Long story short symptoms and conditions

90% BLOCKAGE OF MY SUPERIOR SAGITTAL VEIN IN MY BRAIN..... HUGE BLOOD CLOT IN MY BRAIN DUE TO LOESTRIN 24FE........... THANK GOD I AM ALIVE!!!!!! PLEASE READ BELOW ....................... I was placed on Loestrin 24fe Feb. of this year, after taking it for a month and a half I got a terrible headache on a Tuesday and no matter how much Advil or Tylenol I took it wouldn't go away, well finally I went to the 24hr urgent care center at about 1a.m.Thursday morning. after 3 shots of morphine that didn't work, a Dr. (MALE) trying to tell me that it was just a migraine (from birth control and I should switch to the Depro shot) and I didn't treat it fast enough, so I had to stick it out, mind you they had given me three shots of morphine by this time and my head still felt like it was going to explode. needless to say he discharged me and the nurse that was caring for me said against her better judgment she was letting me go home but grabbed my hands looked me square in the eyes and made me promise if I didn't feel any better or my headache got worse by the morning I would go to the nearest E.R and make them scan my head because at this point she said you don't have to tell me that the medication isn't relieving the pain I can look at you and tell you it isn't working... long story short.. I kept my promise to her and ended up back at the E.R less then 12hrs later, they to put me in minor care and said it was just a migraine headache, gave me morphine again (Which didn't work this time either) until I gave the run down of being at the urgent care center just a few hours earlier and the nurse making me promise to make them scan my head because her concern was what was causing the headaches that wasn't responding to the morphine?? Finally the Dr. (Male) listened to me and ordered a cat scan, said something looked abnormal the Dr. moved me to the real E.R. and then ordered an MRI then B4 they could wheel me back to my room in the regular hooked back up to my i.v. the wheeled me back and did MRV's with and with out contrast. A neurologist came and gave me my diagnosis and told me i was lucky to be alive that I was at extreme risk 4 seizures and strokes and that i needed to notify someone at home of what was going on. I was admitted from the e.r directly to ICU. My diagnosis was Superior sagittal venous thrombosis. I had a 90% (blood clot) blockage of the main vein that runs down the center of your brain (Dr. say its from the Birth control) feel free to write me with any questions, just be careful, with any birth control choice that involves hormones. theres more to this story I am not some crazy lady I am very lucky to be alive and would never want anyone else to go through the hell I have been going through since April of this year.my email address is ****** Thank you again Nurse ***, Fl for saving my life..... You are truly one of God's angels walking among us.

Check this out below... I cut this from a posting on the internet about cerebral venous thrombosis which they also refer to the blood clots of the veins in ones brain. take care, hope to hear from you soon. Headache is the most frequent symptom in patients with cerebral venous thrombosis. However, patients presenting with headache due to cerebral venous thrombosis are uncommon. The association between oral contraceptives and cerebral venous thrombosis is well known. We report the case of a young woman who was admitted to our department for sudden onset of headache. She had been taking oral contraceptives for 6 months. Early pharmacological approach with analgesics failed to alleviate symptoms. Magnetic resonance imaging (MRI) showed thrombosis of the posterior and middle thirds of the superior sagittal sinus (SSS). Because the patient was oligosymptomatic, medical treatment with high-dose heparin was started. A clinical follow-up showed headache regression after 2 weeks of therapy. Subsequent MRI showed partial re canalization of the SSS. The patient continued oral anticoagulants for 3 months. Eighteen months after discharge, the patient was symptom-free. We conclude that new, persistent or atypical headaches in patients taking oral contraceptives should be carefully evaluated for cerebral venous thrombosis.

