Thyroid :: Reverse T3 - Any Improvement In Symptoms?
Jun 27, 2013
just wondering if anyone here has a reverse T3 problem and if so, how long did it take before you saw an improvement in symptoms after taking medication?
View 3 Repliesjust wondering if anyone here has a reverse T3 problem and if so, how long did it take before you saw an improvement in symptoms after taking medication?
View 3 RepliesHere are my test results, should I seek treatment? My other thyroid labs look okay. Not sure what to think....
RT3 22.5 (9.2-24.1)
FT3 3.6 (2.2-4.4)
Ratio 16
Also any thoughts on these antibody tests?
TPO 15 (0-34)
Thyroglobulin antibodies < 1 (0-.9)
TSI 42 (0-139)
Also for reference, here are my thyroid labs and b-12 Vit D labs. I've started to supplement b-12 and vit d. But should I ask for anything else? Any other meds or tests?
TSH 1.32 (.45-4.5)
FT4 1.24 (.82-1.77)
FT3 3.4 (2.0-4.4)
B-12 267 (211-946)
D 37.4 (30-100)
Symptoms, fatigue, muscle and joint pain and stiffness, numbness in my hands, cold all the time, low temperature, low bp, no sex drive, losing my eyebrows, low metabolism, have trouble losing weight or gain weight for no reason, depressed mood, easily irritable, can't handle stress or I don't handle stress well, high cholesterol despite healthy diet...I'm sure there are others but these are the worst ones..
I'm just so confused... It appears that it's not my thyroid although, thyroid explains alot of my symptoms and I have a strong family history. Just not sure where to go from here. It's been suggested on another board that I have adrenal fatigue, but I'm not sure what to think about that either. Trying to get some ideas.
I was recently diagnosed with a T3 Reverse High of 35 ng/dl and the range should be 8-25. This test was done by an Integrated Internal Medicine Dr. that is insisting that most of my symptoms like ringing in the head, twitches in my legs or sometimes throughout my body, brain fog and fatigue could be coming from that number being high. I brought this test to two Endocrinologists that refuse to even look at the number saying that it has noting to do with how I feel and because all my other numbers are fine, I shouldn't worry about that number being high. Currently I am taking Synthroid 112 mcg and the Integrated Dr. suggested I switch to Nature Thyroid 97.5 mg. and on the third day of taking this, I felt like a drug addict without their drug and chickened out and went back to Synthroid again. Does anyone have any suggestions on what to do and if there is another medication I can take together with Synthroid to lower the T3 Reverse?
View 1 RepliesThis is my lab results:
TSH = 2.91 (0.45 - 4.5)
T4 = 3.0 (4.5 - 12.0) -- low
Free T4 = 1.05 (0.82 - 1.77)
Free T3 = 2.6 (2.0 - 4.4)
Rev T3 = 8.2 (9.2 - 24.1)
I have all the hypothyroidism symptoms like fatigue, cold hands & feet, losing hair & eyebrow, brain fog. I was tested for thyroid antibodies (TBA & TPO), and they are all negative. Recently I have increased my carbs intake and felt much better. I believe I also have adrenal fatigue as my daily cortisol cycle are inverted so I wake up several times during sleep.
My question is do I have subclinical hypothyroidism? Why my reverse T3 is low? Or I have iodide deficiency?
TSH and free T4 were in range and free T3 was high at 4.35. I have some symptoms of hyperthyroid. Heat intolerance, anxiety, stress, hypoglycemia but no weight loss. I attribute the no weight loss to eating all the time to keep my blood sugar from getting to low and I have actually gained some weight over the last few years. I started getting these symptoms 5 years ago and they can kind of come and go but the heat intolerance is always there. If I go out in the heat and work it just zaps my energy.
Also my red counts are just a tad high and liver enzymes are always elevated and in the 70-80 ranged. Non drinker and non smoker.
I am 33 years old and have just been diagnosed with having OA Thyroid, but have symptoms of UA Thyroid. I have always struggled with my weight and bloating (from having food intolerances), but have recently gained a lot more weight than normal, despite eating sensibly, walking everywhere (as I don't drive) and swimming.
I have days where I feel really thirsty and have to drink lots and lots of water, unable to concentrate, have a husky voice and morning coughing/ gunk on my chest, rapid heart rate, anxiety, feel achey and exhausted all the time. I also have Fibromyalgia (was diagnosed in 2005). I used to work full time for 17 years, but recently had to reduce my hours to part time, where I constantly felt ill...and I have now had to leave work altogether.
