Home » Press release on the founding of the Moroccan Federation of Trisomy 21 Associations Eight associations unite their efforts to make a common voice heard

Press release on the founding of the Moroccan Federation of Trisomy 21 Associations Eight associations unite their efforts to make a common voice heard

By the grace of God, on Saturday, September 26, 2026, the founding general assembly of the Moroccan Federation of Trisomy 21 Associations was held, in a pioneering step seeking to enhance the status of people with Trisomy 21 and their families, and to support their fundamental rights in a society that believes in the values of justice and equal opportunity. The Youth Center Youssoufia in Rabat hosted this event, which began at eleven o’clock in the morning.Speeches then addressed the Federation’s objectives, which seek to establish a comprehensive vision to serve people with Trisomy 21, enhance their support and rehabilitation pathways and support their families, in a way that achieves their aspirations towards a more equitable and empowering future.Eight associations, one will
The Federation includes associations from several cities in the Kingdom, each contributing with its expertise, commitment and territorial anchorage:Angels Association — Mr. El Mekki Benamrou, Rabat-Salé;Al-Himam Association for Trisomy 21 — Ms. Rachida Dada, Safi;Al-Amane Association for Trisomic Children — Ms. Noura Sekhiri, Al Hoceima;Ichraqat Qalb Association for People with Trisomy 21 — Mr. Raed Al-Moualem Chouaib, Tetouan;Moroccan Association for Treasures 21 — Dr. Nezha Iraqi, of national scope;Abnaouna Association — Ms. Fatima Rkani, Marrakech;Nour Al Mostaqbal Association for Trisomy 21 — Ms. Najia Ahssine, Agadir;Association of Parents and Friends of Adolescents with Trisomy 21 — Ms. Naima Qouraich, Agadir.A federation carrying the voice of people with Trisomy 21
The session opened with a blessed recitation of verses from the Holy Quran by people with Trisomy 21, followed by a solemn atmosphere for the performance of the national anthem, to express great pride in the distinguished attendance through welcome words.Then the floor was given to the child Malak Iraqi, who spoke on behalf of people with Trisomy 21:
“I am very happy to be here today for the founding of the Moroccan Federation of Trisomy 21 Associations. We are here to make our voice heard, to have our abilities recognized, and to achieve our dreams.
We were born like you, like all Moroccans. We are citizens, we have personality and identity and feelings and ambition and dreams. We want to progress and reach the highest ranks, God willing.
Hand in hand and step by step, we will go far.”Federation officially founded
During the meeting, the Federation’s statutes were read and discussed extensively, where attendees provided valuable observations that contributed to amendments to some of its articles, then it was unanimously approved to form the solid foundation for the Federation’s work and achieving its desired goals.And the composition of the board came as follows:President: Dr. Nezha Iraqi (Moroccan Association for Treasures 21)First Vice-President: Ms. Najia Ahssine (Nour Al Mostaqbal Association for Trisomy 21 in Agadir)Second Vice-President: Ms. Rachida Dada (Al-Himam Association for Trisomy 21 in Safi)Secretary General: Mr. Ahmed Moussa (Ichraqat Qalb Association in Tetouan)Deputy Secretary General: Ms. Fatima Rkani (Abnaouna Association in Marrakech)Treasurer: Ms. Hind El Fajri (Moroccan Association for Treasures 21)Deputy Treasurer: Ms. Noura El Fdili (Moroccan Association for Treasures 21)Advisors:
◦ Ms. Noura Sekhiri (Al-Amane Association for Trisomic Children in Al Hoceima)
◦ Mr. Raed Al-Moualem Chouaib (Ichraqat Qalb Association in Tetouan)
◦ Ms. Naima Qouraich (Association of Parents and Friends of Adolescents with Trisomy 21 in Agadir)
◦ Ms. Khadija Jaouad (Nour Al Mostaqbal Association for Trisomy 21 in Agadir)The work of the founding general assembly concluded with the recitation of words of loyalty and devotion raised to His Majesty, His High Majesty King Mohammed VI, may God grant him victory and support.This meeting ended in a fraternal atmosphere, where a tea reception was held in honor of the attendees, and commemorative photos were taken documenting this important event.Word of the President, Dr. Nezha Iraqi
After the formation of the executive board, the word of the President Ms. Dr. Nezha Iraqi, who spoke on behalf of all members of the executive board declaring:
“The idea of founding the Moroccan Federation of Trisomy 21 Associations was born from our closeness to people with Trisomy 21 and their families. And through contact with them we learned deep human values. We touched their suffering from marginalization and inferior view, and we discovered above all their competencies, and the strength of their ambitions, and their great will to move forward.
And based on our deep belief in their capabilities, we decided to establish the Moroccan Federation of Trisomy 21 Associations, to unify efforts and visions in order to support and rehabilitate them.
And if these people carry an extra chromosome, it represents a part of their personality that enriches it without defining it, and therefore they are citizens with full rights.
And the Federation’s vision comes in full harmony with the Royal Vision of His Majesty King Mohammed VI, may God grant him victory and support, which places the human being at the heart of sustainable development, by enhancing his capabilities and enabling him with opportunities that allow him to be an active member in society, and ensure his right to a dignified life, equity and equal opportunity.”Clear and practical tasks
The Moroccan Federation of Trisomy 21 Associations aims in particular to:Unify the efforts of Moroccan associations working in the field of Trisomy 21, and strengthen coordination and cooperation among them;Support families from the announcement of the diagnosis, and provide guidance and necessary support at various stages of the pathway;Facilitate access to health care and treatments, and contribute to improving the quality of services provided to people with Trisomy 21;Contribute to producing and compiling national data and statistics related to Trisomy 21, to support planning and decision-making;Work for effective school inclusion, ensuring for each child with Trisomy 21 his right to learn and develop within school;Open wider horizons for people with Trisomy 21 in the fields of training, higher education and employment;Valorize success paths and capabilities and achievements, and make them known as inspiring models for society;Raise joint recommendations to public authorities;Develop partnerships with various actors and institutions and concerned sectors, in a way that serves the Federation’s objectives;Sensitize Moroccan society to the importance of difference as a value that enriches society, and entrench a culture of effective inclusion of people with Trisomy 21 in various fields and spheres of social life.A first step, and a common path
The founding general assembly on September 26, 2026 formed the official launch of this new dynamic.
Through this press release, the Moroccan Federation of Trisomy 21 Associations extends an invitation to all governmental and community entities to support its blessed journey, and support its diligent efforts towards empowering people of determination, and building a society that embraces all its members with dignity and equity.About the Moroccan Federation of Trisomy 21 Associations
The Moroccan Federation of Trisomy 21 Associations was founded on September 26, 2026 in Rabat, and includes eight founding associations: seven from Rabat-Salé, Safi, Al Hoceima, Tetouan, Marrakech and Agadir, and an association of national scope. Its mission is to coordinate associative action for the benefit of people with Trisomy 21, support their families, and raise their recommendations to public authorities. It is chaired by Dr. Nezha Iraqi.
For press contact: Dr. Nezha Iraqi
WhatsApp: +212 6 68 30 31 12
Email: fedemarocassotrisomie@gmail.com
Instagram: @federation_marocaine_trisomie
Facebook: Fédération Marocaine des Associations de Trisomie