ME/CFS: Recognition, medical care & protection for affected persons and research funding

My child has ME

I have M.E

ME patients need recognition

I have ME and want it to be studied a cure found!

I suffer from ME/CFS.

My husband is severely ill. This disease has drastically reduced his quality of life. The local medical fraternity is of no help. We live in a broken cycle of doctors visits, tests and no positive change. Research needs to get done to advance our approach and help those suffering.

ME patients have been ignored and treated dreadfully by doctors. Much more research is need to find causes and potential treatments for this awful illness. Sufferers need to access medical care without worrying if they can afford it.

ME/CFS needs funding for biomedical research and treatments commensurate with the severe levels of sickness and disability caused by this WHO, CDC and NIH classified multisystem physical disabling disease.

I have ME - the lack of care, treatments and social support is destroying people's lives. We need support and funding for biomedical research. How else do we remedy the EUR 40 BILLION estimated annual disease burden across Europe?

I have Austrian friends.
Austria, UK and most other countries need better awareness, diagnosis and treatment for people suffering from ME.

I’m directly affected with MECFS, and wish to help Austria people.

I have M.E and hope that all M.E patients get the funding and treatment they deserve.

ME patients in Austria need better care

The urgent need for proper care and fundings for research in the me-field

I have been ill with ME/CFS since 2005

Because people with ME have been through hell. With no option of recovery that really works...never mind doesn't do harm...we have been marginalized and rideculed but not helped

I have ME CFS.

As a Long Covid patient I feel it is my obligation to show solidarity with those suffering with ME/CFS which is a very similar disease that has been overlooked by the medical field for decades.

People with ME have suffered for decades from lack of recognition of the complex biomedical nature of our condition, failure to adequately research that condition and unsatisfactory levels if support.

I have CFS and Ehlers Danlos

Because I have m.e and we need it fully recognised

M.e has destroyed my life

I have friends with ME that are bedridden. I have long covid myself. I have hope of recovering. The ME patients do not have this same hope, as research was slow and hugely under funded. Please help the ME community. They have a right to be helped.

I suffer from ME/CFS

Suffering from this disease is unbearable we need help! There is currently no help, no treatments, nothing! We desperately need research into the illness and education so that everyone in society understands how serious and debilitating this disease is. It is such a burden on us to have to keep using our limited energy having to educate others in the face of continual disbelief. Society as a whole needs to recognize that ME is just as serious as other debilitating illnesses such as multiple sclerosis.

I want everyone who suffers with chronic illness to have the support they deserve.

I have been housebound with ME/cfs for a decade.

people with Me/CFS desperae;y need biomedical research, treatment, and recognition.

I have ME - it is almost impossible to describe how much harder an already severe illness is made through the bias ME patients have to face. For many of us our own families believe the official dogma as opposed to us because they trust doctors and the establishment. When you need help the most, there is none. It causes trauma for many of us, on top of all the debilitating symptoms we try to learn how to deal with alone. We are forced to become our own doctors, trying all sorts of things in desperation. This is a medical scandal. Please act to protect your citizens from further harm. Thank you.

För jag själv har denna sjukdom