One person symptoms and conditions

My mother and I have both been diagnosed with Hashimoto's Thyroiditis and we both take levothyroxine. We both experience extreme pain and she has been diagnosed with fibromyalgia. I have not been diagnosed with fibromyalgia but I experience the pain body also. Another thing. I have been losing my hair. No reason, it's falling out from the root and I have some serious thinning. Memory...what memory. I can't remember anything. Has anyone received advise from a MD? Thanks

I'm a 26 year old female and I've been on Topamax since March 2007. It has completely gotten rid of the debilitating headaches I experienced 3-6 times a week. It also got rid of my anxiety. I got my life back, my antidepressant kicked in at the same time. I experienced all the usual side-effects, tingling hands and feet, forgetting words, memory problems, loss of appetite, but was COMPLETELY pain-free. I still am. However, I never remember anything now, forget whether or not I did something, paid my bills, etc, lose things constantly, and I have lost about 20 lbs. Not good. I look anorexic. I have bones sticking out. Eating is hard. I forget to eat and drink all day and food is just unappealing. I feel fuzzy and stupid and slow. Not sharp like I used to be. It has killed my confidence and self-esteem. But I was wondering if any women out there got yeast infections while they were on Topamax. I've had one monthly since I started it, and my doc said it's a rare side effect. Oh yeah, I've had mild hair loss and mild to moderate acne now. This drug, it is such a 50-50. Living with chronic pain, those headaches were awful. But doubting yourself is awful too. Anyone have similar experiences?

I got the Mirena fitted 2 weeks ago and find it was the worst thing I ever did in my life, I feel I am not the same person anymore,whats worse is it was made to sound like the best contraception out there I was so unaware of the side effects and feel so angry for not being warned, I just want to have it removed and maybe I can feel more like myself again like I did before I got the thing in first place, please can anyone get back to me and tell me there stories of how you felt when it was taken out,just so I have some hope that I will feel better.my side effects are depression, weight loss, anxiety, shakes, heart palpitations, insomnia, and this is on a daily basis too I am just not dealing with this thing at all, please be sure to look into this nasty coil before you decide its for you because I really wish I had of done my home work but its to late for me, I just hope I can save at least one person from going through what I am right now. Mandy

I just started Topamax for Bi Polar. I replaced the Seroquel I was on with it. I have been having some really bad headaches before I went on it, and I am still having them. I have lost 6 pounds in a week. Can someone tell me from their experience does the headaches seem to go away with more dosage. I was on 50mg of Seroquel and with the Topamax I am only on 25mg right now.

I am hoping that this will help at least one person, to get off of lisinopril
There is a big difference between "side effects" and actual symtoms that are happening to most of us that take lisinopril.
Side effects usually occur shortly after taking a certain medication.
i took lisinopril for 2 years and gradually all the symptoms escallated and continued to get worse over time. i tought i was dying, i did so many test to find out what was wrong with me, cost a fortune, eventually i realised that all of these things were being caused by lisinopril.
I had shortness of breath,muscle weakness, joint pain, after every meal i was so bloated and a very heavy feeling at night , i could hardly turn in my bed because of being so weak and felling heavy, and the worse was this lump in my throat that got worse every day until i could not swallow or even breath i decided to do MRI ,found nothing , i ran out of lisinopril medication and this immediately got better, i have stopped taking for 1 month and i feel a lot better but still trying to recover from these "side Effects"

I too experienced an indentation from a kenalog shot. My experience is a little different though, because I received the shots on my face for acne. I received four shots and two out of the four depressed / indented. I was EXTREMELY depressed and felt hopeless after reading it would take 6 months to a year (or more) to have my skin gash-free. I stayed up for two days straight searching for some sort of help on the internet and found a medical article about something called saline infiltration. It is a relatively new procedure and was created by "one of the best dermatologists in the country". I was so desperate, that the next morning I drove to see him in La Jolla, Ca (I live in LA). I received shots in the problem areas. It is now two days later and my indents are about 80% better!! He told me to give it another couple of days to see complete restoration, and if not, said that one more treatment should make everything 100% normal again. Needless to say, I am thrilled!! I do not know if this will work for any of your situations (being that the dr. is a dermatologist and the shot was initially given for acne), but I thought I would share my great news and hopefully help at least one person out there dealing with this mess.

