Hi all, I'm new to the forums so please excuse me if these questions have been asked before. My 2 year old son was recently diagnosed with unilateral Wilms Tumour and starts chemo this week. I know side-effects can vary from person to person and drug to drug, I'm just wandering what other people's experiences are with regards to hair loss and skin and mouth changes and immunity and so on goes. Our 5 year old is at school so she comes home with everything that's going around just now! And our son likes to play with his hair, it's a little comfort habit he's got when he's sad or tired.
Thanks in advance.