Report: 3,000 people with hemophilia in Morocco

This article was automatically translated from HIBAPRESS, the Arabic version:

This article was automatically translated from Hibapress, the Arabic version:

Heba Press

Similar to the international community, the Ministry of Health and Social Protection famous, on April 17, 2025, the International Day of Hophilia, which is held this year under the slogan: “Elastic to All: women and girls are also breaking down”, the slogan adopted by the World Himophia Federation.

On the occasion of celebrating this day, the ministry is organizing a national campaign to raise awareness, in addition to a scientific symposium which brings together parties and actors anxious to fight against blood coagulation disorders.

This campaign is the framework of continuous efforts to improve early diagnosis, to extend the scope of fair access to treatments and improve sponsorship, especially for women and girls who suffer from a lack of interest for their health needs linked to these unknown disorders.

Celebrating this day is an opportunity to highlight the importance of joint work in the face of this disease, which aims to overcome the challenges facing people with hemophilia and their families in a way that guarantees their healthy and healthy life.

In addition, the awareness and consciousness of hemophilia and other blood clotting disorders, which are rare genetic diseases that affect blood capacity to coagulate naturally.

According to the World Hemophilia Federation, around 1,125,000 people with hemophilia worldwide live, only 30% of them have been diagnosed and received the necessary care, i.

Hemophilia is the most common type, because it represents 4 to 5 times the cases of hemophilia B.

Hemophilia is estimated to affect around 3,000 people in Morocco, receiving centers specializing in its treatment more than 1,000 of them because they benefit from sponsorship, diagnosis and processing services.

Given the challenge represented by hemophilia as a general health problem, since 2010, the national program for the prevention and sponsorship of hemophilia has been launched, which aims to improve the sponsorship of the wounded, and this program has made it possible to reach remarkable progress, in particular demonstrated at the level of 17 specialized specialized centers, including six; Although there are 11 proximity centers for hemophilia treatment in terms of regional and regional hospitals that are available on equipment and equipment to ensure sponsorship and improve the skills and capacities of health professionals through directed training courses, in addition to improving access to anti-sugar drugs, which are necessary to reduce complications and improve the quality of patients.

Despite these achievements, the need is always urgent to double, in particular with regard to other coagulation disorders, such as the disease “Phone Willberland”, the lack of rare coagulation factors and genetic platelet disorders, which are still not well known and often diagnosed late, especially in women and girls.

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