Blindness symptoms and conditions

I took Cipro for 3 days back in March 2009. After 24 hrs, I was completely disoriented, had HUGE blisters appear on my feet (they are scars now) and lost my memory. Thank God my husband realized something was very wrong and took me to my Dr (the ER had prescribed the meds) He took me off of it, and my symptoms got better.

Since then, I have had pervasive short term memory loss, loss of vision (periods of blindness), and extreme exhaustion, joint pain, and body aches. My doctor is getting ready to send me for an MRI and EEG- this is after full body X-rays and huge amounts of bloodwork.

My life is not what it used to be. I have 3 small children, and I am terrified to be alone with them for fear of forgetting something crucial. My grades have suffered, and I can barely function.

Hi there
Apart from all the above mentioned,
Pitting Edema in arms and legs
Headaches
Severe abdominal pain
Severe backache
Heart palpitations
Constipation
Lack of appetite
SEVERE WEIGHT GAIN (how can this be, I have been a diet for three years...and I am sticking to it) MY PANTS won't fit anymore.
NO energy
Fatigue
Nightmares
Nausea
Dizziness
Unable to concentrate
Slight double vision (right eye only)
Anger
Depression
Fainting followed by temporarily blindness (my studies n that scary matter came up with an explanation that this only occurs when your body organs are switching off. Scary thought.
I have also developed Polycycstic Ovarian Syndrome very serious case
I only had it for 6 month and would recommend to ant woman to take in out NOW!!!!!!!!!!!!!!!!!!!!!!!!!! I hope the manufacturer will pay for slowly killing us or making a whole generation of females sterile, let's face it who like to have their health tempered with?
M. AM
Australia

A year ago I was diagnosed with Sarcoidosis and began taking 50mg Prednisone per day. The worst side effects in the beginning were weight gain, moon face, facial hair, hump-back neck, bruising (for example, just by my knees being together while I sleep,) excruciating joint pain and water retention to the point I felt my skin would split open. And poor vision which could have led to glaucoma, but an eye specialist put me on eye drops to reduce the pressure to normal levels. I've felt horrified and embarrassed by the change in my appearance but relieved that my sarcoid was being treated.
I feel confident in my case that Prednisone was the necessary treatment. My pulmonologist, opthamologist and regular doctor all agreed on a course of treatment. But I really advise people to get a second or third opinion before they take it. A friend of mine was prescribed a weeks course of Prednisone for a severe sinus infection. Luckily she didn't have any side effects but I really question if it was necessary. I'd also like to stress that if you're on Prednisone and experience worsening vision, please see an opthamologist who is a glaucoma specialist because it can lead to blindness if not treated.
And lastly, sorry this became a novel! I have been tapering off and I'm down to 20mg. But recently I've noticed my hair is thinning so much. I lose a ton when I brush it and it clogs the drain when I shower. Also my skin is shedding. When I shower and use a loofah sponge like I've always done and I lose layers of skin like a snake. I would really like to know if my hair will start to grow back when I'm finally off the Prednisone or am I going to lose it completely??

Thank you so much for all your posts guys!! I just googled Mirena side effects today just trying to check ANYTHING that would explain my recent experiences. I sat her bawling while calling my doctor to insist it's removed immediately.

I had it inserted in December after having baby #3 in October. I finally got my girl after 2 boys and a few miscarriages and wasn't certain what to expect. I am only 25 and didn't want something permanent or really any drugs put into me on a consistent basis. When the doctor pushed Mirena I happily said okay! Sounded like a god send. I have extremely high blood pressure and his strong sale point would be that it would remove the need for meds. Liar! My regular doctor flipped out when she found that he had removed me and of course, I went back on meds a few weeks after having it inserted, after 4 readings 200+/110+... amazing he didn't cause me a stroke. That should have been red flag #1 but I figured it was just an error in judgment on his part.

I felt no pain with it going in and didn't cramp at all.. spotted for a few hours then it was over.. My first cycle lasted 2 1/2 weeks and the next started a week later.. All side effects I was warned of so didn't really concern myself.

I started having phantom kicks (uterus contractions) and stabbing labor pains back in February which I figure was it doing its job trying to get my system on track. I had numbness and pain down my left side and would constantly find myself hunched over in pain.. The bleeding had slowed down so much that I was so grateful and just kept popping pain pills like candy hoping it would go away soon.