I too experienced an indentation from a kenalog shot. My experience is a little different though, because I received the shots on my face for acne. I received four shots and two out of the four depressed / indented. I was EXTREMELY depressed and felt hopeless after reading it would take 6 months to a year (or more) to have my skin gash-free. I stayed up for two days straight searching for some sort of help on the internet and found a medical article about something called saline infiltration. It is a relatively new procedure and was created by "one of the best dermatologists in the country". I was so desperate, that the next morning I drove to see him in La Jolla, Ca (I live in LA). I received shots in the problem areas. It is now two days later and my indents are about 80% better!! He told me to give it another couple of days to see complete restoration, and if not, said that one more treatment should make everything 100% normal again. Needless to say, I am thrilled!! I do not know if this will work for any of your situations (being that the dr. is a dermatologist and the shot was initially given for acne), but I thought I would share my great news and hopefully help at least one person out there dealing with this mess. Good luck to you all - I feel for your situations.

I have just come across this site, while looking to find out why I have been experiencing heart palpitations for the past two months - out of the blue!!! and usually "exercise" induced. I had some tests and have been told they are Premature Atrial Contractions "PACs". I started taking Yasmin in April, after having tried others over the past year (tri-cyclen lo and alesse) which did not work for me as the progestin was not strong enough. I am in my 40s and never took the pill before. Yasmin was great, it significantly reduced my "physical" pms (severe inflamation, severe bloating, severe sore breasts) which I experience for 2-3 weeks a month. However, sometime in mid to late June, I started getting palpitations/tremors out of the blue. The first episode freaked me out and lasted for about two weeks. At first I thought it was allergy medication mixed with my thyroid med, which can happen - but I cut out the allergy meds and still got them. They seem to come about 6hrs to a day after I fexercise/figure skate and they last from 2 to 5 five days. It's very irritating and nerve wracking, and I feel very agitated. I am also out of breath more than usual when walking up stairs, a little light headed and have some tightness in the chest. My legs also are weak, which makes no sense given my exercise regimen. I then lowered my thyroid replacement from .125 synthroid to .100 - too much thyroid med can cause some palpitations. Anyone who has mistakenly taken a second thyroid pill having forgotten that they already took one will understand. Even with the lower dose I am still getting the palpilations. I am totally at a loss as to why all of a sudden this is happening to me (perhaps perimenopause??). I have had the odd flutter here and there in my live, but nothing like this. It just doesn't make any sense ag ll. Can one's health just change like this overnight?. I am otherwise healthy, slim, have "lower" blood pressure (apprx 100-90/70-60)I skate 3 to 5 times a week, I have a full time job and yes I do push myself, but this is getting ridiculous. The only thing I can attribute it to is the Yasmin, ... but my symptoms only started after a few months not instantly, whereas it would seem that most of the the women here noticed the side effects faster. I hate to stop the Yasmin because I will have to return to pms "hell", but I suppose I will give it a try to see if the palpitations subside. At this point, I have been offered a low dose "beta blocker" and have refused. I am stunned to think that all of a sudden I have heart issues, especially since my Dr has always kidded me my that I will never have heart problems with my blood pressure. I will stop the Yasmin tonight and post another message in a few weeks one it is out my system. Here's hoping it is the Yasmin.
KarenSkaterGirl

LEVAQUIN is a FLURO quinelone. The fluoride replaces the iron in metalloproteases in your tendons. Remodelling to stress thus fails to occur. It is a molecule shapped like a horseshoe. The base is the formula for an INHIBITORY neurotransmmitter: GABA. It also causes cardiac hyperpolarization. If these dangers are not carefully examined before taking the drug, you are playing Russian Roulette.

But don't just be hysterical. Read. America can't survive as a nation of hedge fund BSers with no grasp of science or math. Doctors are drowning in HMO paperwork and 5 mins. per patient. They can't be thorough and don't have time to read other than the BS of drug salesmen. So don't go by the stupid TV ads. READ-->LEARN-->READ--> and contact the FDA and drug company to get their info on your side effects. If they lie, you have a case. Fight for yourselves instead of just panicking over symptoms. That could kill you whether you stop or not the drugs.

