Graves disease rashes
Common Questions and Answers about Graves disease rashes
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Hi. I am hoping someone can help me. I found out that I have Graves Disease in May of 2009. I have all the symptoms and I am currently looking for the best procedure for me. I came down with a rash on my back a few months ago. It is an open rash. Now it has spread to my chin and arms. Does anyone know what it can be? I am not on any meds for the Thyroid. It almost looks like Chicken Pox??
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 found out via an email that I have Graves' disease . 4 weeks ago I learned I had hyperthyroidism and was placed on methimazole 10mg2x a day. The email for the type came 3 weeks later and it was frightening to read about. I felt exhausted for months had stomach issues and lost 15 pounds in a month.
4 weeks into the medication I have a distended stomach with pains and horrible rashes.
All that said I'm completely stressed about the eye issues that come with graves.
"In conditions of chronic urticaria, thyroid antibodies are not only indicators of chronic inflammation, but they appear to play a role in the disease process. In most cases, improvement of urticaria with thyroxine replacement hormone suggests that chronic thyroid inflammation may initiate a hypersensitivity reaction and an underlying thyroid hormone deficiency.
However, rarely, patients with chronic urticaria have undiagnosed conditions of Graves' disease.
2 weeks ago I was diagnosed with a auto immune thryoid disease after i was at the doctors commonly with issues such as being very tired, getting rashes,loseing hair and then my period came half way through a cycle on the pill and it was so heavy for weeks without stopping so I was given a thyroid test as we usually watch it (I was told at 17 I had early graves disease) now 27 i'm racking my brain trying to understand what it all means what do I have ??
I was treated for graves disease several years ago and have since been taking synthroid. the problem is in the last month or two, i have been suffering from an unsightly rash on my face which won't go away. I cannot figure out what is causing it and i suspect it may be related to my thyroid condition. i do not think it has to do with any other conditions other than my thyroid problem. has anyone experienced the same type of problem with rashes?? what can i do to get rid of it??
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.
Info from Elaine Moore's website...
"rash after a few months on methimazole...
I really appreciate all the feedback I'm getting! Now, that I'm aware that I don't necessarily have to stop the methimazole after 18 months-- I've only been taking 10mg/day & did fine until I went off. I just have a concern re: this rash I developed after about 8 months on the drug. My MD doesn't think it's from the med since it took so long to develop.
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.
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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