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Funding period

Showing all data for 2014–2021

Civil Society Completed

EMPOWERare

Bulgarian Huntington Association ·Bulgaria

€72k
Grant awarded
Civil Society
Programme
2 October 2019
Signed

About this project

<p style="text-align: justify"><span style="font-size: 11pt"><span style="font-family: &quot;Calibri&quot;, &quot;sans-serif&quot;">Social services tailored according to the needs of people with rare diseases are almost non-existent in Bulgaria. Rare diseases are not included in any national or local strategy to develop social services or long-term care. The project aims at contributing to reduction of the social gap by empowering the vulnerable group of people with rare diseases for civic engagement, initiation of reforms in social policies, introduction of an innovative contemporary social service and strengthening of bilateral relations between the donor states and the beneficiary states. Our project will help activate for civic engagement people with rare diseases, some of them living in less-developed geographic regions and groups (Roma), to formulate recommendations based on their experience about desired reforms and services. The project will contribute to solving the above issue through boosting the capacity of people with rare diseases for civic engagement, preparing training and information materials appropriate for multiplication of training sessions among other vulnerable groups, transferring information about good practices of social services from the donor states, proposals from users to the institutions to improve and reform social services, piloting of an innovative tele-rehabilitation service with an assessment by practitioners and users, an innovative increase of access to services through&nbsp; a weekly Open-door day accessible for external users and identified “lessons learnt”.&nbsp; The direct beneficiaries are people with rare diseases, including Roma, and public institutions responsible in the area of social policy and services.&nbsp;The partner will share experiences and good practices from Norway, where there are long-standing models of services and experience in empowering people with rare diseases. To this end</span><span style="font-family: &quot;Times New Roman&quot;, serif"><span style="font-family: &quot;Calibri&quot;, sans-serif">, trainings, exchange of good practices with the Norwegian partner organization and an advocacy campaign for social policy reforms will be carried out.</span></span></span></p>

Bilateral cooperation results

During the project, trainings, exchange of good practices with the Norwegian partner organization and an advocacy campaign for social policy reforms were carried out. During the activities, a number of written and video materials were created, available for use to stakeholders. Due to the pandemic, all planned trainings and events took place online, and the planned regional meetings were held with reduced frequency and a small number of participants. However, on the whole a large number of participants joined the project and an Advisory Board of active and motivated citizens with rare diseases was set up.

Project partners