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Thalasemia Society Mauritius

  • 230 5920 5210

  • 1st Floor, C/R Joory and Seebaruth Lane, C/r Joory Ln, Floreal, Vacoas/Phoenix, Mauritius

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Description:

Thalassemia is a genetic blood disorder which is not contagious. In  Mauritius, we have about 150 patients and those patients need  a life long blood transfusion for their survival.

Thalassemia Society is a registered NGO (Reg No 11194) created in 2009 to help those who are affected. The broad objectives of the association are

1. To support the patients and their families and counsel and educate them on the management of Thalassemia

2. To campaign for blood collection for Thalassemic patients

3. To advocate for the creation of better transfusion and treatment facilities

4. To raise funds and provide equipment and medicines for underpriviledged thalassemic patients.

5. To create awareness among public and advocate for screening and counselling programmes for the control of Thalassemia

6. To promote collaboration with the Ministry of Health and Quality of Life, WHO, and Regional and International thalassemia groups societies like Thalassemia International Federation.

7. To provide support to patients with other genetic haematological disorders such as Sickle Cell Anaemia and other blood disorders

E-ZY(Easy) Search

IMPROVE YOUR BUSINESS STRATEGIES

We Will Show You the Way to Success!

Thalasemia Society Mauritius

  • 230 5920 5210

  • 1st Floor, C/R Joory and Seebaruth Lane, C/r Joory Ln, Floreal, Vacoas/Phoenix, Mauritius

    • mail
    • facebook
    • twitter
    • googlePlus
    • LinkedIn

Description:

Thalassemia is a genetic blood disorder which is not contagious. In  Mauritius, we have about 150 patients and those patients need  a life long blood transfusion for their survival.

Thalassemia Society is a registered NGO (Reg No 11194) created in 2009 to help those who are affected. The broad objectives of the association are

1. To support the patients and their families and counsel and educate them on the management of Thalassemia

2. To campaign for blood collection for Thalassemic patients

3. To advocate for the creation of better transfusion and treatment facilities

4. To raise funds and provide equipment and medicines for underpriviledged thalassemic patients.

5. To create awareness among public and advocate for screening and counselling programmes for the control of Thalassemia

6. To promote collaboration with the Ministry of Health and Quality of Life, WHO, and Regional and International thalassemia groups societies like Thalassemia International Federation.

7. To provide support to patients with other genetic haematological disorders such as Sickle Cell Anaemia and other blood disorders

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  (230) 5973 5303/5758 8633   Ave des Sardes, Morc. Anna, Flic en Flac   info@e-zysearch.com