Dizziness, fainting, rapid fall in blood pressure.
Not sure that this is a problem with Lisinopril, but would be interested in any comments. Have been taking Lisinopril for about 15 years, 10mg/day, BP been stable in the 130/75-85 range until it rose to 140/102, between Sep'06/Jan'07. Was spending the winter months in Spain and on returning to UK in May 2007 agreed with doctor to increase dose to 20mg/day. BP, diastolic reading remained high in 95/98 range. To cut a long story short doctor suggested 10mg Amlovasc (Amiodipine) which is a Calcium Antagonist in addition to the 20mg Lisinopril. This 'worked' and BP was then down to 130/84 range. No particular side effects apart from some dry cough. However 5 days ago I collapsed, fainted for a short period, poor vision, comforted by first aiders until ambulance arrived. Was sick before ambulance arrived and then felt much better but they measured my BP as 80/40. Had various checks in emergency (this is in Spain) ECG etc and now waiting for appointment with cardiologist. Since this event I have seen on the Amlovasc info sheet that it may interact with ACE inhibitors which is what Lisinopril is. I wonder if this possible interaction was the reason for the collapse etc? I have also been taking Benecol (Stanol Ester) since August 2007 to maintain my cholesterol at an acceptable level. This has been successful. Once I have had the consultation with the cardiologist I hope to know more.

I am a 54 year old male who has a chronic a-fib. My cholesterol was a wee bit high so my now retired MD put me on Zetia, which just about killed me- constant stomach pains and associated GI problems-we all can guess. So I went to see my cardiologist- he took me off Zetia and put me on Lipitor. It dropped my cholesterol levels significantly but the side effects are horrendous. My new MD was gooing to look into it because I was on 80 mg a day- but never did and never lowered the dose-229 is not all that high to warrant 80 mg a day.
I am now experiencing severe pain in my right rib-cage area, making sleep an event every night. Also have severe leg cramps the size of golf balls constanlty at night while sleeping. Pain in both elbows, and in the right foot, which when I can sleep wakes me up with a severe pounding pain. I am also experiencing severe neck and shoulder pain and am generally fatigued all the time- So I quit taking the stuff as of today on my own, I am seeing my MD in two week and I want to see what the difference is pain wise being off of the med for two weeks. I have always been a strong physical guy, played football all the way through college and am in pretty good shape for my age, but this stuff is killing me!! Hope this helps someone else also-Thanks for listening-John in Napa, CA.

I am 26 yrs old and I have been on Nuvaring for about 3-3 1/2 years. I thought this was the greatest thing not having to remember the pill and the short light periods. I have always sworn by this BC! I have been having side effects I never thought came from the ring until now. I have read a lot of the side effects others are having and I think my lack of sexual desire for the past 1 1/2 yrs. MAY be due to Nuvaring and not my getting married 2 yrs. ago. (lol) I also have headaches often, not bad ones but enough to carry Tylenol in my purse. And another is dryness before intercourse, that I never had a problem with 2 yrs. ago. I never put two and two together until I racked my brain and wondered why I struggled so badly with my lack of sexual desire. I could care less if I have sex or not! That just wasn't me 2 yrs ago! I just couldn't figure out what had changed, going back on any medicines I had taken the past 2 yrs., the Nuvaring is the only thing that was constant. I have a Dr. Appt today and I am going to discontinue use of the ring and see if the side effects subside like they have for some others. I will post again when I have an update. Please let me know if anyone else is having the side effects more than a year after using the Nuvaring!! Thanks!

