At first I blamed stress, then the tremors and weight change made me see a GP. A clear diagnosis of Graves’ disease gave me answers and a plan
- Apr 12
- 4 min read
When I first noticed my hands trembling, I thought it was just stress. Life had been hectic, and I assumed my body was reacting to pressure. But when the tremors worsened and I started losing weight without trying, I knew something else was going on. That’s when I decided to see my GP. The diagnosis was clear: Graves’ disease. Finally, I had answers and a plan to manage my health.
Recognising the signs that something was wrong
At first, the symptoms were subtle. I felt anxious and restless, but I put it down to work and personal stress. Then the tremors began. My hands shook when I tried to hold a cup or write. I also noticed my heart racing even when I was resting. The most alarming change was the weight loss. I wasn’t dieting or exercising more, yet the pounds dropped off.
I also experienced heat intolerance and sweating more than usual. My eyes felt dry and irritated, and sometimes they looked a bit bulgy. These symptoms made me uneasy, but I still hesitated to seek medical advice. I thought it might pass or be related to stress.
Eventually, the combination of symptoms became too much to ignore. I booked an appointment with my GP to find out what was happening.

Close-up of trembling hands holding a cup, showing early signs of Graves’ disease.
What happened at the GP appointment
During the appointment, I described all my symptoms in detail. The GP listened carefully and asked questions about my medical history and family health. They examined my neck and noticed an enlarged thyroid gland, which felt unusual.
The GP ordered blood tests to check my thyroid hormone levels and antibodies. These tests are essential to diagnose Graves’ disease, an autoimmune condition where the immune system attacks the thyroid, causing it to produce too much hormone.
A few days later, the results confirmed the diagnosis. My thyroid hormone levels were high, and the antibodies specific to Graves’ disease were present. The GP explained what this meant and discussed treatment options.
Understanding Graves’ disease and its impact
Graves’ disease affects the thyroid gland, which controls metabolism and energy use in the body. When the thyroid produces too much hormone, it speeds up many body functions. This causes symptoms like:
Tremors
Weight loss
Rapid heartbeat
Heat intolerance
Anxiety and irritability
Eye problems, including bulging eyes (Graves’ orbitopathy)
The condition can affect anyone but is more common in women and often appears between ages 30 and 50. It is important to diagnose and treat Graves’ disease early to avoid complications such as heart problems or bone loss.
Treatment options and managing the condition
The GP explained that treatment aims to reduce thyroid hormone levels and control symptoms. There are three main approaches:
Antithyroid medications: These drugs reduce hormone production. They are often the first treatment and can be effective in many cases.
Radioactive iodine therapy: This treatment destroys part of the thyroid gland to lower hormone levels. It is usually considered if medications don’t work or cause side effects.
Surgery: Removing part or all of the thyroid gland is an option in some cases, especially if there is a large goitre or suspicion of cancer.
My GP prescribed antithyroid medication and advised regular blood tests to monitor progress. They also recommended lifestyle changes to help manage symptoms, such as avoiding caffeine and managing stress.
Support and resources that helped me
Learning about Graves’ disease was overwhelming at first. I found it helpful to access reliable information and support. The Robert James Graves Foundation offers valuable resources for people affected by this condition. Their website provides clear explanations, advice on treatment, and updates on research.
I also found it useful to track my symptoms and medication side effects. This helped me communicate better with my healthcare team and adjust my plan as needed.
One product that made a difference was a digital blood pressure monitor. It allowed me to keep an eye on my heart rate and blood pressure at home, which is important because Graves’ disease can affect the heart. I used the Omron M3 Blood Pressure Monitor for its accuracy and ease of use.

Digital blood pressure monitor used to track heart health during Graves’ disease treatment.
Living with Graves’ disease day to day
Managing Graves’ disease is a journey. Some days are better than others. I learned to listen to my body and rest when needed. Regular check-ups with my GP and endocrinologist keep my treatment on track.
Diet and exercise also play a role. I focus on balanced meals and gentle activities like walking or yoga. Avoiding stimulants like caffeine helps reduce tremors and anxiety.
I also use a symptom diary app called MyGraves, which helps me record how I feel each day. This information is useful during medical appointments and helps me notice patterns.
The importance of early diagnosis and support
Looking back, I wish I had seen a doctor sooner. Early diagnosis can prevent complications and improve quality of life. If you notice unexplained tremors, weight changes, or other symptoms, it is important to seek medical advice.
Support from healthcare professionals, family, and organisations like the Robert James Graves Foundation makes a big difference. They provide guidance, emotional support, and up-to-date information.
If you or someone you know is dealing with Graves’ disease, remember that you are not alone. There are resources and treatments available to help manage the condition effectively.
Living with Graves’ disease means adapting to new challenges, but with the right diagnosis and plan, it is possible to regain control. My experience taught me the value of listening to my body and seeking help when something feels wrong. The clear diagnosis gave me answers and a path forward. If you notice similar symptoms, don’t wait to see your GP. Early action can make all the difference.
For more information and support, visit the Robert James Graves Foundation.


























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