Levaquin cured my pneumonia but I'm now having trouble with my knees and shoulders. I can hardly bear my weight and am having trouble performing simple tasks such as reaching to answer the phone. Has anyone else suffered this way? Otherwise I feel well. I discontinued using Levequin on my doctor’s advice but when I explained my symptoms was told this was not a problem associated with Levaquin. I wonder. I'm 60 years old, very active and hope this problem is only temporary. I've got life to live!!!!

I have been on topamax for almost a year now. I had been having a nearly constant migraine cycle for three months which had to be broken with migranol nasal spray. I then started on escalating dosages of topamax. By 100mg I realized that life was wonderful but that I couldn't retain much information which was a problem as I had just gone back to school for an advanced degree. Upon consultation with my doctor, we reduced my dosage to 50mg and things improved dramatically.

I have experienced some fingertip and toe tingling which have been completely tolerable. I take the medication right before bed so that I don't have problems with fatigue during the day. I do get out of breath easily when I exert myself and carbonated beverages taste horrible. But my migraines are under control.

I have a Ph.D. in molecular biology and a few years of neuroscience research under my belt. I would like to say that it is EXTREMELY important for people to understand that no medication is going to work identically for any two people. What works for one person, may not work for everyone. I know people who swear by imitrex but this medication does absolutely nothing for me. You have to be your own advocate when it comes to medications and treatments. Your genetics will also determine how well, if at all, you respond to any medication. For some topamax is a life saver, for others it will be the bane of their existence. This will always be the case for any medication. Be tolerant of others' experiences and understanding of each others' pain and progress will be made.

I just pulled the ring out tonight in the middle of my 3 weeks because it finally hit me!!! The light bulb just came on for me. I had been feeling incredibly sad and depressed for the last 6 months since I have been on the ring. I thought it was not like me, but I thought it was job stress. I was moody with everyone around me all month long...very irritated and not wanting to be bothered. I am a teacher and even my students noticed my moods. I had no desire to enjoy the things I use to enjoy. I walked into my school 2 days in a row and had sharp pains in my chest. I thought I was having a heart attack or something, but then it went away. I am on summer break now with a lot of time to think. Something told me to check out the side effects of the ring. Maybe it was divine intervention. I was shocked and almost cried when I found out that I was not alone. I even saw one person report swollen and red eyes. I had this also and thought it was allergies or pink eye, but now I understand that it was probably the ring since I have never had this reaction before. I enjoyed the freedom of not remembering the pill, but I don't think I will ever use the ring again. It definitely affected my personality and judgement.

I have a history of stomach problems (H. pylori infections and acid reflux) and was doing great until I started the nuva ring. Since then, I get sick every night- my stomach hurts and i feel nauseous and I just feel cruddy. I don't know if these things are connected- anyone else have stomach pain with the ring? I also tried to skip a period with the ring and my period has been going on for a week now, when it usually lasts about 4 days. grrrrrrr...

All you are Hypochondriacs. If one person says this medicine is causing this, then of course; you all have the same problem "some how." Isn't this weird? It is called the "placebo effect." Normally all the people involved in the testing are given "Lisinopril" (or some other drug), then the placebo group is given a vitamin supplement, the group receving the vitamin supplement is being told they are receving "Lisinopril." Mysteriously?, the "placebo group" is all feeling better and their symptoms are gone. This is due to the fact that all these people in the "placebo group" have interacted with eachother and have told eachother "I feel better" than of course everybody feels better. So WEIRD!! So, my point is this forum is all your peoples "placebo group." If you guys never heard of these side effects from this forum you would have never experinced them. Hypochondriacs all of you are. This is a very good medicine that is helping all of you make up for your peoples lack of self-disipline to control your diet or exercise enough to lower your blood pressure naturally. So be thankful. Lets not complain about false side effects because John has them. I wonder what the side-effects of that cheese burger are that caused high blood pressure. It is funny, I don't see a forum for that. So deal with your so called "side-effects" that are associsted with "Lisinopril" or go on a diet people. Get over it!!

Several years ago I took prednisone and it causes severe psychological disturbances. I started crying because a pet frog I had back when I was a kid had died. Remember, it had already been dead for over 10 years! I would blurt things out that normally would never be said, especially in public. My moods would range from scared to death, to abysmally sad, to extraordinarily confident. It took well over a year for me to feel "mentally" better. The symptoms I experienced had long lasting effects on my reputation and probably my career. After all, if you know 20 people who took it without problems, why believe one person did? I will never ever ever take it again.

