Graves disease named after
Common Questions and Answers about Graves disease named after
graves-disease
I always thought I had an anxiety or panic disorder because my heart was going haywire all the time. I found out I had Graves Disease and hypothyroid disease shortly after the birth of my 1st child at age 19. I wonder if my thyroid did kinda burn itself out and I ended up with hypo? I saw an endo back when I was 19 and I dont exactly remember what bloodtests were ran but he did say Graves Disease and I was on levo given from my regular Dr. at the time.
why after almost two years do I still have graves symptoms.
Graves is an autoimmune disease and unfortunately for life. Controlling whether they raise or suppress is key to beating the symptoms of the disease.
If you are on Levo now - your labs must be abnormal and now lean towards hypoT levels. You would feel like cr@p right now with the swinging patterns you have been on.
"Once Graves.... always Graves" is the saying here. But I am positive your endo or ???
I am a 25 y/o female diagnosed with hyperthyroidism at 16 and later with Graves Disease and Goiter. I have been on Tapazol along with Atenelol (for the Tachacardia) off and on for the past 9 years with no results. Every doc I see wants to discuss nothing but RAI or surgery. My husband and I have been trying to conceive for a few years with no success. I finally found out that I was pregnant the beginning of last year and made it to 4 months and suffered a miscarriage for no apparent reason.
iam apatient who suffers graves disease. My question is : Although I am almost 4 months on Carbamizole treatment 60 mg + Taking inderal ( propanalol), but the levels of my T4 & T3 are still high and the levels of TSH is less than 0.01.
what do you think , should i sstop the medication and think of the other allternatives like the radioactive iodine or surgical removal?
my son was a newly diagnosed "graves disease" pt. he was given tatazole tablet 5mg. to be taken after breakfast for one month, what are the side effect of tatazole, the things he have to avoid and if you can give me more/additional information about the disease. thanks!
Hi, I am a 28 year old woman and was diagnosed with graves disease 3 years ago. I have commented o many forums regarding my problem but would like your advice. I was treated with radio active iodine in 2006 and then became hypothyroid, I now take 150mg of levothyroxine daily. I have never suffered from graves opthalmology as far as i'm aware.
For the last 6 months I have had a chronic daily headache. This started 3 days after purchasing new glasses.
Graves Disease is never cured BUT it is managed better without a thyroid or after RAI.
You still have the antibodies but no thyroid for it to attack.
As for meds, you swap one lot for another.
You go from anti-thyroid meds to a T4 medication so basically you are on meds for life.
The thyroid regulates every organ in your body and if no thyroid, meds have to do the job.
Hyperthyroidism is a lot easier to manage without a thyroid.
I have been going to an Endocrinologist for almost 1 year. He has done several ultrasounds showing that I have 5 tumors on my thyroid. I have a biopsy which showed they were benign. I recently had another ultrasound which showed one of the tumors had shrunk but another one appeared.
I really thought I was losing my mind, I have had this for about 4 yrs and just now was diagnosed with Graves disease. My Dr put me on Methimazole and after 3 weeks had a severe reaction and was covered head to toe with a horrible insanely itchy rash. Mr Endo told me I have a couple options radio active iodine or somthing else which he did not tell me what. My question is how has the radio active iodine worked for others?
I am glad I found this site, I found out today that I have graves disease, I also have a multinodular goiter and I had a thyroid scan and it showed a cold area, so I have to have a biopsy. I am so scared, I have never really been sick and now all of a sudden I get this. Has anyone had a biopsy on a nodule and how long does it take for the results to get back? Any help is greatly appreciated!
I just went to a new doctor. I saw 2 doctors(endos) they said continue taking these meds and test in 6 weeks. They also agreed that my tests really don't fit Graves disease anymore. WHAT IS WRONG WITH ME? I had my cortisol tested in August and it was normal 17 after a fast. Maybe it's piuitary related. All I know is I don't feel well at all.
Thanks.
Have you been tested for thyroid antibodies to make sure you do, in fact, have Graves disease and are not simply in a hyper phase of Hashimoto's? Both Graves and Hashimoto's are autoimmune.
While Graves is always connected with hyperthyroidism, Hashimoto's is most often connected with hypothyroidism, however it's not uncommon for one to have periods of hyperthyroidism in the beginning stages.
You should ask for thyroid antibody tests.
If you don't mind. I see you posts starts out as Graves Disease and you are looking for a surgeon?
While I would have to do some checking around on this can you post the reason for the removal? - Is it for Graves disease?
Has your doctor told you, you have Graves Disease? Yes, your TSH is extremely low and your FT4 is extremely high, indicating that you are hyper, but your antibody tests indicate Hashimoto's. TSI is the definitive test for Graves Disease and I don't see that listed.
Have you been put on antithyroid med?
Did I develop neutropenia from the Graves disease and how do I stop the neutropenia from getting worse? Also, what are some things that I should avoid as a result of my neutropenia? In addition, my heart rate ranges from 120-140 and I feel very tired and confused. Are these feelings a result of my heart rate? Thank you in advance.
ve been having these severe migraines for over 2 months now, my eyes hurt terribly from all the pressure, im not sure if its the pressure in my nerves from all the spasms and intense pain and weakness im having in my limbs but im scared that its ocular migraines, i could not read properly with having bad pain in my head, i have graves disease but with my doctors appoinment yesterday at the endocrinologist the doc says im 'normal' when im everything but the muscle weakness is so sever i
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