The lack of qualified physicians to treat chronic pain is a challenge on which the SIP platform also focuses. Over the next 10 years, Francoise Thomas from the French Association Against Pain and a member of Pain Alliance Europe is hoping for more physicians to...
The joint statement has been prepared by the SIP Portugal platform in March 2019 and presents the common position of all those involved and proposes actions to be taken, relevant to pain, in two categories: employment and education. There is a need to develop policies...
On March 20, the Portuguese Social Pain Platform (SIP Portugal) organized a meeting with eight companies from different sectors of activity to present measures that aim to promote the maintenance of work or professional reintegration of the person with chronic pain,...
On 6 March, the Interest Group on Brain, Mind and Pain held a meeting in the European Parliament bringing together patient organisations, institutions and industry to discuss the stigma and discrimination attached to long-term neurological disorders (i.e. migraine,...
The 2018 SIP Thematic Network provided a unique opportunity to create new synergies and break silos. SIP is now collaborating with the Joint Action of the European Commission CHRODIS Plus which aims to implement pilot projects and generate practical lessons in the...
There are of course multiple things that matter to chronic pain patients, but if I would have to make a choice I would say the heaviest is losing their independence in society. In other words, their economic dependency, as they depend on others to survive financially...
