November 11th
2008
8:49 PM
I'm writing in behalf of my 15 year old daughter who is trying loestrin24fe to get some relief from her back pain and migraine headaches (which she inherited from me). She had a full period after just 10 days and has had a non-stop headache since starting this pill that won't stop even with her migraine medicine. I know it takes time for bodies to adjust, each is different and the doctor says give it 3 months- but she is considering just stopping because her headaches are so bad. I'm just not sure she can hold out for 2 and a half more months to give it a good try. Her acne is a lot worse too. Moody- yes, this was another thing we were hoping the pill would help with but hasn't. I'm sure this site is biased for people having problems since if it's working okay- why look up information on it? In any case, 30 years ago the lowest dose pill made me depressed, I barely made the 3 month mark before I stopped and I thought it would be different now. I have spent years before and after having kids using an IUD, and for me, that has always been the greatest birth control!
-- By jpzs | Reply | (3) replies | Private Message me
October 10th
2008
11:24 PM
I have chronic migraine headaches and I was first prescribed Imitrex. All 4 times I gave it a chance it did not work. Since then, I have been prescribed 1 other migraine medicine which didn't work, a barbiturate to be taken just for headaches, which didn't work for the headache but made me very loopy then depressed, then a strong pain pill that did nothing for my headache but made me very relaxed, so I just layed on the bed for 4 hours. My doctor wanted me to get an MRI then go to a specialist who wanted to prescribe a medication that I would have to take 5 days a week. Now, I get kelation therapy once a month, which gets rid of high levels of metals and toxins in your body, and I have not had a bad migraine since, only a slight headache every once in a while.
-- By kimmiller112 | Reply | Private Message me
July 8th
2008
11:46 AM
Thank goodness for this sight. If you are thinking you're crazy and can't figure out what's wrong while you're on Nuva, scroll down, you will feel like you're getting a big hug!
I am 27 and have been on the NuvaRing for coming on 8 months and everything has changed. At first I had severe migraines with nausea, a day after starting, that kept going and still occur. They will last all day long and I can take 8 of my migraine medicine and nothing will help. The headaches ruin days, make work difficult, and ruin weekends.
Second: I gained weight around my middle, so perceptibly, I thought I was pregnant. The bloat and gas is constant, I'm always popping Gas-X extra strength but the gas doesn't quit. It was funny at first (yes, I'm immature) but now I'm so uncomfortable, and my pants are tight around the middle but nowhere else. Boo!
Third: ANXIETY. I've been the most relaxed, calm person until I started on NuvaRing, and now I have a prescription for Valium just to keep me from having nervous butterflies all day. The anxiety goes hand in hand with depression, which sucks because I got engaged literally 2 weeks after starting NuvaRing and am always nervous, anxious and sad, and I'm so in love with my fiance but our home life is strained! I sometimes wonder if it's cold feet, but I know it's not. Which leads me to:
Fourth: NO SEX DRIVE. Gone. Dead. Zilch. Zero. I have been the horniest person I know my whole life. I love sex. But I am almost scared of it now. I have no desire to have sex, recoil when my fiance touches me, and get butterflies when I think he's going to try to have sex with me. I sleep as far away as possible, never masturbate anymore, never feel sexy and the idea of sex just doesn't even pop into my head. So unlike me. This causes anxiety, too.
Fifth: Yeast infections and pain during sex. I've never had either of these before. I'm extremely hygienic, and my underwear are constantly filled with discharge. So gross and painful.
I'm going off of it in 5 days and I cannot wait!
-- By cwodehou | Reply | (2) replies | Private Message me
September 24th
2007
5:25 AM
Hello,
I read about how YAZ birth control pill affects the body and psych and I am now scared. This is my 2nd day of YAZ (I've never been on birth control pills ever and I am 27 years old), it's all new to me but after reading all these negative posts about Yaz I don't know what to do. Before the birth control pills, I was depressed, annoying, serious weight problems - 210 lbs :~~((, low energy, low libido, always tired, terrible migraines every 2nd day, ridiculously increased appetite and excessive hunger, hair where it shouldn't be, menstrual blood clots, excessive cramping etc
I have all these problems for 3 years now and now that the family doc. put me on YAZ birth control pill I am even more scared - mainly of more weight gain, it would be a tragedy for me, I am fat enough already and what's worse I can't lose the weight, exercise doesn't help, diet doesn't help, NOTHING. Will YAZ birth control pill worsen my already tragic condition? I just don't know what to do and what to believe ... I appreciate any advice or help you can give me ... Thank You to all!
