Cytomel symptoms and conditions

Since on 0.175mcg of synthyroid after thyroidectomy and neck dissection two years ago, I have started to feel great fatigue? I can go to sleep at anytime during the afternoon. I also have a lethargy and malaise of the mind! If you mention this to the G.P., nurse or consultant you get vague looks!! Can anyone help?

I've been on levothyroxine 150mcg for about 3 months before that it was 100mcg and so on. I have gain lots of weight and tired all the time. depression also, headaches. I hate this gaining weight, sleepy all the time and depression is from gaining weight. I thought this med is to up boost my thryiode but it doesn't seem to be working. my dr. said I'm on the highest dose there is. I don't know what to do any more. I was thinking about taking myself off this but not sure what will happen if i do. I hope there is someone out there that might be able to let me know if they are going through the same things what they are doing and how they feel now.

Wow! Let me tell you my story: I was first diagnosed with HBP (170/140) during a high school sports physical in the beginning of 8th grade (I was about 14 years old). I was in top shape and a very healthy eater. I had probably (from what I remember) every test done to see what was the cause of this hypertension - and the only thing found was that my kidney's produce too much rennin (the hormone that increases BP). I was then put on Lisinopril 10mg. Everything continued well for about 6 years - I also stayed in shape and ate healthy. However, throughout those 6 years, I did notice my curly hair turning straight and my incredibly (can't do nothing with) thick hair started to thin and become style able. Now...I do know this is my fault, but in the past 2 years my healthy eating habits have slipped, I've gained weight and started smoking - plus have a sit down, don't move kind of job. However, about 1 year ago, I had a slight spike in my pressure and my doctor added a diuretic (HCTZ 12.5mg) to my lisinopril. Ok, that brought the pressure down and all seemed well. Then..... In December 2008, not long ago, I started not feeling well. Thinking I was sick, I went to the doctor's to find my blood pressure to be 190/140. Immediately, my does was increased to 30-12.5mg. That brought a quick drop in my BP down to 110/66 - I was so darn dizzy I could barely function. I was also but on short-term disability because all this caused me to be off work for so long. Unfortunately, when my dose was adjusted to 20-12.5mg and the dizziness stopped I went back to work. Now, I can't go back on S.T.D. for many, many weeks. And....... The past month has been complete HELL!! My hands (mainly fingers) and toes are almost always cold, I've been dieting for over a month and am struggling to lose weight, my hands and feet go numb more often than usual - I never used to find myself waking up in the middle of the night because of pins/needles feeling, my hair is thinner than ever and stick straight - I'm afraid I'm not going to have any left, I have UNBEARABLE headaches (sometimes all I want to do is sleep and sometimes, like tonight -it's 4:12am- I can't sleep), I have acne like a teenager - mind you, I never had more than 1 to 2 pimples at a time growing up, and that was rare (I was lucky)... Thank god for FMLA or I would have lost my job since I've spent so much time home since I thought all was good and went back to work. Only wish I could make a dollar again. Now to top it off...I was referred to a nephrologist (kidney specialist) who after seeing me only once for about 30min and reviewing blood work from the end of January (I had a high calcium level as well as some others that deal with the kidneys) wants to take away the diuretic (HCTZ) part of my medication (hopefully to reduce the calcium level) BUT DOUBLE MY MG OF LISINOPRIL. HE WANTS ME TO TAKE 20MG TWO TIMES A DAY. I was starting to think all these new symptoms that came on so quick were a result from the increase of lisinopril - now I think I'm sure. I'm not changing my medications until I can talk this over with my PCP - I'm going to ask we try a medication change. Does anyone have any suggestions? Or any suggestions why a 20-year-old has blood pressure as high as 190/140 with no family history of HBP or really any health problems? Any suggestions why the kidneys are producing too much rennin? Any meds that drop the pressure and we don't get headaches - I can live with cold limbs and numbness - it's the headaches that are rendering this 24-year-old helpless :(

