Welcome word – PAE Newsletter March 2021
Dear readers, With some melancholy feelings, I’m writing this welcome word for PAE’s newsletter. It will be my last one. I looked back through my archive and found our very first newsletter,Read More…
All posts by Pain Alliance EU
PAE General Assembly Meeting – Save the Date : 23 June 2021
PAE members are invited to save the date of June 23 for the organisation’s virtual General Assembly meeting. This meeting will be chaired by PAE current President (Joop Van Griensven) and byRead More…
ENFA launches the campaign “The Faces of Fibromyalgia
It is estimated that 4.7% of the European population suffers from Fibromyalgia (5.8% women and 3.5% men). Despite being a disease recognized by the World Health Organization and some European countries, mostRead More…
European Civic Prize on Chronic Pain – Collecting Good Practices – third edition 2020-2021. The application period is still open!
The Active Citizenship Network is glad to share with you the third edition of its bi-annual project at the European level “EU Civic Prize on Chronic Pain – Collection of good practices”Read More…
PAE Member the Hellenic League Against Rheumatism and HELAR’s project is one of the winners of the EFIC and Pfizer-Lilly Alliance Grant for Education in Pain Associated with Osteoarthritis
Τhe Hellenic League Against Rheumatism and HELAR’s project aims to integrate contemporary, evidence-based, digital and physical intervention, education and outreach approaches into a patient centered, m-Health supported, digitally enhanced and socially innovativeRead More…
Updates from our member: The Liga Reumtolóxica Galega
The Liga Reumtolóxica Galega is drawing up agreements with the management of the Galician Hospital Centers, to participate actively with the hospital procedures and protocols. At the same time, it offers itsRead More…
News from ADDCA : Addressing chronic pain conditions in Europe in the age of Covid-19 – Please complete this questionnaire!
Chronic pain is a serious health condition that affects patients’ quality of life both physically and psychologically and has social implications for the family and society. This questionnaire aims to: identify howRead More…
#EFICPlainTalking: A new campaign on health literacy!
The ‘Plain Talking’ health literacy campaign is aimed at both clinicians and people living with pain. Over the next three years, the Health Literacy Working Group will raise awareness of the conceptRead More…
Gathering insights from patients with cancer-related neuropathic pain!
Neuropathic pain is a common long-term effect of cancer and its treatment– and can have a big impact on patients’ lives. A new online survey is now gathering patients’ perspectives, giving themRead More…
The article “Digital Health Tools for Managing Noncommunicable Diseases During and After the COVID-19 Pandemic: Perspectives of Patients and Caregivers” is now published in the Journal of Medical Internet Research
The article “Digital Health Tools for Managing Noncommunicable Diseases During and After the COVID-19 Pandemic: Perspectives of Patients and Caregivers” is now published in the Journal of Medical Internet Research. We, PainRead More…
