We have had a few fevers after octagam as well but according to Jason's nephrologist he is not concerned as octagam is a foreign protein in his body so pretty normal.
I have been working closely with Jason's dieticians making sure that he is getting enough calories, fluid requirements and not too much protein. According to the calculations we are giving enough fluids and the calories are fine as well. They are very pleased with his eating and not too worried with what he is eating. The main thing is he is eating and as he develops his eating we can make some changes to his diet. I am hoping I can add some potato and pureed stews into his daily foods soon. Texture is something we will have to work on. He loves his onion still and that isn't the easiest thing to eat. I have tried sneaking other foods in but at the moment he is not budging.
Otherwise over all Jason is doing really well. He has a lot more energy which is more than likely due to the oral eating and extra fluids. His speech has improved SO much - his vocabulary has improved as well as the pronunciation of the words he is saying. His sister is definitely helping here as well. He now has serious competition. We are even noticing some naughtiness which is fantastic to see. School is going great - they are now on a weeks break but his special needs school was the best move ever. I had our parent meeting last week and they are SO pleased with Jason's progress as are we. We are working together and this help has been awesome for me, a huge weight has been lifted off my shoulders. To have the help and assistance we are getting at school is an answer to prayers.