thanks and I hope everyone else is okay soon! This drug should be off the market. I received no help for my neck pain at all!!

I took Levaquin on multiple occasions for a severe prostate infection. I took a 15 day supply...then off for 1 week...another 15 day supply...off for two weeks...and then a 30 day supply. I took another 30 day supply when the infection resurfaced about a year later. During the time I was on it I experienced extreme "arthritis like" pain in my ankles, wrists, shoulders, and especially my back. The infection was over 3 years ago and I have not taken Levaguin since. However, the joint pain has never went away. I can barely climb stairs as my right knee feels like it is going to pop out of socket. The bone pain in my neck and between my shoulder blades is horrible. I visited a doctor (I never even considered the Levaguin as a possible antagonist) and was told that I had spinal degeneration and needed physical therapy. Protect yourself and your family from this drug.

I can't believe that after months of searching for an answer to my daughter's health problems I may have found it! My daughter was a healthy, active happy child until recently. She is 17 and started experiencing joint, bone and muscle pain and swelling, unexplained rashes, migraines, tingling in her hands and feet and was diagnosed with neurocardiogenic synchrony (heart rate and bp out of synch) shortly after her first shot (she was 14).

We have been to a rheumatologist for the joint pains, they did blood work and there is a marker for some sort of auto immune disorder, but nothing specific.

I never connected the dots to the shots. In January of this year she started having severe diarrhea, stomach and intestinal pains. She has no energy, the most basic activities wear her out. We ended up at a gastroenterologist looking for a diagnosis (they thought it was Crohn's or lupus). All the tests have come back negative, they said she had gastritis and blew us off. She is on medicine for the intestinal pain, a prescription for an antacid for gastritis and an anti-inflammatory for the joint and bone pain.

She was a straight "A" student up to January and has had to finish her junior year at home. It has been a very stressful experience for all of us.

I am 26 years old and I was diagnosed with endometriosis last year (2008). I had pain in my lower abdomen for years and doctors always told me nothing was wrong but I knew there was. Finally a doctor did an ultrasound and found a 7cm mass on my left ovary. I also had a slightly smaller mass on my right ovary. My doctor told me that he would need to do a lap to remove the masses and possibly remove my left ovary because he could hardly see any ovarian tissue on the ultrasound. Thank goodness when he did the lap I was able to keep but ovary but he told me that I had one of the worst cases of endo he had seen. My right ovary was stuck to the wall of my abdomen due to the endo and I even had endo on my bowel. He removed what he could but not all of it was removable. He suggested that I go on Lupron for 6 months to "shrink" the rest of the endo. I have been on Lupron for 3 months. I just went and got my second 3 month injection. I have had some side effects such as Headaches, Bone pain, Hot Flashes, Insomnia, Drowsiness, Increased appetite and major Mood Swings. All of which come and go. I try to stay active but I don't over do it. It seems to help with the joint pain. Most of my side effects were in the first 2 months of getting the injections. I am told all the time that everyone reacts differently to Lupron and there is a pill you can take to reduce the side effects of Lupron but it does reduce the effects of the Lupron so my doctor suggested that I not take it unless the side effects were unbearable. I don't remember what it is called but if you are one of those people having major side effects ask your doctor.

I am 46 years old. I first started taking Levothyrox 11 years ago during a pregnancy. Now I currently take 200 a day. I have been suffering chest pains. I also suffer bone pain. My hair has not grown in nearly 3 years. I am borderline diabetic and each day when I take the drug, I immediately sleep due to the immediate sugar elevation I feel.

Six months ago my femur broke. It seems due to a Vitamin D deficiency. Now I discover that a few of the nasty side effects that no one ever told me about is Vitamin D Deficiency and also Osteoporosis. Due to the strict bed rest that I have been on from my fractured femur, located near my pelvic, I have suffered muscle atrophy. I am too weak to even stand. So for 6 months now I have not even been able to leave my bed.

