VIDEO DOCUMENTARY

ON CHRONIC FATIGUE SYNDROME

*castellano

 

 

what is SFC?

video documentary

interviews

producción

contacto

 

There exists an illness which disables 0.5% of the population, and for which there is no cure. Most people who have it are not diagnosed but feel very ill and are on a pilgrimage from doctor to doctor trying to find out what is wrong with them. Unfortunatly, because of the lack of medical training about this illness, most people who have it are told that it is “all in their heads”. This makes them suffer even more as they do not understand what is happening to them and they cannot give an explanation to their family or at their work places. This results in economic, social and emotional strife.


Chronic Fatigue Syndrome is a multi-sytemic illness which affects the immune, the neurologic, the cardiovascular and the endocrinological systems. Although people who suffer from it look well, they live with many symptoms, among them, a severe flu-like feeling which does not go away, fatigue, memory loss, constant infections, muscle pain, visual disturbances, dizziness, fainting. Most are house-bound and many spend years in bed. In the words of CFS specialist Dr.David Bell, “It is truly remarkable that a patient can feel so bad yet look relatively well.”

It´s chronic, it doesn't have a cure.

 

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VIDEO DOCUMENTARY (50min. PAL)


This 50-minute documentary in Spanish, captures the voices and the stories of those who live with CFS, their doctors and their lawyers. The people interviewed who have CFS speak of their daily suffering, of how this illness has interrupted their lives permanently, of the lack of understanding from their loved ones and society, of their isolation and of how they are denied goverment pensions after having worked for years. At the peak of their lives, usually between the ages of 30 and 40, everything comes to a halt. They go through years of abandonment by the health care system as most doctors are not familiar with CFS, as well as economic hardship because they are unable to move, let alone, work. Their reality, their desperation, the injustice they live and their amazing coping skills come through in this video.

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INTERVIEWS (work in progress)

 

If this illness cannot be cured, then the day I got sick was the day I died.” Alfonso, 40 year-old father of two, ex-construction worker.

 

 

"I feel so bad all the time, but the worst is not knowing if I will be even sicker tomorrow.”

Anna G., 42 year-old ex-nurse’s aide

“I could not even hold a book in my hand.

But the doctor said that there was nothing wrong with me.”
Nuria, ex-CPA

“This illness cannot be faked. I know. I have been working with people who have it for years and I can tell.”
Teresa Sol, labour lawyer

“How can I have an illness with such a superficial name when I feel so ill all the time?”
C. ex-university professor.

 

 

 

“The Medical Board inspector did not even look at the CFS specialist’s reports and said that all I needed to do was to cheer up.”
Ana G., ex-supermarket employee

 

Dr. Pablo Arnold Llamosas M.D. Immunologist

Patients arrive scared and tired. Their families don't believe them. The uncertainty that the patients live with is a nightmare. As doctors, the most important thing is to believe the patients and to accompany them on their long voyage.

 

 

 

 

 

Dr. Ferran J. García Fructuoso M.D. Rheumatologist

This is an organic disease. When the patients arrive to our clinic, they have already seen many doctors, spent a lot of money and years looking for an answer.

 

 

 

 

 

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PRODUCTION

Directed by:

Clara Valverde
Ana de Quadras

DZIGA PRODUCTIONS (datos de producción: ana@dziga.net)

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Video registered in the Barcelona (Spain) Intellectual Property Registry:
B-1683-05

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