Guest guest Posted July 15, 2007 Report Share Posted July 15, 2007 Shirl, First, how were you feeling before the decrease? That was a decrease of almost 1/2. By the looks of the second set of labs you were about right. Second, have you tried a natural desicated thyroid med like Armour? Synthroid is known to have all sorts of side effects including hair loss. Doesn't make any sence does it? Third, are you of an age where menopause could be a factor. Lots of hypo women are deficent in all hormones especially when they approach meno. I was on Synthroid or the like for 20 years. It was like I didn't take any med at all. I am now on Armour and feel great. Darla > > Hi Everyone I haven't been on here for quite a while. I have been > having a very hard time. To much to explain right now. Anyone have any > ideas on my June and July labs? For June they didn't do my Ft's don't > know why. T4 10.5 (4.5-12.0) T3 186 (85-205) TSH 0.041L (0.350-5.500) > Thyroid Peroxidase (TPO) Ab >1000H (0-34) Antithyroglobulin Ab 2762H (0- > 40). Endo put me on 75mgs of snythroid . July Ft3 499H (230-420) Ft4 1.8 > (0.7-1.8) TSH L<0.03 (0.50-6.00) TSI 282H % baseline <=125 He reduced > my snythroid to 37.5 My hair is falling out my eyes are still very > swollen, I'm depressed and tired but don't know if it's my levels or > stress. Can anyone help? Shirl > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 15, 2007 Report Share Posted July 15, 2007 Shirl, HOLY COW WOMAN! (pun intended!) Your antibodies are very high and from the sounds of it you are hyper. I say that in a very careful, walking on egg shells, kind of way because your blood work shows hyper and with your eyes being swollen my guess is you have Graves Disease. Forgive me if you have already posted that but you either have that or Hashimoto's or both. I think you are hyper, hyper, hyper with antibodies running amok! I wouldn't have you on Synthoid, I would have you on the ant-Graves disease medications which I know nothing about. I believe you have TOO much thyroid hormones and you need to have less. The only way for that to happen is to take the anti-thyroid medicines they give Graves's people. Now, with that said...I spent months listening to people tell me where my labs should be and that I was hypothyroid and I should take this medication or that medication and one was poison and one was the miracle cure. I just happen to be one of the odd ducks where my TSH is suppressed (almost all the time now) and my Free T3 and Free T4 are on the lower end of the normal scale. I actually had people screaming at me that I HAD to have my Free's in upper part of the range, believed it, tried to get it there and went totally hyper. I think I am a tiny bit hypo now but I feel a lot better than when I was hyper. Do you have the shakes or tremors? Heart palpitations, little hot flashes or inability to stand the heat? Are you gaining weight and hungry like crazy? Bone tired where every cell in your body just wants to sleep? This is how I felt when I went hyper. Oh, my hair was falling out then and now it is falling out like crazy. Pretty soon I am going to be bald if it doesn't stop! Dead serious because so much is coming out I have to go around my hair 4 times with a pony tail holder and I only use to go around twice. I am going to cut about 4 " off next week and hope it gets better or helps it some. I have pretty long brown hair but thin, thin, thin. Anyway, I ramble...do your research and I know it is very difficult to do when you feel like crap. Don't believe anyone or everything. Take it all and do what feels right for you. I know I need a tiny bit more thyroid medicine but not much and definetly not enough to get me to the high end of normal for my labs. I thought I was going to die there! That is where you are by the way. Each of us is different and there are some people who are very serious about their opinions of what works for them. It sure didn't work for me even if it worked for 90% of the thyroid people out there. It worries me that your doctor only ran regular T3 and T4 instead of Free T's. That is a sign that he may not know what he is doing because the Free T's are what is available to your cells and that is the truer picture. The TSH? Well, I don't put a lot of stock into TSH BUT it has value and yours screams hyper. Mine does too but I am NOT hyper at this point. I don't have any antibodies left because they have destroyed all they can and they are gone. If you have Hashimoto's then you could be doing the see-saw that the last few posts talked about where your thyroid sputters and works too well then doesn't work much then kicks in and over works