The perspective of a caregiver and my connection with the NMCB
I am Markus, father of three daughters and caregiver of two family members, both bedridden.
ME/CFS has a huge impact on patient’s lives. Read some experiences in the patient stories below.
The perspective of a caregiver and my connection with the NMCB
I am Markus, father of three daughters and caregiver of two family members, both bedridden.
In this process, co-creation between patient and scientist was the 'modus operandi', which honors the approach of the Research Program.
My name is Evelien van den Brink. I fell ill when I was 14 and I am now 40.
I fell ill when I was 14 and I am now 40. I got pneumonia and did not recover well. A few months later, I got the flu and after that I was never healthy again.
What I admire about our ME community is the resilience of the patients and the drive to share knowledge. Despite everything, there is a great willingness to work together with a focus on the future.
My name is Hannah.
I have been living with ME/CFS for more than half my life. On behalf of people with ME/CFS, I am now helping with the NMCB. This is a collaboration of researchers and others involved. We want to better understand ME/CFS and improve the lives of people who have it.
Hopefully, people with ME/CFS will indeed be properly understood and helped in the future.