Guest guest Posted December 17, 2004 Report Share Posted December 17, 2004 In a message dated 12/17/2004 1:19:05 PM Eastern Standard Time, bcbmsts@... writes: > Thyroid Peroxidase >70.0 > Did the doctor tell you that you have Hashimotos? Cindi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2004 Report Share Posted December 17, 2004 In a message dated 12/17/2004 1:28:57 PM Eastern Standard Time, bcbmsts@... writes: > Is it common for > Hypo's to have PCOS also? PCOS is often found with folks with Hashi's. cindi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2004 Report Share Posted December 17, 2004 > In a message dated 12/17/2004 12:54:44 AM Eastern Standard Time, > bcbmsts@y... writes: > > > I now missing some other > > hormone or getting too much of something to cause all this? Or am I > > not being treated fully for the hypo? Would Armour help me? > > > > I don't know about the fuzzy hair...but the cholestrol is probably hypo > related. What I do know is that Armour usually works better for anybody. I would > encourage you to ask for it. Do you have your recent labs ....and hopefully > they did Free T4 and Free T3? If so, post any labs you have. > Cindi > Thyroid Peroxidase >70.0 Thyroglobulin 4.9 This was done approx. 6 weeks after starting meds: T uptake 27.80 T4 8.4 T4 Free 1.17 TSH 3.68 And a sonogram that showed a Multinuodular goiter with lobes minimially enlarged. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2004 Report Share Posted December 17, 2004 Yes, I do have Hashimotos Chris > In a message dated 12/17/2004 1:19:05 PM Eastern Standard Time, > bcbmsts@y... writes: > > > Thyroid Peroxidase >70.0 > > > > Did the doctor tell you that you have Hashimotos? > Cindi > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2004 Report Share Posted December 17, 2004 I've never had Hashimotos even diagnosed or tested for. Where do you people get doctors who test & diagnose for that or Graves disease or whatever else? I was lucky to get a doctor who thought to test me for thyroid dysfunction when none other even thought to years ago. But after putting me on Synthroid, she never suggested any other tests for anything else. I must pick doctors like I picked men......bad track record....'nuff said about that. Re: New to group with questions Yes, I do have Hashimotos Chris Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 In a message dated 12/18/2004 1:44:37 AM Eastern Standard Time, MamaMaha@... writes: > . Where do you people get doctors who test & diagnose for that or Graves > disease or whatever else? a regular doctor can order the blood tests for thyroid antibodies which indicates hashi's. cindi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 In a message dated 12/18/2004 5:32:36 AM Eastern Standard Time, artisticgroom@... writes: > I have often wondered if other illnesses have this same lack of care or if > we're just too easy to shove under the table as we forget and go to sleep in > between our doctor visits. valerie, i don't think it's just us. my daughter has PKD (polycystic kidney disease) and all that forum there are people all the time complaining about the lack of caring and good care from their nephrologists. it's an epidemic i think. doctors who could care less about their patients. cindi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 >>I must pick doctors like I picked men<< No believe me it is not your choice of doctors! it is that there are so FEW doctors out there that even have a CLUE about thyroid disease. I lucked out WAY long ago when I first went severely hypo and by accident went to a DO. A GOOD one. He put me on Armour without even a test and told me how to adjust my meds myself by symptoms. I was about 19 years old! Had he not died and then I was convinced to take Synthroid for so many years oh how much different my life would have been! But in all those years since then till I turned 44 I was in hypo HELL and was convinced by my doctors either NONE of them had succeeded in finding my optimal Synthroid dosage or it was " something else " wrong as my labs were " normal " ...TWENTY-FIVE years of my life gone and in that time I saw SO many doctors and so many diets and so many pain pills, muscle relaxants, anti-depressants, diet pills and yes, shrinks too. I even tried street drugs to feel normal and became a speed addict for a few years trying to feel like I had some energy. Very sad what poor medicine caused me to do with my life. I am just thankful I finally got wise to the horrid lack of medical care we thyroid people actually have. I have often wondered if other illnesses have this same lack of care or if we're just too easy to shove under the table as we forget and go to sleep in between our doctor visits. Lets face it, we are not demanding about our own health till we learn there is a possibility for a better life. I think more of us that HAVE gotten better need to start raising a real stink about our prior care, but we are so grateful to have a life back we don't fuss about it even then. *Artistic Grooming * Hurricane, WV Fat