I was placed on loestrin 24fe Feb. of this year, after taking it for a month and a half I got a terrible headache on a Tuesday and no matter how much advil or tylenol i took it wouldnt go away, well finally i went to the 24hr urgent care center at about 1a.m.thursday morning. after 3 shots of morphine that didnt work, a Dr trying to tell me that it was just a migraine (from birth control and i should switch to the depro shot) and i didnt treat it fast enough, so i had to stick it out, mind you they had given me three shots of morphine by this time and my head still felt like it was going to explode. needless to say he discharged me and the nurse that was caring for me said against her better judgment she was letting me go home but grabbed my hands looked me square in the eyes and made me promise if i didnt feel any better or my headache got worse by the morning i would go to the nearest E.R and make them scan my head because at this point she said you dont have to tell me that the medication isnt relieving the pain i can look at you and tell you it isnt working... long story short.. i kept my promise to her and ended up back at the E.R less then 12hrs later, they to put me in minor care and said it was just a migraine headache, gave me morphine again (Which didnt work this time either) until i gave the run down of being at the urgent care center just a few hours earlier and the nurse making me promise to make them scan my head because her concern was what was causing the headaches that wasnt responding to the morphine?? Finally the Dr. (Male) listened to me and ordered a catscan, said something looked abnormal the Dr. moved me to the real E.R. and then ordered an MRI then B4 they could wheel me back to my room in the regular hooked back up to my i.v. the wheeled me back and did MRV's with and with out contrast. A neurologist came and gave me my diagnosis and told me i was lucky to be alive that i was at extreem risk 4 seizures and strokes and that i needed to notify someone at home of what was going on. I was admitted from the e.r directly to ICU. My diagnosis was Superior sagittal venous thrombosis. I had a 90% (blood clot) blockage of the main vein that runs down the center of your brain (Dr. say its from the Birth control) feel free to write me with any questions, just be careful, with any birth control choice that involves hormones. theres more to this story I am not some crazy lady i am very lucky to be alive and would never want anyone else to go through the hell i have been going through since April of this year.my email address is ***** check this out below... i cut this from a posting on the internet about cerebral venous thrombosis which they also refer to the blood clots of the veins in ones brain. take care, hope to hear from you soon.

Headache is the most frequent symptom in patients with cerebral venous thrombosis. However, patients presenting with headache due to cerebral venous thrombosis are uncommon. The association between oral contraceptives and cerebral venous thrombosis is well known. We report the case of a young woman who was admitted to our department for sudden onset of headache. She had been taking oral contraceptives for 6 months. Early pharmacological approach with analgesics failed to alleviate symptoms. Magnetic resonance imaging (MRI) showed thrombosis of the posterior and middle thirds of the superior sagittal sinus (SSS). Because the patient was oligosymptomatic, medical treatment with high-dose heparin was started. A clinical follow-up showed headache regression after 2 weeks of therapy. Subsequent MRI showed partial recanalization of the SSS. The patient continued oral anticoagulants for 3 months. Eighteen months after discharge, the patient was symptom-free. We conclude that new, persistent or atypical headaches in patients taking oral contraceptives should be carefully evaluated for cerebral venous thrombosis.

I can not thank-you all enough for sharing your experiences with the mirena IUD! I know some have had a positive experience and that is wonderful, I am not one of them. Although it has not been horrible, I will not use this form of birth control again!

It started with insertion, which was uncomfortable followed cramping and weeks of bleeding. However, this did decrease and I would spot occasionally. I haven't had the weight gain or really the acne problems some of you have had but I have definitely experienced mood swings, hair loss and decreased libido!! When I asked physician about this, she said that I should go on dates with my husband and maybe I wasn't sleeping through the night. When I explained to her that I do in fact have time alone with my husband, that we go out on "dates" and my children have been sleeping through the night for close to 2 years, she said nothing!

Long story short, I am having it removed tomorrow.! Althoguh I am looking forward to, I know there will be more weeks of having a heavy period. Right now we are thinking of trying for our third but my alternatives for birth control are slim to none...

I have been taking 300mg for 4 years. The first negative side effect was I passed out. The doctor reduced it to 225mg a day. I also take imdur, norvasc,lasex,altace and quite a few more. I am only 38 and I am surprised I don't have any more side effects. Oh I have experienced weight gain. Has anyone else noticed that? If curious I take all these meds for Hcm with ventricular tachycardia. Had an ICD put in in 2003. Man now that I type this all out sounds like I am in really bad shape. ok I am done babbling. To make a long story short I just want to know if anyone has had some weight gain?

