Experiences with

Graves' disease

does anybody else still get symptoms from graves diesese months after being on medication? I was diagnosed in September and I am still suffering from palpitations. Shakes, anxiety and a sore mouth?

Now they are suggesting it could be the Graves Disease causing these symptoms. I have found a lot of information on Graves’ disease with overactive thyroid but nothing for Graves Disease with under active thyroid! Does anyone have any information on this?

I've had 4 episodes of graves disease in 13 years. Each time I'm treated with 40mg carbimazole per day for 6 months. Each time I go into remission for a 3-4 years. With my last/current episodes of graves I was also tested for antibody levels.

Diagnosed with Graves disease in Sept 2018 and have been taking Carbimazole ever since. My Endo suggests avoiding surgery for a couple of years and revisiting if there is still the need.

(August 05, 2022) Fluctuating Hyperthyroidism and Hypothyroidism in Graves’ Disease: The Swinging Between Two Clinical Entities.

hi im new got diagnosed recently with overactive thyroid and Graves disease still going through tests feel crap every day have a infected throat that I have had since this started and my blood results show a infection every time could of been diagnosed earlier but they dont seem to do thyroid in normal

I was diagnosed with active thyroid GRAVES disease by specialist then diagnosed Underactive 10 years later by GP ?????? Is that normal

Hi, I have Graves Disease and my overactive thyroid has returned...my tsh is 0.01 and t4 is 3.5. Just wondering if that's mild or severe? Really not sure. Thanks

Can I eat fish with Graves disease an active thyroid

Hello. My husband was just diagnosed with Covid on Sunday. He is on Paxlovid. Has anyone in the group taken Paxlovid for Covid and if so we’re there any problems with it? I also have multiple sclerosis and another autoimmune disease called Polymyalgia Rheumatica. Thanks!

Has anyone been told that their Graves’ disease contributed to their kidney disease. I had untreated Graves for 5 years and researched that it could cause CKD

I had subclinical Graves' Disease 19 years ago, which was successfully treated with block replacement therapy. I've tested my thyroid every year or so since then, all fine, until recently.

how much milk thistle to take for your liver, I have Graves' disease and raised alkaline phosphates?

I have had GCA for 10 years, and continue taking Pred. " montha ago I saw a %kg weight loss ( 85 -80), and now it is 8Kg. My Rheumy suggested Graves leding to Hyperthyroidism. Blood tests have confirmed Hyper. I am taking Beta Blocker to regulate heart since Cardio says that an effect of Hyper. is a

I was diagnosed with Graves’ disease in 2018. This was medically managed and my thyroid came back into normal range in mid-late 2019. I have been monitored and was off carbimazole from late 2020. In March this year, I contracted Covid.

Hi, I had graves disease and had my thyroid removed. My thyroglobulin antibodies are high three years after removal does that mean I now have hashimoto disease?

Wondered if anyone had looked into managing Graves' disease naturally?

I was wondering if anyone has experienced the same thing as I have, I’m a little worried but not sure if it is normal 😊 I was diagnosed with Graves’ disease almost two years ago. My T3 and T4 levels were bought under control with PTU. I was eventually on 300mg daily.

I have always suspected that I have Graves' disease as well as Hashimoto's but every doctor I ever had told me that was impossible. Well, my latest labs came back positive for Graves', which makes sense to me because I have always been underweight, tremorous, and had other hyperthyroid symptoms.

Hi there just wondered if anybody has any advise or stories to share about having Graves disease at a very young age . My daughter was diagnosed 6 years ago when she was 9 and is currently on carbizamole tablets .