Day + 59

Posted on: 26/05/2014

We went back to the hospital today at 9am for our routine medication and checks. Dr Biffi was so pleased with Ava's progress that she decided to reduce our hospital visits to twice weekly, which is terrific. We now have capsules (wish me luck) instead of some of the regular IV medication, which is another step towards her independence. We have approximately 6 weeks left in Milan and will now have 5 free days every week. So I think it is time to step up the school work... At this rate Ava may even be allowed to return to school at 6 months post-transplant, i.e. the end of September, which is far earlier than we imagined possible. Provided that she has an adequate immune system, this will certainly be the best place for her, back amongst her friends.