Vision problems symptoms and conditions

I have been on yasmin for about 5 years. I loved it to begin with but just recently I have been having horrible side effects that i just realized could be related. I just thought i was a 21 yr old with problems. i am having heart palpitations, hair loss, insomnia, anxiety, vision problems, UTI's, lightheadedness and blackouts, and CHRONIC migraines. I am having about 3 migraines a week! they are disrupting my life. it is weird that i was fine on the meds for so long and they are just now resulting in this. I am stopping the pill as of today and i am going to talk to my doctor about other options. i am thinking about ortho tri cyclin lo. i have to be on a birth control because i have had endometriosis and my doctor said it is less possible to come back if i am on a birth control. she mentioned the shot but i have heard bad stories about that too and i don't think i want to go there.

Just to start of, I just got out of the emergency room for heart attack symptoms which I later found out were caused by my cholesterol med that I was just put on 2 weeks ago, Litportal. Well after looking this up on google and found out many people had the same affects I figured well if that made me have so much pain maybe I should look up Lisinopril w/ body pain. OMG, was I speechless. After reading the blogs I was sure that the Lisinopril was causing all my pain which doctors had diagnosed as Fibromyalgia after 8 years of testing. I was put on Lisinopril 8 years ago after my reg brand was not covered by my health insurance. Didn't think much at the time because it was suppose to be the no name brand of what I was taking. Well, it started off with weird things happening. Pain in my ankle and wrist like I sprained them. Shooting pain in arms and legs. Vision problems, numbness on one side of face, stomach pain, just feeling like crap. Months past then other weird things happening, not feeling like I slept at all even though I did for 8-9 hours, body aches all over, anything I did made me hurt. Then years past and it was everyday, wake up with pain and go to bed with pain. Not able to do simple stuff like play with my kids or go grocery shopping knowing I was going to hurt even more and that percocet was all that would relieve it. After 8 years of this I am totaling drained. Just cleaning my house kills me. Everything got even worse after the years and still gets worse. Going to the doctors knowing they think I am crazy and it's all in my head. Family members questioning my pain. I would always say, if you could be in my body for one day, just one day, you would know the hell that I have been through. But today, a new life came into me, after reading tons of blogs on the side affects of Lisinopril. I am just hoping that this is what it is caused from. I am 39 years old now, my 30's completely wasted, and do I mean wasted. To think that this has all been due to a little pill taken daily for 8 years. I thank everyone who has posted on this blog, because if it wasn't for you, I would have no hope. Now I do. And I am schedule for an appointment in 3 weeks to change my meds. What I thought I would have forever may soon be gone. Or at least some of it. Thank you.

I was on Yaz for years with no serious problems, but after my baby was born 6 months ago my insurance put me on Yasmin. I hate it! I'm starting to have vision problems and my eyes burn horrible when I get into the sun. I am 37 years old and am in good health. I find myself having mood swings and crying for no reason at all. My concern is my eyes and how bad they hurt. Anyone else having problems like this?

I am so annoyed that this medication is still on the market.
What is it going to take for it to be banned??? It took me almost one year to get my life back together. The side effects from this medication are horrible. Only the people who have gone through them know how severe it is. I had anxiety, insomnia, chills, numbing in the hands and feet, palpitations, vomiting, tremors, twitching, vision problems and the list goes on. My body was out of control. My blood tests were even coming back with all sort of problems thyroid, high blood sugar etc. When retested a few months later, everything was normal.
It took me lots of hard work to get myself back to normal. Thanks to Chinese medicine/acupuncture I now have my life back.
Please don't take Avelox!!!!!

