Average person symptoms and conditions

I am so glad that I found this site! I have been on the NuvaRing for about a year and have noticed side effects that I couldn't pinpoint the cause of.

I'm a very petite girl. Only 5 feet tall and usually about 94 lbs. Well since going on the NuvaRing my weight has gone up to 112! Not a big increase to the average person. But I am so small boned and so short, that all of this extra weight went straight to my tummy, butt and thighs and now I look so un-proportioned that it's ridiculous! 18 lbs. is a HUGE amount of weight for me to gain.

I've also had terrible headaches that (if I don't take anything right away for them) sometimes cause me to pass out or vomit because the pain is so intense. I have crazy mood swings that go up and down minute by minute and this has caused many fights between my fiance and I that start over stupid little things.

Also, my periods are alot heavier since I've gone on the ring. I used to have to change my tampon once every five hours or maybe even every six and never, ever leaked. Since going on the ring my periods have changed drastically and now I'm lucky if I can go two hours without leaking through a tampon! When I have my period I'm on constant guard.

Lastly, my sex drive is non-existent. Completely 100% gone. It's awful! I never, ever feel like having sex and that is NOT the normal me. Normally my sex drive is through the roof, but since going on NR I've noticed my sex drive drop more and more every month, every week, every day. This has hurt my fiance because he thinks it's him, which obviously it never was. Now after finding this site at least I can assure him of that.

After all of these side effects I decided to go off the NuvaRing. It's a form of birth control that I don't feel is safe for my body and is damaging to my relationship. I was on Ortho-Tri Lo before and will happily be going back on it again. After all I've gone through with NuvaRing, taking a little pill every day doesn't seem like that much of a hassle anymore.

Ran into friend at grocery store with mystery illness. Docs attribute it to Agent Orange exposure. Been at death's doorstep for a year. Hands were extremely cold and has little energy. Showed up one day at golf course with oxygen bottle! Asked him if he had taken Levaquin. Unfortunately had. Docs again fail to link antibiotic exposure to his ailments.
I wonder how many illnesses and deaths this poison has caused? Why does the FDA allow this crap? Do you people realize that the average person is clueless about the side effects of drugs like this. Put total confidence and their well being in the hands of ignorant docs and profit crazed drug companies.
Ignorant oncologist failed to link my dad's symptoms to Levaquin, instead attributed them to b-cell lymphoma which just happened to suddenly appear. Rituxan and numerous other drugs (Heparin, Lasix, Gamma globulin, Tylenol, antibiotics, Insulin, steroids, Flowmax, etc.) was too much. A fiasco, people think he died of lymphoma. Was walking three miles a day before taking Levaquin, for an undiagnosed lung infection.

Hi. I was just told I had low Vitamin D. I have been doing some research on what might cause this and what issues low Vitamin D could cause. I am finding that all acid inhibitors can cause this condition. Many of the side effect all of you have listed along with many others have been reported with use of these type drugs. Some research also shows that softing of the bones or brittle bones can be a side effect after long term use. This is where the Vitamin D comes in. The acid inhibitors keep your stomach from breaking down Vit. D which is distributed in your body as a hormone. Vit. D or lack there of can cause so many deceases that are life threating that it is unreal. I am not an expert by no means, but now when I go back to my doctor for the follow up for the low Vit. D I fill much more informed by doing my homework. I have took Nexium for about 3 years and then Aciphex for about 3 years; so a total of 6 years on the acid inhibitors. During this time I have been diagnosed with clinical depression, degenerative bone decease, and now Low Vit. D. I have had the dry mouth, cold feet, leg cramps, unexplained abdominal pain, cannot control my hunger, anxiety, lumps in my throat, skin rash that comes and goes and is untreatable, heart palpitations, trouble sleeping, pain in my kidneys.....OH how I could go on. In the official PDF file on the side effects of Aciphex there are no studies past one year to substantiate any claims of long term side effects. I have heard in the past 18 months little stories on the TV news about how Nexium can cause bone fractures but it is not played up very big. I have gone to the doctor more then the average person and I have felt as if I am a HUGE hypocondriac. Yesterday was the first time I have been able to breath and I actual stated to my husband that I feel as if suddenly the hypocondriac weight I have been bearing has somewhat been lifted off my shoulders.

