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David's Stem Cell Transplant

David's Stem Cell Transplant. Friday, January 11, 2008. Always looking for solutions. Since the first day that we found out that I might have Scleroderma, Robbi and I have looked at every treatment that we have heard about. When you look for ideas - boy can you find them. Then, once you go public with your diagnosis, you are inundated with information from all over the world. About 1 1/2 years ago, when my lung function deteriorated at a faster rate, I had conversations with my doctors. I was, then, ...

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David's Stem Cell Transplant | desktopdavid.blogspot.com Reviews

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David's Stem Cell Transplant. Friday, January 11, 2008. Always looking for solutions. Since the first day that we found out that I might have Scleroderma, Robbi and I have looked at every treatment that we have heard about. When you look for ideas - boy can you find them. Then, once you go public with your diagnosis, you are inundated with information from all over the world. About 1 1/2 years ago, when my lung function deteriorated at a faster rate, I had conversations with my doctors. I was, then, ...

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David's Stem Cell Transplant | desktopdavid.blogspot.com Reviews

https://desktopdavid.blogspot.com

David's Stem Cell Transplant. Friday, January 11, 2008. Always looking for solutions. Since the first day that we found out that I might have Scleroderma, Robbi and I have looked at every treatment that we have heard about. When you look for ideas - boy can you find them. Then, once you go public with your diagnosis, you are inundated with information from all over the world. About 1 1/2 years ago, when my lung function deteriorated at a faster rate, I had conversations with my doctors. I was, then, ...

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desktopdavid.blogspot.com

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David's Stem Cell Transplant: February 2007

http://desktopdavid.blogspot.com/2007_02_01_archive.html

David's Stem Cell Transplant. Sunday, February 25, 2007. HEALING - DAY 23 - 022507. Yesterday I thought I had an accomplishment worthy of a posting, all to itself. but then, today happened. Not only had I begun a series of exercises, so that I can begin to strengthen my arms; but I walked the length of our road TWICE! The second lap was tougher to complete but I made it, and kept the pace at a steady and regular pace. I did this at a steady pace and arrived home without any severe side affects. I was...

2

David's Stem Cell Transplant: January 2007

http://desktopdavid.blogspot.com/2007_01_01_archive.html

David's Stem Cell Transplant. Wednesday, January 31, 2007. THERE’S A MAN IN MY ROOM! And it’s so good to have him in here! It’s amazing that he’s here! It’s amazing that he’s anywhere! Wonder of wonderwhat an unbelivable day! David is wiped out emotionally as well as physically. It’s a great wiped out. Last nite, he talked with Heather, (awesome nurse) for 3 hours going over everything that happened over the past month and he cried. Yes, THIS MONDAY 2/5! 3 WEEKS EARLIER THAN EXPECTED! Posted by DesktopDa...

3

David's Stem Cell Transplant: To Be, or Want To Be, or Don't Get It Be

http://desktopdavid.blogspot.com/2007/12/to-be-or-want-to-be-or-dont-get-it-be.html

David's Stem Cell Transplant. Thursday, December 27, 2007. To Be, or Want To Be, or Don't Get It Be. Hey, I've got it better than many others no one is bombing my neighborhood, and my family, (thanks to so many of you), has never lacked a single thing to sustain our lives. So please read the following posting in this light. This one addresses a challenge I’ve been working thru, that deals with relationships. Please comment early and often. There are those who come to visit and are quick to say, "You look...

4

David's Stem Cell Transplant: December 2006

http://desktopdavid.blogspot.com/2006_12_01_archive.html

David's Stem Cell Transplant. Sunday, December 31, 2006. Day by Day w/ Robbi and David. Stay with us, as Robbi writes the basic updates (as only Robbi can! David will provide some details when ever he feels up to it. Posted by DesktopDavid at 7:55 PM. Links to this post. DAY 5 - 123106. Yes of course I packed it. Last day of 2006. How do I begin to put this year into words? I wish you a year filled with love and laughter. Because with love and laughter you can get through anything. Several visits to 3-No...

5

David's Stem Cell Transplant: April 2007

http://desktopdavid.blogspot.com/2007_04_01_archive.html

David's Stem Cell Transplant. Monday, April 02, 2007. WHY CAN'T I BREATHE AS WELL? This is the question that I've become consumed with these last few days. The examine showed that my oxygen levels were down significantly. I was always in the high 90's (98-99%) but today I was running in the 88-90% level. This is a bad thing! The possibilities are many, so I won't list them now. none are good. some are more treatable than others. Right now we are in the midst of blood tests (for kidney function), and echo...

