Multiple sclerosis symptoms and conditions

I had my Mirena placed in the first of may, it was very very very painful. The following months I had spotting and bleeding EVERY day, I had no energy what so ever. Some days I even felt pregnant, and not to mention my face, I looked like a teenager again, horrible acne!

Then I started having this tingling and stinging sensation in my hands and feet, I googled it and all I could find was MS(multiple sclerosis)! In shock I did a search in English(I'm from Norway) and found that I was NOT the only one having MS symptoms with the Mirena! I had the Mirena removed this week, but I still have the symptoms, but I guess it takes a little time for the hormones to leave the body completely!! My boyfriend said to me "let`s hope you didn't get MS from the Mirena".. And I am of course terrified... I have an appointment with the doctor at the end of the week!

I just don't think that this is a coincident!

I started to take Atenolol after my kidney disease caused my bp to be extremely high. I'm on Avapro 150 mgs a day but at my last doctor's visit my doctor decided to put me on Atenolol for a rapid heartbeat. After about a week I began to feel extreme fatigue consulted doctor and he said it's not the Atenolol so I continued taking until my I started to feel pins and needles in my hands and feet. One morning I got out of bed and my left foot was swollen and curled up into a ball, the pain was excruciating. I was rushed to the emergency room where they said I pulled a muscle, I didn't. I asked the emergency room doctor could this be the Atenolol since I only started taking the drug for a few weeks when these symptoms began. He stated no that's not one of the side affects. After looking online I found that it is one of the side affects. So I stopped the Atenolol and after a few days was able to regain feeling back into my toes and slowly my foot. I still have pain and have trouble walking but hopefully I will recover. DO NOT TAKE THIS AWFUL DRUG. Either the Doctors know the side affects and are allowing us to be used as quinny pigs or their receiving some type of kickback from the pharmaceutical companies for prescribing this drug. If you know anyone taking this drug who is experiencing the above side affects stop the drug immediately before it's too late. If I had continued the drug I would have become paralyzed or worse stopped breathing. Another thing they are telling people that they have MS Multiple Sclerosis so they can treat you for yet another disease you don't have.

I am so glad I'm not the only one that has the crazy symptoms. I am being treated for an inflammation in my optic nerve. I woke up over a month ago now with double-vision. I was on 100mg a day for seven days then went down to 60mg. I feel like I'm high all the time though. I have to take my pills at 7 in the morning and they are still effecting me until about 2 or 3 in the afternoon. I can't drive or do anything that would take a lot of concentration cause I just feel out of it around my eyes. Also I have tingling in my face and arm. Not sure if this is a side effect or if its the possibility that I may have Multiple Sclerosis. (getting an M.R.I. done for further testing) Does anyone else have those tingling sensations?
My vision has almost come back to normal now. The Prednisone has done wonders for that, but I really hate taking it.

I am a 56 yr old female, placed on Lisinopril in lieu of Atelenol, which I have been taking along with HCTZ for a least 5 years. BP was 148/83, Dr. thinks still too high so Lisinopril it is. I was on it for a week and I, too, developed some really annoying side effects. Dry, almost spastic cough, especially at night when I attempt to sleep. Have been on the sofa for over two weeks to avoid disturbing my other half's sleep with my constant coughing. The Lisinopril makes me tired anyway but with the lack of sleep, I am exhausted. I am also an Multiple Sclerosis patient and fatigue is a big factor of the disease so lack of sleep is not good. I had the perpetual headache everyday, not debilitating but enough to ruin your day. Also felt extremely dizzy, to the point of feeling like I could pass out when I raised my head. The newest symptom, is a sore tongue. Feels like I have many cuts on the front of my tongue which foods and drink irritate but there is nothing there. Dr. has taken me off saying that I am experiencing an allergy to Ace Inhibitors and switched me over to another med called Benecare. Have not taken one yet and will do so along with the Atelenol so don't know how it will be but just wanted to share the allergy concept about Ace Inhibitors.
Take Care All

I had mirena inserted in August. The insertion was painful, but quick. I was problem free until my period arrived. I bled profusely for 13 days! Even after the bleeding subsided, I continued having severe stomach cramps. For the past 2 weeks, I have had numbness/lack of sensation in both feet. I also have numbness in my left hand and spasm on the left side of my face (around my mouth and eye). I initially thought the worst might be happening to me (multiple sclerosis). I am 29 years old and in good physical condition. After reading all of your posts, I believe my symptoms may be Mirena related.

MY STORY

My Mirena was removed on 29th May 2008.

