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  • Create a database of children with Moebius Syndrome;
    (listing details of patient, diagnostic data, ie symptoms present, where and when diagnosed; medical support
    ie, network of doctors and examinations needed; family history
  • Spread the awareness through campaigns, media, posters.
  • Provide reading material in the three official languages;
  • Offer support to children and parents - this could be offered via the website, e-mail and printed form;
  • Obtain funding for a special need feeder (Haberman Feeder) and to supply parents of new-born babies with a feeder.
  • Offer assistance with recruitment for adults with Moebius Syndrome
  • Educating the community and educators.
  • To set up a trust fund of bursaries for children with Moebius Syndrome who wish to further their studies.

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The official website of the Moebius Syndrome Foundation-Africa

This is the official website of the Moebius Syndrome Foundation-Africa (MSFA), a NPO organization. Donations are used to achieve the goals of the Moebius Syndrome Foundation-Africa (MSFA) and are not for personal use. The Moebius Syndrome Foundation-Africa (MSFA) and its Board does not diagnose Moebius Syndrome/ Sequence in individuals nor does it endorse particular medical professionals/treatments/organisations. However, with the consent of an individual, we could put him/her in contact with a Medical Professional(s) for correct medical evaluation.