I was prescribed Bactrim for 10 days due to ear/throat/cough issues. After day 2 I had 102 fever, chills, sweats, extreme fatigue, and headache. After day 3/4 I started feeling severe doom and gloom. After day 5 I had insomnia and began having vision problems and felt like my eyes were "loose" in their sockets. I went back in, and saw a different practitioner, and reported my symptoms she thought it was my blood sugar and checked me for diabetes (which it wasn't). She ran more lab work, and chest xrays. Nothing came of it. On day 6 I began feeling a burning and itching sensation on my face, and throughout my head. Nothing helped. During all of this time I could not eat, and was extremely nauseated. I got online, and found all of my symptoms of Bactrim side effects. Needless to say, the bactrim is in the trash. In addition, last year my husband was prescribed bactrim for bronchitis, and ended up in the hospital. At the time they told us he had Scarlet Fever, but when we both went in this week, they stated it was an allergic reaction to Bactrim. He looked like he has a sunburn from head to toe, with a rash. He had 105 fever, and was severely dehydrated. I wish we would have been told that last year. They gave him a zpack this time, saying he was allergic to bactrim. I will never take this medication again, or have my family on it.

Started taking Lisinopril approx. 6 years. ago. Shortly afterwards I started a spiral downwards for no apparent reason. Did not connect this med. Shortly after starting it I was put on Synthroid for low thyroid. Started having loss of balance, dizziness, vision problems, muscle and nerve pain. B/P went up instead of going down. Have been to every type of Dr. (Neurologist, Dermatologist, Endocrinologist, Internist) and every nerve & muscle test and blood work came back negative. I have extreme cold in my hands and feet, increased back pain. headaches. This past week I have broken out in a rash on my torso and down both legs. The doctors answers are that I'm suffering from depression. The irony is that when the symptoms first started I questioned if I could be having a reaction to the medication and they flat out said no. After reading some of the comments as of today I am discontinuing the Lisinopril and will searce for something natural. I'm fed up with doctors and really short on cash from all the money spent trying to find an answer.

Extreme Fatigue, Anxiety, Muscle and Joint Pain, Extreme Hair Loss, Chest Pain, Heart Palpitations, Vision Problems, Vibrating sensation on my insides, Tingling and burning in all extremities.

For any person that got the Gardasil vaccinations and did NOT have any side effects or symptoms, PLEASE go and have a pap test done immediately! We are getting reports of these girls that had no side effects to the vaccine that are now getting cervical lesions and cervical cancer. So if you know of anyone that received Gardasil with NO side effects, PLEASE tell them to get a pap test done immediately!

My 16 yr old daughter was also injured by Gardasil. She had 2 of the 3 injections (Jan 9th and March 9th, 2009). Before Gardasil, she was a happy, healthy and vibrant teenager. Since Gardasil she is sick every day of her life. She has dizziness, overall weakness, numbness and tingling in both legs and left arm, back pain, neck pain, pressure headaches, vision problems, breathing problems, chest pains, racing heartbeats, brain fog, stomach problems, nausea, diarrhea, weight loss, hair loss, jerking all over spells...the list goes on and on.

She was an A/B student but failed her 10th grade year because she was too sick to retain what she was trying to learn (brain fog). She no longer has the energy to go off with her friends. Most days she lays in bed, in pain.

This just doesn't happen to a healthy teenager!! And it just doesn't happen to THOUSANDS of other girls with no connection except they all had the Gardasil vaccine.

It doesn't take a rocket scientist to figure this one out.

Please educate yourself as much as you can before you allow anyone to push this unproven and unsafe vaccine on your daughter! The guilt is overwhelming from a mothers' standpoint! I thought I was doing something to protect my daughter. Instead, I allowed the doctor to inject poison into my child and take away her life!

These 'side effects' are NOT rare! They are happening every day to literally hundreds of thousands of young girls after receiving Gardasil. The numbers in VAERS is estimated to only be between 1-10% of the true numbers! Try asking some of us moms who have to deal with these horrible side effects every day if we consider it to be RARE!

Everyone should look at the other side of the fence and research this. There are thousands of girls that are coming down with strange illnesses, paralysis, gran mal seizures, etc. after receiving Gardasil.

