Graves disease and anger

Common Questions and Answers about Graves disease and anger

graves-disease

Can you have graves disease so bad that it would seem like bipolar and I thought Graves disease was an overactive thyroid, so how can you be hypro?
I have a Q about graves disease , my husband was diagnosed with it a few yrs ago . he had his thyroid killed wuth radiation and is on synthroid . i noticed a comment in a post earlier about graves rage , just wanting to know what this means . my husband has very crazy mood swings , blows up easily ( not as bad as before his diagnosis ) can act a little , okay alot .erratic at times !!
i recently put a post on a different forum and someone mentioned graves disease. im a 21 year old guy. i do suffer from depression and ocd. i just wanna throw that out there before i start. but im a very irritable person. i get mad at people sometimes and wonder why im so angry. my anger is on a whole other level. i get so mad my blood pressure goes up. some other symptoms are i cant get to sleep good at night. i get very wrestless and pace the floor. i sweat way more than i should.
Two years ago he was diagnosed with Hashimotos disease and was on synthroid for treatment. This past December he was diagnosed as having graves disease AS well. Currently, he is being treated for the graves. Being in stage 5 puberty, and having both diseases, he is a train wreck. He is beyond moody, gets angry at the drop of a hat, has memory loss, depression, anxiety, hyper, tired, attention problems, acts out, and the list goes on.
So first off i'd like to state that i have graves disease' and i get the really bad mood swings. For the past 2 years i've been getting angry and frustrated over the littlest things' sometimes i get so angry i break things, punch walls, bang my head on the wall or physically hurt myself. I can't really say what triggers my anger because, even little things people say make me snap; i get frustrated if i can't do something, i'm the worst when people accuse me of something or accuse me of lieing.
Maybe both of you need to come to this website to see what patients and their care givers go through. In the past year sinc I found out about my Graves disease and then thyca. My personality has changes...some for the better. a lot for the worse. My motivation to do simple things like keep a budge it just too hard for me to focus on. However, as a thyca survivor, I am a little more tolerant of some idiot drives on I-95 in Northe VA.
My name is Bec I am 35 year old Australian who is living and was working here until I got diagnosed with Graves disease 1.5 years ago. The foreign doctors here are well let's just say c***, so I fly to Bangkok every 3 months to see an Endo at Bumrungrad hospital.
i was diagnosed with graves disease in may of 2006 when i was 24, i had went into a thyroid storm 2 days in a roll before they figured out it was my thyroid so now i also have heart problems.I was planning on surgery to remove my thyroid but i found out i was pregnant so it got delayed.In 2009 i took the radioactive pill to kill it off and 6 months later my levels bottomed out in the process of all this i went from weighing 141lbs in 2006 to 239lbs in 2009.
I'll join the group that has told you that this is a very common symptom of Graves'. I've heard it called "Graves' rage". Many symptoms "cross over" and are symptoms of both hypo and hyper. While it's more usual to lose weight when hyper and gain when hypo, some people lose or gain either way. You might ask your doctor about a beta blocker for your tachycardia. Beta blockers will slow your HR.
based on your labs, you don't appear to have graves disease. graves disease is when your tsh is low and your ft3 and/or ft4 are high. however, you may have hashimotos (slow destruction of thyroid that leads to overt hypothyroidism). ask the docs to run all the antibodies. that'll give you the info you need.
get yr FT3, FT4 , TSH and a TSI test done to check for Graves Disease. I too...blamed my symptoms on the Menopause and I am now 6 years post menopause.
Twitches not caused by disease or disorders - Often affecting the eyelids, calf, or thumb. Normal and quite common, often triggered by stress or anxiety. A diet deficiency, Drug overdose (caffeine), Drug side effect (such as diuretics, corticosteroids and estrogens) and Exercise. Symptoms suggestive of a neurological cause of fasciculation's include: Wasting of muscle, Weakness (both could be thyroid) and Other findings of nerve dysfunction.
He has a pretty tough case of acne but not on meds for it. He is very outgoing and in ROTC and loves it and the people he lives with. I feel pretty confident that he is telling me everything as he is the one that wants answers. I had Graves Disease at 25 and I remember feeling like I was going to loose my mind at times but everything I read says it is a mostly female disorder. Could this be happening to him also? What about testosterone levels?
Hi, I am a new/old person female-54. I am in the pits of dispare and I have no where else to turn. This is my last stop. I have several Doctors that I see regularly, a headDoc for Bipolar and and ENDO for Graves and my GYN who never looks UP far enough to see if I am "crazy" or not but ultimately he has been the one to DX me over the years with serious Thyroid issues. I guess because he doesn't see me ALL THE TIME and he noticed right away that I had lost 45 lbs <grin>.
Have you been diagnosed with either Graves Disease or Hashimoto's? Are you being treated for the Cushing's and are there plans to remove the adrenal tumor? I'm not familiar with hirschprung's, but I know it's an intestinal blockage that requires surgical removal of a portion of the intestine and the colon. Are there plans to have this surgery?
