Lupus – what are the signs and symptoms of Lupus?

Signs of Lupus

Signs of Lupus

Symptoms

Symptoms of systemic lupus erythematosus (SLE) can vary widely from person to person. Some people may only experience a few mild symptoms, whereas others may be more severely affected.

Even if you usually have mild symptoms, SLE can “flare up”, with symptoms becoming more severe or new symptoms developing.

The three main symptoms of SLE are:

fatigue (extreme tiredness)

joint pain and swelling

rashes – particularly on the face, wrists and hands

Fatigue

Fatigue is one of the most common symptoms of SLE. You may feel very tired even though you get plenty of sleep. Carrying out everyday tasks, such as housework or office work, can leave you feeling exhausted.

Many people with SLE find that fatigue is the most distressing and disruptive aspect of the condition because it has a negative impact on their work and social life.

Joint pain

If you have SLE, you’re likely to experience joint pain in your hands and feet. You may find the pain changes from one set of joints to another quite quickly, and is usually worse in the morning.

Unlike some other conditions that affect the joints, SLE is unlikely to cause your joints to become permanently damaged or deformed.

Rashes

Many people with SLE develop rashes on their skin – most commonly on the face, wrists and hands. A rash over the cheeks and the bridge of the nose is particularly common and is known as a “butterfly rash” or “malar rash”.

Rashes caused by SLE may get better after a few days or weeks, but can last longer or even be permanent.

Rashes caused by SLE can sometimes be itchy or painful. They may get worse if they are exposed to sunlight.

Other symptoms

SLE can also cause a wide range of other symptoms. However, you’re unlikely to have all of the symptoms listed below, and many people with the condition only experience the above main symptoms.

Other features of SLE may include:

a fever (high temperature)

swollen lymph glands (small glands found throughout your body, including in your neck, armpits and groin)

recurring mouth ulcers

hair loss (alopecia)

high blood pressure (hypertension)

headaches and migraines

stomach (abdominal) pain

chest pain

depression

dry eyes

memory loss

seizures (fits)

problems thinking clearly and difficulty telling the difference between reality and imagination (psychosis)

shortness of breath

Raynaud’s phenomenon – a condition that limits the blood supply to your hands and feet when it is cold

ankle swelling and fluid retention (oedema)

When to seek medical advice

You should see your GP if you have persistent or troublesome symptoms that you think could be caused by SLE.

While it is likely that your symptoms are being caused by a more common condition, it’s important to see a doctor for a diagnosis.

Understanding and Lupus – Vision 2043 and World Arthritis Day #worldarthritisday


World Arthritis Day

World Arthritis Day

As promised in our last post on World Arthritis Day here are the results of the Vision 2043 competition.

For this competition people what one thing would make their lives with a rheumatic or musculoskeletal disease easier.

And today sees the winners announced.

The EU winning vision for 2043 is ‘Understanding’ which explains that for Argyri Stara “What has made living with an RMD easier? When I was being given my first blood transfusion the stabbing pain penetrated my heart so violently that I covered my face with the pillow to hide the tears, and just when I thought I was about to faint, I felt someone remove the needle and put it in the other arm. My mom had brought in the nurse. When, for the first time, I needed to give myself injections and thought I could not do it, my sister said she would drive over and do it although she had never done anything like it before. Just hearing that gave me the courage to give myself the first shot. When I was terrified that I might need a kidney transplant, my husband selflessly offered his. It’s excruciatingly difficult living with a severe form of Systemic Lupus Erythematosus and its unexpected twists. Love, UNDERSTANDING and the support of my family have given me the strength to live with it.”

Argyri Stara is from Greece and has had arthritis for 14 years.

Help us raise awareness of arthritis and rheumatic or musculoskeletal diseases (RMDs) by sharing them with your friends on social media using the hashtag #worldarthritisday.