February 4, 2009: Jill is still coughing but it has changed to a looser cough instead of dry one. Her breathing is much better though. She saw Dr Burt at 4:30 p m after having her blood drawn in the lab. He seemed very pleased with her in spite of the RSV. He asked her if she noticed any difference from before the transplant and now and she did say that she feels stronger and isn't as tired, which is amazing for a person with MS. Most of the time being exhausted is part of their every day routine.
I don't know if I am imagining it or not , but I think that she is speaking better. Her speech is not as delayed and she is thinking clearer. I know it is much too early to tell.
Love
Doreen
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That's wonderful news, Doreen!! I hope she continues to improve every day!! I'm so happy you'll both be coming home though it will be a real challenge to keep her so isolated for those 3 months, I'm sure! I hope the time flies by and you're able to find lots of creative ways to keep Jill happy and entertained while she recuperates! :-)
ReplyDeleteLove,
Carol