mattwillsjourney.blogspot.com

Matthew's Journey

Monday, August 15, 2011. Matthew's condition continues to deteriorate. The doctors have stopped therapy as there is nothing more they can do for him. The leukemia has spread to his central nervous system and other sanctuary sites that would not be reversed through a BMT. He will spend his remaining time either here at Stanford or possibly at home. We want to insure he is comfortable and free from as much pain as possible. Thursday, August 11, 2011. We are praying for a miracle. Wednesday, August 3, 2011.

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Monday, August 15, 2011. Matthew's condition continues to deteriorate. The doctors have stopped therapy as there is nothing more they can do for him. The leukemia has spread to his central nervous system and other sanctuary sites that would not be reversed through a BMT. He will spend his remaining time either here at Stanford or possibly at home. We want to insure he is comfortable and free from as much pain as possible. Thursday, August 11, 2011. We are praying for a miracle. Wednesday, August 3, 2011.

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Matthew's Journey | mattwillsjourney.blogspot.com Reviews

https://mattwillsjourney.blogspot.com

Monday, August 15, 2011. Matthew's condition continues to deteriorate. The doctors have stopped therapy as there is nothing more they can do for him. The leukemia has spread to his central nervous system and other sanctuary sites that would not be reversed through a BMT. He will spend his remaining time either here at Stanford or possibly at home. We want to insure he is comfortable and free from as much pain as possible. Thursday, August 11, 2011. We are praying for a miracle. Wednesday, August 3, 2011.

INTERNAL PAGES

mattwillsjourney.blogspot.com

1

Matthew's Journey: Fianlly some good news!

http://mattwillsjourney.blogspot.com/2011/07/fianlly-some-good-news.html

Sunday, July 24, 2011. Fianlly some good news! A recent bone marrow biopsy on Wednesday revealed no cancer cells so the Doctor's are confident that he is in temporary remission. He also received a new pic line on Friday which eliminates the need for IV's in both hands and forarms. He slept for the fist time in two months on his stomach Friday night. If he resumes eating, counts come up, no fevor or bacteria infections for a few weeks the Doctor's. July 25, 2011 at 8:02 AM. July 28, 2011 at 11:13 AM.

2

Matthew's Journey: July 15

http://mattwillsjourney.blogspot.com/2011/07/july-15.html

Friday, July 15, 2011. Matthew had his mediport and pic line removed a few days ago and has been infection free. The high fevers he had from the infection must have taken a lot out of him because he has been sleeping most of the time. We just continue to wait for Matt to get stronger so he. Can receive a bone marrow transplant still weeks away. Both sisters are evenly suited to be Matts BMT donor. The decision will be up to us. July 18, 2011 at 6:59 PM. You can do it! Subscribe to: Post Comments (Atom).

3

Matthew's Journey: August 2011

http://mattwillsjourney.blogspot.com/2011_08_01_archive.html

Monday, August 15, 2011. Matthew's condition continues to deteriorate. The doctors have stopped therapy as there is nothing more they can do for him. The leukemia has spread to his central nervous system and other sanctuary sites that would not be reversed through a BMT. He will spend his remaining time either here at Stanford or possibly at home. We want to insure he is comfortable and free from as much pain as possible. Thursday, August 11, 2011. We are praying for a miracle. Wednesday, August 3, 2011.

4

Matthew's Journey: May 2011

http://mattwillsjourney.blogspot.com/2011_05_01_archive.html

Tuesday, May 31, 2011. Matthew is watching the NBA finals with his uncle Anthony. Subscribe to: Posts (Atom). View my complete profile. Watermark template. Powered by Blogger.

5

Matthew's Journey: July 10th

http://mattwillsjourney.blogspot.com/2011/07/july-10th.html

Sunday, July 10, 2011. Subscribe to: Post Comments (Atom). Fianlly some good news! View my complete profile. Watermark template. Powered by Blogger.

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