Interview to Verónica Zofío — Affected by lymphangioleiomyomatosis
Verónica Zofío is the marketing manager of an environmental laboratory. She is 40 years old and was born and raised in La Vall d'Uixó, Castellón (Spain). Six years ago she had a pneumothorax
The Share4Rare End Event was a successful closure meeting
Loretta Anania , Programme Officer with the European Commission and DG CONNECT, opened the meeting. “ Having a patient-centred approach was something really exceptional. [Share4Rare] was part of the
Share4Rare launches the 1st open call for patient-driven research projects
Share4Rare invites patient organisations and researchers in the field of rare diseases to apply for conducting their patient-centred studies within the platform. The ambition of Share4Rare is to put
Share4Rare End Event: setting the path for next generation data sharing in rare diseases
Rare disease patients and their families have the right to be part of a community, wherever they are in the world. It is equally important that research that is performed will benefit the patient
Meeting the partners — The Synergist
They say it takes a village, and the rare diseases community is just that - a tight knit group with a sense of camaraderie and fellowship. This is the power of Share4Rare - creating a platform where
Interview to Joan Carles — Father of a girl with retinoblastoma
Joan Carles does not forget that day: “ Júlia was diagnosed on May 29 th 2018, when she was a few months old. The symptom that she presented at that time was the strabismus of the left eye. That was
COVID-19, an additional burden for melanoma and all cancer patients
Violeta, thank you for taking the time for this interview. You have recently conducted a research study into how COVID affected melanoma patients in Romania. Can you tell us something about what you
The burden of care
Gilly, thank you for taking the time for this interview. When thinking about cancer, many will think about the burden of disease- you have however argued for a long time that there is also a burden of
Meeting the partners — Cliclab
Cliclab is a transformative agent whose objective is to innovate the approach of entrepreneurs and companies with new methods. Cliclab is a personal and corporate transformation agency or, as they
Interview to Àngels Puigvert — Mother of a girl with megalencephaly-capillary malformation syndrome
Àngels Puigvert's life is anything but calm, but he was able to find some time to answer some questions about her daughter and the work carried out by her association. Thank you Àngels! " Queralt was
Research study on neuromuscular diseases: interactive session with families
In this session we will explain the Share4Rare research project on neuromuscular diseases . This study collects information about quality of life/burden of the pathology and the impact of the disease
Research Study for NMD: interactive session with UK families
In this session we will explain the Share4Rare research project on neuromuscular diseases . This study collects information about quality of life/burden of the pathology and the impact of the disease