These last few days have been a flu from hell. Can't leave bed, can't speak, constantly throwing up, loose stools followed by extreme constipation, achy muscle tingling skin.. you name it!! Went to the bathroom earlier and when I wiped, had a small bout of black blood.. Old blood that sometimes you will find at the end of your cycle! I checked the calendar and had indeed finally skipped a cycle.. The cramps and pains have been there as though I was going to start, but no bleeding for a week now.. So apparently to skip a cycle I'm going to be bed ridden with the flu.. I have a 5 year old, a 2 year old and a 7 month old who can't have mommy sick. This has been hell..

I too have experienced
terrible headaches, stomach pains, DEPRESSION, short fused tantrums, sitting and crying for hours on end, no passion for life, numbness of limbs, tingling skin, sinus infections, yeast infections, temporary blindness and now spots in my eyes which aren't regaining vision, 5 months ago I dyed my hair and it came out by the chunks, now that the dye is gone, I'm still losing hair and have bawling spots which I blamed on the dye.. Now I wonder..I also look like I'm about 6 months pregnant and people keep asking.. I HATE IT!! its been devastating to my self esteem. I lost so much weight after my boys so I blamed the weight gain on having a girl.. Now I wonder about that too.. The weight is only about 10 pounds but ALL in my belly..

I wonder so much..

I got about 5 posts into this horrified before I called to insist it will come out.. I have to wait 4 weeks.. but I can't wait to find me again.. I'm gonna just stick with condoms until I get my body back.

Thank you so much for speaking out on this.. I know the doctor is going to insist that it's not to blame.. but I now know better.. Thank you so much for helping me find answers.

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 am writing on behalf of my elderly parent, Carmela, who has been diagnosed with Lupus since 1991. She has been on a small dose of prednisone since her diagnosis in 1991. In the last several months she has developed very many odd hazey type grey spots all over her body. Dermatologists and doctors are not giving her any answers. They took her off predisone because they THINK this may be the cause. She is on an inhaler and does not like it. She wants to go back on the prednisone as she is feeling chest congestion and lethargy. I read an article on the internet that describes prednisone may cause unusual bruising. I'm not sure if this is what her spots are. They are only the color grey and appear to be beneath the skins surface. They are soft or hazy looking. They are small, about the size of a dime. Has anyone heard of this before in Lupus (prednisone) patience. Any info you have is sure appreciated. S. ******

I started taking Yaz about a year and a half ago. I'm no longer continuing this pill after this month's pack is finished. I have to say that at first, it was a really great pill. The first month was hell. I bled for a month straight, and I was so irritable, and emotional, and my bf would talk about silly shit, like beached whales and I would start bawling. I spent four months living overseas after starting the pill so I didn't notice the loss of sex drive and sensitivity at first. But when I came back I started to notice all the little things that were becoming huge issues. My sex drive is more or less gone. I actually fell asleep last night while my boyfriend was trying to get me aroused. That's awful. I always feel tired lately. I get a lot of headaches. I read that this pill increase your potassium, and my mother's told me she has a lot of potassium so when she eats bananas she gets splitting headaches, and I'm the same way, so I'm starting to realize where all these headaches are coming from. Sometimes they are so bad that Advil does nothing at all and I end up having to rub between my thumb and forefinger while trying to fell asleep to make the pain stop. I've become extremely moody. My moods change so often now. I'm irritable. I am coming off of two really tough years of my life, and things are really great for me right now, and I don't feel great. I never want to have sex. Foreplay doesn't feel as good as it used to. I don't get aroused quickly, and I have a lot of trouble climaxing. I smoke weed and was smoking mixed spliffs with my bf for some time not even thinking about it, and the reaction the tobacco had with the pill was horrible. I'm certain that if I didn't stop I would have ended up in the ER. I would experience fainting spells, momentary blindness!!, I'd go really pale after getting very hot. I nearly passed out on at least four occasions before discovering the link. After I stopped, I felt much better. But now I can feel all the emotional side effects. I've also been sleepless for a long time, and I think that has to do with the pill, too. Lately I've been getting very nauseated if I eat shortly after taking the pill. And it doesn't matter what I eat. I'm constantly burping like I have a nervous stomach, but I've been calming my mind lately so there's really no reason for it. I've got a lot going on with life and whatnot, but I'm usually able to handle a lot of pressure and stress without breaking down, and this pill has made me almost incapable to dealing with the slightest bit of stress. It's horrible. And I don't want any part in it, or in the pharmaceutical business. I'm going to try tracking my own ovulation. At least I won't have some crazy hormones messing up my system.

