Stress fracture symptoms and conditions

I love prednisone, at least so far. I have a rash that occurs only on the back of my upper arms and shoulder blades in the deep of winter...then reoccurs EVERY SUMMER as soon as I get in the pool. In summer though, it's all over my arms, my hands, my thighs and my upper back, even my neck a bit. It starts out as a medium tingle (like pins on my skin), lots of itching..which scratching definitely makes things worse. I apply sunscreen 70 and no help. I use anti itch cream which helps to keep me from scratching...but I can't bathe in it! If I don't scratch, the little bumps are still there, but they of course get red when I scratch.

I tried meds for hot tub foliculitis...no help. I start the prednisone and VOILA! It's gone within a day or two..or quickly disappearing. Two days after the last pill, I get in the pool..and the itching starts.

I have never noticed trouble with breathing or any kind of anger / rage issues...I do wonder if those are other folks symptoms of something else. I would really look into that before blaming prednisone and not addressing the real issue.

I have been on prednisone (tapering from 5 tabs a day to one over time) and it's the ONLY thing that helps with this rash and it's cleared the rash one hundred percent of the time. LOVE prednisone, came here to see if I could be on it all summer. I have three kids, no babysitter and my pool is my only true pleasure....I live for it all year as I hate winter and fall...I'm a summer girl!

I commenced Lipitor 14 years ago at age 47. At that time I was a regular tennis player, walker and generally fit for my age. No problem with Lipitor for the first couple of years until I began to experience hip and low back pain. My GP diagnosed arthritis. Gradually became worse and I started to gather injuries (over stretched ligament in right knee which refused to heal, plantar fasciitis twice) My back pain became far worse, I persevered with tennis believing that exercise would help. I began to "trip" on the carpet and going up stairs (foot drop). I was sent for a CT scan in 2002 which showed spondylolisthesis and root canal stenosisss. On advice from doctor I stopped tennis. Referred to a neurosurgeon who after several months carried out a laminectomy in July 03. Cleared to recommence exercise in December 03 which is when my nightmare commenced. I developed bursitis in one hip, stopped walking until it settled, then excruciating pain in feet, and then bursitis in the other hip and continuing foot pain. I developed rib/back pain, again diagnosed as arthritis even though I felt the pain was muscular. I had one session of aqua aerobics and woke the next morning with plantar fasciitis which continued for 3 months even with doctor, physio and acupuncture treatment. I was then referred to a Spots Medicine Dr who ordered bone scans/x-rays which revealed a stress fracture in my foot. In 2006 I began to notice that my right arm had a tense feeling all the time, I had a loss of dexterity in my right hand which assumed a claw like appearance and my normally neat handwriting became practically illegible. My physio recommended I see a Rheumatologist who said I had "no more arthritis than I would see in any 62 yo", he sent me to a Neurologist who after 5 mins diagnosed Parkinson's Disease. Within 7 weeks of commencing the PD medication I was experiencing Restless Leg Syndrome every night. The neurologist said that my condition had "progressed" and increased the medication - twice. I was then getting RLS DAY AND NIGHT and getting no relief OR SLEEP!!! Finally after 12 months misery my GP suggested that I try coming off Lipitor to see if that was causing my body pain. Within 6 days I felt better, my muscles became less stiff and relax. I went back to my Neurologist who refused to accept my claims, he insists I still have atypical PD (because I do not have tremors). I told him the cure is worse than the complaint and against his advice I weaned myself off PD medication and Lipitor. It was hard going but I NO LONGER SUFFER FROM RLS AND MY DEXTERITY IS SLOWLY IMPROVING. I still have dexterity problems with my right fingers but the tense feeling in my right arm has gone and my "claw" hand is starting to relax My muscles feel bruised all the time. I am still taking my blood pressure tablets and 150mg of Co-Q10 a day. I have been off Lipitor 9 months. It has been a painful journed for the last 8 years and a nightmare for 12 months. My GP has marked my records as "allergy to statins" but says she just doesn't know if I have Parkinson's. I know that I will never take this awful drug again. My cholesterol has skyrocketed but I will have to try and lower it naturally and take the risk. I constantly feel like I have worked too long and hard in the garden, all my muscles are so sore. I really need to know if this damage is permanent and if this drug has caused Parkinson's Disease itself or just PD like symptoms. I guess I will just have to wait and see. I don't think doctor's believe us when we say Lipitor is doing damage to thousands of people. They love it!! When we are aging we are not surprised to get diagnosed with arthritis and this is why we take this medication unwittingly for so long.

