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A letter to JHC about DylanJuly 15, 2003 | |||
Dear JHC,|
Dylan sleeps a lot and he has a "G"-tube so he can eat.
Before he received his transplant he was eating everything, such as potatoes, bread, vegetables, and candy.
The chemotherapy has been very hard for him, just like other children who have had a transplant. He is on 14 medicines per day. | His favorite toys are his monkey and Bert and Ernie, you can see them in the picture. He goes six times a week to physical therapy because he lost his motor skills (due to the disease). We have to stay 5 to 6 more months because we can't fly overseas. Dylan's has no immune system and we cannot risk his geting an illness. This is also why we have to be careful that no one who is sick comes around him because something like the flu will kill him. He has a mask for going outside. We clean everything with Lysol and alcohol wipes and vacuum everyday. Greetings, Michel, Angelique and Dylan 
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