What I don't understand is how I can have the symptoms of UA but be OA. The Doctor has prescribed me 5mg of Carbimazole to take 3 times a day. No Propranolol yet, but I have taken these before as I used to suffer with high blood pressure.
I am worried that I am going to gain even more weight on this medication, when I have already gone up nearly two dress sizes from being so ill. Is this medication usually only given for people with OA? Will the effects be reversed in my case, where I have UA? Are there many of you out there who have the same symptoms as me and who are taking this medication and if so, what has happened in your situation?
i had 2 cold nodules in my thyroid and had a total Thyroid lobectomy on 16 sep (8 days ago) and still waiting for the results if the they were benign or malignant so that i start take the hormone replacement in case if benign or start to go into 6 weeks hypo in preparation for the RAI treatment in case if malignant problem is, i fear the result will take more days to finish, and my body is completely without thyroxine now if benign than this wait & deprivation was pointless, and i fear i will need many weeks to fix the damage the hyop state will impose on me so my question is, when will the hypo symptoms start to show in my case (no thyroid at all) ? considering my TSH levels were normal at 2 before the surgery i'm feeling really anxious about this whole thing, and i need your knowledge, i can't even get in touch with my doctor before tomorrow.
View 1 RepliesI'm 30 yrs old and i have a left-eye amblyopia. I undergone squint surgery last year's August. My eye barely improve and i really feel very down because i was expecting my eye will be at last okay but it didn't. The surgeon said it will require my right eye (which is okay) if i want further improvement in my left eye. I want to know what's will be the downside once my right eye get operated. Please help! My surgeon doesn't talk too much aside from telling me what else i need to do. I really wanted my left eye to be aligned correctly as greatly as possible. I suffered too much.
View 2 RepliesJust wondering how long it took people to get any kind of improvement in their colitis symptoms with renicade. I had my first loading dose today and the dr said it would take some time to see any kind of result.
Also did you experience any itching or headaches after? About two hours after i started expiencing itchy eyes and started to get a headache, now 8 hrs after the infusion finished my hands, arms and face are itchy. My eyes are still itchy and my headache is still there.
I had an allergic reaction to 6mp but it was far more intense itching than this.
I've reluctantly started Zoloft (SSRI antidepressant), being encouraged to do so by my GP due to the depression of diagnosis and the possibility I also have fibromyalgia.
(Pain isn't just limited to joints and fatigue is crippling) ie: I've slept 18 hours of the last 24 and still so very tired.
I'm having awful start up side effects which I understand will pass and understand there will be no benefit until 4-8 weeks, if at all.
I've tried Lexapro a while back with no real success.
Has anyone had any improvement at any level with ADs? I really hate mucking around with my brain chemistry.
I was virtually deaf in one ear and very little hearing in the other ear, have worn hearing aids for 25 years. Recently (all happened so quickly, within 6 weeks) got diagnosed with Otosclerosis in both ears. 6 weeks after seeing doctor, i had the op. I had a stapedectomy/stapedotomy on 04/01/2016. Noticed a faint improvement in hearing when lying on the ward after the op, could faintly hear trolleys being moved about. But nothing drastic...... I've had dizziness, (not room spinning dizziness) which now only remains if i read, do jigsaws, scan shop shelves from side to side etc, weird! I've been through the heart pulsating, creaking, the rain dripping onto a metal plate sound etc.
I've had no real explanation of what to expect, i didn't really ask the surgeon any questions as i wasn't sure what would happen after and was unaware i'd have so many unanswered questions come up.
I assumed, and read some on the internet, and was told by a friend who'd had it done, that once the packing was removed, i'd be able to hear. Had packing removed 6 days ago, i'd built myself up SO much, that i stood and sobbed when i still couldn't hear! Surgeon looked a bit puzzled, but he said he wasn't worried at this point and to see him again in 6 weeks and that it'd be fluid behind my ear. He said i need to have some popping before i'll hear.
So, here i am now, with no change in my hearing for the last 6 days. I'm sure when i swallow, i sound as if fluid is in there? I also get like a thunder noise mainly in the morning when i wake up and my throat moves. But what's worrying me most after reading up on the internet again, is when i put headphones on, i can hear the music, (have to have it on loud to hear it), but the loud thumps/beats in the music make my ear crackle like a loose wire on a radio. I read last night that this is because the op hasn't worked and the prosthesis needs tightening/shortening/revising. But then on the other hand i've read that this may be normal?