May 10th
2007
7:40 AM
I have only been on it for 8 days, but it has been wonderful for me. I suffer from nearly daily migraines. My migraines are brought on by strong smells like smoke, or perfume. The first day I was on Singulair, I went on a field trip to a farming community with my daughter. This is usually enough to have me in bed with an aching headache for a week, but instead I got a mild migraine late that afternoon. My imitrex knocked it right out. The next day, I cleaned house all day, no headache even with cleaning chemicals. Now 8 days later, I haven't had to take any migraine medicine at all. Three nights this week, my neighbor has burnt grass (a major trigger for me) and still no headache. I may get side effects later, but for now, this has been a godsend to me. It has my allergies under control and I can now go out to dinner without fear of smelling smoke, or too much perfume. I can work in my yard again.
If you are having side effects, try something else. I have had terrible side effects from medicines before so I know they do exist. I wish you luck in finding the one that works for you.
May 20th
2006
6:57 PM
Hey all! I started Yasmin in February '06 so it's been a few months now. The first month was great, I had never felt better. Around the second month I started crying pretty much everyday and was ready to quit school and move away from everyone and everything. A few weeks ago I had a horrible headache that lasted for a week, which is very unusual for me, I don't get headaches. I was also having the worst vaginal itch imaginable. I went to the gyno and she gave me some samples of migraine medicine...which made everything about 10 times worse and told me I had a yeast infection..which I had also never had before going on Yasmin. 3 weeks later the itching is back with pain as well. I of course jumped to the conclusion of having an STD but I don't have any other symptoms and my boyfriend and I are very careful about using condoms. Has anyone else had any of these symtoms? I'm thinking about stopping Yasmin all together.
-- By krysti_lynn85 | Reply | Private Message me
February 17th
2006
1:53 PM
The the girl who posted about the migraines. I was on it for a yr. and then I started having the migraines. I went to the doctor and he prescribed me migraine medicine, it helped but eventually my side effects got worse and I had most of what the other girls posted. It's good you got off of it.
-- By hill721 | Reply | Private Message me
Yasmin (3) Topamax (1) Singulair (1) NuvaRing (1) Loestrin 24 Fe (1) Imitrex (1)
May 19th
2009
3:03 AM
I am a 38 year old male suffering from a combination of occipital neuralgia and migraines. For 20 years, until a year ago, i would endure pain that was only manageable with narcotic pain relievers (imagine all the gamut of such kind). I would have neck and head aches typically 3-4 times a week, accompanied by vomiting, dizziness which would put me to bed for the entire day. Work and family suffered in magnitude comparable to my own suffering. So then I finally saw my GP for that. The pain meds went up the roof, imitrex, maxalt was added to the equation with only marginal side effect. I saw a neurologist. He had me do an MRI and put me on Topamax starting from 25 mg, which I upped to 200 mg within 6 weeks. Past the initial side effects, the headaches subsided, the frequency reduced and i was able to enjoy weeks at a time with no episodes. Stayed at 200 mg for 5 months. In the meantime, the MRI came back positive for some brain inflammation. False positive they said, does not fit the clinical picture. Second MRI, same positive, this time proceeded with LP, which was negative. Third, MRI still positive; making the neurologist uncomfortable. While dealing with MRI results, the topomax had yielded positive results as far as pain management was concerned. But little by little I noticed that I was becoming more irritable, more impatient and more forgetful. Someone would have to remind me of something several times before it would even register in my mind. I empathize will all the posts that mention feeling like having Alzheimer's. I didn't care in the meantime. As long as I didn't have to deal with the pain it was ok with me. But the situation became worst and worst. I couldn't concentrate on anything, the mere task of remembering to do something was insurmountable. I would wake in the middle of the night and find myself staring at the bathroom mirror for no reason. I would have terrible panic attacks which i control with valium. But yet i continued on with topamax convincing myself and being convinced by other people around me that i just had a "personality disorder". Finally, work begun to suffer. I was loosing track of meetings, deadlines and when this happens someone knocks on your door (boss) telling you that something just doesn't click, something just doesn't feel like a personality quirk. Other people playing doctor would slap on my face that i just had ADD, that I should take something for that and get on with my life. But something was wrong. Pain or dizziness or lack of concentration etc are all electrochemical processes in your brain. It turns out that topamax was helping my headaches but it was not slowly deteriorating other cognitive abilities. Finally, the neurologist decided I should wean of the topamax, stepping down from 200 - 150 and then we go to 100 and so on. I dread the re-occurrence of the headaches. I am waiting for them to happen again at some point as I drop the dosage. But in the end of the day, I'd rather be in pain and in control of my life rather pain free and absent minded.
-- By sithpadawan | Reply | (2) replies | Private Message me