I am weaning off Zoloft. I began taking it in Nov. 2001 because I knew I would have post-partum depression since I had it with my first two. Zoloft changed my life so much for the better. That was almost 6 years ago. The past year I have decided that I can do w/o Zoloft. One, because I’ve learned how to choose to be happy. Two, because I don’t like being addicted to a pill. I know I’m addicted (or somewhat addicted to) because if I forgot to take the pill, several hours later, I would get weird feelings, like when I turn my head and move my eyes at the same time, a weird slightly dizzy feeling.
Here’s how I did it. In May and June, I took a whole pill (50 mg) every other day and every other day I took half a pill. That’s 2 months of that. Then, July and August, I took a half a pill EVERY day. Now that it’s Sept., I’m taking a half a pill every other day and NO pill every other day. I must say, this has been the hardest. It’s just 4 days into Sept. and I’m having those weird sensations a lot. My toes and fingers are tingly, too. I was planning on doing this for 2 months but I'm on the 4th day (2nd day of no pill) and I'm having too many tingles and weird dizzy sensations. So, I guess I'll continue taking a half pill every day and take NO pill ONE day a week for this month of Sept. Then, in October, I will take NO pill TWO days a week (but not 2 days in a row). Then, in November, I'll go to THREE days a week of no pill (but not 3 days in a row). And so on. I had hoped to be off by Christmas or Jan. 2008, but I see that it won't work unless I wean to a NO pill gradually. I knew all along that it would have to be gradual, and that's what I've been doing, but I had no idea that just missing a mere 25 mg. for 2 days (but not in a row, mind you) would make such a difference.
Now, if I get too many really sad days, I will consider going back on. But I’ve done really well so far. I know that God is helping me. He can lick it; I can’t. I have had just a handful of occasions where I was told something slightly disturbing or something happened to me that was slightly upsetting and it got me down, but only for the rest of that day. AND, I gave it to God and let Him deal with it. He wants to take care of my problems; He doesn’t want me worrying about it. I know that medicine like Zoloft may be the answer and if that is what I ultimately do, then I’ll just continue leave it to Him. I hope this helps someone.

I started with 25 mgs of topamax about 5 months ago for migraine prevention. I very gradually increased the dosage to 50 mgs and started having the usual side effects of tingling in hands, metal soda taste, concentration problems; but not bad enought to make me stop as my migraines were stopping as well! Then I upped the dosage to 75 mgs, and the side effects were sudsiding. My nurologist had me up the dosage to 100mg, and that very night I awoke from sleep having my first partial conscious siezure. At the time I didn't know what the heck was happening to me and thought I may be having a stroke. I am only 44 years old and I ran across the street at 2:30 in the morning to my neighbors house who is a nurse. Long story short, it took uppin the dosgae two more times and having this happen each time I upped the dose, to finally realize that it was the topamax that was causing the seizures. Now my nurologist is gradually decreasing my dosage to wean me off the topamax, and hopefully the siezures will stop! Has anyone had any experiences like this? Or am I the only one who get s siezures from an anti sewizure medication?

Hello,
I am soooooo happy to have found this post!!! I have been on Yasmin for approximately six months for very irregular or non-existent periods. About four months ago I began having dizzy spells where I could not walk or move my head without vommitting. I have now had one each month, this last one occuring for three days. I have also experience nausea, stomach aches, vommitting, etc... intermitent from the other symtoms. Long long story short I was referred to an ENT specialist and was diagnosed with Meniere's Disease (Inner Ear.) I didn't buy it so I began searching for side effects of Yasmin - I am stopping it today! I have my fingers crossed this is the problem>

I am normally a very physically fit specimen, working outside every day. One 500 mg. tab of this poisencompletely debilitated me. Within six hours of taking levaquin I experienced excruciation soreness in my arms and shoulders. My throat swelled up and I could barely breath. I was perscribed steroids to stop the swelling - I took only ONE 500 mg time release tab 7 days ago and today I am still experiencing incredible pain.I am so sore I can't sleep. If anyone wants to start a call action suit I am in - I have NEVER sued anyone - but I am furious.Any advise out there as to how I can flush this poisen out of my system?
Chris