We are now getting reports of girls as young as age 9 that are breaking out with genital warts and severe cases of cervical cancer AFTER receiving Gardasil. Some of these girls/women did not initially have any side effects from the vaccine.

There are perfectly healthy girls all of a sudden come down with all of these strange sicknesses (some that I cant even pronounce) after getting jabbed with Gardasil. All within hours/days/weeks?

Just like Merck's 'wonderful' Vioxx...what will it take? How many dead/injured before someone takes notice?

The doctor that literally pushed this vaccine on us at a routine doctor visit told us that there were no side effects except for soreness or redness at injection site.

She also told us that it would protect her from a whole LIST of things! I had seen the commercials but had not researched it.

As a matter of fact, I never really THOUGHT about vaccines until my daughter suddenly started having all of these strange health issues.

She was ALWAYS a healthy child, happy and outgoing, active and just a joy to be around.

Now, she is a totally different child. She is always sick..always in pain..and cries a LOT, so scared that she will die in her sleep from the breathing problems. She describes it as breathing through a blanket or that an elephant is sitting on her chest.

She has SO many of the exact same symptoms as all of the other girls that have been injured.

It is NOT a coincidence! All of these Gardasil girls have the same symptoms, some worse than others, but the bottom line is the one thing they all have in common is Gardasil.

These symptoms are NOT in their heads!

My daughter started having dizziness, overall weakness, pain and numbness in both legs and left arm BEFORE we found out about any of these other girls having the same issues.

When I called her doctor that gave her the vaccine (as soon as she started with these symptoms) she said it was NOT the Gardasil vaccine that is causing it. How could she be so sure? This is such a NEW vaccine...a DANGEROUS and UNNECESSARY vaccine!

HPV is not an STD (research this!).

Cervical cancers have gone down 70% since the PAP smear came along.

This is NOT an epidemic! Why are they mandating this vaccine for as young as 9 year old girls for a vaccine that doesnt even do what they claim it will do?

Girls are now coming down with cervical lesions and HPV AFTER receiving Gardasil! I'm talking about healthy young girls that did NOT have these things BEFORE getting Gardasil.

Young girls dropping dead within hours of getting the vaccine and they think we are all stupid enough to believe it was a huge tumor that was in her heart and had spread to her lungs? (I'm speaking of the 14 yr old that just recently died after receiving Cervarix).

If that young and healthy and active young girl really DID have this so called huge tumor, she would have had symptoms. A tumor like that doesnt just up and kill it's host without a 'wasting away and painful period'.

That is a complete cover-up!

Just like the young girl that has been paralyzed and hospitalized for the last year, Ashleigh Cave. Because her mother was trying to speak out and find out what exactly happened to her daughter, they have now placed that child under protective orders! To shut the mother up?

This is all about $$$$$ at the expense of our young daughters (and now sons) health and lives!

It is an outrage!!!

Please see my posts at ******

And this website:

******

There, you can see other girls' stories and their pictures..there is also a memorial document with pictures and stories of young girls that have died after receiving Gardasil.

Educate Before You Vaccinate!!

I have had the Mirena IUD for 2 years. I have notice lately that I have had vaginal dryness during intercourse. I have extreme dry scalp, and I have had about three bacterial infections in that time. I have been irritable for so long everyone in my house has gotten use to it. I am getting the IUD out next week. I am looking forward to the change.

I HAVE EXPERIENCED RESTLESSNESS, HYPERNESS, ANXIETY, DEPRESSION, HEADACHES AND VISION PROBLEMS SINCE I STARTED ON THE YAZ, I WONDER IF IT IS THE MEDICATION OR JUST ME

I have used Nasonex for about two years. Last spring, I developed vision problems which I didn't attribute to the Nasonex. In the fall, I was diagnosed with a cataract and glaucoma in my left eye.
I did not have any known risk factors and take very few medicines, so I believe the Nasonex caused the cataract and glaucoma. The first eye doctor never mentioned that the Nasonex could be causing my eye problems so I continued to take it until recently when I discovered it was probably to blame. I am now facing cataract surgery and the new eye doctor I went to told me I have the eye of someone 20 years older.

