Prayers symptoms and conditions

I HAD KNEE SURGERY ON 11/02/2009. MY DOCTOR PRESCRIBED PERCOCET FOR THE PAIN. I DIDN'T KNOW WHAT TO EXPECT OR WHAT EFFECT THE NARC WOULD HAVE ON ME. ALL I KNEW .....IS THAT I WANTED SOMETHING THAT WOULD KEEP ME FROM FEELING THE PAIN. AT 1ST I WAS TAKING IT EVERY 8HRS & I WOULD WAKE UP IN GREAT PAIN. THEN MY SON READ THE BOTTLE & SAW THAT I WASN'T TAKING IT AS PRESCRIBED. I SHOULD HAVE BEEN TAKING IT EVERY 3HRS. SO I STARTED TO TAKE IT EVERY 3HRS & INSTANTLY I FELT A DIFFERENCE. (MY NOSE STARTED TO RUN) I WOULD BE (TALKING 1 MINUTE THEN DEAD SLEEP THE NEXT) MY SKIN WAS (ITCHY) ALL THE TIME (LIKE I WAS AN ADDICT) I STARTED GETTING (ABDOMINAL PAIN) (SEEING SPOTS) VERY PERKY THOUGH. THEN THE (CONSTIPATION) CAME. THIS WAS ALL IN A MATTER OF 4 DAYS. BY THAT EVENING OF THE 4TH DAY THE CONSTIPATION & ABDOMINAL PAIN WORSENED & I DECIDED I WASN'T GOING TO TAKE THE NARC ANYMORE. I DIDN'T TAKE IT YESTERDAY & HAD A (HARD TIME GETTING TO SLEEP) THANK GOD IT WASN'T DUE TO THE PAIN. I DIDN'T TAKE ANY TODAY BUT THOUGHT ABOUT IT SO I CAN GET TO SLEEP BEFORE 5AM. PLEASE KEEP ME IN YOUR PRAYERS FOR I WILL KEEP ALL OF YOU (THE COMMENTS IVE READ) IN MINE. GOD BLESS

Marini IUD side effects and marina crash side effects for my daughter….still going

February- pregnant 19 by 25 yr old first pregnancy...
Abortion first ever
IUD marina same day insertions as abortion
Yr later Sept bloated tummy, anxiety attacks, paranoid, tummy flutters, pushing sensation.. Odor, discharge something’s wrong
Next day….Marina removed, antibiotics, bacteria infection
Lab test all negative.
Next four weeks…. Barley any sleep, barley any food, depression, anxiety, out burst, rage anger, sadness, self verbal destruction, blaming self, tossing turning, moaning, soul hurts, very moody up and down, no patience, confusion, face breaking out…looking pale, skinny, unhealthy….It’s like a drug addict addicted to drugs but this is addicted to the guy who got her pregnant… no drugs ,no alcohol,
Call radio station, ask why are they not making sense…
TV.. fate/Destiny, symbolic meaning meant to be…..
Reality. .NOT an option….
25 yr old who got me pregnant was a fling off and on a yr..
Convinced self…… had to be with him ,loved him,
Drove over to his house daily,
Called daily, text daily,
Believe the earth was putting signs of fate and destiny to be together with him