Now the only solution I feel in order to possibly save my life is to immediately discontinue the use of Levothyrox. My boyfriend is a little concerned for me doing this but I see no other way. Any feedback appreciated. Thank you.

Hey all. I have had asthmatic bronchitis for about 6-7 weeks now and I have never had asthma or bronchitis before. It started off as a normal flu for 3 days with fever. Then when the flu went away, I started having trouble breathing and shortness of breath. It felt like I ran a marathon walking to the bathroom. I never had that before. The doctor told me it was bronchitis. All tests were fine. I was taking azithromycin (took 3 paks of them) and that was the only thing that made me feel normal, but it did not get rid of the infection. Then I was placed on cipro and steroids. Now I'm not on any antibiotics. I'm taking prednisone and just started the advair inhaler. I was having asthma attacks that I never had before. Very scary. Did anyone have asthmatic bronchitis before??? What did you do to get over it and how long??? Please help!!!

I had a similar and horrifying reaction to Avelox after taking only ONE PILL. I took one pill and within four hours had to crawl into the room to my husband to get me into the ER. For probably five months I suffered severe reactions all caused by this ONE LITTLE PILL. I couldn't walk or move without pulling muscles and tendons, my tendons felt so stretched that merely moving my leg felt like I would snap my tendon. I literally could NOT WALK or STAND. I also had eye involvement, chest pain, bone pain, shortness of breath, and just extremely odd and random different reactions to this ONE pill and I can only THANK GOD that I did not take more than that. I was told this IS a very rare possible side effect and NEVER to take any FLOROQUINOLONES again. I have the bottle marked POISON - DO NOT TAKE in my counter to remind me never ever to take anything like this again. Luckily, by 6 months and I was able to gain full motion again in my limbs after rehabilitating myself slowly and carefully without pushing myself to cause any further damage. If you have similar reactions DO NOT PUSH YOURSELF, wait and listen to your body, because you can snap tendons like rubber bands. I have also come to find out that this side effect was not as rare as they made it out to be, just do a search "levaquin and muscle pain" "avelox and muscle pain" "floroquinolones serious side effects" - and you will see that you are not alone. This was over 4 years ago when I had my reaction and at that point they statistically knew and had documented that 70,000 people had this severe reaction (not to mention the countless others who probably went undocumented.) Tell everyone you can and everyone you know about this drug. I do. Be careful with Sulfa drugs as well. Many people who cannot take Floroquinolones cannot take Sulfa drugs, and the worst thing about that is, you might take them successfully three or four times and on the fifth - get bad reactions. I can now not take Floroquinolones, Sulfa or Macrobid. Please take care of yourselves, I sympathize with everyones situation. If anyone has any questions, feel free to write me at ****** my name is N. What's worse is you feel CRAZY when you tell people "I took one pill and I can't walk...." But it is a FACT that's what it can do to you!

I was given Avelox at my clinic for bacterial pneumonia, the doctor said it was a wonder drug and I'd be up and running in a couple of days. I took the medicine that night and I got very dizzy and started sweating, felt like an anxiety attack so I took my xanax and it helped a bit. The next day I tried to get up and about 15 min. later my head started buzzing and my ears were ringing, I tried to walk up the stairs and dropped to my knees at the top step and fell to the ground. I didn't lose consciousness but I couldn't move or speak for several min. when I started to come to, I crawled to my bed and everything was spinning, I started to have severe chest pain and was rushed back to the clinic. The doctor said to stay on the Avelox and take it before bed and finish all the dose, so I did, and gradually got worse and worse. I went to my doctor the day after Christmas and told him what happened, he said I still had crackling in my chest and my cough was still bad, he put me back on Avelox for 3 days, so I've now been on it for 10 days. I became so weak and couldn't eat, it felt like the food wouldn't go down, I was sweating, dizzy, still had cough so I called my doctor again and he put me on prednisone taper and another 5 days of Avelox. Two days later I ended up in the hospital with severe abdominal pain, diarrhea, muscle weakness(felt like I had lost muscle), severe bone pain to the touch, sweating, extreme fatigue, decreased mental ability, confusion, headaches and chills in my legs. It has been over three months since I first got sick and I feel worse today, my doctor's have no answers or solutions, just let it run its course. I feel trapped in my body, I'm 33 and a mother of two active kids, and I can barely get out of bed most days. I feel like my life has been taken from me and I want it back.