Oh. I also had a fibroadenoma (breast cyst) this summer that I had to have a biopsy on (which was really fun, let me tell you...), and I can't say that the pill caused it, but I've never had cysts in my breasts before... The pill did inflate them an extra cup size, and during the third week of pills they are so tender I can't even let my boyfriend touch them or hug me tightly because they hurt so badly. And I live in NYC and there are a lot of stairs to bounce down and it's painful.

I see all the same symptoms with everyone who takes this pill and has a bad experience, and I've decided that it's not for me. The man can wear a condom for a while, while I try to regain my normal self again.

Topamax can cause blindness. Please read about all of the side effects of your antipsychotic meds carefully, and never think you are immune to them. These are powerful drugs, and no one truly knows how they will effect each individual brain.

I've been taking lisinopril for about 4 months for HBP which I have had since I was 18 and I am 40 now. My blood pressure went down immediately--I can never remember the number but before nurses testing my bp would always say I was "a little high" and now they always say "it's normal." When i first started taking it I noticed I felt a little depressed, and I always felt lethargic on lisinopril. I believe that's just normal from taking something which reduces BP. I had bad diarrhea and got pretty sick for a short while a couple weeks ago but there was a flu that was going around. I noticed some dizziness and was pretty out of it, but I have felt those symptoms before I started on lisinopril. I am now worried from reading your complaints about this drug.I ran out of pills a few days ago and I feel much more energetic and with-it now, generally better although now I worry about the long-term effects on my body of my HBP. I currently have a headache and to be honest I still don't feel 100%. While I was on it I noticed some dryness in my belly and my poop seemed weird not normal--I had some bad flatulence and my poop would come out sometimes pretty sparse. I definitely felt different, especially in my digestion and lethargy, but did not have very very bad side effects. Still I'm thinking twice before taking it again. My father had some blindness in one eye that was apparently from long-term HBP, so I am concerned about long term effects of not doing anything about my BP--so I may go back to lisinopril or whatever else my doctor prescribes.

I was put on Prednisonsone for Uveitis, inflammation of the eye. He started me on 20mg at 9 pills a day, then each week it was lowered to 6 pills then now i'm on 3 pills and then next week it will be 1 1/2 pill and i'll be off. I got the puffy face, my feet swelled, everytime i hate my stomach bloated and hurt, my face and neck turns red, i stayed hungry although i fought the temptation of eating for not wanting to gain a lot of weight, which I don't think I've gained any. But now I wake up in the middle of the night and severe knee pain, it feels like my knees they are in some kind of device that is crushing my bones they hurt so bad. i caught a bad cough and it's been around now for about 2 weeks and won't go away, i told the nurse about it and she says, i probably just got what everyone else has gotten, just a bad cough, well what's if it's some kind of infection? I look like a chipmunk, my face is so puffy. When i get off these prednisone in another week I WON'T BE going back on them, no matter what the case. I'm in more pain being on them and have more side effects while on them than the problem i was having with uveitis. I think some co workers thank I'm over reacting, but they're not here they don't see all the pain and frustration i'm going through while on this drug. The leg pain just started this weekend and i Know i can't deal with waking up everynight like this in severe pain. Everyone just makes me feel like i'm over reactin and it's nice to know that somebody out there is going through the same thing. Any comments will be great.

Hi everyone,

I am a 25 year old female who was diagnosed with Crohn's disease one year ago. I stumbled on this website and wanted to share my experiences to let others know they are not alone and that their side effects due to Prednisone are completely normal.

In Nov of 2007, I was in the hospital for a Crohn's flare up and was put on prednisone through IV (240mg/day). After a three days I was released, but one week later, had another flare up and was back in the hospital in December of 2007. This time, I stayed for 6 days and was on 240mg/day again through IV, along with taking Flagyl and fluids for my flare up and infection.