cat? Diabetes? Listowner for overweight or hypothyroid cats http://groups.yahoo.com/group/hypokitties/ ---------- No virus found in this outgoing message. Checked by AVG Anti-Virus. Version: 7.0.296 / Virus Database: 265.6.0 - Release Date: 12/17/2004 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 Caroline, it took 3 dr's for anybody to even consider testing for antibodies for me. #3 Dr Poophead is the one who wanted to know about the antibodies because I was self medicating with Armour. If not for that, I don't think anybody would have honestly cared. She was just trying to prove me 'wrong' for self medicating. SandyE~Houston Re: New to group with questions Yes, I do have Hashimotos Chris Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 In a message dated 12/18/2004 5:38:32 PM Eastern Standard Time, bcbmsts@... writes: > It wasn't until > I went to the ER for an asthma attack & I started telling the doc > about how sick I've been that she decided to run the test for the > thyroid....and sure enough, I was right. > wow. I was also in the ER room with an asthma attack in the year before being diagnosed...but no one mentioned thyroid. I haven't had any problem with asthma since being on Armour. Cindi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 Caroline wrote: >>I must pick doctors like I picked men<< s replied: >>>No believe me it is not your choice of doctors! it is that there are so FEW doctors out there that even have a CLUE about thyroid disease.<<< Yes I know. I haven't found any truly good thyroid or endocrine doctors either. Does this mean that there are too few good men out there too then? No wonder I had such bad luck with them then...LOL! Gee what does that say about male doctors? Which is why I've chosen female drs as much as possible the past many years. Specially gyns & GPs. I know its sad when we find an understanding (if not knowledgeable) doctor & then they either retire, get sick, disabled or die or move away to another town. That's sad & specially when you've been misdiagnosed all those many years...how horrible. I'm sure there's thousands of others on street drugs too because pf undiagnosed or misdiagnosed illnesses by doctors. People then often turn to self-medicating trying anything to feel better, lacking the medical knowledge of their condition themselves. I've also gone the route (for over 40 years) of OTC & Rx pain pills, muscle relaxors, antidepressants, experimented with scads of natural supplements, did juice fasting, enemas, had colonics, chiropractic, accupuncture, Reiki healings, learned hatha yoga, Feldenkrais, aerobics, self-massage, Chi Qong, chanting, meditation, self-hypnosis & also smoked pot for a number of years to ease the pain & depression/anxiety & carry on with life as best I could. And it was only about 6 years ago one lady doctor finally said I had low thyroid & put me on Synthroid which was better than a kick in the head but made me worse after the first year or so on it which I didn't even realize back then. Because heck, I didn't know enough to even question if my thyroid was still a problem when my test results were " normal " . Or if it was the original problem for that matter, since a childhood neck injury which I've recently learned can cause thyroid problems due to pinched nerves & lack of proper energy flow. So my health concerns since 1995, except for occasional chiropractic adjustments, mostly went undertreated is maltreated when the worst of my symptoms were surfacing Big Time again. Mostly because I was so wrapped up in caregiving my mentally/physically disabled ailing husband & trying to find ways to help him & keep track of his medical & health needs & records so I could speak coherently about them at his doctors & with his Workers Compensation attorney because with his Dementia, he had memory loss & wasn't very coherent most of the time which kept getting worse & then he became increasingly violent & verbally abusive too. With all that super stress my health went down the tubes even further so that I was beginning to feel like a hypochonriac & doctors who kept pushing antidepressants, sleep aid Rx, other drugs & advising counseling & more exercise were convincing me it was true. I'm sure my thyroid dysfunctioned even more then & I never knew it & my doctor at that time never put 2+2 together to figure it out either. And neither did future doctors I had to see when I had to move/relocate for a few years until I finally bought this place & settled here & have seen several doctors since being here too & never knew what to even ask them about related to the endorcrine system or thyroid until the last couple of months from this group & the HRT group. I just figured the Synthroid & Estradiol I was on were doing their jobs & the doctors knew to increase or decrease my dosage depending on the blood test results. So what a waste of my life time & money on these know-nothing doctors all these many years!!It makes me sick with rage to even think about it. Caroline ----- Original Message ----- From: T >>I must pick doctors