Massage therapy symptoms and conditions

I am so annoyed that this medication is still on the market.
What is it going to take for it to be banned??? It took me almost one year to get my life back together. The side effects from this medication are horrible. Only the people who have gone through them know how severe it is. I had anxiety, insomnia, chills, numbing in the hands and feet, palpitations, vomiting, tremors, twitching, vision problems and the list goes on. My body was out of control. My blood tests were even coming back with all sort of problems thyroid, high blood sugar etc. When retested a few months later, everything was normal.
It took me lots of hard work to get myself back to normal. Thanks to Chinese medicine/acupuncture I now have my life back.
Please don't take Avelox!!!!!

Wow... I'm glad I stumbled upon this site. I'm 24 years old and had been on NuvaRing for the last 2 1/2 years. I had used the pill until then since I was 16 to regulate my horrible periods, but I decided to switch when I got married because I was always forgetting to take the pill and since I was starting medical school a few months later, we didn't want to become pregnant at that point in our lives (and with NuvaRing I was much more likely to forget it once a month compared to everyday!).
I was always very happy with NuvaRing: my periods stayed regular and manageable, which was all I expected from BC. But oddly, over the next year I gradually developed symptoms which greatly affected my life (and my new marriage): VERY tired & exhausted all the time, horrible IBS symptoms, an aching pain throughout my body, especially in my hips/lower back and shoulders, inability to get a good night's sleep from this aching, HUGE weight gain (25 lbs in 2 years - can't shed it no matter what I do between gym/diet... Dr. doesn't understand of course), NO sex drive, and worst of all, when we did have sex it was very painful. It was horrible. I keep seeing my primary and he insisted it was from medical school & the stress. Being a rational person in med school, I understood the logic in that, but I still felt like it was more... I've always been a "busy" person, and with the increase in symptoms I gradually let other activities go in my life, leaving the only thing left to be med school; to be honest, it was the "least stressed" and most "health conscious" I'd felt in a while. But when we kept going back in my history, it all seemed to start right after I got married / around the time I started med school. So to him it always made the most sense that med school/stress was the cause of it all (of course, I never put 2 and 2 together that it's the same time I started NuvaRing!)
It became so bad I finally took a year off from medical school to spend time to figure it out. After seeing LOTS of specialists and getting lots of tests, the best anyone could come up with was Fibromyalgia. So, I took steps to feel better w/o drugs (water therapy, massage therapy, etc). I didn't like the idea of a synthetic chemical fixing something that doesn't have an exact known cause (drugs can be dangerous when not well studied - as I'm sure you're figuring out), so that's why I went the holistic route. But it never really got 100% better but it was good enough that when my leave of absence was finished, I was thankfully well enough to return to medical school a few months ago.
Oddly enough, in that time off, my husband and I had a lot of time to think about our future, and we've happily decided to try to get pregnant! So a month ago, I stopped NuvaRing. And ironically (I'm sure you can guess where this is going), things have improved over the last 2-3 weeks: I've had lots of energy, and while I still get tired, I feel like it's the "normal" kind of tired, the kind someone in med school should have (not total complete exhaustion like I used to). And wow, the sex drive... we've gone from once every 2-3 weeks (if that) to 2-3 times per week at least (or more! which seems huge for us after what we've been through!).... and the best part, no pain during sex... for anyone knows what I'm talking about, as I've seen in other posts, that's a huge and wonderful improvement!
I always kind of thought NuvaRing might be the problem (I even asked my gyno about it when I had my annual exam during that year off... she said no, most likely not of course)... it was just this odd suspicion, but I have access to all the med journals I want, and when I looked it up, I couldn't ever find any studies that reported these kind of symptoms, so I kept looking for another answer.
So, for anyone who is experiencing these symptoms and others similar to the ones others have posted, I highly recommend you consider NuvaRing as a possible cause. Everyone's different and everyone reacts differently to the same drug. Also, keep in mind lots of other things can cause these symptoms (such as thyroid or anemia issues) so definitely see your doctor about these things first, but if all of that comes out clear, consider giving yourself a break from NuvaRing, and if things improve, at least you'll have your answer finally! Drugs have lots of effects that aren't life-threatening and therefore usually go unstudied (and therefore unreported), but when this many people report similar possible side effects on a post , it's definitely worth considering!