Im from Cork,Ireland.I was put on Seroquel to treat my Body Dismorphic Disorder.I have really disliked the way i look for years.Hated the way i look in fact.I was very badly bullied all through my school life and teenage years because i was very heavy at that time.Needless to say i ended up hating myself with a passion.When i left school i went on mission to lose the weight and i lost about 6 stone by eating healthy and fast walking.I can't tell you how proud i felt and iv never felt proud of myself in my life.Then the effects of my teenage years started to creep up on me.I needed to face them.That was a very,very painful time and to make a long story short i got severly depressed and BDD set in.And guess what?I was put on a drug that put the 6 stone back on again and even more.Even though the Doctor's have noticed this they have continued to keep me on this drug.Every time i bring up the issue with my doctor's there response is 'Oh you need to watch the diet'.Now I tell you, I DO NOT eat alot nor do i eat rubbish.And this drug is ment to make me feel better.Now how stupid is that.

My daughter was born with a breathing condition(never pinpointed) that kept her in intensive care for almost 2 weeks. As she grew she seemed ok. Then pneumonia appeared at 1 1/2yrs. and she has been hospitalized 5 times since with various forms of pneumonia(walking, single, double) since. We moved from the city to the 'burbs and all seemed well. She would take the occasional Xopenex(Abuterol made her nuts). To make a long story short, after 2 years in the new house new symptoms appeared. All of a sudden there was coughing at night that would not stop. We went to a new Dr. and he prescribed Singulair. This was October of '06. Soon thereafter, the behavior began to get worse. Tantrums and extreme moodiness began to become more frequent and her school work began to suffer. We've just been informed that the school is recommending holding her back. When I talked to the teacher, she indicated that my daughter has gotten "worse" since Christmas. Teacher also does not believe that there are any learning disabilities. I know that it is the Singulair. She has the constant stomach ache and no appetite to speak of. All of the professionals are assurring me that Singulair is safe. She is not on this nasty drug any longer... Waiting for changes...

I have taken some sort of medication for hypothyroidism for many years, perhaps as many as 22 (I am 51).

Over the last few years, I feel like my health has deteriorated. Frequent, severe headaches, irritability, moodiness. My face had a sunken look.

I asked an expert in alternatives about the headaches and she immediately said that Levothyroxine has headaches as a side effect. I had not really considered the side effects of this medicine at all--I thought of it as completely safe. (The side effects didn't pertain to me--silly thinking, I know.)

Well, except for the thinning bones! Just a few months before, I read in *Strong Women Stay Young* that levothyroxine causes thinning bones. My doctor had diagnoses osteopenia, which is the beginning of osteoporosis. I don't want that, but it may be too late. (I am started a strength training program to strengthen my bones.)

I decided to stop the med. and try alternatives. The headaches lessened, but did not cease. Ran out of the alternative. Now I have what one site called "moon face." Puffy. Eyes look smaller. Very interesting -- makes me think I was taking too much before, because I looked haggard.

But even more interesting to me was the level of my general anxiety (and thus, my irritability) is down. Yes, I am tired, but I am also calmer!

Long story short (I know, too late for that!), side effects: headaches, anxiety, irritability, haggard expression, depression, thinning bones.

Here's to hoping that the alternatives work! I want to clear this med. out of my body (especially my brain) and try to feel better with healthy alternatives.

Kim
Hi BitterRN here.
All I can tell you about your hormone levels is what I too have experienced myself.
I had my hormones tested by blood and saliva 3 months after I quit bcp.
Both tests showed estrogen and progesterone levels as normal.........HOWEVER
On my saliva test My level was 11... Normal is 20-50 (I am sure I run on the higher end of that scale as I have or should say HAD the oily skin, oily hair, smalller breasts before yasmin..) This level is extremely low, and the test level stated LOW.
My blood tests drawn at exactly the same time on the SAME EXACT DAY, read normal (at the very lowest end of the scale) so my gyn said, all levels are normal.
NOT!!!!!!!!!!!!!
When I had the results evaluated by a bioidentical Dr. later she said no, the blood levels were not "normal" and her words were "for an 80yr old maybe, but not for you"

So long story short, I kept testing, with saliva tests month after month (they have to be done at a specific time every month) and here is what happened.....

