ararecancerjourney.blogspot.com
A Rare Cancer Journey: August 2014
http://ararecancerjourney.blogspot.com/2014_08_01_archive.html
A Rare Cancer Journey. Sunday, August 3, 2014. On November 17, 2010, when my new bone marrow came to live with me, one of my transplant doctors wished me, "New beginnings! See December 5, 2010 post. New beginnings it certainly was - new chances, new opportunities, a new future. Now that it's been almost 5 years since my Acute Myeloid Leukemia. Adventure began, my attention for the last few years returned to my 14 year battle with metastatic Adenoid Cystic Carcinoma. The radiofrequency ablation ( RFA.
hopeandheart.blogspot.com
hope and heart
http://hopeandheart.blogspot.com/2010/11/i-havent-been-writing-in-my-blog-for.html
Nov 18, 2010. I haven't been writing in my blog for a long time, I have been busy with rehab and just trying to stay warm. The foot doctor gave me shots in my feet to help them and it was so so so painful. Dr. Thacker says that I need special shoes or orthopedic shoes because I am so very hard on my feet and medicare or insurance won't cover it. I think one shoe is wider because of my amputation. O well. Subscribe to: Post Comments (Atom). Wild Beasties, 3rd Edition published my Me! What are stem cells?
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,.
supportshazza.blogspot.com
support shazza: Awaiting an Imminent Arrival
http://supportshazza.blogspot.com/2008/12/awaiting-imminent-arrival.html
Wednesday, December 3, 2008. Awaiting an Imminent Arrival. We had high hopes for today but I guess giving birth to a new immune system can vary from person to person. Sharon’s white cell count is still 0.1 and no neutophils. Thanks for your support. Think of you two daily-you are in my daily prayers-love and kissess to both of you-love, pat bal. December 3, 2008 at 1:48 PM. Without you Pat and your help Shazza would not have had this chance of a new life, Cheers Craig and Sharon. View my complete profile.
supportshazza.blogspot.com
support shazza: Long Days of Isolation
http://supportshazza.blogspot.com/2008/11/long-days-of-isolation.html
Friday, November 28, 2008. Long Days of Isolation. Hope everyone had a good thanksgiving thanks to Sue and Gille. For helping Mom and the Boys participate in the holiday festivities. We felt apart of it as we could see and talk to them on the web cams on our lap top from the hospital isolation room. Well I am still Neutropenic. Is an issue but I am still allowed to walk with a mask and gloves three times a day in circuits around the BMT. Cheers Sharon and Craig. Hi Sharon and Craig,. I am glad your mom h...
supportshazza.blogspot.com
support shazza: Return to the Windy City
http://supportshazza.blogspot.com/2008/11/return-to-windy-city.html
Saturday, November 22, 2008. Return to the Windy City. We arrived back on Wednesday after our fleeting visit back to Phoenix. We had a great time catching up with the boys and getting things ready for Christmas as we don`t know what issues may lay ahead. Mom has been doing a great job and our friends have been fantastic. Especially. Mark and Emily. Thank you all for helping out. The boys are more used to Moms routine than mine. She has it well organised. Winter has come to Chicago. Wipes that kill everyt...
frozen-oranges.blogspot.com
frozen.oranges: September 2008
http://frozen-oranges.blogspot.com/2008_09_01_archive.html
Monday, September 29, 2008. It's the high holidays, folks! That means the service is coming to a conclusion. Unfortunately, the holidays (like the other 98.3% of the population's) come with stress and part of that stress always. 160;involves food in one way, shape, or form (no pun intended). Tonight, my mother received the infamous, "You gotta put some meat on her bones! 160;Girls these days don't eat enough! To which she replied, "Oh, haha! Like enjoying our sweet new year. Thursday, September 25, 2008.