Couldn’t be in public, took time off from work, saw counselor, who said needed anti- psychotic pills, depression pills, and sleep pills have hormones checked, thyroid level…. Alice in wonderland can’t separate reality from fantasy.
Saw another doctor, had test….white blood cells moderately high have to go do more testing. doctor said doesn’t need hormones checked…. said ADHD need meds again…
Feel crazy, feel like losing mind, drifting in and out of thought conversation, space out get into trance like sate, and feel as if I can’t control self,
Have to be with this guy, have to protect him. Pregnant because of him,
Convincing self destine to be together, family marriage future with guy..
Other times acceptance of rejection from him, never wanted to be together.
Lost three weeks of work., keys to car taken, keep texting him calling him…Girlfriends tell to stop….Ignore her..
What’s real and what’s not. Keep repeating questions seeing signs, from TV, radio, he wants me……he needs me…All in my head??? Everyone tells me…All in my head..
Can’t take ADHD pill, can’t sleep,….Confusion, blurry vision, see colors…..What’s real???
Snapping at family, angry, disbelief,he wants me….
Reality. Is he doesn’t can’t accept it….
Family thinks I’m loosing my mind…am I?
Over a guy? Who was just a fling? Who I thought was the One….
The reality shows, We are meant to be together…..But told It’sall in my head…
No family history of mental disorder, never have gone though this..
Always had confidence before marina IUD…..
Never chased guys, never had too…what’s wrong??? Why this behavior??
know’s better, he wants me,
Began Sept 26th..anxiety,flutters,pushing,bloating….swollen belly..
Still going Oct 28th..Removed Sept 28th 09…..after removal instantly feel better then BOOM!!! Downhill spiral of emotions began’s…..Still feel very clouded in her head, confusion expression......head tells her the opposite of what the family tell's her...
What can I do as a mother with great concern???? How do I get her back to the happy,outgoing,confident 19 yr old she was????

I was literally in tears when I found this site and read all of your posts. It was as if I was reading something I HAD WRITTEN. Having just returned from getting a CT scan of my head, I started researching "causes of severe headaches not related to migraines" and lo and behold this site popped up in my search. What caught my attention was the word "Mirena". Up until today I had never even considered that all of the issues I have been having since the birth of my daughter in August 2008, were in any way related to Mirena. When my daughter was about 2 months old (after my 8 week check up and insertion of the implant) I became extremely moody, sad, social anxiety kicked in, I cried for no reason, had no desire to talk to anyone, not even my husband - VERY unlike my personality. After talking to my doctor it was determined I had post partum depression so I was prescribed zoloft. Didn't work. Was still irritable and lethargic but maternity leave was up so I went back to work. I was exhausted, couldn't process my thoughts, was constantly dizzy and had blurred vision and it was all attributed to the "baby schedule (nightly feedings, no solid sleep, adjusting to schedule, etc.). My mood swings were out of control and it got to the point that I even through a knive (albeit a butter knife) at my husband. I began seeing a psychiatrist who determined I had mild bipolar disorder so he put me on medication for that. It has helped some but still doesn't control my crying spells or occasional outbursts. Recently I was so dizzy that I saw my ENT doctor who said I had vertigo. I was prescribed something for that. Still, I am dizzy and feel off balance. Most recently, I have had severe, severe, severe headaches and though there is a great possibility it is a viral issue, I was ordered to have blood drawn and to obtain a CT scan. Nothing much revealed so we set an appointment to see an neurologist next week. So, because of the worry over it, I started doing an internet search and her I am. Reading these posts brought on an overwhelming sadness because my poor family has had to endure my wrath for past 12 months. I am so angry that I didn't see this sooner and moreso that their !@#@#$% side effects didn't list ANY OF THESE discussed here. Additionally, my hair has been falling out in clumps and I can't seem to lose weight despite my 1500 calorie diet and exercise.
I made an appointment TODAY to have it removed. If I could yank it out myself I would. Thank you all for your posts. You may have just saved my marriage and my life.

What a MISTAKE! I had my dreadful Mirena INSTALLED September 2. My doctor had me convinced this was the answer to my prayers. It was suppose to control my heavy painful periods. I was not using it for birth control. Unfortunately the effects were exactly the opposite. I have a very high pain tolerance, but when I got home from the dr. office the pain was more like labor pains than menstrual cramps. When the excessive bleeding, cramping, bloating, lower back pain persisted I started to look for answers. I was so grateful to find this site! It has been pure torture trying to live with this thing in me. I am happy to share I just had it removed. I only lasted 15 days! My husband came with me because he has never seen me so weak, in pain, dizzy and light headed. All symptoms from the excessive amount of blood loss. I am confident that the women who shared their stories truly helped me to make the right decision today. Thank you

chronic diarrhea x2 weeks-began 4 days after initial dose of lisinopril.....
diarrhea x 12+daily.....
also, experienced headaches, nervousness, waking at night, sweats, acid-like taste in mouth. I discontinued usage, went to dr-she gave me an RX for procardia via nurse without even seeing me on the sole complaint of chronic diarrhea X2weeks......I surely hope this is the solution, and from the postings here, it does appear that Lisinopril is poisonous.
Good luck everyone. My prayers are with all experiencing similar ill effects.