Month 4 after stopping,
My estradiol went to 0.8 now in the low range
Progesterone dropped to 72 now in the low range
Testosterone went UP to 15 still low range but higher.
Cortisol went up to 9.3 High ranges are 3-8. So just a little high probably from stress.
Symptoms, still feeling up and down with ? improvement.

Month 6 after stopping, (I skipped a month due to expense, I pay out of pocket for all these tests)
MY estradiol is range but still all of my symptoms are not gone
Cortisol still a little high at 8.9.
I am feeling better than before and symptoms are resolving, but I am not feeling getting better as quickly as I would like, so I do something REALLY REALLY stupid...

I try to start my old bcp ortho novum, thinking I did well on it all those years (12 yrs) and my hormones are pretty well getting to be more normal...or so I thought, now looking back not really, still had a ways to go, but I was not thinking clearly, and started them, at first I felt like things were getting back to normal, but about 12-15 after being on it, I felt the anxiety coming back. I stopped them on day 15, and it was like all the symptoms started over again (really wanted to die, How could I have been so stupid?) I believe I would have really felt better by now if I had not tried to do this.

Anyway, I saliva tested 1 month after and I already knew before the tests came back that my testosterone had fallen again to 17
My estrogen was normal at 1.3
Progesterone was really low at 16!!!!!! normal is 100-600
cortisol high at 11.

Next month after stopping
estrogen low again at 0.9,
Progesterone coming up at 52
testosterone 15 whaaaaaaaaaaaaaaaaa!!!! somebody shoot me!
still feeling like sh*!
I really tried supplementing with bioidentical hormones at my doctors suggestion at this point, but It is really hard to find a dose because they are used to caring for much older women so it was a guessing game, consequently, I think i used a little too much testosterone,

Next month testing
progesterone dropped and testosterone shot up to 80!!
I called the lab and they said this indicated the dose I was using was too high, that since I tested while using this high dose, the test was registering high (in other words this was not my true level and it would come back down as soon as I stopped using it.) I asked why my progesterone went down as I was supplementing with progesterone creme as well, she said when one hormone is too high the other hormones become suppressed. Ahh.
So I quit supplementing altogether.
And now I am waiting for the next results, I should have them by monday or tuesday.
Just a side note, I am feeling better just as I was before I tried to take the bcp the 2nd time. It seems like this time I may be getting better faster? I dont know, depends on the day you ask me.
This is why i have been asking silke about her hormone levels and why I think that it may be her testosterone that is the problem, as some women have trouble getting their testosterone up after being on bcp or after pregnancy. I really feel this may be the problem as I did not feel better until this particular hormone started going up, as i felt crappy again as it dropped (especially with the anxiety) However, a doctor not familiar with hormones will say a Low normal level is normal. Its NOT.
This is just my experience. I cannot write it in stone. Hope it helps.
BitterRN

Silke
Hi, did you get copies of your labs?
Anxious to hear from you.
BitterRN

Hello again,
Sarah-thank you so much, once again, for your comforting words. It is amazing that after I read your post telling me that where I am in the process (and what I am currently experiencing) is normal, I actually feel physically calmer and less anxious! I feel now that I know what to expect. Do you have any idea how long that second "phase"--when your own hormones take over--will last? Thank you thank you for comforting me!

Silke-as I was reading your post, something struck me. You mentioned a few times that you feel like something is missing in your body. Ever since my Yasmin nightmare started I have been reading up on Eastern medicine (like Ayurveda) and Chinese medicine because I do not trust Western medicine at the moment. Anyway, have you ever studied it? There is an idea that your lifeforce, or "chi", runs through your body and that each of your systems are connected to each other, instead of operating exclusively from one another. If one system is sick, Western doctors simply provide a pill that will make it better, never thinking that it might not be treating the root problem. In Eastern/Chinese medicine, this idea of chi brings everything togther holistically. There are several different areas in your body that this chi may be centered. If one of the centers is "blocked," it can drain your life force from smoothly running throughout your body at all times. (Anybody who knows about Eastern and Chinese medicine...please feel free to chime in or say it better than me--the amateur!)