Just wanted to add another little bit of fun side effects for everyone.

Last month, I woke up with a pain in my right groin. Since no gymnastics were involved, I treated with ice and ignored it. After a few days, pain was worse, so went to the ER (My home away from home) where a bone density scan was ordered. 4 weeks later I find out that I have a stress fracture of the lesser trochanter (part of the femour just below the femoral head - English translation hip fracture).

Turns out that long term therapy on warfarin (ie. over 1 year) also increases your risk of fractures.

And what does one do for this? Nothing. Orthopedic guy said just go as usual and no physio required. Easy for him to say since he does not have groin pain, and associated thigh/Knee/calf pain associated with accommodating my gait. Needless to say, seeing a new orthopedic guy.

I have started iron infusions monthly as my iron and ferritin levels are low (but hemoglobin is fine).

Still wondering which came first - the insanity or the warfarin!

Fiona

I'm a 47 year old male and have been on 20Mg Daily Lipitor for about 4 years. Everything was mostly fine until about 1 year ago when I started experiencing severe hip and groin pain. I played hockey regularly up until that time and assumed the problem was a hockey related injury, though never remember any specific incident that may have been directly responsible. I told my doctor I thought it was a sports hernia because the symptoms and suspected cause held a close resemblance. X-Rays, MRI and Bone Scans were all negative. Physical Therapy was a useless waste of money. I was in agony for over a year and barely able to walk some days. Could no longer participate in hockey or other sports. Even coaching youth sports was a challenge due to the pain that greatly limited my mobility. The maddening part of it all was the doctor's had no explanation and just wanted me to continue with Physical Therapy. My wife casually suggested to me that maybe it was the Lipitor as she had heard some recent news on TV related to Lipitor and muscle pain. I told her she was being ridiculous and that's when I started to do some internet research and came across this site. It's all starting to add up. I've been off Lipitor for a week and the pain on my left hip is almost completely gone while the pain on the right side has shown significant improvement. While I am seriously happy that I think I have found the cause of my pain, I am incredibly angry that not a single doctor (I saw a total of 3) even suggested the possibility that the problem might be the Lipitor. They all new I was taking it. I know the drug has had highly positive affect on most people and saves lives but I feel that I've lost a year of my life to it.

I have been on Warfarin since Sept 2004 when I had multiple blood clots in both lungs. Since then I have had two more PE's (one with a therapeutic INR) and a blood clot in my left arm (INR was also therapeutic). Genetic tests show nothing.

Since starting Warfarin I have had
- dizziness issues,
- eternal extreme fatigue
- hair loss
- short term memory and cognitive issues,
- joint pain and
- head aches all the time. I think the headaches are the worse since I can't take any NSAID's for them.

I have lost weight and push myself to exercise because it is supposed to make you feel better, right? Well not yet. I keep waiting.

I have not been able to return to work and worry about the long term implications of this.

Many times I have wondered about my sanity and if I was imagining all of this, so finding this forum at least lets me know that there is a possibility that it is not all in my mind.

I have been seeing a psychiatrist to help me work through the almost dying 3 times thing, but it is hard to accept since no one knows why I throw the clots. My INR is not stable in spite of close monitoring of Vit K and other drugs, and my INR must be taken twice a week.