It's 4:42 a.m. Can't sleep. Keep coughing when start to doze off then. Shortness of breath. Was cold now hot.. Started searching internet for side effects found this site. I am taking 40mg of this started only 4 days ago. coughing up the clear stuff. started today. runny nose. have the same spitting episodes. I may go to ER. Trying to make it through the night to call dr. in the morning. I am unemployed...can't afford ER. have to visit clinic. Very hot. I wish I had known about these side effects would never have taken this medicine.

54 year old Male, Retired Marine, Very physically active, with Type II Diabetes; 5mg. Thanks for this Website. Started Lisinopril 3/25/09. Took it for 25 days, found this website and stopped taking it immediately. I had severe JOINT PAIN. It started in my hands, then feet, knees were next, then moved into my shoulders. The pain was the worst I've ever felt. Approximately 60 days after stopping the drug I went to see the Dr. after the Pharmacist told me Lisinopril should have been out of my system after 2 weeks. The Dr gave me Steroids (Prednisol) which completely eliminated ALL pain in 2 days . I was tested for Polymyalgia Rheumatica, however the my Sed Rate was normal. The blood tests did reveal that my RHEUMATIOD FACTOR is elevated (34.3 where the normal range is 0.0-20.1 IU/ML). Was told that if the pain returned, then I would be referred to a Rheumatologist. 3 Days after finishing the dosage pack of Prednisol, the pain/swelling in my hands and shoulder has returned. Going back to see the Dr today to discuss next steps.

Although the doctors don't agree, I believe Lisinopril caused this pain, and although out of my system now, triggered something that isn't going away.

The rest of this describes the roving pains I experienced.

Hand pain included swollen fingers, inability to make a fist or type on a keyboard. After light yard work on Sat., shooting burning pain up the inside of both arms. Trying to close your hands into a fist, you can feel the tendons up your arm burn with pain. Motrin did not alleviate the pain. Hot water did not help.

Pain in my knees each morning. The pain worsened over night and frequently causes you to wake up. The pain was like your knees were being squeezed in a vice. No position is comfortable. Motrin sometimes helped, but after awoken, getting back to sleep was impossible.

Feet swollen. Couldn't wear any shoes for extended periods. Loosening the laces helps, but still caused pressure which becomes unbearable and the shoes have to come off.

Shoulders; This is the strangest one. First pain was in the left shoulder, like I had impacted a brick wall at a full run (actually no trauma occurred). The pain felt like someone had stabbed it in my shoulder in the socket. At it's worst, no position is comfortable. Had to put my arm in a sling. 5 Days later, the same type pain moved to the right shoulder.

Ladies,

I hope you don’t mind a male posting on this forum but I do have a reason for doing so. I am a Coroner’s Officer in England. I will not at this time disclose whereexactly I am based as I need to protect the identity of the family. I would however like to use you as a sounding board in the hope that you can help me, help the family and perhaps, just perhaps, I can help you.

Sadly I am dealing with a suicide. The lady in question, who has taken her own life is in her 40’s, married and has children (all over 11 years). The lady has no history what so ever of any form of depression during her life.

The lady has described her life as being perfect with a family that loves her and who she loves in return and as the Investigator I believe she is truthful in that comment. She states she has been extremely happy until last week. She makes comments of - I am just very ill, cannot sleep, feel dizzy, cannot concentrate, sometimes lose my vision, feel sick all the time and sweat at night. She cannot understand, but it makes her feel bad. I am not myself, something has made me ill which means I can’t be my normal positive, active busy self. I can’t bring myself to do anything that I normally love, like gardening, cooking etc. I am losing my memory badly going fuzzy in the head.

Her final comment, which is the one that has prompted me to post on this forum (with the permission of the family) is ‘I just don’t understand this – I’m so sorry . I can’t understand myself or what is wrong with me or what I’m doing so sorry. Just remember I’m not myself somebody else has taken over – I don’t know if it is all the anti-histamine pills that has mixed up my chemical balance along with the Mirena coil or is it just me’.

