Guest guest Posted October 12, 2003 Report Share Posted October 12, 2003 Well, my last mercury-filled filling is gone, but what a long and painful process it turned out to be. I am finally free of the throbbing pain after having a root canal done on that tooth. Finally, the throbbing from the root canal went away and I now have the permanent crown in place and no discomfort. I had complained about depression while all of this was going on and hadn't had my lab tests done. I now have the latest from blood drawn at the end of September: FT3 4.6 (Range 2.3 - 4.2) FT4 1.4 (Range 0.8 - 1.8) TSH <0.004 (Range .35 - 5.50) (Says new reference range, but doesn't show a new reference range, just says new reference range for 3rd generation TSH has replaced the 2nd generation test.) Since my blood tests don't show hypothyroidism, I am ruling out that as the cause of my depression and as each day goes by, free of throbbing pain, I am beginning to see that the depression may have been caused by the dental situation. I have been taking 5HTP for about 3 weeks, which I started after reading that someone, here, was trying it. That may also be a reason why I am feeling much less depressed than I had been. I am being more consistent with my exercise program, I am less irritated by simple daily chores, my surroundings seem less unacceptably shabby and now look simply shabby, I am less irritated by people and I have more energy to get on with some of the things I want and need to do. I am going to continue with the 10mg of Methimazole and 40mg of Inderal for the next three months unless symptoms pop up that indicate I need to have labs done sooner. I will have the FT3, FT4 and the TSI done. I made sure I would have the TSI on the lab slip so I could get a good idea of whether the Armour did cause the dramatic rise from 248 to 730% from April to August. I imagine if there has been a dramatic drop, then the Armour must have been causing the dramatic rise. I asked my GP two questions; whether he would allow long-term use of ATD's and whether he uses the disappearance of the antibodies to indicate remission. He said that it would depend on whether problems arose, such as liver or WBC problems, if long-term use of ATD's would be acceptable. He said he does use the antibodies as an indicator for remission, but did not know much about it when it came to the numbers. When I tried to share with him what I learned, here, he was unreceptive. My overall experience with him has been, though, that we will be able to discuss any issue that comes up and he will accept some input from me. I feel positive that things are going well, right now. I have come to some level of acceptance of the fact that I have a chronic disease. I am very aware that this disease is very complex and needs a lot of studying to reach understanding about it, but I am also aware that it is not the worst thing that could happen to a person. I don't feel sorry for myself as much as I just wish that I could go back to having my health as the best thing about myself. I am not an attractive person, I have no talents nor riches. At one time, I did have my health and a body that I thought could be fine- tuned by exercise, nutrition and mind-control. Now, I have to be constantly alert for unexpected twists and turns in the road that may lead to battle with dragons and monsters. Today, I accept the challenge. Tomorrow, I may be depressed, again. 54 (soon to be 55 - October 21). Diagnosed 8-20-02. Tried natural remedies for three months. Thyroid hormones still very high. December 7, started on ATD's. (Had been on Inderal from the very beginning to control 114 resting pulse). April 11, tried BRT with Armour. Antibodies rose from 248 to 730%. Stopped the Armour. Continued on with 10mg Methimazole, 40mg Inderal. (Some say that betablockers are " addictive " and struggle to free themselves from them. My experience shows that some people need them longer than others do. I feel my body will signal when it is time to stop the Inderal. My pulse is steadily going down and I don't experience the discomfort of a pounding heart when I regularly take the Inderal). As I indicated, I will continue with the 10mg Methimazole, 40mg Inderal until either symptoms show a need for a blood test or I have the blood test done in January of 2004. Lab tests have shown that I have a severe case of Grave's Disease. Except for my episodes of depression, I have been one of the lucky ones for whom the ATD's are working, albeit very slowly. I don't want to destroy my thyroid, so I am very glad. I realize, though, that not everyone is as fortunate as I am. If, for whatever reason, destroying the thyroid seems to be the only alternative, then that is the way that you must go. Not only is this disease complex, but the inner workings of everyone who is afflicted by it, are also very, very complex, and only that person can decide what they must do to be able to feel good, again. Quote Link to comment Share on other sites More sharing options...
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