Tears of joy Its only been 7 months since the first Spinraza treatment…but even I couldn’t dare to hope to see Abris like this. After being told a year ago – by Hungarian doctors – that he only has a couple of months to live, this kid is pushing himself in a tiny wheelchair – even if just a little bit. This counts as a miracle to us. The irony is that one of these doctors was at the conference in Krakow today. I wish she saw in person what the child who she passed on is capable of now. I can only encourage […]
Second day Abril’s expression tells all… 😀 Some of the presentations go beyond my genetic knowledge, but we still are learning a lot. Thankfully, some members of SMA Hungary are bigger experts in the topic. Our Belgian neurologist and Italian physiotherapist are also here, so we have some familiar faces to see. Have a great weekend everyone!