then stops. It can be pure hell when that happens. If you are taking Synthroid or another Thyroid hormone then when your own thyroid kicks in you are getting too much. There isn't a lot you can do except get through it. I have read that the Synthroid can help calm the antibodies down so they don't do as much damage so quickly but then I have heard the opposite. If you have Graves then you don't need any extra thyroid medicine. You need a good doctor who knows what is going on. Do you know if you have Graves or Hashis? I hope I didn't confuse you. I get passionate about this because some pretty bad advise from a whole lot of folks (from what seemed like the best thyroid forums around) messed me up and I lost most of a year being sick and almost unable to function because I followed their advise. Don't follow mine, just listen and follow your own. Beware of your doctor too. Most of us have seen many, many doctors who don't have a clue and I have one of those right now. Long story. BJ knows, she had him for a doctor too. Please let us know how you are and more information if you have it and I apologize if you have posted it already but I can't seem to view the latest post. a > > Hi Everyone I haven't been on here for quite a while. I have been > having a very hard time. To much to explain right now. Anyone have any > ideas on my June and July labs? For June they didn't do my Ft's don't > know why. T4 10.5 (4.5-12.0) T3 186 (85-205) TSH 0.041L (0.350-5.500) > Thyroid Peroxidase (TPO) Ab >1000H (0-34) Antithyroglobulin Ab 2762H (0- > 40). Endo put me on 75mgs of snythroid . July Ft3 499H (230-420) Ft4 1.8 > (0.7-1.8) TSH L<0.03 (0.50-6.00) TSI 282H % baseline <=125 He reduced > my snythroid to 37.5 My hair is falling out my eyes are still very > swollen, I'm depressed and tired but don't know if it's my levels or > stress. Can anyone help? Shirl > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 15, 2007 Report Share Posted July 15, 2007 Shirl, I went back and read your old posts. I do have a life but it is Sunday afternoon and way too hot to do a darn thing. Honestly, I think there is a high likelihood you have Graves too. You have had a mess on your hands and I personally, as I said in the last post, don't think Free T3 and Free T4 should be as high as most people say they should be and it can be dangerous. For me, the best way to determine if you are hypo or hyper is your symptoms. Since you are on a beta-blocker that means you may be having heart palpitations and they are probably better because of the medicine. Are you shakey? My pulse and blood pressure were low but I shook like a wet dog and my heart was having several palpitations a minute. I didn't have many clues I was hyper and I will say it again, my Free T's were low normal. My TSH was .02 but this is my normal. Most folks said I couldn't have low Free T's and a suppressed TSH at the same time but my labs for the last 6 months have been the same over and over. I couldn't go by the lab results at all. My doctor (whom I loved and retired in April) asked me to consider the fact that possibly I was hyper. I nearly fell off the chair in disbelieve but I trusted her. I KNEW I was hypo. Shows me what I know. She asked me to stop my thyroid medicine for 7 days and see what happens. In 7 days I was substantially better. I was extremely skeptical but I did it and it worked. The one thing I learned in all of that, back in April, was I am not like most of the others on the thyroid groups and I want others to know that they may not be like all of the others on the thyroid groups. When I became sick (long story) my TSH was >75 and I had myxadema so badly I couldn't go up stairs or hold a pencil. I was 33 years old and thought I was dying. I could barely function and had made a suicide plan with my husband. He agreed to help me kill myself because the idiot doctors couldn't figure out what was wrong with me. I was so depressed and so tired of trying to live my life. It was very sad. Instead of taking me out into the dessert like my husband said he was doing he drove me to the emergency room but I didn't know because I was asleep. The emergency room doctor figured it out right away. I spent a few days in the hospital and then they sent me home. It took 9 months for my body to get my thyroid levels back to normal. I don't believe my body has ever gotten back to where it use to be. My point is that it takes a long time to get back from hypo (at least at that level) and it doesn't take long to get back from hyper. I am not talking about the being on the far ends of the spectrum, just a little high or a little low, enough to feel crappy and have