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victoriasmiracle.blogspot.com

VICTORIA'S MIRACLE: January 2011

http://victoriasmiracle.blogspot.com/2011_01_01_archive.html

DIARY OF A STEM CELL TRANSPLANT. Friday, January 28, 2011. I hope you're having a good day too. Saturday, January 22, 2011. Blip in the Road. Subscribe to: Posts (Atom). Bob and I (post-transplant). Victoria by the Pond, August 2008. Happy Mother's Day, Mom," by Gaby. Some of my angels. The Field Museum, Chicago. Walk Along Lake Michigan. How to Reach Victoria. National Foundation for Transplants. Dr Richard K. Burt. Not the ending, but happiness to report (follow-up article on Victoria Chavez). Please m...

victoriasmiracle.blogspot.com

VICTORIA'S MIRACLE: July 2010

http://victoriasmiracle.blogspot.com/2010_07_01_archive.html

DIARY OF A STEM CELL TRANSPLANT. Monday, July 26, 2010. Scleroderma Support Group Summer Party. It has helped me so much to volunteer, to get outside myself and focus my concern on the needs of others with this disease. I am a lucky one. To have had the opportunity to have a stem cell transplant which saved my life is how I was blessed. I am forever grateful to the Foundation for being there for me. National Scleroderma Foundation Conference. Again I would like to thank everyone for their support. Sacram...

victoriasmiracle.blogspot.com

VICTORIA'S MIRACLE: October 2009

http://victoriasmiracle.blogspot.com/2009_10_01_archive.html

DIARY OF A STEM CELL TRANSPLANT. Sunday, October 11, 2009. Yesterday Bob and I and Karin and Sheldon went to the Sacramento State Football Game.we won! It was a great fall day! Also, My daughter, Gaby, went to her boyfriend, Phil's, homecoming dance. As you can see I'm out and about so there may not be as many updates before. This is a good thing! Saturday, October 3, 2009. Hey, I'm back! Yesterday, I gave my best friend a ride to a very important interview and she got the job on the spot! I love life,.

desktopdevona.blogspot.com

My experience: 6/24/07 - 7/1/07

http://desktopdevona.blogspot.com/2007_06_24_archive.html

Thursday, June 28, 2007. So I go back tomorrow to see how it is healing. This is Gods way of slowing me down. Hope your all well. Mom and Joe are coming down tomorrow. I have not seen her since we got home. Links to this post. Subscribe to: Posts (Atom). View my complete profile. My friend Amy's website.

desktopdevona.blogspot.com

My experience: what a time

http://desktopdevona.blogspot.com/2007/06/what-time.html

Tuesday, June 19, 2007. So to let you know a little about what happened. 1 I learned I am allergic to platelets that are not washed first. 2 Any tape they use is not friendly to my skin. Because of this the picc line they put in so that they do not have to stick you all the time got infected and they had to pull it out. 3 I got pneumonia in my left lung after my transplant and was released early despite this.which mom had to turn around and take me back the next day and I got admitted again. Ok, so I am ...

desktopdevona.blogspot.com

My experience: 5/20/07 - 5/27/07

http://desktopdevona.blogspot.com/2007_05_20_archive.html

Friday, May 25, 2007. The doctor said I have five more days of "bad days" then I should be on an upscale then. I can hardly wait for those days to come! I am still not eating the food they bring and my taste for "sweets" has disappeared but the nurse assures me that my taste for it will return. Hope everyone is doing well and God Bless all of you! Links to this post. Subscribe to: Posts (Atom). View my complete profile. My friend Amy's website.

desktopdevona.blogspot.com

My experience: 9/2/07 - 9/9/07

http://desktopdevona.blogspot.com/2007_09_02_archive.html

Friday, September 7, 2007. Ok, so I decided that while I am recovering that I would do something productive. I signed up for school! Ok, so I decided to get an education in medical coding. I should know enough at this point about the medical field to know that this is what I want to do. Let me just say that medical terminology and anatomy suck. I am getting through it and made a 96 on my first test, but it is hard. At least it gives me something to do! Links to this post. Subscribe to: Posts (Atom).

desktopdevona.blogspot.com

My experience: pics

http://desktopdevona.blogspot.com/2007/06/pics.html

Friday, June 22, 2007. Subscribe to: Post Comments (Atom). View my complete profile. My friend Amy's website.

desktopdevona.blogspot.com

My experience: 4/15/07 - 4/22/07

http://desktopdevona.blogspot.com/2007_04_15_archive.html

Saturday, April 21, 2007. Well I was hoping to be released today to my hotel room to rest after a 24 hour molization? I know is ready to get out of here because she forgot her makeup bag and is about to go nuts without it. Leave it to her to leave something. She said she would have rather left her meds.lol. Links to this post. Friday, April 20, 2007. The strongest women I know. Woo hoo thanks for the distraction Teri. Pics are down below. I finally got to meet the beautiful Amy! Links to this post.

desktopdevona.blogspot.com

My experience: Dancing

http://desktopdevona.blogspot.com/2007/10/dancing.html

Tuesday, October 16, 2007. Star in Your Own JibJab! Subscribe to: Post Comments (Atom). View my complete profile. My friend Amy's website.

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David's Stem Cell Transplant

David's Stem Cell Transplant. Friday, January 11, 2008. Always looking for solutions. Since the first day that we found out that I might have Scleroderma, Robbi and I have looked at every treatment that we have heard about. When you look for ideas - boy can you find them. Then, once you go public with your diagnosis, you are inundated with information from all over the world. About 1 1/2 years ago, when my lung function deteriorated at a faster rate, I had conversations with my doctors. I was, then, ...

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