Orthopod symptoms and conditions

I have been on Fosamax since 2003. In 2004 my left hip starting hurting so bad it would wake me up during the night. I had dislocated my left hip in 1994 so we put the pain down to complications from the accident. The x-rays were fine however so she sent me to a Rheumatologist to see if something else was going on. He told me I had Inflammatory Arthritis (even tho there were no markers in my blood) and put me on Plaquenil. After 6 months, the Plaquenil had done nothing but the Rheumy wanted me to stay on, and truthfully, I was afraid if I went off, the pain would become worse. Next came wrist pain so severe at times I couldn't lift a glass without wincing.To make a long story short, the joint pain has continued to migrate throughout my body. My thumb joints (where they join the palm) are so painful I can't undo jars or bottles, the small bones in my fingers ache all the time. I also get shooting pains in the long bones of my left leg and both arms. Back to the Rheumatologist last week. He said the Plaquenil was not working so he gave me an RX for Methotrexate 20 Mg once per week. This drug is one of the first-line chemo drugs for Cancer and it's effects on the body can be devastating. I have been crying since last Wednesday and had just decided yesterday to start taking this medication. I sat down at the computer to just test the drugs I am currently taking and one by one entered the drug name with "and joint pain". Plaquenil came up with only good things such as "less joint pain" etc. Mobicox also came up with good things. I entered Fosamax "and joint pain" and the top 15 hits were unbelievable. It was my problem in each and every article. I am dumbfounded. I have been seeking Dr.s help with my pain for 4 years, a GP, a Rheumatologist (2 actually) and an Orthopod, not one of these people ever mentioned a problem with Fosamax! What is going on. I am NOT going to be starting the Methotrexate and I feel I have been given dangerous medications over the past four years which I should not have been taking. I was a Personal Trainer and aerobics instructor for 12 years - now I can barely get through a yoga class without modifying the stretches because the pain is so severe.

Thank goodness for this site. I have made an appointment with my GP but I am stopping the Fosamax today (it was my day to take it). I pray I can regain some of the pain-free movement I used to have. In closing, I do have to say that I have regained some bone mass on Fosamax but...was it worth it? Was there another way I could have done this? Who knows. How long does it take for the pain to lessen after dropping Fosamax?

On Wed, My orthopod's PA gave me 80mg into the left side of the knee for fairly constant knee pain post arthoscopy. The knee pain is gone from 1st day. Have been using hot spa treatment followed by ice pack for 3 days. There was some facial flushing on the 2nd day. Today I have severe abdominal cramping and wondered if this is a side effect of the kenalog.

I have experienced severe pain at injection site along with awful nausea and vomiting the first few weeks following the injections; unsightly rash/acne over neck, chest and shoulders that is taking over a month to clear; irregular and quite heavy menstruation...even midcycle... equaling three periods in 6 weeks. Palpitations sent me to my primary care md. These side effects have been an insult to injury and embarrassing. The rash has left scars and the constant bleeding has left me exhausted and a little scared. I use an SPF on my face...maybe why it was spared from the breakout. I told my orthopod about the breakout and he and his assistant laughed at me pretty much and said they never ever heard that before. I have been in to see my OBGYN, last week, and will speak to her soon about the likely correllation between Kenalog and my heavy/irregular and never ending periods. I did not make the OBGYN connection until after I read some testimonials. I was going to have some pretty uncomfortable obgyn tests done and they would have been in vain. It sounds like the pharm reps selling Kenalog...or a generic brand...have not been educating their docs on these awful and life changing side effects. I feel that the physicians choosing to use a specific corticosteroid should informl every patient what it is exactly they are injecting into them. Each woman shoud be told of the potential menstrual irregularities and major inconvenience. My husband and I have been trying to conceive and now it seems impossible.