Foo symptoms and conditions

I've been taking Yaz for the past 5, almost 6 months. I was struggling with PMDD symptoms. There were times when, for a week or more, I would become incredibly depressed, full of rage and anger, I craved anything within chomping distance, and felt like the ugliest human being in the world. My periods were so painful, and I would bleed so much, that all of this just began to control my life. I was literally planning my life around this time during each month. The YAZ has really made a difference in helping solve a lot of these problems, but now I've new problems.

My husband and I have always been very sexually active. We try to make time for sex during the week if we can squeeze it in (we work different shifts), but whether we do or not, we always make up for it a lot on the weekends. However, now, I find myself with no interest. I even encourage him to just skip the foreplay and get down to the deed so I can get it over with. I dry up halfway through, become frustrated if he loses his erection (usually due to my personal lack of interest. I can't imagine that's very arousing. lol) because that just means we will have to work harder to get through this ordeal, and I don't want him kissing on me or doing much of anything to me while we are in the act. It's really damaging our relationship. We are 30 and 31 years old...way too young for this nonsense. I dare say I've even thought a time or two, "Why can't he just have an affair like every other husband and leave me alone?" Yeah, I don't mean that at all, but it's crossed my mind.

That's my biggest issue with it, well, that and the monthly cost. The other side affects I had were dry mouth, dry hair (?? - not sure if this is directly related), lower abdominal pain, mild weight gain, and a rash that broke out on my lower legs and left forearm. These are the CONS so far. I'll list my pro's, too, just to be fair.

PROS" Periods, while still very painful, last about 2 to 2.5 days. The painful part only the first day. The food cravings usually only a couple of days instead of a week or more. Mood swings, if any, are not as severe and are shorter in duration. I feel like a normal woman just having normal PMS mood swings now instead of mood swings you see in those crazy women on those Lifetime for Women movies or something. lol I also suffer from migraines, and these pills don't seem to have affected them one way or another. This is actually good enough for me because usually BCPs have caused them to worsen over time.

So there you have it. It's my own long, personal experience with YAZ.

I've been taking Fosamax once a week for about 4 months. During that time what began-before taking Fosamax-as mild pain in my lower back-has gotten progressively worse. This is the only negative possible symptom I’ve experienced, but of late it has increased and spread to my hips. I decided to stop taking it today, and see if it makes any difference. If it does, I will post another reply here with details.

I think all reading these personal accounts should consider this: obviously many medical professionals see far more benefit than loss in the majority of users. My osteoporosis was only diagnosed via a bone scan 6 months ago. -2.5 The increased pain and worsening conditions in my back might in fact be much worse if I hadn’t started taking the Fosamax. One must beware of apophenia setting in with self diagnosis.

Most posting here already had serious medical needs to have Fosamax prescribed in the first place, given a small percentage of diagnostic errors. Most of the conditions I’ve seen described vary greatly, and without a serious study are purely antidotal. I suspect there are legitimate adverse reactions, but for now the percentage and severity remains a big unknown. There seem to be some activists here, so get a campaign going for publicly funded analysis of the now considerable amount of data on file.

If my back gets better, I’ll still be unsure as it might have been a delayed benefit from the drug. Likely I will take Fosamax again either way. If it doesn’t improve in several months I’ll assume F-max wasn’t the cause and begin taking it again. If it gets better, I will take F-max again to see if the problems return when I do. If they don’t I’ll keep taking it. If they do, that will red-line my ‘coincidence meter’ and I’ll never touch the stuff again.

I hope some will find my approach to our common dilemma helpful. We all have to be our own advocates within the modern health care cabal. I worry about the old adage that when we do so, we have a fool for a client. Feel free to criticize my reasoning, and thanks to all the others that took the time to share your experience. It helped me make my decision, and I’ll share the results in about 6 months.

I have been using Lantus for about 3 weeks and my eating habits are not an different and I have noticably been gaing weight,

I have cusining's disease. I was on Kenalog for arthritis in nec and shoulders for almost two years. The doctor stopped the shots abruptly and put me on VIIOX till it was taken foo the market. I have been on predisone for a year now and continue to decrease my dose. I have every symptom of Cushing's from Moon face, buffalo back and neck. And weak muscles, joints and so much pain. My wuestion is my teeth. I have lost 3 molars and have 4 more indanger. Can you give me some documented information on steroids and my teeth after prolong use. I need my dentist to receive this info so the insurance company will help with the expense. Any web sites, written documents would be appreciated

Regards,
P.J.