Guest guest Posted September 6, 2003 Report Share Posted September 6, 2003 Hi all, I hope everyone is doing as well as can be expected. I wanted to run by some new symptoms I am having and would like any and all input as to if anyone knows or thinks they are a correlation with CP, which I do have. I do have hypothyroidism, but my blood work was just checked and everything is the same. No change in medication at this time. Does anyone know if TMJ is a problem with CP? I have had it for many years, but lately it has gotten exceptionally bad. I have been having body aches all over. When I wake up in the night or in the morning it takes me several minutes just to turn over or try to get up. I hurt everywhere. My heels have cramps in them and everything hurts?!!!! I am also having increased pain on a daily basis. I have an attack every afternoon between 3 and 4 o'clock just like clockwork? I am taking OxyContin 40 mg b.i.d. and Oxycodone 5 mg twice a day. I just been on these meds for 2 1/2 months now. Does this mean that maybe things are progressing? I have always had the most pain in my upper middle chest area and then around, but lately it has started in my left side and gone to my back more. When does one know if things are progressing? Should one have a CAT scan or some other testing done every so often to check for progression? Thanks for listening/answering. Take care, all are in my prayers. in Ohio Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 6, 2003 Report Share Posted September 6, 2003 , Hyprothryoidism is also one of my problems. It was just discovered this year. My recent test in July was 11.9, much increased from a 5.88 six months ago, so I started on .088 mg. of Synthroid to combat this. At least this is an explanation for why I am always cold!!! I don't know that this has a relationship to chronic pancreatitis or not. I would suspect that your increased pain indicates more progression of your CP. That's the way mine progressed. When I was first diagnosed I could go without problems or pain for weeks at a time, and then when I had it, it only lasted a few hours. As the months passed, though, the pain episodes quickly increased, and lasted longer each time. By the start of my second year I was experiencing daily annoying pain with bad episodes lasting 5-7 days. In less than 2 years since diagnosis, I've had 12 CT-scans, but these were done mainly to monitor the status of my two pseudocysts. I don't think CT-scans are done on a regular basis for CP patients without pseudocysts unless the doctor suspects some new damaging development. I hope this information is of some help to you. With hope and prayers, Heidi Heidi H. Griffeth South Carolina SC & SE Regional Rep. PAI, Intl. Note: All comments and advice are personal opinion only, and should not be substituted for professional medical consultation. " What lies behind us and what lies before us are tiny matters compared to what lies within us. " - Ralph Waldo Emerson Quote Link to comment Share on other sites More sharing options...
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