your hair falling out but able to more or less function. Usually, for me, I can skip one or two doses of medicine and I notice that I feel better in a couple of days. What I am trying to say is that if you think you are hyper then you can skip your medication for a few days and see if there is a difference. If you are hypo you won't notice it much right away but hyper, you should notice in a few days. I can't imagine why your doctors took you off medicine for an entire month and that happened to me too. I was a disaster in 30 short days. A few days of experementing won't hurt much. A month can set you back a long time! I may not be very popular voicing my opinion here but that is all that it is, my opinion. I think you are hyper and the folks that are saying you are right were you should be are not right. But then, they are probably saying I am wrong so we have freedom of speech working right here and now. If I had labs like yours I would be a total disaster hyper mess. Do you feel like you are right where you should be? I agree with Darla in wondering how you felt during your June labs before they lowered your dose? From what I gathered your eyes have been an issue for several months. My eyes never got swollen but they were so sore and dry and I felt as if I was loosing my vision to a slight degree. My ears weren't working right either. Below I posted a few things I found on the web about your antibody tests. Read them carefully. The last sentence in the last paragraph says statistically you probably have Graves as well as Hashi's. Again, forgive me if you have already established this with us. I didn't see anything in your old posts except that you said they tested you for Graves but no results and that you do have Hashi's. Antithyroglobulin Antibodies (Anti-TG Ab) " The prevalence of Anti-TG Abs in thyroid autoimmune disease is significant (85 percent and 30 percent in Hashimito's thyroiditis and Graves' disease, respectively) but it is much lower than the prevalence of the Anti-TPO Abs. The diagnostic information provided by Anti-TPO assays is rarely improved upon by the addition of an Anti-TG determination. The growing trend is to adopt the anti-TPO Ab test as the front-line test for autoimmune disease and no longer to routinely use the anti-TG assay routinely for this purpose. " Antithyroid Peroxidase Antibody (Anti-TPO) " Anti-TPO Abs mediate antibody-dependent thyroid cell destruction; levels correlate with the active phase of the disease. Measurement of this autoantibody is useful for resolving the diagnostic dilemma presented by the apparent inconsistency between elevated TSH and normal free T4 results. Given abnormally elevated TSH and euthyroid T4 results, a positive anti-TPO Ab test provides strong evidence for early, subclinical autoimmune disease. This assay is also used to monitor response to immunotherapy, to identify at-risk individuals (with family history of thyroid disease), and as a predictor of postpartum thyroiditis. Elevated levels are found in virtually all cases of Hashimoto's thyroiditis and in approximately 85 percent of Graves' disease cases. " Hope that gives you more food for thought. Once again, only my humble opinion from my small nightmare. Rather, plural, nightmares... I wear a lot of " Life is Good " T-shirts by the way. a > > Hi Everyone I haven't been on here for quite a while. I have been > having a very hard time. To much to explain right now. Anyone have any > ideas on my June and July labs? For June they didn't do my Ft's don't > know why. T4 10.5 (4.5-12.0) T3 186 (85-205) TSH 0.041L (0.350-5.500) > Thyroid Peroxidase (TPO) Ab >1000H (0-34) Antithyroglobulin Ab 2762H (0- > 40). Endo put me on 75mgs of snythroid . July Ft3 499H (230-420) Ft4 1.8 > (0.7-1.8) TSH L<0.03 (0.50-6.00) TSI 282H % baseline <=125 He reduced > my snythroid to 37.5 My hair is falling out my eyes are still very > swollen, I'm depressed and tired but don't know if it's my levels or > stress. Can anyone help? Shirl > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 15, 2007 Report Share Posted July 15, 2007 > > > > Hi Everyone I haven't been on here for quite a while. I have been > > having a very hard time. To much to explain right now. Anyone have any > > ideas on my June and July labs? For June they didn't do my Ft's don't > > know why. T4 10.5 (4.5-12.0) T3 186 (85-205) TSH 0.041L (0.350- 5.500) > > Thyroid Peroxidase (TPO) Ab >1000H (0-34) Antithyroglobulin Ab 2762H (0- > > 40). Endo put me on 75mgs of snythroid . July Ft3 499H (230-420) Ft4 1.8 > > (0.7-1.8) TSH L<0.03 (0.50-6.00) TSI 282H % baseline <=125 He reduced > > my snythroid to 37.5 My hair is falling