I am not on it for BC, but to help with my severe cramping during my period. I had only been taking this for one week when I started experiencing chest pains, horrible cramping as if I have my period, extreme breast tenderness, sinus problems (nose is constantly running - almost instantly after I take the pill), lack of lubrication and drive, extreme fatigue, vision problems and leg cramping. I'm glad that I now realize that it must have been Yasmin, as everyone is experiencing the same problems. I stuck with it for 2 more weeks thinking it would subside, but it has only gotten worse. I am calling my doctor today to get something else.

I have been on prednisone for 8 weeks, the first two at 40 mg., then 30. I have sarcoidosis and had a cough for several years, then shortness of breath, a fever for three weeks, very low energy, headaches every day, vision problems, mental fuzziness, fatigue, leg cramps, weight loss, a host of symptoms that were impacting my life. With the prednisone, I have had some jitteriness and occasional insomnia, though not bad. I have had increased energy, clearer mind, no cough, the sarcoid symptoms have almost disappeared. I do have increased appetite and have gained maybe 5 pounds. I occasionally have a day when I have low energy and am depressed, but most often, my energy is a lot better since taking the prednisone. So, for me, prednisone is most definitely NOT a devil drug. In fact, I believe that thinking of it this way is very harmful both to the person thinking that way and to others who come to this site looking for help. It is helpful to know that there are other people having similar problems to yours. But focusing on all the negatives without acknowleging the vast array of positives can only hurt. When I take the pills, I remind myself to be grateful that there is something that can help me fight the sarcoid. When I start being fearful of the side effects (from reading these internet sites), I remind myself of all the many people who have taken prednisone and gotten better and lived a long, good life as a result. My sister-in-law took it years ago for Crohns and loved it. My friend's daughter took it and had a few side effects, primarily the moon face, but it helped her and she now is as thin as ever and doing well. Focus on the positives, people! Where your mind goes, your body will follow. Be aware of the possible effects and work to offset them. Exercise, eat less, find reasons to laugh and be with people. It sucks to have any disease that would cause you to have to be on prednisone, but we are lucky to have medicine and people to help us. Be thankful for what is good in your lives.

****Are you having severe headaches, vision problems, dizziness, ear pain, nausea?? If so, you may be experiencing what my daughter did. Please, please seek immediate treatment from your physician and request a CT or MRI. This is the only way to detect blood clots. Unfortunately, my daughter did not have that chance. She was 18 years old. I do NOT want to scare anyone! I want to raise awareness of the side effects and prevent any of you going through what my daughter did. Listen to your body and go with your gut. If something doesn't feel right, you need to get it checked out. You may need to be very persistent with your doctors too. Don't give up & give in to them. If you are having any of the side effects I listed above daily, you need to follow-up with your physician immediately!!****

I had my Mirena put in back in June of 2008 right after I got married. I, too, was lead to believe that the effects of the progesterone were purely "localized" to the uterus and would not cause any symptoms at all.

Since then I've experienced SEVERE migraines and dizziness, loss of libido, greasy skin and hair, weight gain (size 6 to size 10/12), numbness/tingling in my feet, crying, irritability, and SEVERE brain fog. For the migraines, I went to a neurologist who wanted to prescribe me topamax and said the only major side effect is cognitive difficulties! HA!!! I already have the worst brain fog, can't remember anything, am tired.... rather..... exhausted all the time, and can't function.

This Mirena surely works well as birth control, seeing as I have NO SEX DRIVE at all! LOL. But seriously, it's great not to have a period, but I knew something was wrong when I was needing medication (antidepressants for the mood swings, provigil for the fatigue, botox nerve injections for the menstrual migraines) for this medication IUD!