PLEASE if you have took any of these types medications and you have these symptoms insist that you have your Vitamin D levels check before it is too late. Continue to persue this avenue even if your doctor is reluctant. AND write the FDA about your experiences. STAND UP FOR YOUR HEALTH!

Hi,
I have been on Warfarin since 2002. I suffered multiple pulmonary embolism's in both lungs. My first was in May 2002 and even though I had excruciating pain in my left shoulder area & could not lay down as this worsened the pain, the NHS x-rayed my torso!!!! & sent me home with medication for a kidney infection. I gave it a few weeks but the pain did not go completely & was moving to my right side, I was coughing up 'tablespoon' size clots of blood. My GP was not happy & spoke to a colleague at the hospital. I was sent straight in,(July) thorough tests done & I was found to have suffered multiple PE's.
I tried to sue them for medical negligence but it was turned away by the court as there was not enough evidence on my notes ie; some info was not written down & most was unreadable to even other medical professionals.
Since Aug 2002 I have been on Warfarin & am on this for life.
A blood test showed that I had a genetic blood disorder called 'Factor V (5) Leiden heterozygote'. This causes my blood to form clots much easier & quicker than the average person. If you have this disorder, as a woman it is important that each time you have a child you are treated with Heperin after each birth. I had 5 children & was not treated therefore I suffered with my PE's.My children have been tested for this & 3 of them have it. My daughter was glad she found out before having children as she hasn't had to suffer what I went through.
I ask one thing.... Please TELL your GP that you want a test for the above disorder. As I suffered my PE's & that I have this blood disorder I have to stay on Warfarin for life.
If you need any more info I will tell you as much as I know. Feel free to ask questions. my email is; ******

Hello, I've never been on birth control before, but i recently had an abortion and decided I really need to get on some kind of birth control. I am 27, married, and I am a NON-SMOKER. Nuvaring seemed to be the best option for me, easiest, effective and practical. I'm only on my first ring, it comes out for the week break in few days. So far I have NOT had any irritability or headaches, or anything like that. I have gotten a little "spotting" which to me can still be linked to the abortion or even sex. What I DID notice, however, is that I had a few sharp chest pains here and there, quick and not consistent, my husband thinks that could be from stress. I also noticed what I thought to be a pulled muscle in my lower calf could be a sign of a blood clot, which totally scares me. A persistent issue I HAVE had so far, is that I have that numb "pins and needles" feeling in my limbs a bit more often than usual. I do sit odd and my limbs tend to fall asleep more than the average person, but I actually notice it happening more frequently, like my blood circulation isn't as good as it was. I have NOT had high blood pressure. I ALSO noticed I wake sometimes with severe leg pain (cramping) that reminds me of those "growing pains" one would get as a child. I haven't had those since I was a child, wondering if it could be due to the NuvaRing. If anyone has felt similar pains let me know. I am visiting the clinic tomorrow to discuss these things and to see what could be a safer method of BC 4 me!

My thyroid troubles started in 1993. I am not sure how long before the discovery I had the problem. Mine started as a nodule on one side. I was immediately put on Synthroid and had to go see the Endo every 6 months for a biopsy. In 1995 I became pregnant. I had one more biopsy until after the birth of my daughter. The Endo told me he wanted to see me right away after she was born to do another biopsy. I had my suspisions, but didn't think anyhing until after she was born and went for my biopsy. Well, I had cancer. I went through the whole thyroidectomy, the 3 days isolation with radio-iodine, and every year to every few years after I had to go back and get the radio-iodine treatment, while not the high dose as the first time, it went with the complete body scan. In fact, I am due now, but don't have health insurance. My dose has been switched a lot, I have probably been on every dose from the lowest up to .200mcg, which has been the highest for myself.

Symptoms: pre-thyroid disease, I am 5'2. I was always 110-115 lbs, I was 22 yrs old and 120 lbs. when I married in 1993. I did notice gradual weight gain, probably because of my thyroid problems. I am sad to say that now I am around 180 lbs. I cannot seem to lose the weight unless I go on a total starvation diet. I managed to lose 10-15 lbs over the past summer, but unfortunately for me it has come back over the winter. I tried to stay as active as possible by going to stores and malls to walk around. I do for a fact notice that when my dosage for Synthroid goes higher, so does my weight gain. I was on .137mcg over the summer, and I think that was a good dose for me, that was through the regular dr. The Endo is the one who put me back up to .150mcg. My Endo told me the thyroid is a regenerative organ, so it CAN grow back. I guess they don't want that in case of cancer again, and I guess that is why he keeps me on higher doses.

