- 2020: ENFA became involved in a project developing a fibromyalgia position paper/consensus document.
- 2020: ENFA developed a new 2025/2026 strategy encompassing holistic, person- and family-centred care across the life course.
- 2020: ENFA undertook a project to explore the needs and expectations of ENFA members.
- 2020: ENFA’s membership surpassed 20 organisations.
- 2020: ENFA refreshed it’s branding and visual content, accompanied by changes in its governance and transparency.
- 2019: ENFA was part of a founding group of healthcare professionals, researchers and non-for-profit organisations involved in establishing a Europe-wide network of patient registries for fibromyalgia.
- 2019: ENFA launched a new project to identify and share self-management strategies that people with fibromyalgia use.
- 2018: ENFA entered into a new collaboration with Active Citizenship Network.
- 2018: ENFA was invited to host a two-day programme in Malta under the distinguished patronage of Her Excellency, Marie-Louise Coleiro Preca, President of Malta. The two-day programme consisted of a hearing in the Parliament of Malta, followed by a conference at the Presidential Palace, San Anton.
- 2017: ENFA hosted a lunch meeting at the Societal Impact of Pain (SIP) Conference in Malta on the topic of the position of fibromyalgia patients in society, which was hosted by Member of the European Parliament for Cyprus, Mr Takis Hadjigeorgiou.
- 2017: ENFA published a video on chronic pain and fibromyalgia titled ‘Monique fibromyalgie’.
- 2017: ENFA engaged in dialogue with the EU Commissioner on a series of questions about fibromyalgia.
- 2016: ENFA was represented on the European League Against Rheumatism (EULAR) Task Force, developing updated recommendations for the management of fibromyalgia.
- 2015: ENFA was registered on the transparency register of the European Parliament. This means that ENFA are informed when there is any mention of fibromyalgia within the parliament, alongside invitation of ENFA to comment on various health related issues.
- 2015: ENFA became a member of the European Patients’ Forum (EPF).
- 2014: ENFA became involved as an eligible organisation of the European Medicines Agency (EMA).
- 2013: ENFA became a member of Pain Alliance Europe (PAE).
- 2008: ENFA was involved in the acceptance of the written declaration 69/2008 on fibromyalgia by the European Parliament in December 2008.
- 2008: ENFA initiated a round table discussion in the European Parliament on May 6, 2008.
- 2008: ENFA supported the launch of a petition on fibromyalgia and the presentation of the first 10,000 signatures to the European Parliament.
- 2008: Announcement of the ‘year of fibromyalgia’ in cooperation with the European Pain Federation (formerly EFIC). This was done during a press conference in the European Parliament on October 8, 2008.
- 2008: ENFA was involved in the development of the Fibromyalgia Global Impact Survey.
[vc_row][vc_column][vc_column_text]Please find below some achievements for ENFA, since the organisation was established in 2008.