I have read all of these post and I have also taken 1 dose of this drug and now I know all of my issues, including migraines and memory loss, and bone pain and I could go on and on, are all related to this crap drug. I am mad as hell. My OB even told me when I called the office because I actually thought I got a (let me think because my memory is so bad I can't even think when I type anymore) tainted, yeah, thats the word, or infected dose of LUPRON, it made me sick. But, no, it's just the stuff itself. She even told me, LUPRON doesn't cause headaches. You betcha I'll never return to that office. When, and if my memory fully recovers, including when I'm cooking in the kitchen and I can remember what it was I was cooking in the first place, I'd like to try to start a support group for all the women who took this stuff. It has almost ruined my life. I can't tell you the number of times I have sat in the shower and prayed to God to answer me why, and what is was wrong with me. He finally told me what was wrong with me...and it wasn't me. LL

The reason is when you stop taking the Lipitor, and your symptoms don't go away is this: Lipitor cause hearing loss, which is what causes the Tinnitus! I have been having severe tinnitus for months now, seen all kinds of Dr.s who didn't have a clue. And I finally went to the House Ear Clinic, and they told me what it was, but they didn't know how I got it. I got Tinnitus a few months after my Dr. upped my dose. It's taken me this long to put the puzzle together. The Physician's Desk Reference lists hearing loss, tinnitus, and dizziness as side effects of Lipitor. I am appalled that not one Dr. asked me what kind of medication I was taking!

I was giving prednisone for only 5 days (not sure about dose, but it tapered to one pill on the last day) for a bronchitis induced severe asthma attack. I have only had asthma twice in my 50 years, both times associated with a bad case of bronchitis. The "doc in the box" reduced his original dosage due to the 3 corisone injections I recently had in my spine. After reading these posts I feel grateful I wasn't on a higher, longer term dose. I have some of the same side effects listed here including uncontrollable appetite, fat gain around the middle, water weight gain, constantly having to urinate, superhuman energy, heart palpitations, and approximately two weeks after finishing, I began to get a mustache (hairs that were previously white became brown over a two week period). I have read on the internet and been told by my pharmacist that this is temporary. I have also read and been told that the 2mg estradiol I take every day since my hysterectomy causes the body to retain and not rid itself of the steroids as it normally would (estrogen is actually listed as drug interaction with prednisone). The doctor in the box apparently just ignored this interaction and prescribed it anyway. However the main reason I am posting is a very strange possible side effect that occurred approximately 1 week after my final dose. I was awakened in the middle of the night with SEVERE pain (felt like bone pain, not muscle) in my right knee that lasted until morning. By mid morning it was gone. The next night I had the same experience but in both knees. It lasted about 5 more days, gradually tapering in intensity, and then just went away. I do have severe arthritis in my lumbar and cervical spine, having had surgeries to repair injuries from a snowmobiling accident. I have normal arthritis elsewhere for a 50 year old, but have NEVER had issues with my knees. Has anyone had this strange symptom? None of my doctors (internist, rheumatologist, physiatrist - who gave me the injections and prescribed physical therapy for my spine) had any explanation. The only explanation I have is the prednisone because I had taken the Z-pac (antibiotic) with no side effects several times in the past. Weird!

Incidentally, I am off the prednisone for about 5 weeks, am still hungry all the time, still fat, still bloated. Unfortunately the extra energy is gone. Best of luck to everyone on this strange drug. My heart sincerely goes out to all of you on long term therapy. God bless.