If i go to do a burp movement when i have music in the headphones, i get a millisecond of a loud noise, but then it goes again as my throat can't seem to hold the noise open if you get what i mean. I have soooo many questions but don't want to bore you with them, maybe later. So, should i be hearing by now, is the crackling loose wire sound normal, and if you have any other advice that might stop me worrying please. I'm just sitting waiting day by day thinking today might be the day that i hear.
After my dad who is 85 was diagnosed with Osteoporosis, I started doing some research. Most if not all these meds have so many side effects and are even thought to cause further damage to the bone. There are a lot of doctors starting to promote healthy diet changes as opposed to taking meds. The old theory that milk and dairy promotes bone health is now thought to be a scam funded with trillions of dollars by the dairy industry. So I'm curious, has anyone tried a plant based or starch based diet to reduce symptoms or even reverse their Osteoporosis?
View 1 RepliesThe doctor prescribed me Trimethoprim 300 Mg for 7 days. I am having it since last 3 days now but nothing has improved.
The dipstick test showed blood in my urine...though I have been having some other health issues as well...but this medicine was prescribed when the urine sample had blood.
I am worried that I might be having the wrong medicine, as nothing is improving.
I need to understand, how long should I wait for the improvement signs. I am worried. I feel dizzy after this medicine, and my health is getting worse.
I have taking Amiodarone 200mg for about 35 days for my AF .However, I still get irregular occasional especially after taking hot food. The improvement to my condition is marginal. Can anyone advise me if I should continue with Amiodarone. Also,I have been on warfarin for the past 3 years . Due to the interaction of Amiodarone with Warfarin, my doctor has reduced my Warfarin dosage from 4.5 to 3.5 to maintain my INR between 2 to 3.
View 7 RepliesThe researchers say a certain way to eat fruit can reverse diabetes Read Here ....
View 2 RepliesAny solution that can possibly reverse the diabetes. How can I prove this, I also suffered from diabetes for over 15 years with blood sugar that sometimes rose to 400,then in 2015,I discovered a natural herbal supplement which I had to mix with lime. In less than 2 months of usage I began to see significant positive changes which ultimately led to me being diabetes free.
View 1 RepliesI m diagnosed neurocysticercosis on left optic nerve n m having blurring of vision.
Drs have put me on steroids past one year ,but no Improvement is seen.
My Surgery was July 7th (3 months back) to repair torn ligaments and tendons and also to align my ankle. I have a metal plate on one side and 6 screws on the other. I have been going to PT 3x a week for the last month and I feel like I am not seeing any kind of improvement. They keep telling me that I am making progress and I am walking and wearing sneakers but the pain is and has been so bad. I am also back at work with some limited restrictions. Standing is painful and I find I have to shift my weight around a lot. I am getting to a point where I am always in pain and I don't know what to do. I can't really talk to my family anymore cause they just dismiss me...pretty much since I started walking in two shoes they figure I must be well and I don't know how to tell them that I don't feel well. I still have a lot of swelling but they say that it is all normal. I feel like I really shouldn't be back to work but I had no choice. How do I deal with the chronic pain all the time...I can't keep popping pain meds cause I just fall right to sleep and I need to be able to function at work and not be in so much pain that I am just angry all the time. Am I foolish to think that I will be better soon?
View 6 RepliesAfter what feels like a lifetime of side effects and then nothing, I think things are looking up. Had a great day today, and I haven't said that in a while, particularly on a Monday. I have counted hours, days and weeks. Like everyone else I have questioned my dose and the medication on many occasions and felt like giving up a million times. To everyone who encouraged me to keep going and give it time, thank you, because it does get better in its own good time. I have no doubt that there will be ups and downs to come, but hey, I think I'm going to make it! Yes it really has taken 20 mg this long to start to work on my head , so keep at it during the early weeks. I hope everyone is letting a little more light in every day.
View 50 RepliesJust about every time I bend my neck forward I have pain that extends upward to the base of my skull and tingling up my head to envelope mostly the upper left side of my head. I am guessing I am having a relapse. I was unable to see my neurologist as its impossible to get in to see him for months. So a local clinic doctor gave me prednisone. So far it's the only thing helping. I have already been diagnosed with Ms but the only thing I have found is people speaking of Lhermitte's that run down the spine. Do I need a new MRI?
View 14 RepliesWhen I received my diagnosis a month or so ago, I spent a lot of time reading this forum and learned an overwhelming amount of information. One post that stood out was someone who had managed to somewhat reverse their fusion with a baking soda spray treatment. I can't find that post, or remember what thread it was posted on, and I'm hoping someone can point me in the right direction. If there is anyone else who has managed to reverse their fusion.
View 4 Replies