Hi,
Does anyone have any experience of pulmonary AVM please? I had a contrast CT scan today, as I had pneumonia at the beginning of November, but I’m still extremely breathless and my heart rate is extremely elevated. CT report came back saying they’ve identified a pulmonary AVM.
I’ve got a doctor’s appointment for the 27th, but I’m just wondering if anyone can give me an idea of what happens now please.
TIA.