Long story short, there are ways to "free" this blocked chi. That might be the answer to what you feel like is "missing." I have a friend who struggled for a long time to heal from being on a terrible oral contraceptive (not Yasmin, actually) and she swears by this alternative medicine. She has an acupunturist and an herbologist and feels so healthy, holistically. So if you feel like traditional medicine, doctors, and tests are not working to help you heal, just google some alternative methods. They have been around a lot longer! I considered it for myself, but unfortunately I cannot afford it at the moment.

I hope everyone reading this is doing well today!
Best, Erykah

I was on Paxil, 20mg then 30mg for about 2 years. My doctor took me off of it slowly, because he knew of the awful withdrawl effects. It took a month of tapering it off, and I still had withdrawl effects: Terrible dizziness, twitching of my legs and arms, itchyness of my feet when I tried to sleep, cold sweats, hot flashes, no appitite, and most scary of all was the nystagmus (uncontrollable jerks of the eye in horizontal directions when you move your eyes or head). My doctor said that not many people have this symptom, but that it was caused by the Paxil withdrawl. If anyone has jerky eyes they can't control while coming off paxil, mail me at ****** and I can tell you more, maybe reassure you that it will get better.
Long story short, about 2 weeks after coming off the last few milligrams of Paxil and everything (even the nystagmus) is gone.

I had a total thyroidectomy last year...long story short, after about 4 months my surgeon said the scar was turning into a keloid ( I now wish I would have just left it alone) So he recommended kenalog injections. I had 3 total over a 3 month period. After a few months the scar had severly indented & it looks horrible...when I swallow it looks like my throat is mangled inside. I hate it & I don't think there is anything I can do about it. I wish I would have been advised about the possible side effects!!! I can 't stand that people stare at my neck when I talk to them...it's very depressing. Not to be so vain, but I'm a young woman!!!

i am a highschool student and have been taking geodon off and on for at least 6 months, i got BPD and have been on other stuff but this is the only one i will put up with, after being on it at least 6 months i still could not wake up in the morning, when i get up my eyes start rollin around the back of my head and i cant stay awake , i cant walk and i slur my words when i talk, at the most i was taking 20mg morning with 40mg riddlin and at night 20mg geodon, well i got pissed off at the side effects and stoped takin it in the morning. i read up on riddilin and i dont like it being narcodic so i stopped that since its summer and i can sleep a little later. long story short i thought i wasnt bipolar and had no problems this was a big mistake, a month after completly stopping geodon i relized all my close relashonships have been destroyed and blame it on not taking meds. one more thing i noticed though, if anyone gets very parinoid on geodon thats what happend to me and when i got off i wasnt parinoid, its now setting back in, i cant stay in my home alone. but anyways just thought id put my two cents in about that stuff its kinda put me through hell.

I started taking toprol after my doctor reccommend it for my fast pulse rate and high blood pressure. Originally went to the doctor for problems caused by a nervous system exhaustion. and realised that my pressure was very high 155/98 anyways to make a long story short after taking the lowest dose 25mg for 2 days I started to feel like i was losing control of my mental state of mind, my mood changed to very dull state. like i was just a zombie inside a body - this medication has a bad effect on the brain , it did get my pressure down fast. but the effects on my mood and mental stability wasnt worth it stopped after 3 days. i am wondering how many people who have been taking this medication for years who are now suffering from depression and cant make the connection.

