Ailments symptoms and conditions

Hello, I can't help but get into the Mirena conversation. Three months after my son was born, I was put on the Mirena IUD. I had a ton of symptoms. My hair was falling out, tired, weak, headaches, stomach cramps, and just all around felt like crap. I went back to the doctors to have the Mirena removed positive that it was the Mirena that was making me feel like crud. The doctor persuaded me to keep it in longer and after much debate and feeling flustered with the doc I agreed for a couple more months. Well symptoms got ten times worse to the point I called and demanded to be seen right away to have it removed. Well after it was removed, I felt better but not completely. I started losing weight, I had periodic migraines which mind you I never had a migraine in my entire life, and felt like a truck ran over my body every morning when I got out of bed. I went to the doctors and they ran a slew of tests and NOTHING! Well about a month after a car ran a stop sign and crashed into me. I hit my head. IT was the best damn thing ever, I got a cat scan and it showed something on my brain. A MRI picked up a right cerebellum hemangioblastoma about 3cms. I had to have brain surgery to have it removed. They decided to do a full scan and I now currently have a kidney hemangioblastoma. Moral of this story. I am 31 years old, I have always been healthy with no migraines, no ailments, nothing. I have the Mirena put in and I feel like shit and they found a brain and kidney tumor. The estimated both my brain and kidney tumor to be about 2 yrs old. THE EXACT TIME I GOT THE MIRENA IN. Hemangioblastomas are either sporadic of VHL. With sporadic, usually you only get 1 and if you get another its later on down the road and my two tumors would not be the same age so it rules that one out. VHL, I had a genetic test done and it came up negative. So anyone of answers for my mishap. I know the Mirena caused this for me. Im just looking for someone with a similar story

I've been on Yasmin for about 5-6 years and have had all sorts of minor (or so I thought) ailments. My boss advised me to stop Yasmin as her daughter died at 28 from a DVT, put down to Dianette and she explained about these forums. After reading this forum, nearly every problem/ailment I've had or have is listed as a side effect of this bloody little white tablet. I am officially stopping it as of today and as I've just read another lady has written, I hope my sex drive returns soon and that I stop being so tired and lethargic and my crippling migraines stop !! I've had heart palpitations, weight gain (gradual so I've not put it down to the pill !) I have down days, migraines complete with auras, fuzzy heads, short tempered and narky, tired ALL the time. I never knew all these things could be down to the pill. I'm just keeping my fingers crossed that coming off it makes me feel human again !!

Good Evening,

My mother has been taking Remicade for several years now. I believe 4 years.
She has ankylosing Spondylitis. Nasty nasty disease. The drug has worked like a charm so far. Aside from the temporary side effects during the first few hours of injection - tiredness, drowsy, etc.

After that, shes as good as a goat.

Recently, shes been experiencing a loss of recent recent, very recent memories. Sometimes a convo here she wont remember or take a while to remember.
Or convo yesterday she wont remember at all. Also her ability to compute math problems in her head on the spot has decreased. She has a hard time doing any simple math. She was never like this.

Being in the medical field, her wit and brain power were her key features. Now that have dwindled, shes having difficulties coping with her loss.

Shes been tested for Dimentia and other ailments when reaching the age of 51. So far, soo good. No such things.

I would like to know, if this side-effect ( if i can call it that) is permanent or temporary

Her doctor in charge of her dosages has reduced her treatment volume to fewer ml and will prolly resort to other meds as well.

See how it fairs in the months to come

If anyone has any cases similar to this. Please relate and re-iterate!

God-bless!

I went to the doctor with complaints of possible mold/fungus in my lungs which got better on it's own - but progressed to a throat infection. Later, my right nostril was runny for a while, which progressed into a blockage/infection of my middle ear. The doctor agreed - I have no compacted wax or anything wrong with my outer ear, so it seems to be a middle ear infection. He prescribes Biaxin XL 500mg for seven days, for my combination of ailments.

By the first day, I had a very vivid wet dream. Awesome, I guess. Then the second day I start with diarrhea, and another vivid dream. Today is the third day, and I slept before work. Had another vivid dream about someone building a house for me - and really runny stool. I can hardly call it diarrhea - more like urinating from my anus. Anyway.

