Guest guest Posted February 20, 2002 Report Share Posted February 20, 2002 Hello, Val, I don't have an answer for you with regard to the lowered white count, but I do have a similar question. My daughter showed a decrease in her WBC after 2 1/2 weeks on PTU. The doctors admitted it might be Graves itself, but wouldn't talk about the fact my daughter had just gotten over a nasty flu running through our family. They thought it was PTU and wanted to take her off. We readily agreed and they said to wait two weeks. It's been two weeks and today we see a new endo (the others were pushing for RAI immediately) and this is my question: Is two weeks enough time to see a difference? I don't want to have unnecessary blood work done if it's too soon. Any experience with this greatly appreciated. And this group is great! Pam In a message dated 2/19/2002 7:23:30 PM Central Standard Time, valkyrie@... writes: > Also does anyone here have further info on the side effects of PTU, if > my WBC is low and my body is not producing enough bone marrow, is it > permanant? I have been completely off PTU for 2 weeks now. > > Phew. I'm done > > Val I want to be the kind of friend Jesus would call, at the end of the day, just to talk about nothing.-Wayne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2002 Report Share Posted February 20, 2002 Hello, Val, I don't have an answer for you with regard to the lowered white count, but I do have a similar question. My daughter showed a decrease in her WBC after 2 1/2 weeks on PTU. The doctors admitted it might be Graves itself, but wouldn't talk about the fact my daughter had just gotten over a nasty flu running through our family. They thought it was PTU and wanted to take her off. We readily agreed and they said to wait two weeks. It's been two weeks and today we see a new endo (the others were pushing for RAI immediately) and this is my question: Is two weeks enough time to see a difference? I don't want to have unnecessary blood work done if it's too soon. Any experience with this greatly appreciated. And this group is great! Pam In a message dated 2/19/2002 7:23:30 PM Central Standard Time, valkyrie@... writes: > Also does anyone here have further info on the side effects of PTU, if > my WBC is low and my body is not producing enough bone marrow, is it > permanant? I have been completely off PTU for 2 weeks now. > > Phew. I'm done > > Val I want to be the kind of friend Jesus would call, at the end of the day, just to talk about nothing.-Wayne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2002 Report Share Posted February 20, 2002 Hello, Val, I don't have an answer for you with regard to the lowered white count, but I do have a similar question. My daughter showed a decrease in her WBC after 2 1/2 weeks on PTU. The doctors admitted it might be Graves itself, but wouldn't talk about the fact my daughter had just gotten over a nasty flu running through our family. They thought it was PTU and wanted to take her off. We readily agreed and they said to wait two weeks. It's been two weeks and today we see a new endo (the others were pushing for RAI immediately) and this is my question: Is two weeks enough time to see a difference? I don't want to have unnecessary blood work done if it's too soon. Any experience with this greatly appreciated. And this group is great! Pam In a message dated 2/19/2002 7:23:30 PM Central Standard Time, valkyrie@... writes: > Also does anyone here have further info on the side effects of PTU, if > my WBC is low and my body is not producing enough bone marrow, is it > permanant? I have been completely off PTU for 2 weeks now. > > Phew. I'm done > > Val I want to be the kind of friend Jesus would call, at the end of the day, just to talk about nothing.-Wayne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2002 Report Share Posted February 20, 2002 Hi Pam - It may very well be too early to see much difference yet. Quoting from The Book (aka Graves' Disease, A Practical Guide), " ATDs are very (at least 90 percent) effective in controlling the symptoms of GD. However, the effects aren't immediate. Although new thyroid synthesis is inhibited when ATDs are initiated, the thyroid gland still has a large store of thyroid hormone. Until these hormone stores are depleted, the effects of ATDs are limited. This is considered the latent period. It duration depends on the amount of stored hormone, its rate of release, and the patient's innate response to the ATD, with larger initial ATD doses decreasing the latent period. In general, euthyroidism is achieved within about six weeks. " So, bottom line, if she's not euthyroid yet, no big surprise. Two weeks might be enough to show some improvement, depending on how high her levels were before, but probably not enough for the levels to be normal range yet. And if the doc wants to push you for RAI again, tell him you'd like to wait some more for the ATD to do its job. If the doc's worried that the WBC cell count is indicative of a reaction to the PTU, you can request to try Tapazole, the other ATD. Most times if people have a reaction to one ATD, they are able to tolerate the other. Hope this helps. Good luck with the new endo! Re: RAI,PTU low white count >Hello, Val, > >I don't have an answer for you with regard to the lowered white count, but I >do have a similar question. My daughter showed a decrease in her WBC after 2 >1/2 weeks on PTU. The doctors admitted it might be Graves itself, but >wouldn't talk about the fact my daughter had just gotten over a nasty flu >running through our family. They thought it was PTU and wanted to take her >off. We readily agreed and they said to wait two weeks. > >It's been two weeks and today we see a new endo (the others were pushing for >RAI immediately) and this is my question: Is two weeks enough time to see a >difference? I don't want to have unnecessary blood work done if it's too >soon. > >Any experience with this greatly appreciated. And this group is great! > >Pam > >In a message dated 2/19/2002 7:23:30 PM Central Standard Time, >valkyrie@... writes: > > >> Also does anyone here have further info on the side effects of PTU, if >> my WBC is low and my body is not producing enough bone marrow, is it >> permanant? I have been completely off PTU for 2 weeks now. >> >> Phew. I'm done >> >> Val > > >I want to be the kind of friend Jesus would call, at the end of the day, just >to talk about nothing.