I personally cannot stand it. I feel it is a horrible curse. I feel very robbed of my previous active life. I have been dealing with this now for 12 years not having a thyroid and being on this medication. I feel angry that I do not have the energy to do things with my 12 yr old and 3 yr old. I miss the way I was before having thyroid disease. I feel very sad when they come up to me asking to do certain things and they (nor anyone else I know for that fact) can understand that I just feel so whooped, and no energy. All I ever seem to want to do is take a nap. I have migraine headaches constantly, I am constantly tired. I cannot concentrate, I have some memory loss. My ex-husband, and my current husband too for that fact think I am just being lazy. Well, that is not so. There are moments when I do feel a burst of energy, but then, I have to use that burst to do the things I need to do around the house.

Pre thyroid disease I was always active, never tired, could do anything. After: TIRED, I was 24 in 1996 and felt like an old lady, dry skin, no matter how much lotion I put on. The tub is full of hair, while it doesn't come out in clumps and I still have thick hair, I have hair all over the place. Irritable, mood swings, happy to angry and the snap of a finger. I can have insomnia some nights, constipation, lots of the same stuff others have listed on this forum. Those side affects are the same no matter what dose I am on. And like I said the higher the dose for me, the more weight I pack on. It is instantanious. Over Christmas, and no, it wasn't from eating all the goodies, I gained a lot of the weight I had lost over summer back, and that was because a few weeks before, the Endo had put me on the .150 mcg.

Hi. I just wanted to let everyone know what has happened since I stopped taking Yasmin 4 days ago. (I only took it for 2 months.) I'm still having heart palpitations, feeling of a lump in my chest, and still a bit dizzy at times. My ears kind of feel like when I'm on an airplane coming in for a landing when the dizziness comes around. I'm also still having an occasional urge to cough. I still have shortness of breath and it's very noticeable when I'm talking and saying a long sentence. I thought the symptoms would really decrease but it seems to come and go. I feel the palpitations more frequently during the evening hours. I don't know why that is though. All of this makes it really hard to concentrate a work. I was reading one blog that said to take extra magnesium and zinc. Has anyone tried that and is it effective?

I haven't had a problem with Kenalog. In fact, it worked very well for me with no side effects at all.

However, I'm surprised at people who would ask if they should just stop going to the doctor who is prescribing this medication. In my opinion, asking a group of non-professional total strangers whether one should take or stop taking a prescribed medication seems extremely dangerous.

If one is worried about side effects, one should ask a different professional. A second, or even a third, opinion from a doctor is much wiser than taking advice from people one has never met.

I'm not a doctor, don't know any doctors socially or by family relationship and deal only with my own doctor. I'm probably as intelligent as the average person and I have experience with Kenalog but I would NEVER suggest that any of you start, stop or change any prescribed medication.

Nor would I ask Internet strangers what I should do about a medication. A site such as this is very useful for gaining many-sided, experiential information but I wouldn't use it in place of a medical professional and I'm sure that the site owners agree.

BTW, I once got a permanent injection site indentation from a simple pain shot. Some people are just prone to get these things. I didn't blame either the doctor or the medication and a dimple on my butt hardly seems earth-shattering.

I've been on Dilantin for approx. 5 years now because I began having seizures after being involved in an airplane crash when I was 14. I suffered a ABI (Aquired Brain Injury) which has had a considerable effect on me. A considerable problem with this is trying to separate what symptoms are a result of what condition.
Since I've been taking Dilantin - I've noticed first of all my gums tend to be a little more sensitive than normal, bleeding at times when I brush.
My ability to learn new activities & study is also diminished, I find I have to study twice as hard & have to do things twice as much as the average person before it finally "sinks in". To the un-trained eye, this can be easily mistaken for laziness or lack of motivation. I had always attributed these learning difficulties to my brain injury, but after looking into Dilantin side-effects, I've discovered that diminished learning has also been associated with taking this drug.
Another side-effect I've noticed is a diminished sex-drive. Only recently have I started looking into this, but I've dealt with this for the past couple of years, and it has really started to have an effect on my relationship with my wife.