Headed for the MSS unit again

We are headed down to the short stay unit again today. My understanding is that Beth is going to have to get another transfusion. I’ve been going in to work each day, and so I don’t get a chance to talk directly with the folks in the hospital, and so I have less information than I’d like. Last I saw, her hemoglobin level was rising slightly, but it’s also been a hallmark of her behavior that, if she’d get a transfusion, she’d feel good, she’d try to do a lot of stuff around the house, and then she’d feel tired again. Maybe that’s what’s happening.

We do have an appointment with Dr Rossetti on Monday, January 9, and we should find out a lot.

Beth is still suffering from itchy, painful blisters on her hands and feet, and she’s itchy in other places as well. She does seem to be having less trouble eating (it’s easy to see that she’s lost some weight during this process).

 

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