Sun. May 26th

On Friday we were down for blood counts and they were great. Her surgery is scheduled for Wed. May 30th for the removal of her port. This is a picutre of Connie who takes Meghan's blood every time and her room is filled with pictures of all the kids, so this one will be posted on her wall. We met with our doctor and he's decided that he will hold off on her one chemo med vincristine because it has caused the nerve damage and now the acrocyanosis, which has been slightly better. She has been looking great and feeling great as well. Her hair is really starting to come in and she looks great with short hair but she's not ready to go without her wig to to many places, unless she has her hood on like in this picture. She has such a beautiful face for short hair, not everyone can get away with it. Her next round of chemo is scheduled for Monday, June 4th. She has still been breaking out in a rash usually the 3rd day of her meds and we've realized that it's the large dose of prednisone that's causing that, she had it when she was in the hospital as well.

I hear from many of you when I see you that you have trouble making comments but you still read this and that's wonderful and we appreciate all your love and prayers.

On Friday, June 8th Meghan is going off to a spa for the day that is organized through the social worker at the hospital and all the teenage girls that are lukemia/lymphoma patients go and she is so looking forward to that, unfortunately she can't take her mom :*( I'll have to go find a spa for myself that day, ha ha!

Michelle