After a year and a half of synthroid because of removal of my thyroid for cancer, I feel worse than I have ever felt in my life. Many tests have shown that there is no recurrence of the cancer. I would think I had fibromyalgia if it weren't that I read the blogs from other sufferers like me. I now take 150 mcg on most days. Some days I have to cut it down or skip it because I just cannot bear the body pain, weakness, brain fog, constant awakening in the night, severe cramping knee and leg pain, and muscle aches (there's no word strong enough to describe this pain -- 'aches' just doesn't do it). On the days I don't take synthroid I begin to feel like my old self. But my old self was 40 pounds thinner and losing. My old self walked three miles a day and hiked into the back country with my son. And my old self felt energetic and woke up every day with happy plans. Now I feel like an invalid. Some days I can barely walk. I cannot stand for longer than 5 minutes. I have tried cytomel, unithroid, and armour with varying problems. Synthroid is all that is left. Those of us who are dependent on this drug really need some good research on its effects. And we also need compassionate physicians who do not dismiss our pain and, it is not overdramatic to say, suffering.

Hello Ladies....I am 56 and diaged Hashimotos disease 3 years ago.At the moment on 112mcg of synthroid....dosage started off low and have gradually worked up....So angry with drs...was seeing endo, but moved and using family practice...so frustrated with weight gain approx 25lbs since diag. Also does the word sweat ....mmmm perspire for all us ladies, mean anything? I can't even wash dishes without breaking out in to a sweat...mmm beads of perspiration....Dry skin, I own stock in Aveeno....Also....does anyone get "boil type" skin eruptions in the nether region...butt, inner thighs etc? Does anyone or has anyone done any serious research on Iodine? I try to eat as well as I can, was doing Weight Watchers and gained weight do ya hear me? I am questioning my idodine intake or lack of....Presently take mulit vit with 150mcg. Considering uping it and dc ing my synthroid...cuz docs have been useless....eat less, (how much more less?) exercise more...I swim so much I look like a freaking prune....Any comments?

Welcome to my hell!

If I could choose to have my thyroid back, I take it and take my chances with the cancer. Well lets see... I take .300mcg of Synthroid and generally feel good only when I forget to take my medication for a couple of days. After about 3 days, I start feeling tired and will eventually start crashing for 10 to 12 hours at a time. OH! Ive heard that it takes weeks to level out, but I can feel the difference in about 3 days. Of course, the doctor says that's not possible, but then - he is holding my thyroid hostage.

I have gained 30 lbs. Have headaches frequently, get moody, AND now I get bloated when I eat. Im ready to try the Armour thing that Ive read about. Cytomel makes my heart race.

Im pretty sure that smoking helps! I read that it lowers your TSH levels.

Im just tired of feeling like sh_t all the time.

Hi,
I am 50 years old. I was diagnosed with as hypo at age 39. My doctor prescribed Synthroid at 25mcg and I have (proudly-ha!) worked my way up to 125mcg. I was always one of the "lucky ones" who could eat any and everything and my weight stayed the same. I am a busy mom of two and a first grade teacher, so the 33 lbs. I have gained since age 39 has not been due to diet changes or sitting around with a bag of chips in front of a TV all day. I also questioned my doctor about this and he just brushed it off. Well, I am tired of not feeling good about myself. My life is in good order except for my weight. I want someone to take this seriously. Should I see a specialist rather than my regular internist?
Wow! I think I just lost a little weight telling you great people about this!
jf

I've been taking levoxyl for 8 years now with mostly good success. My endo doctor recently upped my dose due to lab results (I think the test results were bad). Now I feel horrible. Headache, dizzy/lightheaded, blood pressure increased, tightness in throat, and muscle cramping. I've been to many specialists concerning the dizziness - everyone says I'm OK; cardiologist, ENT, and neurologist. The symptoms started a few weeks after the dose increase, and have worsened in the last week or two (about 2.5 months out).

I've been on 300 mg's of Lamcital since last December. Great drug, really helps my mania get under control. Lithium wasn't cutting it for me with my depression, in fact the side effects were making me even more depressed. My pdoc decided to try out Geodon (at 100 mg's). In the most part, it has been great. I feel alive and like myself again for the first time in years. But...
I wonder if making me so stable has also given my mind way to much time to over- analyze what I see and do. I see things out of the corner of my eye all of the time. I had something appear right in front of me the other day. I can no longer sleep past seven in the morning. And I have three facial twitches: my lower lip, the arc in my left eyebrow and the very top of my forehead where the first of my hair follicles start on my widow's peak. Those drive me nuts.
I am also on 40 mg's of Propranolol (Anderall) and Cytomel for my thyroid. For having such a severe case of BP, it's nice to be on so few medications. Geodon has been a lifesaver and has given me back my creativity and my marriage. I'll take seeing things and facial twitches any day for those.

