Transition support for young people with congenital heart disease (CHD)
Are you a young person who will soon transition to receiving support from an adult multidisciplinary team with congenital heart disease (CHD) specialism?
Please share with CHF about what has worked well for you and what you would like to see improved — literally.
Your here & now reality, experience & views of CHD are really valuable to us so that we can better support you!
- Please email CHF via email@example.com
- Or share your views via our Facebook page https://www.facebook.com/chfed.