Blockage in my ear went away the second day, but it's back again. I searched the net to explain the diarrhea (hopefully find something explaining the expulsion of bacteria causes this, but no, just a 'side effect' I suppose). I'm going to take some Imodium as soon as I can to battle the diarrhea, and hopefully things will get better by the end.

I can't complain about the dreams though. No nightmares yet, and I enjoy remembering my dreams, so...

This drug crosses the blood brain barrier thus the anxiety and depression. It is damaging your brain not to mention all these other ailments. It shrinks the brain and is causing cognitive deficits. All should google the recent article in Sunday paper from the Pittsburgh Post Gazette regarding Mylan Laboratories. Hmmm....maybe this is why so many people are sick from this drug. Here is the website address: *******
I still have tablets although my husband has been off them for 10 months. Guess what...they have a big "M" on them...isn't that interesting. I don't believe a word any doctor or any study has out there on this drug. This drug is tainted with something causing all these issues. This isn't healthy, it's poison straight from a venomous Brazilian pit viper. And if they try to tell you it's the synthetic version...bull crap! It causes the same horrible side affects that over 2500 people have described. I guess WE'RE all nuts and it's not the drugs . Huh!

I was on Yasmin for only a month in November 2008. I quickly got off of it because of the side effects. I wear contact lenses, yet my vision was getting blurry. I was training for a marathon, yet I was gaining weight (and it wasn't the muscle mass I was also gaining from training). I began to have horrible headaches, retaining water and I even got these little red rashes on my arms and breasts. At the time, I didn't know that Yasmin was causing all of this and ruining my life! Now I know it's Yasmin. I went to my doctor, she performed various lab tests (including liver, kidney, thyroid) and I am perfectly healthy. So I did major research on Yasmin and discovered all of my ailments were on there as side effects. My advice for anyone experiencing anything similar is to either change the dosage or just get off of it. It's not worth it. Yasmin is the devil! I mean think about it, we are messing with the natural way our body's hormones function. Oh yeah, and not to mention that I started losing some of my hair as well.

Ran into friend at grocery store with mystery illness. Docs attribute it to Agent Orange exposure. Been at death's doorstep for a year. Hands were extremely cold and has little energy. Showed up one day at golf course with oxygen bottle! Asked him if he had taken Levaquin. Unfortunately had. Docs again fail to link antibiotic exposure to his ailments.
I wonder how many illnesses and deaths this poison has caused? Why does the FDA allow this crap? Do you people realize that the average person is clueless about the side effects of drugs like this. Put total confidence and their well being in the hands of ignorant docs and profit crazed drug companies.
Ignorant oncologist failed to link my dad's symptoms to Levaquin, instead attributed them to b-cell lymphoma which just happened to suddenly appear. Rituxan and numerous other drugs (Heparin, Lasix, Gamma globulin, Tylenol, antibiotics, Insulin, steroids, Flowmax, etc.) was too much. A fiasco, people think he died of lymphoma. Was walking three miles a day before taking Levaquin, for an undiagnosed lung infection.

My 13 year old daughter had her third shot on 02/16/09. Her first two shots did not seem to be a problem. She said her arm hurt really badly after the shot, and the next day she complained of leg pains she hadn't had before. Within a few days, she had a high fever with body aches like the flu, except it wasn't the flu. She felt better, but a week later she still had a low grade fever. She was tested and had strep throat, and was treated with anti-biotics. A week later she started having stomach cramps and diarrhea. It's now March 18th and she still has diarrhea. I think it's criminal this vaccination is being given to our young women. How on earth could anyone think "possibly" preventing HPV and/or cervical cancer is worth the risk of what my daughter and so many others are having to go through?

