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The president highlights the remarkable evolution of the CF community since the foundation of the organization, announces the official opening of membership for the families of people with CF and invites the entire community to become a member in order to strengthen participation, representation and collective support.

The director highlights the resilience of the CF community in the face of the pandemic, the historical access to Trikafta in Quebec, the evolution of the VAFK team and the organization's renewed commitment to supporting members, in view of the 40th anniversary celebrations in 2025.

The data suggests that, despite common inflammatory mechanisms, people with cystic fibrosis may present a form of COVID-19 that is often less severe than expected, possibly thanks to cellular characteristics of CF and the potential protective effect of CFTR modulators.

The Fall 2024 issue of Santé Vous Bien highlights the inspiring journeys of people living with cystic fibrosis, from climbing Mount Kilimanjaro to lung transplantation, sports, literature, and research to show that CF does not set limits to the heights that can be reached.

The inspiring story of Marc-Antoine Pelège, an athlete and osteopath living with cystic fibrosis, who tells the story of his ascent of Kilimanjaro step by step as a symbol of overcoming, resilience and hope for the entire CF community.

Living with Cystic Fibrosis is launching a survey to better understand the needs of the CF community and adapt its services, with a draw for a $50 gift certificate to be won.

This article explores the psychological and identity upheavals experienced by people with cystic fibrosis in the Trikafta era, between immense hope, social pressures, past griefs and the need to reinvent themselves in the face of a suddenly possible future.

The editor takes stock of a significant year for the FK community, marked by access to Trikafta and an issue rich in testimonies, expertise and scientific advances.

A message from the president that highlights the current issues of cystic fibrosis, pays tribute to the community and reaffirms the organization's commitment to those affected.

A series of clear medical answers to common questions from people living with cystic fibrosis, addressing fermented foods, kidney stones, thrush, halitosis, premenopause, and precautions before surgery.

In a context of pandemic and uncertainty, this word highlights the resilience, solidarity and unity of a community that adapts, helps each other and comes out stronger.

The call for applications for the 2020 Michel Paquette Prize is launched in order to recognize a person or organization that has made a remarkable contribution to the field of cystic fibrosis, with a presentation scheduled for October 2020.

Pharmacies recommend limiting renewals to one month, giving priority to delivery, paying without cash and contacting your doctor in case of drug shortages.

Essential measures to be adopted during the COVID-19 pandemic to reduce the risks of infection, manage stress, and ensure continuity of care, especially for vulnerable people.

The death of Thérèse Dion at 92 rekindles the Dion family's connection to cystic fibrosis, a cause supported in memory of their niece who died from the disease.

Two distinctions are awarded in 2019 to recognize the exceptional commitment of individuals and organizations who have made an impact in the cystic fibrosis community, as well as the remarkable contribution of a person living with the disease.

Christian Auclair, a committed communicator and a leading figure in the field of cystic fibrosis, passed away on June 16, 2019 after devoting many years to informing, raising awareness and creating relationships in Quebec and internationally.

CEO Tomy-Richard Leboeuf-McGregor died after several days in a coma, leaving a significant impact within the cystic fibrosis community.

Neonatal screening for cystic fibrosis would allow Quebec to diagnose the disease at birth, to establish early care and to prevent avoidable nutritional and pulmonary complications, as is already the case in the majority of western countries and Canadian provinces.

A practical and educational text on deep physiological breathing and the importance of exhalation in supporting breath, tone and expectoration in people living with CF.

A psychosocial reflection to better understand one's reactions to the disease and to find a balance between responsibility and self-compassion.

A human and political reflection on the end of life, autonomy and the role of elected officials in health.

A critical look at therapeutic progress and inequalities in access to cystic fibrosis treatments.

Boy and girl? Not when the twins are the same! This text explains, in an accessible way, the different types of twin pregnancies, the role of genetics and the particularities of identical twins.

Writing a will and a mandate in case of incapacity makes it possible to ensure that your wishes are respected, to protect your loved ones and to avoid conflicts, delays and unnecessary costs.

The Service Québecois de Changement d'Adresse (SQCA) makes it possible to simultaneously inform several government departments and agencies of a change of address, in a single simple and quick process.

A look back at the history of Living with Cystic Fibrosis, from its foundation to today, highlighting the evolution of its mission, its actions and its commitment to the community.