Commitment to patient associations

For several years, LFB and its teams have been committed day in, day out to patients suffering from rare and serious diseases.
Portrait of Jacques Brom
“I met hundreds of people in various job positions in France and internationally during my first weeks and they all spoke to me about commitment: their commitment to patients. Why? Because we strive to honour our mission to serve patients.”
Jacques Brom CEO of the LFB Group.
THE COMMITMENT OF LFB EMPLOYEES

LFB employees provide support to patient associations in countries where LFB markets its medicinal products. LFB’s representatives and those from patient associations work together to evaluate care pathways and launch initiatives to improve them. Improving the time to a correct diagnostic, increasing the availability of medicinal products, and improving hospital-city care pathways are some of the themes we focus on in our work.
Thus, the activities of patient associations, partially with the financial support of LFB, and LFB’s initiatives for patients work in complementarity, all in the service of patients.

LFB employees took part in the 4th edition of the connected race, organised by the IRIS Association:

PATIENT ASSOCIATIONS

Patient associations are committed to reducing diagnostic errors, ensuring safety, quality and access to care and treatment, and improving patients’ quality of life.
Collectively, they defend the right of patients and users of the health system to take part in decisions that concern them. They represent patients towards public stakeholders and they support research.

Some of the patient associations that support people treated with plasma-derived medicinal products also promote blood or plasma donation.

LFB's historic commitment to patient associations

ADAAT: Association for patients with alpha-1 antitrypsin deficiency

Since the ADAAT was created, the LFB has supported it in its missions which aim to improve knowledge of the deficiency, support families, raise awareness of the disease and advance research in the field.

Visite ADAAT website

Interview with Sandrine Lefrançois, President of the ADAAT.

AF3M: French association for patients with Multiple Myeloma

Myeloma is a rare disease that affects 20,000 people in France. The AF3M’s mission is to provide information on current treatments and research and to provide aid and support by bringing patients and the association together.

Visit AF3M website

AFH: French association of haemophiliacs

As a long-standing partner of the AFH, LFB supports its missions which include to guarantee safety, quality and access to care and treatment for all, improve the quality of life of all and ultimately to cure haemophilia and rare haemorrhagic diseases.

Visit AFH website

EHC : European Haemophilia consortium

The EHC consortium brings together 48 national patient organisations for people with rare bleeding disorders from 27 European countries.
The EHC represents its national member organisations at national and European level, helping them to engage with each other.

Visite EHC website

WFH: World Federation of Hemophilia

The WFH is an international organisation whose goal is to improve and sustain the care of people with inherited bleeding disorders throughout the world.

Visite WFH website

AFNP: French association for peripheral neuropathies

Since the creation of the AFNP, the LFB has supported the association in its missions aimed at people living with inflammatory-dysimmune peripheral neuropathy and in its desire to improve health policies.

Visit AFNP website

Interview with Jean-Philippe Plançon, President of the AFNP.

IRIS: Association for patients with primary immunodeficiencies

Since the IRIS was founded in 1998, LFB has provided its support to improve the diagnosis and management of primary immunodeficiencies, support and represent patients, promote donation and support research.

Visit IRIS website

IPOPI: International Patient Organisation for Primary Immunodeficiencies

The IPOPI is an international association representing patients with primary immunodeficiencies and is dedicated to improving awareness, access to early diagnosis and optimal treatments for patients worldwide.

Visit IPOPI website

EPODIN, European Patients Organisation for Dysimune and Inflammatory Neuropathies

EPODIN is a European association whose members are European patient associations. Its mission is to bring the voice of patients suffering from dysimmune neuropathies to European public health stakeholders.

Visit EPODIN website

Le Rire Médecin

For over 15 years, LFB has been a firm supporter of the 150 professional clowns of Le Rire Médecin, who perform every day to the great delight of hospitalised children. In collaboration with healthcare teams, Le Rire Médecin “hands out” laughter to children with chronic illnesses in their healthcare environment.

Visit Le Rire Médecin website