My 12 yr. old daughter had her first gardasil shot last summer and her 3rd in January. She has been complaining of headaches, nausea, stomach pain, dizziness, confusion, as she put it 'she felt like an alien'. I just figured it was preteen/body change/that time of the month stuff and thought it would pass. She only complained of headaches a few times after the first shot, didn't even think of them being from the shot but then more after the 2nd shot, still didn't make a connection, and now it's an every day thing. This morning again the headache/nausea/stomach pain, crying from the pain and Tylenol isn't helping. I got her to go to school but after 2 hours had to go pick her up. She said it was worse. We will be back at the doctors for the 3rd time in 2 weeks. With the possibility of this being from the gardasil, I wish I had never gotten the shots. The not knowing, is this from the gardasil? will it pass? get worse? and what she is going through. No it's not worth it

I had my mirena inserted about 13 months ago before Christmas after the birth of my 2nd child , I was naturally shedding the baby weight until Mirena came into my life and then I gained 10lbs effortlessly within 2 months! even though my diet is always the same (I am coeliac). I had to start working out running 4 times a week and gradually have lost 8lbs but its been a huge battle.
Last May I woke up one morning bright red covered in a sunburn type rash all over my body it was scary, my joints ached so bad and my hands and feet were really swollen as if my body was reacting to something.. my gp did some blood tests and nothing it kept happening for 2 weeks and then the rash went,..I put it down to a virus at the time but felt as weak as a kitten and suffered night sweats, anxiety and flu like symptoms for months.

Ive had to really fight to keep up my running because most of the time I feel tired and depressed and run down and I have awful PMT the past few months have been dreadful I feel rubbish most of the time..everyone is getting on my nerves, I have little sex drive too and I am sure its down to the Mirena..its side affects remind me of the mini-pill which I took once for a few months it sent me so extremely loopy (paranoid and anxious) that my husband flushed them down the toilet!! well I think its the same/similar type of synthetic hormone that my body DOES NOT agree with.

I saw my Gp the other day and asked her about the side affects and she still said that I shouldn't have any after a year and it was very rare but after reading about it on here I cant believe it... its obvious and Im getting it removed. Ive had over a year of feeling terrible and various ailments so much so that I think my immune system (which is already sensitive) has suffered.

I am as relieved to find this site, after reading this it's like a puzzle where all the pieces have come together. Unfortunatly now I am worried about what this Kenalog has done to my body.

In Aug 2008 I recieved a 40mg Kenalog shot to help stop the swelling in my lips, tongue and throat...which is ironic and funny to me since those happen to be the same symptoms I would have experienced had I had an allergic reaction to the shot. Nice job thinking that one through doc.

The shot did nothing to relieve the swelling (thanks docs!), but apparently has done a number on my body.

Two months later (Oct 2008) I have been left with a visible dent on my right buttocks, where the shot was given. It started as a grey dent about the size of a small thumb, but has now grown to the size of an Ozarka bottle top.

Additionally the non-visible ailments I have been suffering are numbness in the right leg, sometimes it gets so severe that my leg feels tight and paralyzed. I have noticed heart flutters, and about two weeks after the shot I noticed a sudden weight loss of 12lbs in 2 weeks. This might not seem like much, but for a 25 year old who is 5'5'', muscular, and very active my healthy weight is about 125lbs, I am now 111 lbs (I weighed that much in JR. HIGH!! ugh!) it's bothersome. I can't seem to gain weight and instead continue to loose weight. Additionally I get blurred vision randomly and for extended periods of up to 3-4 min.

The dent is bothersome, but it is just a visible ailment. What worries me more than anything else is the fact that the above ailments seem to be related to the Kenalog shot...so what unseen damage has it done to my body??

I called the nurse who gave me the shot and she offered no help what so ever.

I have sent this site to other family and friends so that they can be aware of the side effects of this too commonly used drug. I hope the side effects that we are suffering go away, and that this product is taken off the market.

Wow....sounds like Kenalog is not a drug to be administered without careful consideration of the pros out- weighing the cons. I had a Kenalog injection in my elbow at an urgent care center while on vacation about 8 mos ago (painful elbow was impacting vacation activities). It took my pain away 100%. Never gave it another thought even until just recently when it began hurting again. Did, however, notice the atrophy at injection site...and a grayish tone to skin. Indentation has not grown, but certainly has remained. My elbow is also super sensitive. Feels like the nerve is right there under a thin layer of skin.....so sensitive. I also have leg shakiness, hip weakness, anxiety, nausea, and increased heart rate....I assume these are related as I did not have these issues prior. These issues bother me way more that the indentation on my elbow. Dont like not feeling well. I guess the learning is that all medications are foreign to your body and thus have potential side effects. One needs to ask questions and or do own research on their own prior to consenting to take a mediation to be sure the benefits are worth it.

