Picture och the yellow house and children playing. Picture.

Ågrenska provides programs for children, teenagers and adults with disabilities, their families and professionals supporting the family. Striving to be a progressive and creative meeting place between needs and knowledge, our aim is to contribute to people´s coping with everyday life and empower them to become as independent as possible.


National Competence Centre for Rare Diseases
Family program
Adult program

Respite care

ADHD-consultant
Family Support unit

Courses for professionals

Personal Assistance

The Agrenska Academy

 

For further information please contact
Anders Olauson, Chairman anders.olauson@agrenska.se
Robert Hejdenberg, President robert.hejdenberg@agrenska.se

 

News:


EPF value + conference. 9-10 December 2009. Logotype
Value + Conference
Meaningful Patient Involvements in EU Health Programmes and Policies.

If you were unable to view the conference live, a video is now available for viewing of all plenary sessions. Please follow this link to the recorded webcast.

Socialminister Göran Hägglund. Foto
Göran Hägglunds speech at the European Patients Forum december 9th.


Have a look at the webcast "Future Challenges for Rare Diseases" and the Agrenskas 20th Anniversary (link opens in new window)

To be able to watch the webcast you need to install Microsoft Silverlight. Silverlight powers rich application experiences wherever the Web works.


Terkel Andersen vinnare av Ågrenskas Stora Pris. Foto.
Terkel Andersen winner of The Agrenska Major Award!


Read more about Agrenskas 20th Anniversary hereHM Drottning Silvia är Ågrenskas beskyddare. Foto.

Hovet 
Microsoft
David Lega
GP
GP-Ledare
Föräldrakraft
GT
Funka Nu


Rare disease day

 

Rare Disease Day
28 Februari 2009


HM Drottning Silvia är Ågrenskas beskyddare


Agrenska is a NGO in Special Consultative Status with the Economic and Social Council of the United Nations