Since no OBGYN believes me when I say I think it's the Mirena, I've began to think I was crazy and this was all in my head. So I started on the internet and all my symptoms sounded like MS. So I had thousands of dollars in testing including a full body MRI/MRA. Negative. Had ENT see me for the vertigo. Lots of tests. Negative. Anemic? No. Thyroid? Normal.

HOW MUCH MORE DO WE HAVE TO SPEND ON HEALTH CARE TO FIND OUT WE ARE "FINE" WHEN WE FEEL THE WORST WE'VE EVER FELT???

Then I found this site!!! I think it's the Mirena now! So I want to get it out. But then on the other hand, I feel SO GUILTY that my husband paid $900 for it and I only kept it 1 year. That's expensive birth control! But then again, all the tests, doctor's bills, and feeling lousy cost more! (Not to mention that my doctor cut my strings too short so we can't "check" them each month so to be certain that my IUD is in place he makes me get an ultrasound every 6 months for $250!!!)

My ONLY FEAR is that I will have this out and the symptoms WON'T go away and it was NOT the Mirena after all. Then I will have gone through the pain of putting it in, taking it out, and the cost of "throwing one away" and then what am I supposed to do? I'm 29 but in school and can't get pregnant for a few more years. I don't want to go back on the pill because the mood swings were terrible. But I never had migraines or anything on those, so why is the Mirena causing problems?

Any feedback or encouragement would be helpful right now. I need advise!

My 16 year old daughter has been injured by Gardasil. She was a
healthy, active teenage girl before Gardasil was pushed on us at a
routine doctor visit. After receiving 2 of the 3 shots, my daughter has
experienced severe overall weakness, numbness/tingling in both legs and
left arm, chest pains, racing heart, pressure in head, vision problems,
back pain, abdominal pain, nausea, diarrhea, weight loss, dizziness, just
to name a few. She has been in the ER twice, once by ambulance for
stopping breathing 3 times. She's seen several doctors. She's had a CT
scan done. All tests come back normal (which is typical with all of the
injured 'gardasil girls'). Her blood panel showed high on
immunoglobulin E (131H) and Anti-streptolysin O (208H) which the doctor
'thought' was Rheumatic Fever. Another doctor has said he did not
believe she had Rheumatic Fever.

I'm 38 years old and I started Topamax in July of 2008 for severe migraines. I've had an average of 12-15 migraines per month since my early 20's and nothing was working. While initially adjusting to Topamax I had the tingling in my hands and feet during the first month but then it went away. My neurologist increased the dose very slowly from 50mg to 100mg to 150 mg. The migraines have decreased in response to each dose increase. At 100 mg the migraines reduced to 10 per month and at 150mg they reduced to 6 per month. My dose is now being raised to 200 mg which the Dr. says is the maximum recommended for treating migraines. The worst side effects I've experienced are extremely dry mouth (from 150 mg+) and slight hair loss. My starting weight was 138 and I lost 11 pounds very gradually before my weight stabilized at 127. I haven't noticed any problems with food or drinks tasting different. For some reason, I always have insomnia for the first week after a dose increase but then it goes away. I've only had mild concentration problems but nothing notable or problematic. So far, the medication has been remarkable and I can't believe what it's like to live life without so much migraine pain! I hope other people can have the same benefits from this medication.