At first, I lost about 10 lbs due to the flare up and all of the medication I was on. However, within 3 weeks time, I gained 28 lbs and was a complete mess. I looked different, felt different and was emotionally and mentally drained.

My side effects included: Severe moon face, buffalo hump, increased appetite, hair thinning and severe hair loss, night sweats where I would have to change pajamas 3-4x a night, OCD to the point where I would have to clean my entire apartment (even if it was already clean), restlessness, anxiety, no sleep and sometimes I would go days without sleeping, increased thirst and dehydration, swollen eyes and headaches, depression and mood swings, upper and lower abdomen swelling and weight gain (28 lbs in 3 weeks), suicidal thoughts, unbearable muscle and joint swelling and aching, forgetfulness and memory loss, blurred vision and dark hair growth on my face near my sideburns and underneath my chin and on the bottom portion of my face. Bottom line: it was unbearable and nobody warned me about the harsh side effects of the drug.

When I left the hospital, I was put on 60mg/day and eventually weaned off Prednisone over the course of 2 1/2 months and took my last 5mg dose in mid- February 2008.

It is now 2 months since I have been off Prednisone and as of now, I have only lost 7 lbs, but much of the moon face has gone away and I don't seem as swollen in my chest. My appetite returned to normal the day I stopped taking the drug and my mood swings subsided one week after stopping Prednisone. I still have the buffalo hump, but it stopped hurting and I am now able to sleep through the night. The fluid retention seems to have moved south towards my legs, arms, and lower abdomen. My doctors say that within about 6 months after stopping Prednisone, most of the fluid retention should go away and they recommend walking for 45-60 minutes/day to help with the fluid/weight gain.

Overall, prednisone helped to save my life and put my Crohn's into remission, but is one of the WORST drugs I have ever taken. My heart goes out to anyone who has had to take this drug and trust that you are not alone--and the side effects are real and they are harsh. I am slowly seeing that it takes time for the prednisone to leave your system and my doctors say that every day there is less and less in my body.

Stay positive, stay active & stay Healthy!!

Been on Prednisone for 3 years now for ulcerative colitis. At first tolerated the drug quite well. But after a few months started to gain weight, acne. After 3 years of yo-yoing between large and low doses, each increase in dose made me feel worse. I am now at a state of osteopenia and of extreme tiredness and brain fog. I see 80yo with more energy than I. I cant walk up 10 sets of stairs without feeling tired out. I need to sleep 3-5 hours a day just in order to function. As mentioned before brain fog is amazingly bad. I'm a scientific researcher which can no longer work.

Prednisone has introduced to me what panic attacks are, mood swings, joint pain and swelling, extreme muscle fatigue and wasting, blurry vision, in habitual eating habits, depression.

This drug has ruined my life. I would have preferred having surgery to remove the colon and going to the toilet 10 times a day rather than not living as brain fog and tiredness that makes my life a dream-state nightmare.