-Wayne > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 Hi, , The new endo was very good. Understanding, great manner with my daughter, and not pushing for RAI. He called today to put her on Tapazole, and we hope she doesn't react to this negatively. I've posted a message regarding the difference between Graves' and Hyperthyroidism, since I'm not clear yet on the differences, and they are now saying our daughter has gone into hyperthyroidism. We're also taking our daughter to a facility that focuses on the whole body, the whole person, and approaches things nutritionally. We're hoping this will be a help. Thanks for the input. Oh, and I understand there are least two other " Pams " out there. Since I'm here for my daughter, I'll sign off now as Amy's Pam. :-) In a message dated 2/20/2002 1:32:38 PM Central Standard Time, mlbuck@... writes: > So, bottom line, if she's not euthyroid yet, no big surprise. Two weeks > might be enough to show some improvement, depending on how high her levels > were before, but probably not enough for the levels to be normal range yet. > And if the doc wants to push you for RAI again, tell him you'd like to wait > some more for the ATD to do its job. If the doc's worried that the WBC cell > count is indicative of a reaction to the PTU, you can request to try > Tapazole, the other ATD. Most times if people have a reaction to one ATD, > they are able to tolerate the other. > > Hope this helps. Good luck with the new endo! > > I want to be the kind of friend Jesus would call, at the end of the day, just to talk about nothing.-Wayne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 Hi, , The new endo was very good. Understanding, great manner with my daughter, and not pushing for RAI. He called today to put her on Tapazole, and we hope she doesn't react to this negatively. I've posted a message regarding the difference between Graves' and Hyperthyroidism, since I'm not clear yet on the differences, and they are now saying our daughter has gone into hyperthyroidism. We're also taking our daughter to a facility that focuses on the whole body, the whole person, and approaches things nutritionally. We're hoping this will be a help. Thanks for the input. Oh, and I understand there are least two other " Pams " out there. Since I'm here for my daughter, I'll sign off now as Amy's Pam. :-) In a message dated 2/20/2002 1:32:38 PM Central Standard Time, mlbuck@... writes: > So, bottom line, if she's not euthyroid yet, no big surprise. Two weeks > might be enough to show some improvement, depending on how high her levels > were before, but probably not enough for the levels to be normal range yet. > And if the doc wants to push you for RAI again, tell him you'd like to wait > some more for the ATD to do its job. If the doc's worried that the WBC cell > count is indicative of a reaction to the PTU, you can request to try > Tapazole, the other ATD. Most times if people have a reaction to one ATD, > they are able to tolerate the other. > > Hope this helps. Good luck with the new endo! > > I want to be the kind of friend Jesus would call, at the end of the day, just to talk about nothing.-Wayne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 Hi, , The new endo was very good. Understanding, great manner with my daughter, and not pushing for RAI. He called today to put her on Tapazole, and we hope she doesn't react to this negatively. I've posted a message regarding the difference between Graves' and Hyperthyroidism, since I'm not clear yet on the differences, and they are now saying our daughter has gone into hyperthyroidism. We're also taking our daughter to a facility that focuses on the whole body, the whole person, and approaches things nutritionally. We're hoping this will be a help. Thanks for the input. Oh, and I understand there are least two other " Pams " out there. Since I'm here for my daughter, I'll sign off now as Amy's Pam. :-) In a message dated 2/20/2002 1:32:38 PM Central Standard Time, mlbuck@... writes: > So, bottom line, if she's not euthyroid yet, no big surprise. Two weeks > might be enough to show some improvement, depending on how high her levels > were before, but probably not enough for the levels to be normal range yet. > And if the doc wants to push you for RAI again, tell him you'd like to wait > some more for the ATD to do its job. If the doc's worried that the WBC cell > count is indicative of a reaction to the PTU, you can request to try > Tapazole, the other ATD. Most times if people have a reaction to one ATD, > they are able to tolerate the other. > > Hope this helps. Good luck with the new endo! > > I want to be the kind of friend Jesus would call, at the end of the day, just to talk about nothing.-Wayne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2002 Report Share Posted February 22, 2002 Hi Amy's Mom, If she should have a reaction to TAP, the doctor can try her with PTU. When we react to one of the drugs negatively, we can usually use the other one. On rare occassions some people can not take either. I also think, in the archives from over a year ago, there was a discussion on this, and that sometimes it is the fillers in the TAP or PTU that people react too also. Jody _________________________________________________________________ Chat with friends online, try MSN Messenger: http://messenger.msn.com Quote Link to comment Share on other sites More sharing options...
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