I am a 42 year old woman. I started taking Topamax in March of 2008 for severe migraines. The migraines often caused vomiting and for my body to jerk similar to having seizure. I have had migraines for the last 15 years, but prior to starting Topamax I was having migraines almost every day (for about 6 months). My life had come to a stop. I had been through all of the neurological tests, and CT scans, etc. with no results. Topamax has nearly halted my migraines. I have a severe "head-ache" about every 6 weeks now that last 3 days. A huge improvement! However, my doctor had said that I should not be on Topamax long term so I have tried going off of it twice in the last year, each time on the 5th day to be hit with an all consuming migraine. I had come to this website to find out why I should not be on Topamax long-term to discover that many of the other health problems that I have been complaining about in the last year are probably a result of Topamax and the doctor did not ever suggest that was the case. I have TINGLING IN MY HANDS AND LIPS...the doctor thought this might be my thyroid, but that test was normal. I have had REDUCED VISION, the doctor said it is due to age and working on a computer all day. I have had JOINT PAIN which they are treating with an anti-inflammatory and suggested it’s probably the onset of arthritis. I have had WEIGHT LOSS, SHORTNESS OF BREATH, and the PAIN IN THE BACK OF THE HEAD. These are all things that I see others describe as symptoms of Topamax! Wow! I wish my doctor would have told me this so I didn't think there was something else wrong. I WILL NOT STOP TAKING TOPAMAX. Even if taking Topamax meant that my life would be 2 years shorter or something like that, there is no living in that kind of daily pain. But I am grateful to know that the symptoms are normal. Topamax has giving me back my life.

I had open heart surgery August 23rd 2006 for a conginital heart defeat (Aortic Valve replaced with mechanical St Jude valve). I wanted a bio valve but Drs insisted I should have the mechanical valve because of my age (45 at the time).

Prior to my heart surgery I was a performer, singer/songwriter/actress/comedianne and I loved what I did. It was my life. Now, after 2+ years post-op and on Warfarin (7.5 mg daily for life) I feel like life has ended and I'm just a walking dead person. The effects I feel daily are as follows...

Dizziness
Severe Headaches
Blurred vision
Memory Loss
Fatigue
Weight Gain
Trouble concentating
Fluttering effect in my head/ears- Hard to explain
Hair loss
Unexplained pains in chest & left side of my body
Unable to sleep well
Tiredness- even when I've done nothing to be tired for
Nausea
Gas & Diarrhea off and on
teeth pain- Like I've drank something very cold
feeling in my head similar to a brain freeze- like you ate ice cream too fast
Night bleeds in my month- wake up with a mouth full of blood daily
What do think, is that enough??

I'm going in tomorrow for a cat scan because the headaches have been so bad they feel I need to be checked for brain tumor and/or internal bleeding. When I tell the Drs I think this is due to Wafarin they pratically laugh in my face as if to say, "Silly silly woman, don't be foolish! We know whats best for you. Remember, we saved your life!" Really? Did you?!

I want nothing more than to get off this rat poison and regain my life, but to do so could mean a stroke or heart attack. I would go under the knife again to have the mechanical valve removed and replaced with a biological valve, but do you think my insurance company (Kieser) would pay for a "silly" thing like that? Right!

Welcome to the greatest country in the world!

I'm going to start a website to help people like us. I want your stories, please send me your info, together we might make a change, what can it hurt to try? Email me ******

B.

I was prescribed Dexpak for sudden severe pain in my back. The pain was gone the third day but the side effects of this drug are so horrible that I will never take it again. Besides the common steroid side effect of sleeplessness, on day 4 I started noticing vision problems, cloudiness of my eyes. On day 5 my taste was gone and my tongue felt like I had burned it with hot liquid. The tongue also started blistering. Then my legs started swelling so bad that my socks left about a 1" rim above my ankles. On day 8 I was done with this drug. 2 hours sleep per night, extreme mood swings, depression, heavy acid reflux and stomach pain, constant and excessive urination and incontinence, the skin on my hands extremely dry and cracking and the worst, my tongue and gums so swollen and painful that I could hardly eat right and decided to taper off early. I went 2 more days 2 - 1 and 1 - 1, then I quit. First steroid free day I awoke with a massive candida albicans outbreak under my breast about the size of a dinner plate. By the evening my knees were abnormally swollen and painful and I was scared to fall asleep because my heart was pounding like a hammer. Next day I was hardly able to get out of the bed. My hands were looking worse and I developed very painful bumps on the skin of my skalp. The slightest stroke of the hair brush hurt. All my leg joints were hurting, my face and eyes were swollen, I had pressure behind my eyes and sensitivity to light, and a debilitating headache. I felt so bad, that I thought I would die. Went to the doctor that evening just to hear that all these are side effects (which I was not told when starting this drug) and was released with Lasix for the excessive fluid and Candida medication and the order to have my eyes checked. I have taken steroids before but never ever experienced such serious side effects. Wished I had never started this and had rather dealt with the back pain then going through this cruel ordeal!