i am so happy i have found this site! ive had the mirena coil removed just the other day (Thursday 16th oct) im now hoping that all the symptoms ive been suffering will fade away. i had my coil inserted a year ago last October. since having it inserted i have experienced headache, light periods that last around ten days which seem like forever every two weeks, with spotting in between which i was was told seven months after insertion by the doctor it would calm down and be less frequent but did that happen? NO! slowly but surely around two and a half month ago i started experiencing achey back pains where no matter how hard you try and get comfortable its impossible till it subsides, mild abdominal pain, pain in my neck and shoulder blades, chest pains, breast pain, shortness of breath, tearful, and paranoia thinking that theres something terribly wrong and im going to die and constant moaning about my ailments which im sure my poor boyfriend is secretly tired of! i just thought to myself hopefully putting two add two together that it may be the mirena coil thats making me feel so unwell. i have bled since having it taken out but i think thats the norm. so two days on im looking at this site that i found and its given me hope to know im mot the only one thats suffered with these awful side effect. im still going to get a check up to rule anything els out but im quite sure that its the coil that has done this to me. my advice to anyone would be don't have it fitted or get it taken out! good luck.

I have some of everything above and am in so much pain that I feel as if I am dying a slow, painful death. I am on heavy pain meds and even with those I have severe abdominal cramping. I don't know what I would do if I didn't have this pain relief. I am very worried as to what is happening to me internally. They are scheduling cat scans and I am awaiting a phone call to get something diagnostic done. This all started 8/15 and not only are things not easing up, but I think this is getting worse. I also have a urethral discharge, UTI, and alternating constipation and diarrhea. Initially, I had a 102 degree fever and now my temp is low, only 97.1! my husband plans on calling a lawyer today, 8/26. One day I passed brown urine and it shocked me! I'd appreciate hearing from others as I feel so alone in this horrible nightmare which is unfolding! FYI, my doctor feels that my muscle tissue is breaking down...has anyone heard anything like this from their doctor? The stomach and abdominal pains are like labor!

I have the Mirena since 06/07 and i haven't had one problem. I love it! I have slight cramps right before my personal but nothing major. My sister best friend and 3 sister n laws all have the mirena and we have never had one problem.

this might help anyone who is looking for more information. This site is trying to get the FDA to investigate more into this drug:
******
Under the "documents uncovered" area, it lists SEVERAL woman who have been hospitalized from this shot from Jan. 2008. Very scary stuff.

also, a post the one of my friends sent me from a news story:

10 deaths have been linked to Gardasil since September 2007, and there have been 140 reports so far this year of serious side effects such as miscarriage and Guillain-Barré syndrome.

Well. We’ve already lost 18 girls, some as young as 12, in the effort to spare them from the mere possibility of cervical cancer later in life. Others have developed debilitating and potentially life-threatening ailments within weeks of being vaccinated, and others still have had spontaneous abortions or given birth to babies with birth defects.

Also consider this: Cervical cancer usually develops in your late 20s to mid 30s. The protection period of Gardasil is estimated to be 5 years. That means, if you receive your first set of shots when you’re 10 years old, you’d need at least 2 to 4 additional booster shots to make it through your 30s. And THAT means you’ll have to expose yourself to the potential side effects of Gardasil over and over and over again.

But now to the real clincher, and I want you to read the following section as many times as you need to let this truly sink in…

U.S. statistics show there are 30 to 40 cervical cancer cases per year per one million women between the ages of 9 and 26, which is the age bracket that Gardasil targets (and was tested on).

According to Merck, Gardasil was shown to reduce pre-cancers by 12.2% to 16.5% in the general population. So, instead of ending up with 30 to 40 cases of cancer per million, per year, in that age bracket, the HPV vaccine can potentially bring it down to 26 to 35 cases of cervical cancer.

What that means is that you would have to vaccinate one million girls to prevent cervical cancer in 4 to 5 girls.

Further, about 37 percent of women who develop cervical cancer actually die from the disease, so vaccinating ONE MILLION girls would prevent 1 to 2 DEATHS per year, at the bargain-basement price of $360 million per year, plus potentially lifelong suffering for an untold number of women, which has no price tag.

Is this REASONABLE?

