Graves disease nausea
Common Questions and Answers about Graves disease nausea
graves-disease
hi i'm a 28 yr old woman and have suffered badly with symptoms from graves disease for 3yrs i've been on propylthiouracil for a year now as i had a severe allergic reaction to carbimazole!
my symptoms include insomnia,severe fatigue,anxiety,bouts of depression,poor concentration,memory loss,bruising easily,dizziness,nausea and graves rage and weakened immune system (sick often). the problem is that i've recently had a blood test that read normal at 5.
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.
I ate a huge amounts of food when I was Hyper thryroid - yet I had times when I didn't eat at all -- I forgot. I would get nausea because of eating to much and when I didn't because I was so empty. I am sure the abdominal distress is a part of that too. Has the doctor put her on any meds. I found relief from a nausea/ stomach spasm Rx prescribed to me at that time.
Recently I was diagnosed with Hyperthyroidism due to Graves disease, I experienced the symptoms of nausea, rapid heart beat (over 100) anxiety and panic attacks. I had to stop working due to my symptoms. While I stayed at home I started to feel better, experiencing only discomfort due to heart beat for only few times a day. At that time my endo didn’t prescribe my any thyroid medicine as I was supposed have thyroid uptake scan prior it.
In the U.S. doctors are required, by law, to provide a copy of lab or test results, upon request. I have every one of mine, since about 1999. I use my thyroid test results as a running record of my disease. On each report, I mark my med and dosage, along with any symptoms I was having at the time. If I am symptom free, I know those are the numbers I need to target.
What are the reference ranges for the results? Ranges vary lab to lab and have to come from your own report.
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 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.
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?
What antibodies test was done? With your symptoms it seems like a test for Thyroid Stimulating Immunoglobulin (TSI), to test for Graves' Disease, would have been in order.
It is much ore like what our bodies make. Did you have
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.
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!
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
I've just been diagnosed with Graves' Disease. I have autoimmune thyroid disease that has changed from being primary Hashimoto's thyroiditis to Graves's Disease. I was diagnosed in 1997 with Fibromyalgia. I also have severe osteoarthritis, especially in both hands. What am I doing wrong? The doctor told me I'm a very strange case. What's that mean?
Looks like Graves' disease based on the significant elevation in T3 however to confirm this a TSI blood test or I-123 nuclear uptake would be required.
I was diagnosed with graves disease and had the radioactive treatment to destroy it a few years back. I have had a few times where I did not have my meds for a week at a time. Is it normal to feel so tired and cranky? Also I took Zirtec for my allergies and I felt like I was cloudy and just wanted to sleep and tightness in my chest..... I am currently on 137 mcg of Levothyroxine.
Hello. I'm 36 and I am almost 9 weeks pregnant. I have Graves' disease and had radiation treatment back in 2009. I hadn't been taking my thyroxine constantly for a few months as I was super stressed and now that I am pregnant haven't missed a dose. My thyroid levels are still very high and I'm worried that this will affect my baby's brain development/IQ levels. Has anyone else had similar experiences? I'm scared and worried.
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