I was given Avelox July 2007 .. within a week started getting severe leg pain in both legs .. making walking too difficult and painful... This pain has stayed with me 24/7 since I took the avelox over a year ago.. I have been to over 12 Doctors this past year trying to get help...and spent a small fortune with many tests done..now diagnosed with fibromyagia, osteoarthritis, cardioapathy, torn knee meniscus, adrenal fatigue, and i.b.s. which all developed after given Avelox... Not one will acknowledge that I may be suffering from a severe reaction to Avelox ... though they have no answers and have not been able to help me.. I have tried acupuncture, massage therapy, physical therapy, and steroid injections.. nothing has helped.. I am now seeing a Holistic Dr. and being treated for many hormone vitamin, and mineral deficiencies .. .I It has been a nightmare year with this 24/7 pain.. homebound.. because too painful to walk..and I also have constant gastric discomfort and insomnia. I feel my body has suffered from a very toxic reaction to the Avelox and just want to warn others out there too.... Please think twice before taking any antibiotics from the quinolone family...There are less toxic antibiotics that can be given.. not worth taking the risk of suffering serious reactions from these very poisonous antibiotics..

Hello: Posting about simvastatin. I have been off of the medication for about six weeks. Initially the symptoms led me to hop on an ambulance gurney and visit my local ER due to dizziness, lots of palpitations, and the feeling that I was going to drop on the sidewalk. I followed the ER with two days on the heart unit, and have pretty much have had just about every test but a brain scan (or at least it has seemed that way).

My symptoms progressed to intense burning in my torso, pronounced in the shoulder blade areas, upper chest, and into my forearms. A week after stopping the statin much of the intense burning was gone.

I still have pain and discomfort, but I have not been "white knuckling" to get through the nights like I had been, which is a relief. I read somewhere that someone described the muscle pain as feeling like he had been repeatedly punched with a bag of oranges. I can relate to that feeling, and recently I have felt the symptoms in my thighs as well.

Pain management takes up my days (although I have continued to work). I have begun massage therapy, and I am going to attempt acupuncture next week. I am trying to sort out what supplements may be the best and which ones won't interact with each other or other medications that I take. I am taking CoQ10, Omega 3 capsules, a multivitamin, and a B complex.

Anyone with similar symptoms or comments, please jump in. We are in similar boats, as they say. I have gotten the impression that some people out there (not on this site) don't see this as real. For those people, unless someone is bleeding profusely from an artery, they remain non-supportive or non-believers....

Hello: Posting about simvastatin. I have been off of the medication for about six weeks. Initially the symptoms led me to hop on an ambulance gurney and visit my local ER due to dizziness, lots of palpitations, and the feeling that I was going to drop on the sidewalk. I followed the ER with two days on the heart unit, and have pretty much have had just about every test but a brain scan (or at least it has seemed that way). My symptoms progressed to intense burning in my torso, pronounced in the shoulder blade areas, upper chest, and into my forearms. A week after stopping the statin much of the intense burning was gone. I still have pain and discomfort, but I have not been "white knuckling" to get through the nights like I had been, which is a relief. I read somewhere that someone described the muscle pain as feeling like he had been repeatedly punched with a bag of oranges. I can relate to that feeling, and recently I have felt the symptoms in my thighs as well.

Pain management takes up my days (although I have continued to work). I have begun massage therapy, and I am going to attempt acupuncture next week. I am trying to sort out what supplements may be the best and which ones won't interact with each other or other medications that I take. I am taking CoQ10, Omega 3 capsules, a multivitamin, and a B complex.

Anyone with similar symptoms or comments, please jump in. We are in similar boats, as they say. I have gotten the impression that some people out there (not on this site) don't see this as real. For those people, unless someone is bleeding profusely from an artery, they remain non-supportive or non-believers....

My 16 year old son took Levaquin 6 months ago and had a bad reaction to it. His symptoms were severe muscle weakness (he would get exhausted walking from the parking lot to a store and back, severe joint pain (in thumbs, wrists, elbows, knees, and ankles), dizziness (he felt like the room was moving away from him and would lose balance), and headaches (a severe pressure in the back of his head that was constant and then shooting pains in his his head that would come and go for no reason). I should say he was in top shape before this and wrestling in the 125 pound category. He took Levaquin to prevent an infection after sinus surgery.