Hope this helps some people.
MLM

i think what we need to understand is that all of the posts provide information. maybe its not the information you want to hear but all this information will maybe help us come up with some answers and although one person might feel like certain posts are unnecessary others might find it valuable. i understand its frustrating what we are all going thru, but if you thought you were going to find an answer here you wont, what you will find is thousands of women on yasmin for months or years who have all delveloped serious side effects while on the yasmin, coming off the yasmin and after yasmin even months later. if you are new to this site please take the time to read the posts skip over the ones that dont give you the information your looking for and realize you are not alone and even though the doctors tell you its not the yasmin over 2000 users tend to disagree. we do not have the answers as to why this hell pill put our bodies through such havoc we just are here to communicate about our personal experiences and update others on any progress or any tips as we continue to become more knowledable and refuse to give up one day we might have answers.

My husband had a TIA in July of 2004 and had some short term memory loss and has polycythemia so in fall of 2004 doctor put him on 10 mil of lipitor , I immediately noticed a difference in him he couldn't remembeer things like he did before had skin problems hurt all over but dr. could not believe it was lipitor so in March of 2006 put him on 20 mil. of lipitor to lower his cholesterol more, he started getting hateful, mean and hard to live with. Nov. 15 we got a flu shot and 2 days later he lost it completly didn't know where he was what he was doing and didn't remember me. It came and went for a week and on 24th. put him in hospital. Doctors did all kinds of tests and could not find what was causing his problems so told me to put him in nursing home in the lock down ward, I couldn't do it so brought him home with ativan if I needed it so 2 times in 5 days I had to give it to him and was odd as his problems always came on at night after taking his lipitor. so on the 5th day looked on the computer and immediately knew what his problem was so stopped it right then. He is slowly getting better has good days and bad days. I am hoping it will improve some. The sad thing is the doctors wont agree with me that lipitor has caused all his problems. I wish there was a way to broadcast it so other people could see what can happen and if I could just prevent one person from having to go through wat we have been and still are , I think that would be wonderful
Thank you

im in tears the more i read the posts the more i actually start giving up hope there is not one person online who has said she is 100% better even after a year off this pill and no doctors will help us becuase no one believes us or they think our symptoms are annoying my biggest complaint is my foggy head its been 8 weeks off yasmin and i still go thru everyday with my head not bein clear and my ears feelng blocked some one please tll me it will disappear someday

So saintmorrowind STILL isn't old enough to actually have people 'respect' his 'opinion'. Afterall, he's been on it SO many years and he's still only 23. What did you come toa forum called "singulair side effects" if you weren't searching them yourself? HMMMmmmm.....Don't knock others, if it works for you - fine. Don't judge. What works for one person does not work for another.

My daughter is having neurological 'twitches' from singulair. for the rest of the forum of people who are actually interested in possible side effects, her twitches are coming from the withdrawl of the med. I first noticed it when I forgot to give it to her one saturday night - she got mouth twitches and her throat (uvula) was actually twitching for hours - it was really wierd. Never thought about singulair. It happened again weeks later and same thing. She complains that she can't sleep - has anxiety, feels 'jumpy' - and has very vivid and scary dreams. It's not like her - shes been on it a year - I'm taking her off it - we are weaning - but she is having the withdrawl effects - I pray that it doesnt stick around.

Steve

Attention ladies...especially Silke: (re: response to femalepara's post)

This board is for posting individual experiences while using Yasmin. Amongst the hundreds of posts stating negative effects...you throw a fit because someone has a good experience. Even if it has only been "2 weeks" that is her experience. I think most people that are reading are not going to take one person's opinion and run with it...there are plenty of negative effects information on this board to make one seriously consider taking this medication. You're post seemed very harsh and uncalled for...as if you are the ruler of this board. Chill out and let people share....it doesn't discount other peoples experience, clearly many women have suffered greatly on this medication.

"This registry is a place to share positive or negative side effects of using Yasmin."

HEY SILKE, RITA AND ALL YOU WONDERFUL LADIES WHO POST HERE SO TO SUPPORT EACH OTHER IN THIS TIME OF STRUGGLE....

