65 images for 650,000 ME/CFS patients

Over 650,000 people in Germany suffer from ME/CFS, including at least 80,000 children.

This means that significantly more people suffer from ME/CFS than from MS (250,000), Type 1 Diabetes (350,000) or AIDS (90,700) (Source: https://www.mecfs.de/daten-fakten/)

People living with ME/CFS often have a very low quality of life and frequently a high degree of disability. Approximately 2/3 of all sufferers are unable to work; the severely ill often lie in darkened rooms for years.

Currently, there are no recognized therapies or medications that can effectively treat or cure the underlying disease mechanisms of ME/CFS.

For every picture sold, €10 will be donated to the ME/CFS Research Foundation

The ME/CFS Research Foundation advocates for more biomedical ME/CFS research (incl.
Post-COVID). Its focus is on diagnostic and therapy research.

What is ME/CFS

ME/CFS myalgic encephalomyelitis is a severe multisystem disease whose main symptom is post-exertional malaise (PEM). PEM is a worsening of condition and an increase in symptoms after physical, mental, or emotional exertion.
In addition to post-exertional malaise, affected individuals suffer from symptoms of the autonomic nervous system such as heart palpitations, dizziness, lightheadedness, and blood pressure fluctuations. There are also immunological symptoms such as a severe feeling of illness, painful and swollen lymph nodes, sore throat, respiratory infections, and increased susceptibility to infection. Furthermore, many affected individuals suffer from severe pain such as muscle and joint pain and new-onset headaches. Additionally, there are muscle twitches and cramps, severe sleep disturbances, and neurocognitive symptoms such as difficulties with concentration, memory, and word-finding (often referred to as "brain fog"), as well as hypersensitivity to sensory stimuli.
Therefore, severely affected individuals often have to lie in darkened rooms and can only communicate with relatives in whispers.