I have asthmatic bronchitis. In June 2006 I came down with an infection in my lungs, which also set off my asthma. Between the two I was hospitalized and put on 240 mg of intravenous Prednisone and the antibiotic Levaquin. I was cured of the infection and was able breathe normally again but it took a great toll on my body It took me 3 months to taper off of the Prednisone and almost a whole year to feel myself. I was a strong, physically active person before this happened to me and I have not gotten my energy level and endurance back to what I was before I was sick. When I was released from the hospital I went from 160 mg of intravenous Prednisone to 80 mg of pill Prednisone. That step down was too severe and I went through intense joint and muscle pain in my body that it woke me from a sound sleep in the middle of the night. I luckily had an old Vicodin that I took which only made the pain bearable. I should have upped the Prednisone to make it go away but I wanted off. This pain lasted one week with each day getting less. The side effects I experienced from then on were so plentiful that I almost can't remember them all. The physical problems were, thin skin that bruised or ripped and bled profusely with the slightest bump, blurred vision, sensitivity to light, muscle cramps in my legs and hands, sleeplessness, dry mouth and frequent urination. My stomach bloated and got stretch marks. I didn't have any before that. The muscles in my thighs and upper arms atrophied so bad that I could not walk up stairs w/o using my arms to help. My arms were also very weak and I got hemorrhoids; another muscle that was affected. I had a bad case of the drops. I couldn't hold on to anything and broke many glasses. I got moon face that took a couple of weeks to go away after I was off the Prednisone. Because I was on such high doses, my hair died and stopped growing. About 40% of it fell out in one month. It took 6 months to grow back and it all grew back curly. On January 30, 2008 my bronchial tubes closed again due to a sinus infection. Again I was hospitalized with 240 mg of intravenous Prednisone and Levaquin. This time I responded much better, because I jumped on the infection/asthma instead of waiting. I stepped down from 240 to 180 to 90 to 60 and decrease 5 mg a day until I was off. This time I did no lose my hair land did not get hemorrhoids. The other physical effects were pretty much the same but much less severe. However, this time the emotional effects of Prednisone were much worse than last time. I was not a nice person. I was short tempered and argumentative and even had to stop myself from resorting to violence a couple of times. That is definitely not who I am. Prednisone stops your adrenal glands from working and adrenaline is you chemical way of coping with stress. I have been off of the Prednisone for one week and still find it hard to cope with the slightest controversy. My brain is still in a fog and I get confused easily. I cannot handle too many questions at once and forget things. My face is still round. Both times, I have found it the hardest dealing with the Prednisone at the very end and even after I finished taking it. I think it builds up and even though the chemical is suppose to be out of your body in 24 hours, it's effects stay a lot longer. I thought I knew what to expect but the second time was different again. It is a horrible drug but my trade off was breathing. Sometimes I think, that if I have to go through this a few more times, the side effects will kill me before the asthma. I wish all you Prednisone users loads of luck and stay positive.

This is my second course of Prednisone after several UC flare-ups. First time I was on 40mg for 2 weeks, then tapered down for two weeks. My first few days on Prednisone were great. I finally had energy, I was in a great mood and finally felt like I was living again. After 4-5 days, the weight/bloating began. My fingers and ankles began to swell, then my face. I no longer felt "alive" anymore, more slovenly. None of my clothes were fitting either. I developed a very noticeable "muffin-top" that made buttoning my pants difficult and wearing and snug t-shirts embarrassing. I returned to my doctor after my two week course (prior to tapering) and found that not only did I gain 12 pounds in two weeks, but my blood pressure had increased dramatically. I was assured that once I quit the Prednisone, my weight should return to what it was, as well as my blood pressure. Sure enough, they did.

I would have to say the very worse part of taking this medicine, for me, was not the two weeks that I was on my 40mg course, nor was it the two week taper, but the two weeks after stopping the medication. My energy level was completely zapped, but I couldn't sleep. I also had the worse headaches and mood swings. I would snap at my family for the smallest of reasons. This medicine introduced a side of myself that I never want to meet again.

Unfortunately, here it is 2 months later and I have been prescribed another course of Prednisone due to another colitis flare-up. I thought I was prepared for what this medicine will do to me since I experienced it once before. However, this time is nothing like the last. Unlike last time, I have yet to feel "on top of the world". My bloat came on quicker this time, as did my mood swings. I am depressed and really hating what I have become. Fortunately, I have enough sense to realize a lot of my depressive thoughts and mood swings are a result of the Prednisone, but it doesn't make it easier. My vision is blurred and for the first time I understand what others are talking about when they speak of foggy brain. I am physically present, but definitely not coherent. I just want this medicine out of my system. I would rather deal with the intense cramping and bloody stools from my colitis, then have to ever go on this medicine again.

I don't have a new side affect with Prednisone but just want to share my feelings. I was diagnosed with Temporal Arthritis since last July 2007. I started taking 60 mg of Prednisone for 1 month. Didn't notice the side affects then. Weaned myself off through my doctor's instructions. But relapse occurred when I was only on 2 daily. With Temporal Arthritis, you get delibating and horrendous head pain which is caused due to inflammation of the main artery in the temple. I am back to 3 daily.
Besides my moon face, I am bigger. I really don't have a lot of the other side affects you all talk about. I am sorry you all have to go through that.
My depression is better. My sleep is horrible. Now I am going to a sleep study to see if I have Sleep Apnea.
I consider Prednisone a wonder drug. Although the side affects are horrible, I have to admit, I feel much better, most of the time. I do have inflammation in the neck. Not sure if that is pred or temporal arthritis, but am seeing a rheumatologist for that.

