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UPDATED: Mon Feb 18 16:59:04 2002

Dr Gro Harlem Brundtland        
Director-General
World Health Organization

WHO, Geneva
12 February 2001

 

Launch of the second phase of the Global Campaign Against Epilepsy

Mrs de Boer,

Dr Reynolds,

Dr Engel,

Mr Lee,

Mr Bowis,

Chairman,

Ladies and Gentlemen,

I would like to welcome you all to this launch of the second phase of the Global Campaign Against Epilepsy. I am especially pleased that this event today marks the beginning of a year where mental health and brain disorders will be the global focus of attention.

As you all know, the theme for this year’s World Health Day is mental health and brain disorders, and so is the subject of this year’s World Health Report.

Our advocacy effort will concentrate on reducing stigma associated with mental ill health and neurological disorders on raising awareness about the many effective, affordable treatments that are available but underused, both in developing and industrialized countries.

I will mark the World Health Day twice this year; first in Nairobi on the fourth of April where the Kenyan health authorities for the first time will arrange an "Open Day" at the country’s main mental hospital. Then, we will celebrate again here in this room on 6 April in what we hope will be a warm and forceful celebration of the benefits of inclusion and care.

The World Health Report will give a comprehensive review of what we know: about the current and future global burden of mental ill health and neurological disorders; about the effectiveness of prevention and the availability and restraints to treatment; and about the policies needed to ensure that stigma and discrimination is broken down and effective prevention and treatment are put in place and funded.

I am confident that our efforts this year will take mental health a large step forward towards equal priority and respect with physical aspects of health.

This past century has seen spectacular changes in the way we live and think. Human brilliance and technology have come together to propose solutions we dared not imagine forty years ago. We have conquered diseases that once seemed insurmountable. We have saved millions of people from premature death and disability. And our search for better solutions to health is, as it should be, ceaseless.

Mental health is a central part of overall health. When I took office, two-and-a-half years ago, I was convinced that WHO should devote considerable energies to addressing the challenges posed by mental disorders. Since then, my resolve has only been strengthened.

There is also an increasingly strong evidence confirming the close relationship between health and development. Ill health taxes the economy of whole nations as well as bringing terrible burdens on families. By reducing the burden of disease, we also improve the conditions for reducing poverty.

When we talk about reducing the toll from the diseases that cause and perpetuate poverty, we often focus on malaria, HIV/AIDS, tuberculosis, early childhood diseases and problems linked to pregnancy and birth. But we could also include mental and neurological disorders.

An estimated 400 million people alive today suffer from mental or neurological disorders or from psychosocial problems such as those related to alcohol and drug abuse. Around fifty million of them suffer from epilepsy. Many of them suffer silently. Many of them suffer alone. Beyond the suffering and beyond the absence of care lie the frontiers of stigma, shame, exclusion and, more often than we care to know, death.

Of those who suffer from epilepsy, around 85% live in developing countries. There are two million new cases occurring in the world every year.

What neurological disorders have in common with mental ill health is that these conditions are victims of stigma, ignorance and fear. As a result, these diseases receive low priority by authorities and health personnel in many countries.

Stigma and discrimination have several consequences: they limit the degree to which patients attend treatment; they limit the degree to which health workers are being trained adequately to identify, assess and treat disorders; they may even limit the willingness of mental health care providers to intervene. They also reduce the abilities of the patients to live normal lives in their communities and workplaces and in some circumstances prevent them from earning a living altogether.

Up to 80% of persons with epilepsy could lead normal lives if properly treated, but the overwhelming majority of patients does not get any treatment at all. The WHO Regional Office for the Americas estimates that out of five million people with epilepsy in the Region, 3.5 million are believed to be untreated. A recent survey of 30 Latin American countries revealed that none of them had national policies for epilepsy. In sub-Saharan Africa, there is one neurologist for four million people.

So we are facing the two challenges of reducing stigma and of building up capacity to correctly diagnose and treat epilepsy patients world-wide.

It can be done. Epilepsy is not difficult to diagnose if health personnel have received minimum level of training. And it can be effectively treated with safe and inexpensive medication. The main anti-epileptic drug, phenobarbitone, can be produced and sold for as little as $5 per person per year.

The difference can be between total disability and a fully normal life. Research from the United Kingdom shows that around 70% or the estimated cost of epilepsy are caused by premature mortality and disability, leading to need for care and lost productivity.

As health workers, we know that few opportunities are as gratifying as that of being able to restore someone back from despair to a normal life. The Global Campaign Against Epilepsy, which was so aptly named "Out of the Shadows" is based on that inspiration.

The collaboration between the International Bureau for Epilepsy, the International League Against Epilepsy and WHO has shown that when people with different backgrounds and roles come together with a shared purpose, creativity is released and expertise is used in innovative and constructive ways.

The original objectives of this campaign were:

  • to increase awareness, both among health professionals and the general public, of epilepsy as a universal and treatable disorder;
  • to raise epilepsy to a new plane of acceptability in the public domain;
  • to improve education about epilepsy;
  • to identify the needs of people with epilepsy; and
  • to encourage governments to address the needs of people with epilepsy.

The first three years have focused on the first three objectives: increasing awareness, creating acceptance and improving education. Much work has gone into the campaign and special care has been taken to involve a broad spectrum of experts and professionals. Activities to improve awareness have been held in over 50 countries world-wide. More than 1200 health professionals from more than 100 countries have participated in consultations to shape the work in countries and to formulate regional declarations against epilepsy.

In doing so, the campaign has built the foundations for achieving the last two objectives. How well we have succeeded in creating awareness and reducing stigma – at least among decision makers in countries around the world, will determine to what extent we will succeed in convincing governments to address the needs of those living with epilepsy.

We are here to launch the second phase of the global campaign. And I am pleased to say that judging from the momentum the campaign has created, the considerable efforts from all who are involved have been a success.

We can today announce four demonstration projects against epilepsy in four countries: Argentina, China, Senegal and Zimbabwe.

These four demonstration projects will assess the number of people suffering from epilepsy in the project area and train primary health care workers within the existing primary health service how best to diagnose and treat epilepsy patients. In China, the project will cover a population of nearly three million people.

The projects will run for four to five years. The experiences they will yield will form the basis for developing national programmes in the four countries and to assist other countries in designing their own programmes.

We have come a long way since the campaign started three years ago. We can now enter the second stage reassured that we are making real improvements to the lives of hundreds of thousands of people, and we are laying the foundations for lasting improvements for millions more.

With that inspiration in mind, let us all to do our best to make this second phase of the global campaign a success, and that we can bring epilepsy out of the shadows.

Thank you.

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