I have just been switched to Synthroid (by my Endocrinologist) after being on Armour for 4 years. I have to tell all you out there that think "Armour" is the save all drug..and believe me I am not an advocate of Synthroid either because I have not been on it long enough to know what possible side effects I might have..however when I first started on Armour I felt like I did before I had been diagnosed with Hypothyroidism ..then about 1 yr ago I started to gain rate rapidly like 40lbs in 6 months feeling sluggish, off and on skin problems, puffy hands, face, feet,hives, pimples in the back of my head almost hive like,some hair loss that is noticeable to me as I have had very thick curly hair all my life now it is getting noticeably thin and It is making me very nervous...My Endo put me on .75 mcg Synthroid and .5mcg Cytomel which she calls a "controlled Armour"..Armour does not stay consistent with your T4's and T3 levels and that is what cause my thyroid to become suppressed and these are the symptoms I was experiencing...she also put me on Spironolactone which is a mild diuretic to lose the puffiness in my face,hands,and feet and so far so good...Like I stated earlier, I am not an advocate of Synthroid or Armour our any drug for that matter, I just want to find what is right for me and stick with it..and if Synthroid doesn't work for me, then I will try something else...Just remember one very important thing.."You" are the only one who knows how you feel and Dr's are not God they can't fix everyone that is why its very important to read about your disease and find out what things might work for you..I suggest getting this book I bought that was recommended to me by my Endocrinologist called "Screaming to be Heard" Hormone connections women suspect and doctors still ignore written by Elizabeth Lee Vliet, MD...its a fabulous book and I am sure all you women can relate to this book...its all about us....Most important thing is to stay healthy eat a well balance diet and exercise..also find out about the foods that only worsen thyroid problems...

I have been on Levoxyl 125 mcg for about two months after my thyroid was "killed" with the radioactive pill. Ever since I have been on this medication, I have constant headaches and feel sick on my stomach all the time. I had to go to the ER the past week because of the intense vomiting. The doctors tell me it's not related to my thyroid or the medication. How can this be? I didn't feel this bad when I was hyperactive thyroid. My wife has had to take care of our 18 month old all by herself ever since I have been taking this medicine. I feel like I am missing out on my life! This is terrible!!

I've been on Synthroid for 8 months after gaining 10 pounds in two months. The symptoms started to appear when my Mom was very ill. Doctor said it was caused by stress and started me on 25 mcg of Synthroid. My reading at that time was 5.56. I had blood work done every 4 weeks,and the numbers are going down (1.8 last reading), but so is the quantity of my hair, which I see all over my white tile. My weight hasn't budged even though I am dieting. My doctor upped me to 100 mcgs. My blood work is not good - low white count, low lymphocytes, borderline anemic. Mom died, and I didn't get any better. I feel sick all the time and it's difficult for my husband to understand how bad I feel. I've tried to get my doctor to prescrive Armour, but he doesn't even return my phone calls. When I see him in the office, he keeps telling me it takes time. I hate living this way and want to stop the pills completely.

I have been on Synthroid since about 1995. I had a thyroidectomy and do not have a thyroid anymore. I have been on 0.175 mcg for about 10 years and did not have any side effects except for fatigue and a little depression.Everything else was pretty good. My TSH is registering low so my doctor moved me to 0.1 mcg of Synthroid and 5 micrograms of Cytomel. I took this for about three weeks and for the last 1.5 weeks have had awful headaches and the dryest eyes ever. Something, I have not experienced before. My doctor keeps saying he wants to help me but does not listen to
any of my symptoms. I actually pulled off the symptoms from the list online of hypothyroidism and have 15 out of about 20. I am wondering why I felt so much better on the higher dose than this low dose. Can anyone releate. I am starting to think maybe my body is not processing this right. The funny thing is is that my lab work came back with normal results today, which means my doc is probably going to keep me where I am and I feel the worst I have felt in ten years.