I had the Mirena put in four years ago,I had terrible pain the day after, it was that bad I was going to go to the hospital Emergency to get the thing out but I put up(the worst thing I done in my life, Im paying for it now) with it and it and the pain got a bit better,had a lot of bleeding (spotting) for the first six months and then it finally went away. For the first year I thought Mirena was Great but then the problems started.I started to gain a lot of weight,facial hair,Very sore breasts, I also had a lump removed from my left breast a couple of years ago, but I didn't know until recently that it was most likely caused by Mirena. Some of the other problems I had, My stomach bloated, I look like I'm six months pregnant ,I have a cyst on my left ovary,dry skin,acne,strange depression,headaches,and the Worst of all I had to have my Thyroids REMOVED on 1st Nov 2006 and I'm pretty sure that was caused by Mirena as well, so now I have to take thyroid Medication for the rest of my life,I had the Mirena removed as soon as I done some searching on the internet for my unexplained medical problems, mainly my weight as I had weighed about the same my whole adult life and now I had put on a few stone and now I have to try and lose it,as for my thyroid I have trouble getting the Meds right its a real pain,blood tests all the time.I just don't feel I have much left in my life,depressed,sick all the time. I eat well as I have high cholesterol so its not that I over ate,I noticed you do feel a lot more like eating sweet things. I found a site called ****** and found out there are thousands of woman,girls with the same problems as myself and that there is a class action law suit going on to Sue. Its worth having a look at this site it helped me a lot.I feel so bad I don't go out anymore I don't see friends or family I'm to depressed about my weight now. I am in the process of trying to find out if there is a Class Action Law Suit in Australia.If anyone knows of a Class Action in Australia could they Please let me know. After having the Mirena removed about 6 weeks ago I thought I was doing ok only a bit of spotting,but about 3 weeks after having it removed I got my period and the pain was unbearable,I was in agony stomach cramps and I bleed so much I thought I was going to die from blood loss,also the scariest was the huge blood clots,very scary,must of been four years of period in 1 week I couldn't believe how bad it was, I felt really sick and weak,but thank goodness its eased off now after a week. I just hope now I might slowly start and feel like my old self. Im also on medication for heart palpitations,I get Heart palpitations (SVT) a few times a week,I had my heart palpitations just after my thyroid removal op and was put on ecg and my heart rate was 176 Beats per Minute I was rushed to Intensive Care and I had to have an injection called Impending Doom (It makes you feel you are going to die) to slow my heart rate,it worked and I was kept in intensive car for 3 days,very scary thing to go through I hope I never have to go through that again,my heart palpitations got worse while I was on Mirena and now I also take Magnesium to help control them as well as Metoprolol which I have been on for some years and I recently read that if you are on Mirena it increases the side effects of Metoprolol.

So if you have had any bad experiences with Mirena please let us know,it will help others with their problems, hopefully. I just wish I never got Mirena and my advice is DON'T its not Worth the risk,if the Doctors had of told me about the BAD side effects I would NEVER of had it put in. Sorry about going on so long, Good Luck to you all,

Thanks Net.

google mirena-side-effects.****** (a mirena help,info site)

UPDATE

I have had it out nearly 3 months now my painful breasts feel normal again,I haven't lost any weight yet, but will soon hopefully,I do feel a lot better but still get some of the symptoms back just before my period.

I get sooo mad when i think of what Mirena done to me and all the other women and how bad some of their side effects have been. I get mad when i read some of the other ladies stories and the terrible things they have gone through ,

Perforations,Miscarriages,IUD's lost in their body,

Hystorectomy,and the rest. I want to wish them all the best, and we WILL get Better and Bayer ,Mirena will PAY some day for what they have done to US..

I took Levaquin 500mg for ten days for a UTI, by the 5th day my right shoulder and bicep was hurting and hard to lift. On the 8th day my left arm was doing the same. I went to the doctor and was told it was Osteoarthritis and take Advil. Two days later I called the doctor told her this was not some little minor pain, she ordered an MRI. It showed torn and severed tendons in my biceps and rotator cuff. I had surgery on my right arm to repair all of this plus the tendons in my thumb on 2/26/08. I am scheduled to have the left arm repaired at the end of May. All this has been caused by the Levaquin, I have Multiple Sclerosis and my daily life was tough and this drug has made things twice as bad.
dfwtexan

Does anyone got multiple sclerosis because of yasmin?
i started taking yasmin when i was 19 and took it for almost a year.
i have always been a healthy person never really got sick.
i went off the pill because of the terrible side effects; first my sex drive changed in a bad way, then i had mood swings (i would cry or get mad for any reason) then my leg got numb then my arm got numb then i got speech trouble then chest pressure, then blurry vision on and off for two months. my doc sent me to a neuro doctor, did all the tests everything came up clear except for the mri. He told me it was up to me to start the medication for ms, and that he cannot be sure if i really have ms or not because of the test results. I decided to stop taking yasmin after my leg got numb and since i when off the pill (2yeas ago) i have not felt any numbness, or blurry vision, or speech trouble, or chest pressure, only 2 occasional terrible headaches in the passed 2 years (last year) and anxiety once in awhile).