like I picked men<< No believe me it is not your choice of doctors! it is that there are so FEW doctors out there that even have a CLUE about thyroid disease. I lucked out WAY long ago when I first went severely hypo and by accident went to a DO. A GOOD one. He put me on Armour without even a test and told me how to adjust my meds myself by symptoms. I was about 19 years old! Had he not died and then I was convinced to take Synthroid for so many years oh how much different my life would have been! But in all those years since then till I turned 44 I was in hypo HELL and was convinced by my doctors either NONE of them had succeeded in finding my optimal Synthroid dosage or it was " something else " wrong as my labs were " normal " ...TWENTY-FIVE years of my life gone and in that time I saw SO many doctors and so many diets and so many pain pills, muscle relaxants, anti-depressants, diet pills and yes, shrinks too. I even tried street drugs to feel normal and became a speed addict for a few years trying to feel like I had some energy. Very sad what poor medicine caused me to do with my life. I am just thankful I finally got wise to the horrid lack of medical care we thyroid people actually have. I have often wondered if other illnesses have this same lack of care or if we're just too easy to shove under the table as we forget and go to sleep in between our doctor visits. Lets face it, we are not demanding about our own health till we learn there is a possibility for a better life. I think more of us that HAVE gotten better need to start raising a real stink about our prior care, but we are so grateful to have a life back we don't fuss about it even then. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 Oh that's sad, Sandy. I asked my dr to test for antibodies & other things I learned of from this group a week or so ago but haven't heard back from here yet. She likely hasn't a clue what the results even mean, let alone know how to prescribe for any of it is what I'm figuring since she called me the next day after she got my TSH & T4 results. But I haven't heard Word One from her on these latest tests she never even suggested but which I asked for that include antibodies, FT3/FT3, ferritin & other things. I'm going to have to call her on Monday & no doubt make another appointment to go over the results with her. Tho I don't even know what to discuss or suggest to her that I might need. I will ask her to prescribe at least 2 grains of 'real " Armour for me tho instead of the generic she got the first time in that puny 30mg dose. Re: Re: New to group with questions Caroline, it took 3 dr's for anybody to even consider testing for antibodies for me. #3 Dr Poophead is the one who wanted to know about the antibodies because I was self medicating with Armour. If not for that, I don't think anybody would have honestly cared. She was just trying to prove me 'wrong' for self medicating. SandyE~Houston Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 I guess trying to prove you wrong to get the tests is better than not doing it at all. These doctors....bah humbug!! ----- Original Message ----- From: sandy Caroline, it took 3 dr's for anybody to even consider testing for antibodies for me. #3 Dr Poophead is the one who wanted to know about the antibodies because I was self medicating with Armour. If not for that, I don't think anybody would have honestly cared. She was just trying to prove me 'wrong' for self medicating. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 I just happened to get lucky. I had gone into my regular doctor over a year ago complaining of hypo symptoms & he told me I was fine. Meanwhile I kept getting sicker and sicker. It wasn't until I went to the ER for an asthma attack & I started telling the doc about how sick I've been that she decided to run the test for the thyroid....and sure enough, I was right. > I've never had Hashimotos even diagnosed or tested for. Where do you people get doctors who test & diagnose for that or Graves disease or whatever else? I was lucky to get a doctor who thought to test me for thyroid dysfunction when none other even thought to years ago. But after putting me on Synthroid, she never suggested any other tests for anything else. I must pick doctors like I picked men......bad track record....'nuff said about that. > Re: New to group with questions > Yes, I do have Hashimotos > Chris > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 So that was a lucky trip to the ER for you then. Sometimes that's the way of it. ----- Original Message ----- From: bcbmsts I just happened to get lucky. I had gone into my regular doctor over a year ago complaining of hypo symptoms & he told me I was fine. Meanwhile I kept getting sicker and sicker. It wasn't until I went to the ER for an asthma attack & I started telling the doc about how sick I've been that she decided to run the test for the thyroid....and sure enough, I was right. Quote Link to comment Share on other sites More sharing options...
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