The mention of the Mirena coil has therefore prompted me to investigate it. I am not, by any means suggesting that this is responsible but it would be wrong of me to discount it after having read the posts on this forum and other places on the Internet.

The lady in question had the coil inserted in 2004/5 and it would appear that there were no problems or side effects reported.

I am therefore looking for some help from you. Some comments on what I have posted etc. Some advice on where to obtain expert advice (although I am trying some avenues of my own).

I may also ask, depending on what help you can give me if you would be willing to identify yourself to me.

Thank you

P.

This site is the answer to my prayers. I have been on YAZ for 2 years and at first it was amazing. Regular and light periods, no mood swings, no breast tenderness and no weight gain. The past few months it all changed. I thought it was just a funk I was going through but its to the point it is affecting my life. I have developed severe anxiety and a feeling of sadness for no reason. My life is great; new job, great relationships, financial issues are fantastic. I have been having panic attacks out of the blue and it is getting worse as well as weird muscle twitching daily. I felt like I was losing my mind, because I can't stop feeling that way. I went to the doctors and acupuncture to see if it could help. I noticed it was worse a week before my period and during my period and the week after. It fluctuated all the time. Then one day my eye sight was blurry and couldn't see straight for 20 minutes. I've been thinking about Yaz and if its a side affect so decided to get off of it. Now that I did my own research and seen that people are having similar side affects , it gives me an even more red flag to get off it. I hope and pray that these feelings go away now that I am getting off it.

I have been on prednisone since I was two years old (I am now sixteen) because I have Autoimmune Hepatitis IIa. I would like to point out that there is still a life worth living being on prednisone, maybe I say this because I do not know life without it, but at least we're alive! Last year I had a flare up of the AIH and had to 6x my dose of prednisone. It sent me into a spiraling depression of constant sleep, crying, hopelessness etc....but I made it through. Just PLEASE keep hope that things would get better, because I know what it's like being on the dreaded drug better than most.

My doc prescribed Avelox for a sinus infection after the first round of antibiotics didn't clear it up. The dosage was for 10 days. After taking pills for 4 days, I started getting a strange shoulder pain. It's like I had worked out my shoulder muscles after a loong time and my muscles were recovering, but I had done no exercises of any sort to cause that. I also did feel some dizziness and unable to focus after the 4th pill. I immediately stopped taking any more pills after that. Would rather face the sinus infection than deal with all this.
I was worried after reading the side-effects of others on taking this med. But luckily enough - it's been one week after stopping the meds and my shoulder pain is now completely gone. So, it does look like the side effects will clear up, but just takes sometime. My prayers to all who are suffering that they recover fast.

I am 38 and took YAZ for two years. At first it seemed like a wonder drug. I didn't have a period the entire time I took them and my MD said that was normal for some women. After about a year, I started having night sweats, leg cramps, and increased moodiness...like things that should just aggravate me made me down right angry. I also started having considerable swelling in my hands and feet that was present most of the time. After a night of research on the internet trying to figure out what was wrong with me (my thyroid?) I landed on a few sights about YAZ and felt like my prayers were answered. Every single thing that was happening to me: sweats, swelling, cramps, low sex drive, fatigue, headaches, GI upset...could be attributed to YAZ. I stopped taking it immediately. It's only been about a month and I'm still feeling a little tired and moody, but my legs don't cramp, my rings fit my fingers, no more night sweats, and I have the hots for my hubby again. Life if Good! :)

How can I describe my thanks to this site and everybody telling their stories? Thank you oh soooo much!!!

My not so short story: Im on my second Mirena, in total now for just over 8 years. The first Mirena was all joy, periods stopped, no side effects whatsoever. Then I got the second Mirena after I removed the first after over 5 years (my gyn recommended keeping it in for longer but I didn't want to take the risk).