******

53 year old female who has taken "F" for almost 2 years - the past two months was the generic version. Have noticed a gradual onset of joint pain and heart palpitations, but am not one to see a doc unless I feel like I'm dying... So I wrote it off to aging. (-:
A friend recently mentioned that she had heard that Fosamax causes bones to be brittle, which caused me to wake up, look around and see what people are saying and what new articles or research are out there. Yeah, sure - there are lawsuits. Not a surprise in our litigious society. More importantly, however, are the comments from real people. Thanks to you who've posted your experiences!
I stopped the drug several weeks ago and seem to have an increase in joint paint. But I'm not going back to Fosamax! Also interesting to me is that around the same time I stopped the drug, I experienced an uncharacteristic downward shift in my mood/mental state. Not sure if there's a correlation to the drug or not...
It is reassuring to see some comments from people who indicate they feel better after weeks/months of being Fosamax free. I am a "gym rat" and very fit/weight appropriate. Weight training and nutrition will be my treatment of choose for osteopenia for now. With time, I am confident that the symptoms I'm experiencing will subside. And any future ailments for which I am prescribed a drug will be very carefully researched by me beforehand.
Be careful out there and stay informed!

I stumbled onto this site while trying to find a reason for these headaches I get sometimes for no" apparent" reason. Imagine my surprise to find your testimonies about your lives on warfarin sodium.At 38, I had surgery to repair a congenital defect of the aortic valve and had to have a hema-shield graph to repair an aneurysm of the aorta. That was in Oct.2002. Warfarin has been a part of my life since then. I was also put on anti-depressants because my family Dr. thought I was depressed since I repeatedly complained of not feeling well.(I took myself off the anti-depressants a couple of years ago.) Extreme fatigue , serious memory issues, thinning hair,dizzy spells and numerous other ailments continue to plague me.Add to that a large weight gain ...and, well, you get the picture. If anyone knows of an alternative to taking this "poison", PLEASE, PLEASE let me know. I just WANT MY LIFE BACK!!! I actually cried after reading this blog. As I explained to my husband, I suppose it was from the sheer relief of knowing I was not going insane!!!

Hi All - I have been off prednisone for one week and I am not doing as well as I thought I would be at this stage. My symptoms are not flaring, which is a very good thing but I am so tired and feeling very depressed and low energy. I thought I'd feel great once I was off the evil prednisone but so far I am feeling almost as bad as when I was on it. My moon face has not started to go away, which sucks, but I guess I have to be patient. I am so tired of this situation as it feels never ending. Part of the problem is I have continued to work throughout my ordeal, and it's been very hard at times to carry on like a normal person who is not sick. I have been sick since last November (with an autoimmune disorder) and I had really hoped by this time that I'd be on my way to being better :( Prednisone saved my life but the side effects are horrendous, as are the after affects of it. Good luck to all who are taking it. I share your pain and frustration.

I've taken Ultracet for about 4 years almost every day, morning and night time and sometimes in the afternoon depending how severe my pain is. I take 2 pills each time. It does help take the edge off my pain. My doctor said my Fibromyalgia is as bad as it can get, plus I have severe arthritis through my whole body. I can hardly stand up straight and trouble walking. Ultracet seems to help better then Ultram for me. I'm concerned about how long I've taken Ultracet and damaging my liver or other organs. Does anyone know how long you can continue using Ultracet before it does damage. I'm very concerned about that issue because it does somewhat help with pain. I haven't noticed any side effects using Ultracet. If anyone knows how long you can stay on Ultracet without any harm, please post your knowledge or experience. Should I also have my blood monitored periodically?

I've posted before about the horrible effects this med has had on my daughter. Two months off and she's doing much better.
I received emails from ****** published by web md, it gives reent ifo in the world of medicine, recent studies etc. I just received one and there was an article comparing the long term side effects of varios asthma treatments for children. Of course singular was one of the meds mentiones. Think it said anything about the real side effect, of course not, only focus was on it's ability to control asthma. It makes me so mad, this article doesn't give any indications that doctors shouldn't prescribe it to kids.

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.