I live in Israel, and here in this country not only do the police do their duty incorrectly, but so do psychiatric officials.
I was in a bad state emotional, and that did not result in any obscene or out-of-the-order matter, but me having chosen to move on with my life was a bad idea since moving on meant letting go and kicking out of my life a she-devil that posed as a girlfriend.
she had connections and accused me wrongfully of stuff i didn't do, and since she had friends in the police force, I ended up being admitted to a psychiatric hospital, there I was forced to take 10 mg of ZYPREXA, every day, for a little more than a month and a half, after a couple of weeks i developed a rash on my head, and vibrations with palpitations.
when i stopped taking ZYPREXA, the rash continued, the vibrations when i go to sleep with the palpitations continue but are even worse,
I cant sleep, and when i do fall asleep I wake up every hour, if lucky i sometimes manage to sleep for 2 hours and then only wake up, and i keep waking up until i give up on sleeping, i get headaches, nausea, dizziness, i eat, and after 30 minutes to 1 hour i go the the toilet and diarrhea..
my left eye sees blurry, i hear much less in my left ear, and not to mention that i have no tinnitus, - all day long i hear an electric pulse in my ears, i am disconnected from emotions, cant concentrate, my memory is impaired, i cant seem to make myself do anything, i cant even figure out what i am feeling, my teethes health has gone bad, get mood swings which are not extreme at all, resulting in me not knowing what it is I'm going through, i think this Zyprexa ordeal as resulted in multiple sclerosis which hasn't been diagnosed yet, and i don't know what more else there is, since i am quite handicapped mentally emotional and physically i can do stuff, but for some reason i don't do anything.
bad dreams (when i do manage to get several minutes of sleep), and i feel stoned all the time. and this is not all, but seriously, here in Israel or overseas, who really gives a damn? and who can help these things go away??..Ive been told to wait (I've been waiting a little more that 3 months) for all this to go away, and nothing as gone away, instead more things slowly gather.
too bad there is no death sentence here in Israel, if there was I might try to get it, to end this suffering, though, what can i say, even dying is not something I can manage to get myself to do, I cant seem to actually decide to do anything, I just think of it, and in the meanwhile, my whole life is passing in front of my eyes, making me realize, this might be the ending of my life as I know it, and all i have to do about it is just sit and wait, either for things to change (cause i cant change them), or to die.

I am a 37yr old female. I started on Lamictal Jan.' 07 for severe depression. Which I have battled for years and still do not know why I have it. My doc tried many different antidepressants, but nothing seemed to really work well. In fact Wellbutrin XL made me very sick!! I felt like I hadn't eaten in days and had no appetite and then lost major weight. The doc said it was due to the depression, which I knew wasn't true. I took myself off the Wellbutrin XL and immediately felt better. Remember no doc knows your body better than you do!! I Started with the starter pack of the Lamictal. The doc worked me way up to 200mg. Now I just started 300mg for 3 wks, then the doc said I could take 400mg if I felt the need to do so. Taking 400mg makes me quite nervous to try. All the listings I have read are so interesting and helpful b/c I too have many of the side effects....... acne on face which I never had before, extremely itchy bumps along my jaw line, loss of short term memory ( I will ground my daughter and the next morning I can't remember why), problems concentrating, forget how to spell common words, balance is off, sometimes a little butterfly red rash across the face, loss of libio at times, a little slurred speech, and bad nausea once in awhile. These postings have really helped me b/c I also have Multiple Sclerosis and I wondered if all of these symptoms were from that or the Lamictal. I do believe that it is from the Lamictal b/c I haven't any problems w/ the MS in a long time. It is very comforting to know I am not alone w/ Lamictal problems. God Bless you all.

I started having problems with my voice cracking and throat aching after singing or talking alot. Went to Dr. and he said he thought it was reflux (of which I had no symptoms). Wtihin days I started experiencing fatique, headache, depression, dizziness, ringing in my ears, and my right leg went numb about 3 weeks into taking it. Then about 2 months into taking, my entire right side went numb (thought I was having a stroke). Since that time I have been through CAT scans, MRI's, lumbar punctures. Been to 2 Neurologists, a Neurosurgeon, Cardiologist, Endocrinologist. 3 different Doctors thought I had Multiple Sclerosis or a stroke. All tests negative for both. After researching Prilosec on my own I found that Prilosec and all like meds block the absorption of and strip vitamins out of your body. 2 1/2 months after stoppping it I had B-12 level checked and it was almost non-existent. Started taking B Complex and B-12 shots. Symptoms have tremendously improved but haven't completely left. I still have numbness even 14 months later. The problem is that B-12 deficiency can cause the numbness and if not treated quickly enough the problems can become permanent. IF YOU TAKE any acid reflux medicine have your vitamin levels checked ... especially B-12.

I took half of 750mg i.e 375mg levaquin for 3 days for sinus infection. i have numbness and tingling sensations in my hands and feet. i took the last dose 2 days ago but my symptoms are persistent. i saw a neurologist who does not believe me. he is checking me for multiple sclerosis but does not think that this is the right diagnosis.
please help me....i am convinced that this has something to do with levaquin

I am currently finishing my third week on topamax, I am only up to 75mg a day. I do not sleep right at night, due to tingling from the medication and other Multiple Sclerosis complications. I return to my MS Neurologist next friday and we will again discuss my M.S. and Migrains. The Tingling for me is from head to toe and it is driving me nuts. At least now I know that it is the topamax and not my M.S. causing the tingling. So life does goes on.

Paula