Now 6 months later, his joint pain is completely gone except for his knees. They still hurt when he does squats and they are not good enough for him to go back to wrestling, but he can walk around pain free. His dizziness is also gone as well as his muscle weakness. His headaches are still there and still constant, but not as bad as they once were; however, he has had them 24 hours a day, 7 days a week for 6 months. He is on Lyrica which has helped make the headaches subside.

I have taken him to more than 16 medical doctors of all specialties, had multiple MRIs, CT Scans, blood tests, spinal tap, and an MRA. All come back negative. Thankfully, despite all of this, he still remains happy and positive that he will once again be 100% healthy; it will take lots of time, but he will get better. I know the first three symptoms (joint pain, dizziness, weakness) are clearly Levaquin related, but I haven't heard much about the headaches from people. Anyone else out there that has suffered from a constant headache after Levaquin? I REALLY want to hear about headaches from others!!!!

By the way, we have filed a medwatch already. I also know that Levaquin is not approved for anyone under 18 years old and he never needed such a powerful drug to prevent an infection, but there is nothing I can do about that now except to warn others. One of his UCLA doctors wants to write a case study on him to make this more known to others and I am helping him with that.

If anyone has questions, please feel free to ask. If you have had a headache from Levaquin, please let me know where in the head the pain was, if it is constant, what it feels like (pressure, shooting, throbbing), how long you have had it, and what, if anything, helped. THANKS.

"Free at Last, Free at Last, Thank God I Am Free at Last" - That was my first thought as after two months, the horrible effects of Levaquin finally left my body. Don't give up hope, although with no support for doctors, it is hard not to! I just don't know why they are not interested in how bad the side effects can be with this drug - I received the same story - "out of the millions of prescriptions written, how many people have had adverse reactions"........well, with as severe as a reaction as I had with every joint, muscle and tendon in my body aching as though I had been hit with rheumatoid arthritis, and from all the other testimonials I have read, someone ought to be doing something about the toxic reactions to Levaquin. I was prescribed 750mg for 20 days and threw it in the trash after the 10th day. Honestly, after reading all the postings with people with similar symptoms, I cried not knowing how long this was going to last. I have posted previously that I don't know if it was a time coincidence or the fact that I went to a health food specialty store and was told to take Zyflamend A.M. & P.M, liquid magnesium and another liquid Cal/Mag/Zinc drink. I also took the largest dosage of Fish Oil (Omega 3) that I could find. I did this religiously for at least 3 weeks, so you may want to give it a try - one of my doctors said that it has to "work out of your system", but I can't think that the magnesium based products did help and they are godd for you also.

I am not a person inclined to sue anyone, but if there is a class action suit ever instituted against Levaquin, I would happily participate in the suit - this drug does things that I would never imagine an antibiotic would do.

Make sure to get on all you medical charts that you are allergic to Levaquin and related drugs in this category.

I also thank the day that I found this website as it relieved my mind to find out what was ailing me - I guarantee you that it would be a rare instance to have a doctor concur with the side effects!

My 4 year old son has been taking Sigulair for three weeks. He has started showing signs of restlessness. The past two weeks he jhas becime very aggressive at school. I started questioning this medication a few weeks ago. I decided to research the side effects and I am so pleased to have found this sight. He was even restless in his sleep. The is out of character for him. I am stopping this medication immediately.

DO NOT TAKE THIS MEDICINE IF YOU DONT HAVE TO. I too have experinenced all the negative side effects of lupron. Ladies!! We must stick together. If you have Endo, join a local support group. There are some in almost every town. Search the internet. You will find them. I just want to bring up alternative options that have helped me. Maybe they can help you too. Dont want to sound too new age but yoga has really helped my back pain. Also looking into Acupunture which has helped me before but unfortunitly is not covered by my insurance. (Even though its proven to help). My chiropracter is covered so she is trying to incorporate acupuncture and massage therapy. Evening primrose oil can help. For severe pain, I take Naproxin which helps me much more than than Ibuprofen. There is a convention every year on Endo, Im going to try to go. We must communicate and be vocal to our insurance companies and to the public. There is just not enough press about this female disease. I also found out that I have Hypothyroid, dont know if its
all related. Its all hormonal and would not suprise me.