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History

The Association of People with Multiple Sclerosis (SAmSKP) is a nonprofit organization and has been established solely by patients to services, information and support to patients across the spectrum of their needs and informing the general public about the disease. A founding member of the Panhellenic Federation of People with Multiple Sclerosis.

Nothing can help more on empowerment of MS Association from access to clear and meaningful information about their disease, existing treatments, rehabilitation possibilities are entitled to as well as their rights by the state (social benefits), to improve their living standards.
The Association contributed to it significantly, providing reliable and authoritative information on the issues of MS, counseling, education, psychological support, social events, scientific meetings, and more! It publishes newsletters and quarterly magazine. It refers to the published opinions of experts, but does not represent their proposals for remedies. Each case is different, not to say unique, like the fingerprint. For more specialized knowledge recommend you contact the neurologist.

Our objectives

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The sympathy and support at all levels for people with Multiple Sclerosis and their families.

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Providing reliable and eminent information, regardless of their place of residence, both for developments in science, and pharmaceutical sectors.

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The reception of newly diagnosed so as to remove the original panic” in which the diagnosis is usually associated.

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The support for the treatment of personal, occupational, family difficulties of people with MS and their families.

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Providing space for communication and mutual support for both peopple with MS and for members of their families and their friends.

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Cooperation with all the medical and other scientific disciplines necessary for the treatment of disease.

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Demand for all kinds of welfare benefits and their legislative entrenchment.

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