Hans’s Story
Written by Yolandi Du Plessis My Dad was born with an extremely rare lung disease called “Alpha 1-antitrypsin deficiency (A1AD or AATD)”. This is a genetic disorder which he was unfortunately only diagnosed with at the age of 36. After his diagnosis, he...
Where to Now?
It was only since we entered the New Year that our visits have become twice weekly to Busamed Gateway Private Hospital for regular check-ups post-transplant. Matthew is being given a little more freedom too, as long as he is careful and keeps away from anyone who may...
Along the Road to Recovery
As we approached 3 months post transplant for Matthew, I opened Facebook recently to be reminded of this post that I had written a year ago: “When I opened my eyes this morning, I just knew that today was going to be a battle and that I needed to win it. A battle not...
Matthew’s Transplant Story day T+20 to T+22
Over the next couple of days we watched Matthew getting stronger day by day. We sat with him for many hours talking (from the glass door) about past experiences and what was to come post-operation. I had contacted Matthew’s previous cardiologist, Dr Kenny, and...