And for the past 2 years my ACNE problems started, first only one or two cystic acne once a month or a couple of small ones here and there. Nothing major. But for the past year, my skin / face makes me feel like a freak. So I went to the derm, got put on Accutane, more meds with a yard long list of side affects. Had to go of Accutane cos my right eye's sight deteriorated so bad I couldn't drive home at night. Went to my house doctor, he wanted to take me of the Mirena asap and refered me to a new gyn, cos mine moved away and I was stuck. But the new gyn did not want to take it out, but rather put me on a retinoid cream, cos it wasn't the acne that caused the acne.... yea right. So 5 months I gave this retinoid cream... I feel like a freak with my face, both cheeks inflamed red bumps under the skin, large cystic acne everywhere... sigh.

But during this 5 months I found a web site acne.org and here I made friends and read stories and hoping and praying, even believing things are getting better, but they weren't. If I look at pics I took of myself 5 months ago and now... sadly things are worse. My self confidence is gone, and I don't even want to have sex with my husband with the light on!!! And then last week somebody posted on the acne site some posts regarding zinc supplements, and I read and researched more on zinc and acne and found that your skin needs zinc to be healthy and having no zinc could be because of to much copper or copper toxicity. So then I researched copper toxicity and found some web sites with references to birth control.... and a bright light went on... and I found this site...

I am glad to say I saw my normal trusted house doc again last night, and made an appointment to have the thing, Mirena, removed first thing Monday morning. I have stopped using any meds like the retinoid cream for my face and cant wait for Monday. I just hope my face returns to normal quickly.... time lines anyone? I had no trouble with acne ever until now.... and Im 35!!! Udult acne my @#$ :)

My right eye now needs laser surgery to remove a layer or something, Im seeing an eye specialist soon, and this was caused by the accutane drying up my eyes so much! :(

I will report back to let other ladies know how it went and how I am progressing... thinking of taking a daily photo of my skin for reference purposes.

Pray for me please, I really need it....

C.

My daughter received her first vaccine in Dec. 2007 at 15 y/o. We really didn't notice anything out of the ordinary until she received her second shot in Feb. 2008. In March of that same year she began experiencing severe abdominal pain and an unusual rash on her feet and ankles. We have been through many different tests from acid reflux to testing for Ulcerative colitis to Crohn's disease. We do not have a diagnosis as of yet but I recently realized that all of her symptoms began following her second shot. Her symptoms are severe abdominal pain (more severe while on her period), nausea, diarrhea and spotting between her periods There isn't a day that goes by that she does not have pain. She developed the rash on her feet and ankles and itching under her armpits that comes and goes (one doctor states it may be eczema) Nothing is clear to us as to what is going on. She will not be receiving the third shot! There is nothing worse than watching your child suffer as I have watched her suffer! My heart and prayers to all you moms out there and children going through such a horrible ordeal!

I made my appointment yesterday. It comes out tomorrow. I had my first anxiety attack on Monday Feb 2nd. I thought I was dying and to make it worse I was driving. I'm paranoid. I can't help but cry right now. I have blurry vision I feel awful. I was thinking its only anxiety and nothing to do with the Mirena, but I don't need this in me. I'm not chancing it. I don't want to have children right now especially how things are going, but I'm not willing to go insane just to prevent it. I want my mind back. I want my life back. Even if this isn't the cause of it I won't give it the slightest chance.

I was doing well for a while then this year certain things started changing in my body. I'm not willing to keep it in. I can't feel the strings so I hope nothing bad has happened. I'll find out tomorrow at 3:30 Pray for me. I need your prayers I'm so paranoid.

Ladies (and that is not a sexist greeting. This forum better be women only ;-)---thank you for your contributions!! My oh my. I had a Mirena put in shortly after the birth of my daughter. No pain from insertion, but afterwards, dizzy, nausea, headaches...and CRAZY. I would fly off the handle. We weren't sure if it was postpartum or the Mirena. So, out it came and I straightened out within 24 hours! Now, you may think I'm stupid, BUT I cannot do traditional pills because of the breast cancer history. I spoke with my new physician (switched insurance plans--new doctor) and we decided to try the Mirena one more time (now that I couldn't possibly be post partum). Insurance pays for it, so we will try it. Well, guess what. It has been three weeks. This time around, the doctor PAINFULLY inserted the device. In three weeks, I've been dizzy, nauseated and CRAZY again. Oh--non stop bleeding. So, I'm getting it out as soon as they can give me my appt time. I don't know if this reaction is to a foreign device in my body OR to the chemical. Either way...we have to do what we have to do. Prayers to all of you and do not hesitate to take care of YOU. God bless!