Hi
I posted on this site in Jan 05, after my husband was rushed into hospital 3 days after multiple kenalog shots for his joints ( gout) He was told he was diabetic type 1 and would be using inuslin for the rest of his life. His body had started closing down his organs. He was on drip for 6 days, lost a stone in weight in 3 days prior to getting into hospital. I kept saying it was the injections, Cut a long story short he stopped using insulin injections within a month and his bloods have came to nearly normal. He is still treat as diabetic ( type 2) no medication, diet controlled. You cannot go from Type 1 to Type 2. We are in the process of going to court with the doctor who gave him the shots, we were not warned of any of this side effect. We have been told it will take a long time to sort out, but what really worrys me, if Kenalog came make the pancreas stop making insulin, and thank -god his started working again. What in the future if it is badly damaged and stops altogether? Can I thank the person who put the information on the site about dosage and side effects. Would you believe the hospital has lost my husbands records. I hope if this happens to any-one else this piece of informtation may help. Not only did Kenalog change my husbands life but 4 months later I had a heart attack and they have put it down to stress ( I am 44 and my husband is 45)We both had no serious illnesses ever but now!!!!! WHO KNOWS
Regards
TINA

3/30/06 update

I was referred to a rheumatologist by the ER Dr. and had my appointment on 3/29/06. To make a long story short, I do not have gout. I have a condition called 'reactive arthritis' that the doc could/would not openly say was caused by the Levaquin but that he had seen before in patients who were taking/had taken Levaquin. I am taking celebrex and it seems to have helped slightly (stress on the slightly). I am experiencing more and more problems sleeping. The last two nights have been the worst so far with basically no sleep. I generally come into work at 9:00AM and have been showing up at 6:00-7:00AM as of late because I either do not sleep or wake up around 3:00-4:00AM.

I am as used to the foot pain and numb/tingling/burning sensations as i'm ever going to get and am able to work, although at a severly hampered pace. I am actually having some real fear for my job at this point, having taken three sick days in two weeks because of this. I am beginning to believe that I need to consult a mental health professional. I have learned that drinking lots of water can temporarily alleviate some of the symptoms, which I started doing for gout treatment, but doesn't make you feel normal again in any way. I guess this is going to become normal for me. :-(

Hi, I feel so much better after discovering this site, as I now know I'm not the only one suffering horrible side effects from Yasmin!

I was on it for just over 5 months and last week I just stopped taking it after I realised that the terrible way I was feeling was due to this pill. Anyway, to cut a long story short, the side effects I have are: leg pain and leg/ankle swelling, also cramps, worsening of my bi-polar mood disorder, nausea, increse in severity and frequency of migraines, dizziness, blurred vision, nervousness, fatigue and to me, worse of all, weight gain which is all on my breasts and stomach!

I am 38 years old and I have ALWAYS had a washboard flat stomach, now I have a little pot belly which is freaking me out because I can't fit into or suit my usual clothes which I always chose to emphasise and cling to my waist and stomach! I feel that I want to stop eating, I am so upset, I feel ugly and fat and I just want my flat stomach back! Please tell me I can get it back to normal!

My doctor wants me to start on the mini-pill, but do I need to wait for my side effects to wear off first? Also, does anyone know how long it will teke me to get back to normal, after being on the drug for 6 months? I have been off it now for 6 days and I still suffer from all the side-effects as yet....

i have been on 20mg of celexa for a month now and i was running low last week and tried to call my dr for a few more to get me till monday when i see her to make sure its working for me......sooo long story short i was without my pill yesterday and last night started feeling nause, diarea, and like cold sweats......i thought i might be coming down with somthing but i called and found out that it was probably becouse i didnt have my celexa.......im still not sure but do know that once i got some to last me i took it and felt much better.

HELP!!! I need to know if any has had this side effect of this pill. I am not sure if it is a side effect, please share!!

I started the pill in Nov & in Dec I started getting bad pains in my wrist. the first doctor i went to said it was carpal tunnel and then the pain moved into my hands. To make a long story short the muscels in my hands become inflammed & the only thing that has been helping is steriod shots. However, they have tested me for everything under the sun and everything comes back fine. I have asked the doctors if the pill could cause this. They have said no but they never did ask what pill I was on. Is anyone else out there having this problem.