1. Workshops, Simpósiuns and seminars to raise awareness and promote the spread of the disease and its treatment to society through dissemination and, biannual publication of a newspaper;
  2.  

  3. Intervene with employers and unions sensitizing them to the disease entities and possible disability resulting, derivatives as side effects of medication to patients who are subject to ON;
  4.  

  5. Support and assist in resolving physical problems, psychological, and socio-economic stemming from EM, providing support, by a multidisciplinary team consisting of psychologists, social workers, occupational therapist / physiotherapist, lawyers and volunteers. In active collaboration with other Associations and Public and Private Entities-are held joint actions for people with MS;
  6.  

  7. Collaborate with health services (hospitals, health centers, clinical, among others), so as to sensitize physicians to the pathology, leading to a quicker diagnosis and a systematic monitoring of disease symptoms;
  8.  

  9. Support research and research in the context of MS, thereby promoting the improvement of treatment and a significant improvement in the quality of life of patients;
  10.  

  11. Sensitize them to the needs of laboratory research and development of new medicines;
  12.  

  13. Continue the collection campaign "Bottle Caps" to which we attach to this year from the collection of "plastic" and metal cans to acquire Technical Help to lend to the general community;
  14.  

  15. Domiciliary associates who for health reasons can not move the association visits, contacting up with the reality surrounding each wearer.

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Esperar o inesperado: os sintomas da EM variam de doente para doente e a cada dia, o que os torna em desafios acrescidos. Na luta contra a doença, saber é poder. #ExijaMais da vida com EM.

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