AS I SAID IM NOW 5MNTHS POST PILL AFTER BEING 4MONTHS ON IT..THIS MONTH THE HEART PALPS HAS COME BACK AFTER FINALLY DISAPPEARING.
ALSO THE BLOATING HAS INTENSIFIED DRASTICALLY.
HEY WHAT HAPPENED TO THE FACT THAT THINGS ARE SUPPOSED TO GET BETTER WITH TIME.FOR ME ITS ACTUALLY GETTING WORSE. IVE GONE UP TWO DRESS SIZES AND I DESPISE THE WAY I LOOK..WHICH IS AN OVERSIZED PIMPLE...HE HE..IM SO DEPRESSED ABOUT IT AND ITS REALLY HURTING MY OVERALL DAILY FUNCTION.
I DRINK DANDELION TEA, RED RASPBERRY TEA, VITAMIN SUPPLEMENTS AN
D WHAT NOT. NOTHING SEEMS TO HELP AT ALL. I AM WONDERING IF THERE'S AT LEAST ONE PERSON WHO CAN TELL US....WHEN IF AT ALL IS THERE LIGHT AT THE END OF THE TUNNEL????«
THANKS TO EVERYONE WHO TAKES THE TIME TO POST HERE AND TO HELP EASE OUR PAIN. GOD BLESS U ALL.
SHERRY

After talking to my gyn about Seasonale & Yasmin, last Sunday I went on Seasonale. The Dr. prescribed it for my heavy periods & anemia. He said even with the mega iron supplements (ugh) I've been taking, my body can never catch up. One period every 3 months sounded great to me.

The first pill brought a mild all-day headache - no big deal. With the second pill the headache turned into a 3 a.m. screamer with nausea to boot. When I called simply to ask which pain med was best, the Dr. didn't even call back - just had his nurse tell me to pick up Yasmin samples. So much for Seasonale - the nurse said she didn't know any patient who has stayed on it and she wondered why he still prescribes it. Guess what - I paid $150 for that 3-day headache - Seasonale is not covered by my insurance.

After reading this page I dread trying the Yasmin! This is not just a few unhappy women. I can't believe how many people post & how often. Yasmin works great for at least one person I know, but after the instant reaction to Seasonale and seeing your stories I can't risk screwing up my life/body/head.

Good luck to you all. Thank you for sharing. What next for the anemia? I don't know but I requested an ultrasound. What fun it is, being a girl...

-Grateful in SoCal

ARACHNOIDITIS FOR LIFE, DUE TO EPIDURAL STEROID INJECTIONS OF KENALOG. THEY'RE NEUROTOXIC AND NOT FDA APPROVED OR LICENSED FOR EPIDURAL USE. OR ANYWHERE IN OR AROUND THE SPINE AND SPINAL NERVES. DON'T HAVE EPIDURAL STEROID INJECTIONS OF ANY KIND, WHETHER WITH KENALOG OR DEPO-MEDROL SUSPENSIONS. THEY CONTAIN KNOWN NEUROTOXINS, LIKE BENZYL ALCOHOL AND ETHYLENE GLYCOL, BUT DOCTORS CONTINUE TO PERFORM THESE INJECTIONS BECAUSE THEY RAKE IN SO MUCH MONEY FOR THEMSELVES AND THE PHARMACEUTICAL COMPAINIES. STAY AWAY FOR THEM OR ELSE END UP PERMANENTLY DISABLED AND IN SUCH TERRIBLE NEUROPATHIC PAIN FOR THE REST OF YOUR LIFE. IF THIS MESSAGE HELPS JUST ONE PERSON, MY POSTING IT WAS WORTH IT.

I see one person posted that they get tired from Wellbutrin. After about 4 weeks on it I have started feeling pretty severe fatigue...started in the afternoon the first couple of days but now it is almost all day long. Has anyone else had this experience with it? A little nervous about it and thinking of going off of it to see if that's the reason for the fatigue.

I took (1) Levaquin (500mg) tab for a severe kidney infection at about 7:00 at night, at about 8:00 I started to have terrible, horrible pains near my vaginal area and my anal area. To describe the pain it felt like i was in active labor. The pains came like spazums and lasted for about 2-5 mins localized in that area. Also at 8:00 this morning i felt like i was in an all day workout and/or hung-over. I will not be taking another pill and will call my doctor to be prescribed another antibotic. I am so glad that i am not the only person with these side effects, at least i know that it not just a one person thing.