Hash thyriod disease with vitiligo.Synthroid .88mg. 3 yrs on Synthroid.
NONE OF THESE SYMPTOMS I HAVE HAD BEFORE SYNTHROID.
SEVERE knee pain,ovary pain,joint pain, bone pain,muscle aches, fatigue, sleep apnea, weight gain,depression, anxiety, edema, FIBROMYALGIA / LUPUS SYMPTOMS,chronic inflammation, numbness in left foot,numbness in left hand, lower back pain, headaches,elbow pain,abdominal pain, brain fog,HAIR LOSS and greasy hair (always had thick curly drier hair) greasy skin, white pimple-ish areas on arms, itchy breast, lymph breast pain,increased hunger, strong food cravings, irritability,high blood sugars (I am type 1 diabetic) synthroid is known to mess with insulin in a diabetic, all my symptoms have had one test or another ran and all come back normal. I have no diabetic neuropathys..which surprised the doctors when my nerve tests came back normal...he was blaming my diabetes for most symptoms and told me to eat less in regards to weight gain.Still he brushed off my symptoms. I have asked my (endo doctor) to put me on Armour but she refused, she said I would be taking steps into the dark ages.
As if the symptoms are not enough, I am developing more.
NEW SYMPTOMS..Globus sensation (feels like constant lump in throat) eye twiches, eye floaters (not diabetic related).
I did experience twice after a higher dosage was made I felt great for the first two weeks and then like crap again.
I have oddly noticed I have crazy-fast hair growth, although my hair is thinning and not replaced..I have to shave twice a day.

Also I read a comment about one person switching synthroid to evening and said they felt better. I am pretty sure this is because doing it that way the body absorbs less synthroid. And for any one who doesn't know..synthroid takes calcium from the bones over time.
I am sure the avg person on synthroid complains to a dr about symptoms and doctors never get a clue.

Much of the same, but honestly, not too bad. Hot flashes started one month after the first shot (2 shots/6 mo. treatment), almost to the day. They are tedious but not unbearable. Joint and bone pain, hot flashes, night sweats. I'm now one month past the 6 months, I still have hot flashes and am having a lot of knee pain and some in my left hip.

I gained 20 lbs despite good exercise habits.

But definitely not the horror-stories posted below, I was lucky.

I got my first Lupron shot in Aug and I've had nothing but serious muscle and joint pain and also constant sweating, I'm always hot. I've gained weight, I've also had more anxiety. I'm about to get my 2nd and last shot next week..I'm debating on even getting it....

My daughter, 21yo, took prednisone off/on for 4 months, both oral and IV form, with the highest dose of 90mg over a two week period. The risk of bone death (Osteonecrosis, aka Avascular Necrosis) is not disclosed as a risk and 7,000 people a year get this from steroids! They gloss it over under the guise of "bone pain" or "bone fracture" near the osteoporosis risk so you think that by taking calcium and vit D supplements you're protected. What's really going on here is that the steroids cause the bone to die so if you have pain, PLEASE INSIST on an MRI because a regular x-ray will not show ON until it's in the advanced stages..and then you'll most certainly need joint replacement.
I'm not making light of the weight gain, or loss of hair or any of the myriad of other side effects that come with this drug, but when you're told that the joints in your body are dead...and that they'll eventually become brittle and break and cause so much pain it is often compared to bone cancer, then you'll really want to sue someone. But, I've tried that...it doesn't work. Because the drug is FDA approved...the manufacturer can't be held liable.