Teena

Hi Everyone,
I have been taking Topamax 25 mg for 1 week. I can't stand it. Today I am to up my dosage to 50 mg.I am not sure if I want to do that. The side effects suck.. I think I would rather just deal with my migraines, at least I know how to do that since I have had them for over 25 years. I have tried everything and nothing has worked so the Dr. and I thought we would give this a try.
I am trying to keep my place of employment happy with trying to cut down on the migraines but nothing works.
Most days I just want to give up.
Hopefully we will be able to figure something out.

I can't stand the pickhands and feet, the stumbling like I am drunk( and I dont' drink) nothing tastes right anymore, I have the shakes and I ache.
And all it does is makes me sleepy and like I am in another world.
I went to work today and made it half an hour before I came home because I stumbled and almost fell over. And when the boss talked to me it was like I wasn't there. So I came home. I don't know but I don't like it at all.

I was dianosed with an immune disorder of the inner eye. It was advanced enough that regular treatments were not effective. So the dr. started me at 60 mg of prednisone and started to taper it off at 20 mg. every 2 weeks. At 6 weeks, it was observed that my symptoms had reappeared and so he started back at 60 and the tapering was much, much slower (50 mg, 40 mg 30 mg 25 mg 20 mg 15 mg 10 mg 7.5 mg 5 mg 2.5mg) the first week I had panic attacks and wanted to physically attack people. I couldn't sleep. After that I had mood swings, fuzziness, forgetfulness and confusion, all I wanted to do was lay on the couch. I had heart palpitations, moon face (people thought that I'd had dental surgury) went from a size 6 to a size 12. I had terrible yeast infections, and wanted lots of fluid and had frequent urination. It was horrible. By the time I was done (and I had withdrawel symptoms long after I stopped taking it) I'd lost 2 years to the side effects. I do get to keep my eyesight. Fair trade, I suppose. In the next year and a half I lost weight down to a size 2, not as good as it sounds, all my muscle tone had gone and I'm having to rebuild from being nearly skeletal. The worst part of it is.. at any time I can be put back on prednisone and will probably choose to over losing my sight. At what point does one have to worry about osteoporosis? How much prednisone for how long effects the bones? There are things I'd like to do, but I'm not sure if I should.

My husband was the one put on Levaquin for a chronic infection to his testes and prostate (that incidentally was not taken care the 4 years that he was incarcerated). He was started out on a 8 day supply of 750mg and then cut down to a 30 day supply of 500mg. He has experienced loss of feeling to both hands and feet, severe knee pain, hallucinations, nightmares of the worst kind when he did sleep (which was very rarely) and experienced temporarty total blindness for about 5 hours, at which time his vision slowly returned but was blurry around the edges. He was physically worn out. The medication was stopped after he experienced the blindness. He is doing better but continues to have numbness and tingling in his hands.

I have been on Prednisone since July 3,2006, I agree with all
the side effects that has been mentioned. I have temporal artirites a the age of 58. I was within hours of never getting my sight back. The drug did stop the blindness so far. I am having trouble with my eyes but also I am having so much bladder trouble now. They say I do not have an infection of the bladder, and the pills could be causing the troubles.
Is there anyone out there that is also having bladder troubles?

The head pain was like my head was going to burst open, not just a head ach for me. I put up with for almost two weeks, till my sight was so bad and I couldn't hold my head up and the Dr. on vacation came back and knew I was in trouble and researched it. Other s had been treating me for allergy pain. I knew this was no head ach.

If no one will listen to you just keep pushing for more. I am the one that asked for a blood test and my count was off the charts. We know our bodies the best and I am not usually a sick person or a pill taker, so this has left me with alot of changes going on that I thought was going to disapear, but after reading the letter on this chat line, I am really worried. So many of the feeling are so strong already, mood swings, I am usually easy going and happy, but whow..somethimes I don't know myself. I have a really good business and it is really hard to keep it all together now and like others have said, I feel I am wearing others down with not feeling good from the pills not my condition.

PLEASE....let me know if anyone has experienced the bladder problems.

THANK YOU,
JANET...MO>

Guest # 4041
I really feel sorry for your 3 years old niece. Try something else for her!!!! The prednisone will ruin her little life for ever!!!!!
Blindness, stop growing, diabetes - only a few from a long-long list.