My 17 year old son was diagnosed with MRSA after getting an injury on his knee from playing basketball.After the first does he had a loss of appetite, fatigue, nauseous and severe headache. By the third day he got a fever, chills, neck stiffness and a feeling of doom. We went to the ER because his blood had not been cultured and we were afraid of sepsis in the blood. The ER doctor said it was most likely viral and sent him home. The next night he had a fever of 103, sore throat, trouble swallowing, sun burnt look, swollen eyes and cracked swollen lips.The next day we went to the urgent care and they tested him for mono, strep and the flu...(all negative). He felt awful and was so tired and feverish. The next morning he woke up with a severe rash and itching all over his body and his skin looked like it was scalded. His blood culture came back negative for bacteria and his wound has healed. I have taken him off of this drug Bactrim. This is his first day. His rash is better and his fever was down for a little while. It is 101 tonight and he just feel so tired and achy. I know it will take time for this to get out of his system. Meanwhile he is missing school and is getting depressed because he feels like he will never get better. If someone told me that fever and chills were a side effect from this drug I would not have been so worried that he could die of a blood infection. Ask lots of questions or google this site before taking a new drug.

I was diagnosed with SLE (lupus) when I was 14, I'm 21 now, and I've had to be on prednisone all this while. The dosages alternate between 60mg (the highest) and 2.5mg (the lowest), I just went for a routine check up today and found out that my protein level in my urine is at an all time high. So the doctor is pushing me back up to 30mg of prednisone. Its 2 am, and I am sitting in bed crying because I don't want to have to go through everything again; the weight gain, the moon-face, everything. I know I may sound shallow, because ultimately, the medicine is keeping me alive, but the side effects are terrible. Very few people understand that its not fat that you're gaining, and the remarks that I know I am going to get are enough to drive me insane.Is there anyway the water retention or the weight gain can be stopped or decreased?

I was put into the hospital in March '06 after using a carpet protectant that I purchased at the pet store. The chemicals in the product burned my lungs and I spent about 3 weeks in the hospital and was given prednisone for 10 -12 days. I remained in the hospital after my lung function increased because of the sever pain in my knees. My husband was going nuts trying to tell the doctors that he read on the internet that prednisone causes problems with knees and joints but they didn't believe him and kept running tests. They eventually switched the steroid to solumedrol and the pain decreased. I was sent home with less pain which eventually went away....but not for long. 7 months later, I began to have knee pain, which continued to get worse each day. The 1st Ortho told me that I tore a ligament and that the dead bone on the MRI will grow back. I didn't like that answer and eventually went back to an orthopedic surgeon I saw a few years prior for an injury I had while doing gymnastics. He took one look at my MRI and diagnosed me with AVN in my right knee. I got my 1st total knee replacement in August '07, a manipulation in October '07. While recovering, I noticed that my left knee was hurting and thought it was from using it so much and compensating for the right one......but I was wrong. I got an MRI on my left knee and once again, I have AVN. I got my 2nd knee replacement in January '08, a manipulation in February '08 and a 2nd manipulation in March '08. I'm now 29 years old, with asthma (from the carpet spray) 2 fake knees and have had the worst 3 years ever while going through all of this. I now have pain in my 1st replaced knee......under my knee and toward the inside. I go back to my surgeon tomorrow and am dreading another surgery.

If anyone has any questions, I'll try to help you as much as I can.

J.

Hallucinations, clumsy like a drunk, extreme short term memory loss, my husband recorded me with camera and it shocked me to the core. I had no idea it was effected me. I too as some is taking it for back pain from lower and 2 upper neck surgeries. I am going to Dr. today to discuss other options. My prayers to you all.