My daughter has ON in her right shoulder, both elbows, both wrists, both knees, and both ankles. She's considered "collateral damage" by the medical/legal communities because Prednisone is the "gold standard." This disease is a slow progressing disease which is often found as late as 10 years after stopping the steroid treatment. If you find it early enough, some surgical options exist to prevent the collapse of your bones, so if you have joint pain...PLEASE investigate with an MRI

No, I am not a drug rep,I am simply just being honest.Not everyone has a terrible experience from this drug. I am sorry that so many of you have had so many bad reactions,just like any medication it may not be for everyone,but it does work for some.

please can u tell me does anybody on this site suffer from memory loss cause they are taking simvastatin

Hi, I am a 57 year old female who was just recently put on Fosamax to counteract the bone loss caused by Femera that I am taking to keep my breast cancer from coming back. The first two weeks I felt okay albeit I did have stomach ache for two days and loose bowels. Then the bone pain began and I mean pain, not light, not moderate as the labels say, and it was especially severe at night. I found myself also feeling dizzy, depressed, no energy, kinda weird. I couldn't have relations with my husband because my hips and pelvis were so painful, also my neck, lower back and legs. Not fun. I took myself off it....Bone pain subsiding..also gastric upsets were getting worse. I tend toward gastritis and have IBS so this drug did not agree with me. I hate it! Will not go on any of these again, as I have also had lots of jaw problems in the past, and dental problems and DO NOT WANT that horrible jaw thing to happen. Yike... Love Pam

I just went to the Dr. for my second Lupron injection and to get some help with the side effects. Menopausal/emotional me, started crying!!! Gawd! I went in with my list of side effects from the last 3 months (and it was long!) and wondered what was worse, the pain of endometriosis or the life changing side effects of Lupron. My Dr. is wonderful and spent an hour with me; he decided to put me on Provera (progesterone or add-back therapy) for a week to see if the side effects improve. If they do, I get my second dose of Lupron in a week. If not, we stop it all and let my body slowly try to get back to normal (although I have never known what "normal" is since endometriosis) and see how the "therapy" worked. He is strongly encouraging me to follow through with the 6 month course as that is the recommended length of time for the best results. I'm 5'8" and have lost 10 lbs. in the last three months, I'm down to 107 lbs. He told me to try and eat more if I could (although my nausea is constant 24hrs. a day) and make sure to take a daily vitamin and calcium for bone loss. He said that he has never heard of blurred vision to be a side effect of Lupron, "But every woman is effected differently." I'm really hoping the Provera works - any kind of relief is better than this! I'm still having 3-4 hotflashes every hour with extreme exhaustion/fatigue, night sweats, daily migraine headaches, nausea 24hrs. a day, life changing mood swings, and shaky hands. He kept reminding me that this only 6 months out of my life - it's not forever ... forever feels like an awful long time when you can barely get out of bed!

I gotta tell ya this is scary. I am a 30 yr old guy my wife is 27 we have four children.Our last one was born Mar. 2007 She has been on Yasmin 6months or so.She has never been regular on periods. Well a few weeks ago she started having massive headaches.As of June 31st her doctor said she has migraines. Well by July first her left eye went blurry by the 2nd she has lost vision in both eyes.She only sees light and is very cloudy and can see shadows. We made 3 trips to ER. They did Cat scan and it was neg. the doctor said she might have even had a mild stroke because her left cheek went numb. By the 2nd we were in ER again because of total vision loss. They did a lumbar punture and no Meningitus. cat scan again neg. blood work neg. except UTI sound familiar ladies??? By the 3rd we visited her doctor and she passed out and was rushed by EMT to Hosp. They did and MRI,MRA,had a eye Doctor called an ophthalmologist clear her of vision problems.She has talked to a neurologist. So here is a 27 yr old female with all the test's coming back normal but she can't see.They even had a psychiatrist talk to her because she is on Prozac because she has PCOS and had half her ovaries removed and almost died.They even suggested that she had conversion disorder(google it).Finally I decided to check side effects for all her meds. When I checked this one I almost jumped outta the chair.She has about 10 symptoms. But before I get too excited has anyone had vision loss for a period of time and did it come back once off of it?? I'm throwing these away