out my eyes are still very > > swollen, I'm depressed and tired but don't know if it's my levels or > > stress. Can anyone help? Shirl > > > Hey thanks for the help. I'm glad you found my old post. I just know I don't feel well my stomach feels like I have a rock in it. I have been in other thyroid groups and I think they get upset because I'm still learning about all of this thyroid stuff. I was 14yrs no problems at all I never knew thyroid could cause so many different problems. I think if my eyes weren't like this and it was just my thyroid either hypo or hyper I could handle this. I think right now I am a little hyper but for some reason having hypo symtoms. I deal with a huge deal of stress which is to much to go into. I didn't feel to great in June very very tired which seems to be on going and depressed cold when it was 90 out. I just don't feel good! I heard hashi's and Graves are the same just at didn't ends from each other don't know if that is true. I am worried about my antibodies being so high Endo didn't seem to be. Yes I am a little bit scared because I don't know what is going on. I'm gonna get my hair cut also it's long but maybe it will help. Thanks so much I can use some friends and support. Shirl Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 15, 2007 Report Share Posted July 15, 2007 > > > > Hi Everyone I haven't been on here for quite a while. I have been > > having a very hard time. To much to explain right now. Anyone have > any > > ideas on my June and July labs? For June they didn't do my Ft's don't > > know why. T4 10.5 (4.5-12.0) T3 186 (85-205) TSH 0.041L (0.350- 5.500) > > Thyroid Peroxidase (TPO) Ab >1000H (0-34) Antithyroglobulin Ab 2762H > (0- > > 40). Endo put me on 75mgs of snythroid . July Ft3 499H (230-420) Ft4 > 1.8 > > (0.7-1.8) TSH L<0.03 (0.50-6.00) TSI 282H % baseline <=125 He > reduced > > my snythroid to 37.5 My hair is falling out my eyes are still very > > swollen, I'm depressed and tired but don't know if it's my levels or > > stress. Can anyone help? Shirl > > Hi Darla, No I'm pass menapause I had my last daughter when I was 42 and after her I seemed to go straight threw it I was lucky not even the hot flashes. YEAH! I have six kids four girls 35,25,21,14 and two boys 17,19 like I said I didn't have any problems till Dec. Shirl > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 15, 2007 Report Share Posted July 15, 2007 Shirl, That is the exact same reason I joined this group because I was looking for answers and had hyper AND hypo symptoms. How can you be hyper and hypo at the same time??? How can you have a suppressed TSH and low/normal Free T's??? I have stabilized some I still don't feel right. I am considering going to a doctor that BJ goes to which is 2 1/2 hours one way. I am very tired of going to doctors. My other doctor that retired said that a hyperthyroid person will be the most tired person you ever meet. I had to agree. a > > Hey thanks for the help. I'm glad you found my old post. I just > know I don't feel well my stomach feels like I have a rock in it. I > have been in other thyroid groups and I think they get upset because > I'm still learning about all of this thyroid stuff. I was 14yrs no > problems at all I never knew thyroid could cause so many different > problems. I think if my eyes weren't like this and it was just my > thyroid either hypo or hyper I could handle this. I think right now I > am a little hyper but for some reason having hypo symtoms. I deal > with a huge deal of stress which is to much to go into. I didn't feel > to great in June very very tired which seems to be on going and > depressed cold when it was 90 out. I just don't feel good! I heard > hashi's and Graves are the same just at didn't ends from each other > don't know if that is true. I am worried about my antibodies being so > high Endo didn't seem to be. Yes I am a little bit scared because I > don't know what is going on. I'm gonna get my hair cut also it's long > but maybe it will help. Thanks so much I can use some friends and > support. Shirl > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 15, 2007 Report Share Posted July 15, 2007 > > Shirl, > That is the exact same reason I joined this group because I was > looking for answers and had hyper AND hypo symptoms. How can you be > hyper and hypo at the same time??? How can you have a suppressed TSH > and low/normal Free T's??? I have stabilized some I still don't feel > right. I am considering going to a doctor that BJ goes to which is 2 > 1/2 hours one way. I am very tired of going to doctors. > > My other doctor that retired said that a hyperthyroid person will be > the