I started using the NuvaRing in 2003. I am still on it and now really having second thoughts. When I started usign the nuvaring I was already taking the anti-depressant Lexapro (not sure if it's spelled correctly). Since I started taking both of the medications around the same time, I could not decipher which symptom went with what medication. I was experiencing numbness in my face, hands and legs. I was also very fatigued, had a candida related rash for 6 months, and gained weight.

Yet, through these symptoms my period was easy, painless, and short. So I quickly assumed it was all related to my anti-depressant. My doctor prescribed me Prozac and most of the symptoms I had been experiencing went away. But for the next four years I had numbness in my face and hands the week after my period, the first week I had a new ring in. During that week my doctor prescribed me to double the amount of prozac and it cured most of the numbness and nausea. Yet taking more prozac seemed to really affect my short term memory.

Last November 2008, I decided to ween myself off of the anti-depressant. By January I was totally off of Prozac. It is now February 16th 2009 and it is the week after period and just got a new ring. Today I am experiencing major numbness in my face, hands, and legs. I am having terrible headaches, vision problems and have no energy. After reading all the posts tonight I realized that all these years I have been on the Nuvaring I have mistaken its side-effects for other medications side-effects. I am really trying to cleanse my body of medication b/c my stress level and lifestyle has changed.

I want to go to the doctor and discuss other alternatives since I feel terrible and have been on this for so long. If I hadn't had gone off the other medications I never would have associated my symptoms with the NuvaRing. But now it all makes sense.

Has anyone experienced vision problems ? Seeing red and green dots ?

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..

My 19 year old daughter received the first shot in March 2008. She immediately had a severe back pain. She had her first seizure in April. She got the second shot in May and had more seizures, fatigue, headaches, severe stabbing stomach pains, body aches and pains, tremor, hair loss, vision problems, 2 UTI's, mono like symptoms - swollen glands, bruising and bleeding gums are the most recent symptom. She had daily seizures throughout the summer and they are now about every 5-6 weeks. She is fighting to recover from this horrible nightmare called Gardasil. Thank goodness we figured this out and she did not get the third shot. If you want to sign the petition to get this vaccine in front of Congress go to: http://www.thepetitionsite.com/14/investigate-gardasil-vaccine-risks-now

Mirena is an absolute NIGHTMARE. My sister had this inserted approximately 2.5 years ago and ever since then her life had gone totally down hill. She was another one that could have gotten some kind of award for the most illnesses without a cause ! Her symptoms were so severe that she was sure that she must be dying of some terminal hidden disease. Hair loss, anxiety, panic attacks, depression, headaches, bloating, weight gain, joint aches, muscle aches, vision problems, confusion and the list goes on and on. Lucky someone made the connection that it maybe from the Mirena, so we both got online and googled for days and read all these sites and posts. My sister freaked out when she saw so many of you wonderful ladies with exactly what she was going through. She got the Mirena removed first thing this morning and 12 hours later she absolutely cannot believe that for the first time in God knows how long that she hasn't got a HEADACHE. She thought she was imagining it but she wasn't her headache WAS TOTALLY GONE. Hopefully as the days go by all the other horrid symptoms will go away too. This contraption has robbed my sister of 3 good years of her life and her family's life. I just thank the Good Lord that she made the connection and got rid of this. It is a shame that pharmaceutical companies feel its ok to rob people of their health in order to make more money. Shame on them.