I am a 56 y/o female who started on Fosamax last Sunday. I have a dx of osteopenia. I followed the directions of taking pill with full glass of water and remained upright for 30 minutes before having anything to eat. I was fine on Sunday but on Monday I woke with SEVERE bone pain! My whole rib cage, back, knees and heels were hurting so bad. It felt like I had pain in every bone in my body. I could not take in a full deap breath as my rib cage was hurting so bad. I could not bend or turn without terrible pain. My energy level was zero. I immediately called my doctor who told me to hold the Fosamax (ya think?) and ordered Vit D lab levels. Apparently when you Vit D levels are off (don't know if too high or too low) you can suffer this bone pain. I am awaiting the results. The pain is better today and I was told it takes 5 days to get out of your system. I only wish I had done my homework and found this site before taking this poison. I have to say I'm a registered nurse and know that ALL medications have side effects and everyone responds to meds differently. Some side effects subside as your body gets use to it and some can experience severe allergic reactions. But it's important to weigh the risk vs the benefit. I would rather deal with osteopenia in another way. So my search begins for alternatives to Fosamax for good bone health. Has anyone had good results with other supplements/meds?

I have had so many shots of
Corticosteroids/NSAIDS/Steroids:

Triamcinolone Acetonide, Kenalog, Depo-Mardol, Lidocaine, Marvaine, Toradol, Epinephrine, Bextra, Xylocaine, Isovue.......on and on and now I do not walk hardly anymore.

I am married, no sex whatsoever! I stayed away from my husband for 3 years almost, living at my apartment. I just moved out by Eviction March 2, 2008. I did not pay rent for one year. I applied for disability since 1995. Won ALJ decision September 2006. I appealed the case being opened back to 1995. I wanted it go go back futher. Just appealed it again in 2008.

Okay, I am a simpleton out here needing a HERO to Take A Stand and Advocate for me.

I do not live with my husband. I live at his mother's home so that he comes and takes cares of us at the same time. She is 90 now. Can you imagine this? I have been reduced to a cripple.

I am a prisoner laid to rest by the BIG DRUG COMPANIES MISLEADING ME, IN NOT KNOWING ABOUT THE DISEASES THAT WOULD ATTACK ME IN THE ONLY LIFE THAT I HAVE.

I wonder if my hip bones have collasped. I have terrible bone pain.

I waddle like a duck, side to side with extreme pain until I freeze up and fall, but mostly, I live with a cane at my side when going out and about.

I now need a wheelchair.

From 1980's, 1990's and now all the way to 2008. I have all medicals.

It was not until 2003-2004 that my life took a turn for the worse.

Hips pain, arms pain, shoulders pain, pain in the Thorasic area to the tail bone area, right groin pain/pubic area pain/gentials, stomach sores/cut out, pain on the scalp, calves feel hard in side/stiff at all times, hamstrings are short,open sores have been on my face, arms and neck lasting for 4-6 mths, low back pain....all of me has been injected with the above crap.

I was doing quite well in life until 2004 when this Orthopedic doctor had shot my left shoulder 3 times.

After this June 2004 event above, and by September 2004 I had walking problems, blamed only on Fibromyalgia, DX 1989.

They took one blood test for Polyrheumatica.

I was fed 20 something meds in 2004.

By 2005 I was devestated in life, health and even wanting to be alive. For one full year I lived on the pot, using Lidocaine up the butt 3-4 times a day for the pain.

Now, looking back at this part, no wonder I had extreme skin blisters, hives, rashes, extreme sweating....this Lidocaine for rectum pain was harming me and no one took me off of it. I finally had my pharmacy tell me this was so wrong to be using 134.00 a month for over one year for pain. I stopped!!!! he seemed to say that I was being harmed.

Suddenly, at my clinic, all of my primary doctors began to do trigger point injections weekly, monthly and for 4 years for my Fibromyalgia comlaint. DX in 1989.

Many NSAIDS for one year, 2003-2004.

In 2003 I had a new denture and a few teeth extracted so that I smiled great when got married April 2003.

