Shin splints symptoms and conditions

My symptoms started with aches in my ankles and I thought I should stop wearing heals for a while. But then the tingling pain moved up into my lower legs and then my arms/wrists over a period of a few days. I felt like I was having constant shin-splints. I was heavy joint/muscle pains. Then the back of my head hurt really bad on the left side, just at the top of my neck/bottom of my head, and was also really sore to the touch. Then massive headaches. Probably migraines, although I have never had them before. My MD immediately put me on celebrex, which did nothing. I was eating Advil and Tylenol like candy and couldn’t sleep. So the doc put me on steroids (prednisone). That took the pain away. After a few days, while at work, the vision in my left eye went in and out (perfect vision to completely gone). I have never had any issue with my eyesight before - perfect vision. Then at one point (actually while I was in for my first MRI) my vision never came back. No one thought it was serious enough until I demanded to go to the hospital. I spent three days in the hospital, where they ran tests after tests (including MRI, Lumbar Puncture, blood work, neurological tests, echogardiogram, dobblers, etc). Upon leaving the hospital actually diagnosed me with Optic Neurosis, and gave me a 15% chance of getting MS later in life. We were all relieved it was not MS, like they originally suspected. After going to the Eye Dr, they told me that was not the case. This kind of eye stuff only happens to people in their 80’s! I will never regain my vision. If my diagnosis had been optic neurosis, it would not explain the joint pain. I have seen specialist after specialist over the last two months, and they still have no idea. Every test I have undergone has come back clear and I am perfectly healthy. My doc said we might have to go with the retinal specialists theory - which was a piece of cholesterol that clogged the artery in my eye. I just don’t get why a piece of cholesterol would have caused me so much pain over the rest of my body. After viewing this site and the Mirena pamphlet that I found online they give to the doctors, I really think it was the cause. The packet even notes, if you have symptoms like visual loss and headaches/migraines for the first time, to remove it immediately! I did not get mine removed until a month after my vision loss. Every doc I have seen I have asked if it was Mirena and not one of them thinks that could be the cause. But it is ironic, that when you see someone for the first time, the first question they ask is if you are on birth control or any other medications! I think I need to show them this site, so they can read other women’s symptoms. I did also have all the other symptoms as well - weight gain, irritable, oily skin, cramps, moodiness, vaginal odor, gross discharge, headaches, nausea, low sex drive, hot flashes, anxiety, restlessness at times, fatigue, and the list could really go on and on.

55 yo male. I started Vytorin (20mg zocor) in Jan of 2007 until May of 2007. I lowered the dose to 10mg in March but am still suffering side effects (3/29/08) It did lower my cholesterol dramatically but at what price?
I began having tingling/burning in my feet and shins. Also, muscle pains in my calves and something like shin splints. I had been very active but have not fully recovered. B-12, methylcobalimin, has helped the tingling. I was taking as much as 10mg per day. Also, L-carnitine for the muscles, CoQ10, and Ribose. I do feel like I am gradually improving. The tingling is much less but my legs are weaker than before.

I thought this was a miracle because pill until after about a month ago.....breast tenderness, bloating, fluid retention.......makes you depressed when you are not even having a period. Been on Yasmin for about 6 months......just started skipping the inactive pills and starting a new pack.....that way you don't have a period at all. The edema itself is a nightmare. I have been on Yasmin in the past....with no problem...then 3 years ago I had a child and only started back six months ago. I thought I was gaining weight from overeating until I realized that my eating habits haven't changed at all. And to top that....I have exercised at least 3 times a week for the last six months (which is more than I have in the last 2 years) and I'm not losing any weight? I've also experienced the terrible muscle cramps in my legs.....thought it was shin splints.....but now that I read what people are saying I honestly believe that my problems might be from taking this because pill for way to long. I've taken my last pill this morning and I am not going to finish the pack. Taking a break from the pill period!!

nursehl

I am a 38 yr old female in excellent health--thin and fit, and don't take antibiotics. I had a bacterial infection and was prescribed levaquin. After the first dose, 24 hrs (500 mg 1x day) I experienced joint pain in a place i'd once injured a wrist. A few hours later it was into my hands--a deep ache, with a tight, numb feeling them. By the second dose--48 hrs later, it my joints and forearm area ached as if I'd lifted crazy weights. It moved into my shoulders, neck, hips. By the third dose, I was sleepless. My head ached at the nape of my neck and ears rang. When I got out of bed, I felt shin splints, sore ankles and my fingetips feel like they're asleep. I called the doctor and they told me to discontinue the meds. The bummer is, I was only warned at the doc's ofc of the tummy effects (which didn't happen at all to me since I timed the meals and no booze were ingested). Also the pharmacy did not provide counsel or an informational sheet which floors me after seeing this website. I really hurt. I have faith the symptoms will subside since I'm so early in the dosing. I would never take this again.

This is an additional comment to ershry's question since I am the daughter to which the question refers to. Not only has this rash steadily worsened throughout the past few years, I am now having random chest pains, and it feels as if I have something stuck in the top of my throat and along the tonsils. The doctor says that these new symptoms might be related to the GI tract since I am taking prednisone to keep the rash semi-under control, but it sounds as if numerous people have these symptoms without any other cortisones.

For the people who have been stuck on advair for a while, have you noticed a pattern to how the side effects occur? I started with a rash on my face and neck that has now spread all over my entire body, then severe, debilitating calf pain that the doctor wrote off as shin splints, then the throat irritation, and now the chest pains.