I suffer from cluster headaches as well as several other ailments (Doctors say..."we know it's something we just can't figure it out"...sigh). With my latest bout of cluster headaches they decided to put me on prednisone..60 mg for 4 days...30 for 3 days..etc. until I tapered down. Worked great! Headaches went away and I was feeling wonderful (terribly agitated but physically wonderful) until I went off of it (headaches returned with a vengeance. They immediately started me on a second round of Prednisone at 60 per day. Third day, on this second round, I went to get out of bed and BAM!!! fell straight to the floor. I had absolutely no muscle control below my waist...NONE! Laid there on the floor for about a half hour (trying to get up as I flailed around). Managed to finally raise to a somewhat standing position. Walked (shuffled) down the hallway to the bathroom to try and use the toilet. Went to sit down on it and promptly fell wedging myself between the toilet and the wall...(a disturbing visual). A relative helped me (how humiliating) out from my predicament and we immediately called the doctor. I was told it was not the prednisone but a flaring of my underlying vascular/soft tissue disorder and to stop prednisone. Stopped prednisone, next morning went to get up and low and behold I could stand but I had excruciating pain shooting into my hips, knees and ankles which once again made me fall (from agonizing pain). Day three off of prednisone and the excruciating pain upon rising is better but far from over. Currently, extreme muscle fatigue...so weak my poor little muscles won't even quiver. Headaches are back. Red swollen face...ack!!!...what a nightmare.

Wow. I thought I was going crazy. I have PMDD and go through my 'psychotic' periods the week and a half before my period starts. I had the worst one ever last/this month. I don't think I have experienced anything this bad before. I started YAZ at the beginning of May. I tried Apri before and it caused me to have my period for 18 days, followed by 7 days of brown gunky blood and then my period for 15 days. On YAZ, my period lasted 11 days. I normally have a 5-8 day period which is very heavy. It was not as heavy, but it lasted longer with intermittent days of the brown gunky blood. I have also been experiencing more frequent panic attacks and depression. My stomach has been upset and my head has been hurting constantly. I am used to getting migraines, but not normal headaches. I have also experienced dizziness. One think I did not attribute to the YAZ is the change in my vision. But I read in a prior post that someone has had an issue with that also.

I have had the above symptoms because of other ailments, but they were basically gone, until I started the YAZ.

Like most of you state in your posts.........I cannot begin to describe how relieved I am to have found this site. I honestly thought I was losing my mind. I had Mirena placed in December '06. It was uncomfortable during the actual procedure, but not too bad. Then within a day or two I was in severe pain and bleeding like crazy with severe lower back pain. I was told to take ibuprofen and allow my body to "adjust". I went for my follow-up ultrasound and the placement looked fine although I was still bleeding like crazy and very uncomfortable. After several more calls they brought be back in for another ultrasound, told me that my uterus must have gotten bacteria in it during placement and that I had an infection. They sent me home on antibiotics and pain medicine. I bled pretty regularly for 6 months straight accompanied by lower back pain, fatigue, and headaches. Finally the bleeding let up only to be followed by a multitude of other nasty side effects. Depression, anxiety, fogginess, forgetfulness (severe), waking up with headaches every morning, nausea (to the point that I can't tell you how many pregnancy tests I've taken), weight change (redistribution, thicker waist, tummy, and hips even though actual number only changed by about 5 pounds), feeling swollen and bloated when I wake up in the morning, NO libido whatsoever and feel like crying during sex because it's nearly impossible to reach orgasm (this has never been a problem previously), hair loss (becoming more noticeable over time), dandruff, boil-like acne on my face and back, dry eyes and blurred/double vision, chronic yeast infections and dryness in that area too. The list goes on and on. I went to three different doctors and had tons of bloodwork done, all came back normal (thyroid, hormones etc....) I was told over and over that it couldn't be the Mirena. HA! How can this many women be delusional? I called last week and got an appointment for May 20 to get it removed. After reading this forum my husband called the doctor himself and I don't know what he said, or how he managed to do it.........but I'm going in tomorrow morning at 10:20 am to get it removed and you better believe I'm going in armed with this website and others I've found. Physicians need to be more aware of this! Even if it's not common, it's miserable for the 1 in 1,000 woman who gets the worst of the side effects. It's literally ruining my life and my marriage. It's impossible to be a good wife and mother when you feel terrible everyday.

-Amanda