By August 2003 I was off the State HMO, had housing city of salem voucher for 5 years at my apartment and was planning to move out and be at my husband's home, but...by September 2003 I was already in some medical exams, new meds and was being normal to a point.

By late 2003 to mid-2004 I was feeling strange about my health. I felt as if I was being sucked dry of any fluids, weird to say, but it felt as if...hard to explain.

I was dizzy, vertigo, some balance problems and like itching, sweating and extreme fatigue. I felt like i was melting. My muscles felt like jello. I had no ability to stay upward on my spine.

I did complain to my dentist and doctors that I was feeling numb on my face and gums by may 2003.

After 2 years, leaving room for a possible lawsuit on the dentist/OS, I filed, had one deposition and my lawyer walked.

I had laughing gas for teeth extractions/numbing shots.

I thought that GAS/SHOTS was to be blamed, maybe the tools they used, or the water and I worked this case to the bitter end, sad to say, that a Lawyer Walked On Me.

By 2004 I did not know what hit me with my health issues..dentists/new meds/new marriage/new doctors involved.

I was in a drug stupor, taking almost 30 drugs from this clinic in 2004.

Prescribed and the samples of Vioxx, Mobic, Celebrex and Bextra.

I had so many Toradol shots to my spine and hips at this clinic and thought they had crippled me.

This doctor humiliated me.

Told me that I was a nut.

I now needed long term counseling with all of the body ailments they all told me. My primary doctor told me many times that NONE OF THE SPECIALIST NEEDED OR WANTED TO SEE ME FOR ANYTHING.

Nothing was hardly affecting me when I got married April 2003. I was a knock out!

The Gastro doctor had me on his 3 drugs also, including that daily Lidocaine up my butt. He did the endoscopy and colonscopy, bloodwork and he said I had Atrophic Mucosa.

He was in direct conflict with my Neurologist who did his own work and he claimed that I was Gluten sensitive, a Celiac now. He gave B12 shots and Folic Acid on top of all the other crap that I was taking.

The Hospital did a spinal tap and may tests.

The pain specialist did his epidurals 2 times.

I have had every NSAID they prescribed me.

I had sleeping pills.

I had anti-depressants.

I had Vicodin to Percacets and then they tried to get me on Methadone. One week on that crap was all.

I notice that Depo-Medrol, Marcaine, Lidocaine was mostly used thru out my life.

The pain specialist above that I used in 2006, also shot me with the epidurals 2 times before 2006, and the O.H.S.U. also shot me with all the above when they DX me with Fibromyalgia 1989.

Then many Toradol and Kenalog shots.

I live with daily diarrhea since 2005-2008.

My legs are always red every day with any walking, sleeping, sitting, balance is off, waddling gait.

My feet pain is as if I walk on glass or rocks....sharp pain now for 4 months.

Arachnoiditis fits me well. I have spoken with the doctor/expert that can test me.

I have been searching since early 2004.

I have no way to know who or what to blame.

I even thought that the MRI's Contrast Agents harmed me starting from the past to now.

I left the clinic that stole my life from me and now have a new doctor at Kaiser Permanente.

I am scared of all doctors now.

I have 4-5 meds right now.

Not one doctor or specialist will DX me. I have a thought below...

I fought the medical community WORLD WIDE back in 2002-2003 with the President Dr. Richard Willner, of Retired Association of Physcians and Surgeons. My two other sisters were in this heated debate.

I was told to expect danger at any time after this online 30 page cruel attack by the doctors on my wrongful death of my mother by her doctors/nursing home/hospital.

I proved this case.

The lawyer in Portland, Or. Judy Snyder told me I did extremely well proving this death was murder...but the Medical Consultant who did the summary of this death was hushed up!!! Later on, after another summary by Medical Consultant, she told me that we would be lucky to get $10,000 for a Nusiance Claim. I tried to get one Lawyer before the statues ran, but no luck. I heard that the Elder Abuse Statues ran for 7 years and to try for that. Oh well, I tried.

Joanie K.