Hello-
I am here to share my story about topamax in hopes that others may read this and not have to go through what I did. I went on topamax for the prevention of migraine headaches. It worked great to prevent my headaches but gradually I could not talk, I stuttered severely, and I have memory and other cognition problems. At my doctors recommendation I stayed on the medicine for about 6 months because he assured me that the stuttering would go away. I was in such awful pain that I agreed with him. Needless to say that 6 months was not me. I couldn't talk and I couldn't think. Now when I think back on it, I wish I had just endured the pain. When I went off of the medication I still stuttered. It was not quite as severe but it was bad. It effected my work, my personal life, and daily menial tasks. I could no longer communicate. I was devastated. My doctor was puzzled and said that he had never heard of this before. So to make a long story short I went to a speech clinic, bought casa futura techs small talk device, and tried some anti-stutter meds. My speech now, 2 years later, is much improved thanks to the smalltalk but guess what,? I still stutter. Manageable and not very noticeable to others at times but my speech has not returned to pre-topamax status. I looked into sueing the drug company to bring awareness about this issue but did not get much positive feedback from attorneys. IF YOU ARE ON TOPAMAX AND ARE STUTTERING, STOP TAKING IT. IT MAY NOT GO AWAY WHEN YOU DISCONTINUE THE MEDICINE. It is not worth it. You cannot put a price on speech. I don't care what the physicians desk reference says, what your doctor says, what the corrupt drug companies say. I know my experience and it has been a catastropohic effect from topamax. Find a different med if you have speech problems! Please, for your own sake. Thanks for letting me share my story.

Please, is the anyone who knows of a way to treat the dibilating muscle/joint pain experienced as a result of taking the antibiotic, levaquin?

My son is 12 and has been taking Singulair for the last ten months...he has been getting moody and upset for no good reason over the last 3 months and I put it down to "hormones" starting to kick in. He has now gone to feeling very sad and has even told me last night that he has thought about killing himself several times and feels he can't go on, or cope and feels lost and lonely or unwanted and in the way. He is confused and does not understand what is happening to him. I have just realized it may be the Singulair and will be taking him off it immediately. I'm hoping it is this as if it isn't I feel totally helpless as to how to help my child. Please say a prayer for him. He used to be happy go lucky.

My 7 year old female Siberian Husky, Niceah is suffering with her second serious flare-up of IBD. She was taking 20 mgs. of prednisone every 12 hours for several days. We are now down to 12 mgs. daily and working towards 12mgs. every other day. She is lethargic and her body and belly have swollen frightfully to the point where it is difficult for her to lie down without grunting and sighing. She pants heavily. She drinks and eats constantly. Her nose is dry. Her tummy grumbles all day and night. I have been boiling chicken breast and mixing it with sweet potato and Enzymes & Probiotics. I am currently working with a holistic advisor concerning Niceah's diet once she has weened off the prednisone. The side effects of this drug are frightening and I am so worried that something more permanent and damaging will occur. Has anybody experienced this?? If so, I would appreciate any advise. Robin. copher370@aol.com

So basically this is my story.. I am 19 and have had severe asthma every\ since I can remember. I took prednisone up until I was 14, and from what I can remember I just stopped taking it around then. Then when I was about 18 I started up again because my asthma got worse. Between the time period of 14-18 I still had asthma, but started working out and became very active and healthy.I lost alot of weight had VERY THICK long hair. Then at 18 I got very sick and my doctor put me on prednisone knowing my asthma history. After being on it for a month my hair has become thin, I have gained weight, my face has rounded, my skin used to get tan very easily but now just flushes. I have headaches all the time, can't sleep at all during the night, then crash during the day. I am constantly depressed. I always have to pee. I can't be at the gym for more than 30 mins and then I just die im so tired. I can go on and on. I have tried so many time to get off but like I have read from the above comments,I become very sick and lazy I literally can't move. But what I need answers for, and what I was wondering, has anyone started to get hives/rash after coming off or being on prednisone. Every time I try to wean off of it I get them all over my legs!! NOTHING and I mean NOTHING makes them go away except when I start up prednisone again. My doctor thinks its okay and no other doctor can figure out why im getting these hives but its so obvious its from that because when I go back on it goes away. This is not a good medication to be on. I haven't seen hair loss as one of the major side effects but has that happened to anyone else. im praying to god i can wean of this drug if anyone knows anything pleaaaase let me knowwwwwww