I have been on synthroid for about 3 yrs. I am considered subclinical (can't find hypothyroidism with blood test- normal range).
Grant it, the medicine took away the almost angina pain and loss of breath. However, my body seems to have deteriated structurally. I have tremendous lower back pain, that worsened. I have been in pain every day since. I starve, (veggies - then dinner). It's been very, very difficult. Always looking for help.I'm hoping that a natural hormone will change this, I know my husband will be glad; he won't have to hear me cry anymore.

I HAVE BEEN TAKING LEVOXYL FOR 22YRS AND I FEEL LIKE I CAN NEVER GET SLEEP,I TAKE MY PILL IN THE MORNING AND CAN'T SLEEP ALL NITE AND AM TIRED OF IT,I WISH THEY HAD AN ALTERNATIVE.THAT WAY I CAN SLEEP AND NOT BE DEPRESSED ALL THE TIME

I was born without a thyroid gland so I can't compare the way I feel now to the way I would've felt with a thyroid. I've been on Synthroid my entire life (22 years), and I'm up to 112 mcg now. I am very skinny (5'5", 104 lbs) and feel constantly fatigued no matter how many hours I sleep, what I eat, and how much exercise I get. I periodically get pain in my hip joints, heart palpitations, and intense mood swings. My thoughts race but I have very little physical energy. I feel restless and gloomy almost all the time for absolutely no good reason. My doctor tells me I'm depressed but I honestly have no reason to be depressed and I wish she would see it as a symptom instead of a diagnosis. I graduated from a good college, I've got a job I like, I have friends, I enjoy life and my hobbies, yet I feel overwhelmingly sad. This does not seem like depression to me.

I find that after I do aerobics I get a tightness in my chest, which makes me worry about my heart, but again my doctor doesn't seem to think this is cause for concern. I have been irritable/fatigued for YEARS and I suspect I'll feel this way for the rest of my life. The worst of it started when I hit 16 years old and started the 112 mcg. My tests are always normal and it frustrates me that my doctor disregards my symptoms. I've tried other doctors, but they always send me away with my 'normal' test results. Can anybody help?

I was diagnosed with hypothyroidism in April of this year (2007) kind of by accident through a routine checkup. I had gained a bit of weight over the past two years, but that was really my only symptom. I was begun on 75 mcg of a generic brand of Synthroid, levothyroxine. Since I began this medication, I have rapidly gained another 15 pounds despite a 1,000 calorie per day diet. I retain fluid horribly. My ankles, wrists, hands and face swell daily. My muscles ache, especially my legs, upon walking across a room. I'm fatigued, short of breath. My LDL cholesterol level has skyrocketed in only three months and now I'm being told I need to be on a statin drug. I cry frequently and feel uncharacteristically anxious and irritable, but this could be due to the frustration I am experiencing with the loss of my sense of well-being. In essence, I felt much better before being placed on the medication. I may, in fact, discontinue the medication totally and see if over time I begin to feel better. Like so many other stories I'm hearing, my doctor seems totally unconcerned.

i've been on synthroid for 9 years. started at some low dose and gradually went up to112 mg. get extreme itching all day everyday if i don't take allegra for that.not a rash just itching. that doesn't bother me as much as the fatique. every joint in my body aches all the time. sure there are better days but fo rthe most part it's bad. tried physical therapy and chiripratic care but no avail. they ended my sessions. my legs get sooo weak and my feet burn lower back really aches. sometimes muscle cramps. i'm very negative towards my loving family and it hurts me to do so. can't seem to keep upbeat. soo tired all the time.
is it the syntroid? i used to be very energenic and a doer. now i have spurts of activity in the morning , but then i just can't get motivated. help me any suggestions?