successful in treatment of my particular type of Graves disease. Those odds aren't good enough for me and he didn't recommend it anyways. I have nodules, one thats grown 1 mm in 3 months. the others haven't, but there is always that chance. RAI doesn't kill off the nodules, leaving them to grow, so I'm going for a TT. I've talked to my hubby about it and he supports me in it. (I think he wants my sex drive back..ha ha). I have really good insurance right now that will cover surgery 100%.
The literature also states that before hyperthyroidism was recognized as a disease, many patients with Graves' disease spent their days in asylums. Emotional changes in Graves' disease are primarily caused by the effects of excess thyroid hormone on thyroid receptors in the brain. Emotional disturbances may also result from nutrient deficiencies and exhaustion. Changes in GD caused by hormonal imbalances also weaken the ability to cope with stress.
Well ive read your post, and you sound like ive lived on and off for the last 11 years, ive got graves disease, and i had the same problems, as you, in other words i was fobbed off as having anxiety and depression, even though i had serious tachycardia, were i thought i was having an heart attack. I have just had my second thyroid surgery, due to this hell off a disease, I have never had holistic or natural remedy to treat graves, and dont know if there is one?
I had vision correction surgery 6 years prior and had perfect 20/20 vision until this quack - I was fine even w/ hashi prior to this staying on a lower dose - this jerk wanted me less than 2 tsh - I was bedridden for days, sick in many ways and lost my great vision in a matter of months - anyhow - after 6 years of egotistical doctors I now have a wonderful internist who is very knowledgable about all forms of thyroid disease and attends conferences frequently about these issues - I stay on the
I wouldn't be surprised if the tests are positive as I have lots of allergies, Celiac (inability to digest gluten), sever milk protein intolerance, and some kind of crazy thing going on with visiual auras (some or all of these are autoimmune). I really feel for you if you really do have RA! That is one mean disease and the drugs used to slow down it's effects mean serious business. I pray that your aches and pains end up being just thyroid as that can be treated far easier.
) What better doctor to have than one who is also a patient, they seem to understand the disease much better. So many times I've heard and read doctors say that thyroid disease is 'easy to treat' and oh, if that were true....but we all know that's a myth. Anyway, in answer to your question about the cortisol test, no I did not have a 24 hour cortisol test run. I had the controversial saliva testing done, taking four samples at 8AM, 12PM, 4PM and 8PM.
As a teenager being prayed for depression and for this disease and to be protected I WAS right with God, and he let horrible things happen to me. I did everything, I looked to him and trusted him, and awful things happened to me, not at church but outside of church, so dont say that if you're right w/ him he won't let bad things happen, thats pure bull**it and lies.
I was also told that some do choose to abort because of the drugs and because of the hyperthyroid and graves. I have to take the propranolol because if i don't my heart rate will be in the 120's. Without the propranolol I will have heart problems. Without the methimazole well thats is just dangerous. So I have no choice than to take them. I could take the ptu. but i'll still be on the propranolol which is only giving if it has to be becuase it is not recommended for pregnant women.
I have had heart palps both hyper and hypo and like you, thought it was from being hyper as I was dx with Graves and Hyperthyroidism before RAI 7 months ago. I now know that heart palps comes with BOTH lol.
Hey girl I was on thyroid meds because of graves disease for 18 mths. I went to a specialist and he took me off meds and said no one should take them longer than 18 mths unless their thyroid had been burnt out. Mine is bk to normal now and I have lost 20 lbs.
Welcome to Part 6! Please make yourself at home!
So I dug up some more info that I wanna share ... in case you are dying of curiousity. Or need more info like I do. ---------------------------------------------------------------------------------------------------------------------------------------------------------- http***mb.rxlist.com/rxboard/ultram.pl?noframes;read=3179 not just for breakfast anymore Posted By: mkny Date: Friday, 21 October 2005, at 3:53 a.m.
Graves' disease can be diagnosed using Thyroid Receptor Antibodies (TRAb) / Thyroid-Stimulating Immunoglobulins (TSI). The presence of TRAb/TSI test can confirm Graves' disease, and while experts can't agree, it's thought that from 75 to 95 percent of all Graves' patients will test positive for these antibodies. Practitioners do agree, however, that the presence of TRAb/TSI is considered diagnostic for Graves' disease.
hi, ive just read your post, ive had graves disease for 11years, and i have a high bilirubin level in my blood, it also shows up in my urine as well, but dont know what it means? The doctors dont seem to be interested in it. So i would be interested to know more if you find out please let me know.
On top of that, I keep gaining weight (and I do exercise, I walk and still do my line dance) My gastro doctor did send me for a CT of my abdomen and pelvic area. I don't have the results of that yet. He thinks it is possible that my intestines have twisted again or that I have something going on gynecologically. My only concern with that is, when I went to the ER last summer, they did a CT of my abdomen and they didn't find the twisted intestine.
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