Rheumotologist symptoms and conditions

I want to know if anyone has experienced severe joint pain while on Doxy. I was prescribed this med on a Monday. I (like an idiot) doubled up on my first dose Monday evening because I know you can do that with other antibiotics to jump start the process. What can I say? I don't like being sick. Well....Tuesday morning, I took my 2nd dose and went to work. Very soon after taking the second dose, I broke out into a very itchy rash all over my back that soon spread to other parts of my body. I called my doctor and was immediately taken off the Doxy and prescribed Augmentin. Later that night, I began aching all over. I woke up in severe pain throughout all of my joints, and was in a terrible mood.....obviously. As the day progressed, the pain continued, but seemed to be moving randomly about my joints. My ankles would hurt for a while, then my arms, the my shoulders, etc. That night, I took a Benadryl (still itching from the rash a little), some ibuprofen, and went to bed. I woke up feeling a lot better. A lot less pain in most of my joints. It was a good day. However, today, Friday, I am still in some pretty bad pain in my hands. Anyone else have a similar experience??????

I don't have a new side affect with Prednisone but just want to share my feelings. I was diagnosed with Temporal Arthritis since last July 2007. I started taking 60 mg of Prednisone for 1 month. Didn't notice the side affects then. Weaned myself off through my doctor's instructions. But relapse occurred when I was only on 2 daily. With Temporal Arthritis, you get delibating and horrendous head pain which is caused due to inflammation of the main artery in the temple. I am back to 3 daily.
Besides my moon face, I am bigger. I really don't have a lot of the other side affects you all talk about. I am sorry you all have to go through that.
My depression is better. My sleep is horrible. Now I am going to a sleep study to see if I have Sleep Apnea.
I consider Prednisone a wonder drug. Although the side affects are horrible, I have to admit, I feel much better, most of the time. I do have inflammation in the neck. Not sure if that is pred or temporal arthritis, but am seeing a rheumatologist for that.

Teena

I just returned from seeing a hematologist for bruising and bleeding under and through the skin of my forearms. Luckily, it is not a bleeding problem, but a dermatological condition known as "cutaneous atrophy". I read on this website that is a side effect of the kenalog injections.

I've been getting the injections in both my knees for the past year (shots every four months). The injections help the pain in my knees, but I think I will just take darvocet for the pain and tell my rheumotologist that I do not want any more of these injections. I've also experienced the excessive sweating around my neck and upper back, not knowing why. Scary side effects.

Responding to the latest poster.

No, no improvement for me in 6 months.

So sorry to have to say that. For you and I and the rest of us.

I just came back from a rheumotologist who has done many, many tests on me. I shared with him my belief that this all started within 1 or 2 days of taking only one medicine ( and after not taking "any" other medicine at all for 1 or more years before this ) and that is Levaquin.

Immediately the subjcect of psychiatric help was brought up by him and his feeling that it is very easy to read other peoples emotional responses such are posted on this board into your own situation.

He did give me the time and chance to at least present the idea to him regarding the "fact" that all of this began shortly after I started taking my 6 day dose of Levaquin. When I told him about the thousands of "exactly" matching experiences by you other posters, he shifted in his seat and stopped me and told me what I just recounted in the previous paragraph.

After repeating individually all the medical tests that have come back negative on me and repeating his hope that I get back on anti-depressants, he then shook my hand with a look of pity on his face and said something like, I hope that my allowing you to unload your concerns on me helped.

I am 54. I am not so ignorant that I don't understand and appreciate the importance of relying on well tested, scientifically solid and proven facts when it comes to making decisions about almost everything. But there is something wrong here. I can sense it. And yet no doctor will give "any' weight to what you and I and others are honestly pouring out here on these boards.

The "fact" that thousands of people are saying the same thing after almost all of them report only one thing in common ( the taking of Levaquin and or Cipro and usually just this one medicine alone ) is simply emotionally unstable nonsense motivated
by people who are suffering from something other than Levaquin or Cipro side effects and proabably mental in nature.
And their physical testing results are thier God of logic here.
If 500,000 people were reporting what we are reporting, and they didn't have the 30 different clinical test results to back this up they would probably say this was some form of mass hysteria.

It is a very sad and actually frightening statement about the almost crazy mind closing mentality of our medical community and their educational conditioning.

Of course there aren't many studies and clinical test results of people who have had such serious side effects like ours from Levaquin and Cipro. These powerful antibitoics haven't been around for decades and there is proabably 100,000 times more money behind trying to prove these drugs work and are fine and "not" that dangerous, than the monetary amounts and motivations behind trying to show that they are indeed much more danagerous and damaging than anyone will admit.

My depression and anxiety took off "after" I started taking Levaquin, not before! My leg weakness and soreness and other limb pain is "not" coming from my depression. And all these other unprecedented and extreme cases of insomnia, itching arms and scalp, weird wincing pains, stomach problems, shuddering, tremors, weird pulse rates, incredibly heightened sensitivity to cold and then immediate turns to feeling too hot, uncoordinatided gate and a few other carzy symprtoms started only after 1 or 2 days of a 6 days dose of Levaquin for me. And I have never, ever experienced anything like this before in my life ( with the exception of a few panic attacks, like who hasn't had those ) until I started taking this Levaquin.

I have written to so many major media outlets asking them to start looking into this situation of ours and so many like us. I will "never" just cave and accept my devastatingly changed life by simply accepting every doctors explanation that I am just a loon because their test results aren't shwoing them any results that would explain this.
WRITE...write to everyone you can about this. There is massive money behind trying to make you believe there is nothing wrong here. Stand up and be courageous here. You may have to take anti-depressants in the search for the truth and cure...but what other choice do we all have? JB

I am 36 years old and have been on Yasmin for almost 2 years. My dr. switched me from ortho-cept because of terrible mood swings and said this was a much lower dose bc pill. When I first started, I thought it was the best thing since sliced bread!! Over the last year, however, I started with all types of aches and joint pain and major fatigue. Only being in my mid 30's, I felt as though I was in my 70's. Over the last year, I have been through tests for thyroid, lyme disease, etc. I have even been to a rheumotologist. Within the last 2-3 months, I have started with break through bleeding which I never had before. Also, I am getting severe headaches which seem to be more prominent when I am on the placebo pills. They subside after about the 3rd pill of a new pack. Some headaches have been at the migraine level with my vision also being affected. I have noticed severe dizzy spells, nausea and the cramps has returned with a bang. I have contacted my dr. and they have told me to stop when I finish the next pack and they will put me on another pill. I realize everyone's body is different and there are those that this may be the mriacle pill. But after this roller coaster ride, I think I am going to take a couple of months off and see if my body can or will recoupe and I may feel better.