Help researchers and mental health professionals at the University of Newcastle better understand how Duchenne muscular dystrophy (DMD) impacts families, and be reimbursed for your time.
There are 3 surveys currently available, and participants can take part in any/all for which they are eligible.
A) survey participation (for parents/caregivers and siblings of people with DMD)
B) interview participation for siblings of people with DMD
C) interview participation of parent/caregivers for people with DMD
How to get involved
- Scan the QR code on the flyer.
- Follow the below links or click on the flyers.
- Email Rosie Locke – R.locke1@newcastle.ac.uk
This uptick in research focusing on mental health and well-being is great news and represents a real interest from clinical psychologists. It demonstrated a desire to increase understanding of how Duchenne muscular dystrophy (DMD) impacts families, and support better treatment guidelines that will put DMD higher on the awareness of the next generation of mental health professionals.