I think what a lot of people are posting here are more side effects of thyroid conditions rather than side effects of thyroid medication. After my RAI treatment I started on a generic brand of levothyroxine. I even got my doctor to let me try Armour Thyroid since many people do well with it rather than Synthroid. Armour didn't work well for me, but it definitely is the only way to go for some people. After months of misery, things finally smoothed out. I was a royal pain in the butt to my doctor because I questioned everything. The biggest side effect for me going from hyper to hypo was edema. A clinical name for water retention. It wasn't so much the bloated feeling that bugged me. It was the pain in my hands and feet from the water retention. I have never, ever had a problem with carpal tunnel syptoms even though I have always used my hands a lot for work and I play the guitar. I had to add a small dose of dieuretic to control the edema and relieve the hand and feet pain. Sometimes it does flair up depending upon what I eat and how much I sweat, but that's what goes along with this type of illness. It's not just a magic pill that makes you feel "back to normal". You have to be demanding of your doctor to try other things to get you to feel right. You even have to pay attention to how you feel at different times of the year to figure out how to adjust what you take, eat, or do to feel better. I have noticed that with all things remaining constant, how I feel in terms of energy level and edema is related to the season. The body is weird that way. I still have side effects from the treatment from time to time, but I finally figured out what seems to work best for me. Maybe things could change over time, but I've learned that medicine just doesn't have a black and white treatment plan that works the same for everyone for thyroid related conditions. To sum it up, question everything your doctor tells you, demand to try things that you think would help you feel right, pay attention to what your body is telling you and adjust, and fire your doctor if they treat thyroid problems as black and white. Your doctor is not the one suffering from the condition, you are. It's your life and there's nothing wrong with being demanding about wanting to feel right.

Those of you that are feeling terrible side effects with synthroid, check out (with you doctor of course) adding T3 (cytomel) to your medications. Synthroid is T4 which some doctors claim that's all you need but often that is not the case. With sythroid alone I get very sick.

I have been talking Levoxyl for years. I had my whole thyroid
removed in 99 with a precancerous nodule. For years
I have had trouble with concentration -- always feeling
kind of "out of it," "zombie -like," but just since about
September I have felt very bad. I have noticed this bad
feeling begins bout an hour or so after I take
my med.

I began in Sept on 88 mcg, then went to 100mcg,
then to 112, and then to 125. I cut myself back to 112
because with 125 I was so so so tired, and cried with
strange anxiety every day. Since cutting back to 112, I don't feel a lot better. During the day I feel to tired to do anything,
and I have lost my interest, personality, and sense-of-humor.
But, on days when I completely skip my med. I feel soo
good, but I can't do that two days in a row b/c then I feel
worse. Also, at my last dentist visit, I had 3 cavities and
I brush my teeth twice a day, every day.

I have another apt. tomorrow (with my specialist).
I hope he can fix me.
I have suggested Armour and Cytomel many times,
but he always says "this is rare that anyone needs to take
these" I hate feeling this way. I want to feel like everyone
else so bad, I just feel like I never will. It is very debilitating.
I have recently graduated from college and I feel like
an old woman -- too tired and bad to go after my career
goals.

Write back anyone that feels this way too.

Not sure if this is side effect. Had Thyroid Cancer, Had radiation. became hypoparathroid. Taking large doses of calcium 7200 mg. daily. Taking 200 mcq Synthroid daily. Still hypocalcemic, just increased calcium to 9000 mg. daily. Having heart palpatations so severely, my head feels full. It lasts approximately 1 minute with each episode, skin is really dry, even peeling, leg and feet cramping, finger, hand and arms have episodes of tingling, and hair texture has changed.Doctor has tried to regulate calcium and synthroid for almost 2 years now. Is this normal??

I have taken Levoxyl for over 2 years and am still having big problems with hair loss. I have complained to my doctor numerous times, but she always says that it is the thyroid condition not the drug (I had no problems wtih hair loss until I started taking Levoxyl). I can't believe there are so many people with this problem. I thought I was just sensitive.

Has anyone found a solution? I hate going off it, because before taking Levoxyl, I was always tired.

i have been taking neurontin for about 3 or 4 years now. i am also on several other meds. verapamil 120mg bid,cytomel 25mg 1/2 tab qd,valium 5 mg 1 tab tid,zoloft 100mg 2 tab qd, levoxyl 0.125mg qd and imertrex 100mg at start of migraine plus more later if needed(which i won't do) recently i have been having a burning tounge. my dr. says it could be one of my meds.'turning against me'. i also urinate all of the time. i can't go anywhere! i also can't urinate if i take almost any psytrophic drugs because i can't release it from my bladder. i have been schizo-affective for many years now. only within the last year have the meds.started to bother me. could the neurontin be the cause of my burning tounge and frequent urination? i already know which meds. that i use to be on that caused the inability to release urine from my bladder. i don't take those anymore? any help would be appreciated. my doctors are stumped. oh yes , my kidneys and bladder are ok i had them checked out by specialist. sorry. my neurontin is 300mg qd.