March 27th
2007
4:47 PM
i have been taking it for back pain for about a year, i notice i sleep really great when i take it,
now for the side effects, i noticed that my lower back really hurt if i tryed to walk, or clean, i was in a great deal of pain, also i had pitting edima in the legs, very bad, , and a rash on the neck, and no energy at all, its been a week now since i quit taking it, the back pain is gone, i can walk around the block now, the rash is going away, my blood pressure is going down, i am happier and not mad all the time now. also have more energy
May 3th
2004
8:08 AM
PLease be careful. I have been on a suppression therapy dose of synthroid for over 8 yrs. I had thyroid cancer and my endocrinologist said I needed to keep my tsh between .3-5.6. For the last yr I have been feeling awful. My heart rate was arnd 145, I had shortness of breath, muscle aches, hair falling out, could barely eat but I gained about 30 lbs because I was swelling up from edima. I had almost every symptom of being hyperthyroid. My endo said I ran on high test!! I thought I was going crazy. I was on 2mcgs of synthroid. My tsh level became .009 and then became non-exsistent(.oooo) I now have dialated cardiomyopathy, and congestive heart failure.
So if you are not on the correct dose you can have very serious side effects. Make sure your levels are checked on a regular basis. If you are not feeling right make sure someone , like a dr listens to you and hears your symptoms. I had repeated ly told my dr how I was feeling and he said I needed to be suppressed. to prevent cancer returning, well after almost dying from heart failure how suppressed should someone be????? Now My entire live is suppressed....
April 4th
2007
5:44 AM
I am a 59 yo Male diagnosed with MG Myasthenia Gravis). MG is an autoimmune disease affecting the muscles. At it's worst I couldn't keep my eyes open, my speech was constantly slurred, I had double vision, and I had a hard time walking because my hip muscle sometimes would give out. I was on 60 mg of prednisone/day for 4 months and am on the "weaning off" cycle (decreasing the every other day dosage by -10mg at 3 week intervals then by -10 on the other day when the cycle gets to 60mg/0mg). The side effects are as previously mentioned: The good: My arms are like steel! My MG symptoms are pretty much gone. The bad: My Blood Sugar is so eratic and I have to take diabetes drugs to combat that. I am taking fosimax to combat osteoporosis (just in case as my Dr. says). My feet have swollen up really bad, my hands are swollen, my legs weep from all the edima (water retention), and I have a voratious appetite! The Ugly: My face looks like an Orangutan, My weight sored at least 50 lbs, I am moody as hell but the longer that I am on this drug the more tolerable it seems (by other people's obversations). I am having a hard time walking. I had to have a BiPAP machine so I could sleep at night. My memory is erratic and I hate that part.
Hope this helps someone.
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