most tired person you ever meet. I had to agree. > > a > > > > > Hey thanks for the help. I'm glad you found my old post. I just > > know I don't feel well my stomach feels like I have a rock in it. I > > have been in other thyroid groups and I think they get upset because > > I'm still learning about all of this thyroid stuff. I was 14yrs no > > problems at all I never knew thyroid could cause so many different > > problems. I think if my eyes weren't like this and it was just my > > thyroid either hypo or hyper I could handle this. I think right now I > > am a little hyper but for some reason having hypo symtoms. I deal > > with a huge deal of stress which is to much to go into. I didn't feel > > to great in June very very tired which seems to be on going and > > depressed cold when it was 90 out. I just don't feel good! I heard > > hashi's and Graves are the same just at didn't ends from each other > > don't know if that is true. I am worried about my antibodies being so > > high Endo didn't seem to be. Yes I am a little bit scared because I > > don't know what is going on. I'm gonna get my hair cut also it's long > > but maybe it will help. Thanks so much I can use some friends and > > support. Shirl > > a, > I live in Columbus Ohio, someone gave me a name of a doctor at OSU her husbands eyes were like mine and he has made great progress. I know I'm tired of being tired. I still need to find someone who I feel is doing the right thing for me. I'm just not sure about my endo although he is supposed to be one of the best. I'll give him alittle time but I don't see him again until November and labs are eight weeks away. Shirl Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 3, 2009 Report Share Posted June 3, 2009 I really need help on this problem> I have been dealing with this crap to long and no real results. I have recently depvelope more pain and it can be pretty chronic. feet,calves, wrists/thumb area. Serious fatigue my spine is again getting that agitated feeling I just dont know what to do. I also when I use the massager on my feet and legs have a tingling feeling run thru to my toes. The pain is constant with some shooting stabing going on as well. Is anyone else having the same type of symtoms?? any help out there.... Deb Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 5, 2009 Report Share Posted June 5, 2009 I saw something the other day while standing in line at Walmart. It was in the section for diabetics....it was a cream/lotion and said it was to relieve the pain and numbness associated with diabetes. Do you all think it would be safe to try on our hands and feet? > > I also when I use the massager on my feet and legs have a tingling feeling run thru to my toes. The pain is constant with some shooting stabing going on as well. > > Is anyone else having the same type of symtoms?? any help out there.... > > Deb > > > > Deb, this sounds like neuropathy - poor nerve signals down the legs/arms. It is known to gradually occur when your carbohydrate metabolism is messed up, as it often is with CFS/FM. A low-carb diet can start to help in a few days. > > Plus, have you tried Vitamin B12? When I get my weekly injections regularly, my pain goes way down. The first injection after a break is almost unbearable pain and lasts for days, but by the third or fourth I barely feel it. > > Best wishes, > > Jayne > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2009 Report Share Posted June 9, 2009 Hi! Know what you went through. I had one done about 4 years ago. Most painful test I've ever had. They were testing both sides of my body - right leg & arm, left leg & arm. I only got through one side and was screaming and in tears and it seemed to me the, well I won't dignify the woman who did it by calling her a doctor, she actually appeared to be enjoying the level of pain I was in and would tell the tech to turn up the power each time I screamed. I finally insisted they stop I would not put myself through more pain. I was in excruciating pain before I went in and the pain level ratcheted up and stayed up for many months after this test. Of course since I could not finish the test it was deemed insufficient to determine what was causing the pain. Never, never again. I don't care what is wrong I will not do this type of test again. So take care of yourself and pamper yourself as much as you can until that pain subsides. It could all be Fibro, that's what my dr. says and apparently it can cause all types of nerve pain which is not related to anything else. Kimbal Quote Link to comment Share on other sites More sharing options...
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