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Bledsoe BattleSharing thoughts on living with Chronic Myelogenous Leukemia (CML) in our family
http://bledsoebattle.blogspot.com/
Sharing thoughts on living with Chronic Myelogenous Leukemia (CML) in our family
http://bledsoebattle.blogspot.com/
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Bledsoe Battle | bledsoebattle.blogspot.com Reviews
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Sharing thoughts on living with Chronic Myelogenous Leukemia (CML) in our family
bledsoebattle.blogspot.com
Bledsoe Battle: January 2013
http://bledsoebattle.blogspot.com/2013_01_01_archive.html
Sharing thoughts on living with Chronic Myelogenous Leukemia (CML) in our family. Sunday, January 6, 2013. Two years ago, my husband took his last breath as his body finally gave out after battling leukemia for 4 years. While his memory and his presence live on for me, I am deeply saddened by the fact that someone so loved is gone forever because of cancer. Posted by CML Wife. Labels: Leukemia and Lymphoma Society. Subscribe to: Posts (Atom). Subscribe to Bledsoe Battle by Email. CML Guy and CML Wife.
Bledsoe Battle: Feeling the Loss
http://bledsoebattle.blogspot.com/2012/10/feeling-loss.html
Sharing thoughts on living with Chronic Myelogenous Leukemia (CML) in our family. Tuesday, October 30, 2012. I've been feeling more subdued and more grumpy than normal for the last week or so. I was just blaming it on not getting enough sleep, but today I finally figured out that my emotions are on edge more than usual because Tyler's birthday was Halloween. What can you do to help save the person who will be diagnosed with any form of cancer tomorrow? I've chosen fundraising for the Leukemia and Lymphom...
Bledsoe Battle: Love Lives On
http://bledsoebattle.blogspot.com/2013/02/love-lives-on.html
Sharing thoughts on living with Chronic Myelogenous Leukemia (CML) in our family. Sunday, February 24, 2013. A few weeks ago at our Team in Training practice, each of the runners was given the opportunity to write the name of the person that they run in memory/honor of. I wrote down Tyler's name because my love for him is what inspired me to first start fundraising for the Leukemia and Lymphoma Society. Posted by CML Wife. Subscribe to: Post Comments (Atom). Subscribe to Bledsoe Battle by Email.
Bledsoe Battle: July 2012
http://bledsoebattle.blogspot.com/2012_07_01_archive.html
Sharing thoughts on living with Chronic Myelogenous Leukemia (CML) in our family. Tuesday, July 3, 2012. Light the Night Kickoff Event - July 21st. FUN for EVERYONE and FREE to join! Guest appearance from a Seattle Sounders player! Meet and take your picture for unforgettable memory! Free to attend for everyone - team members, family, friends, and coworkers. Carnival games, festivities, and prizes. Complimentary food and refreshments. Meet your local Honored Heroes. Raise $100 by our Kickoff date AND.
Bledsoe Battle: Tyler lives on in happy memories
http://bledsoebattle.blogspot.com/2013/10/tyler-lives-on-in-happy-memories.html
Sharing thoughts on living with Chronic Myelogenous Leukemia (CML) in our family. Thursday, October 31, 2013. Tyler lives on in happy memories. On the anniversary of his birth, I find myself remembering Tyler in so many different ways. While some cause grief, many more cause smiles and laughter. I'm so very thankful to have had the years that I did with him and hope that each of you has happy memories of him today too. For a slideshow of photos of Tyler, visit http:/ youtu.be/ggeaw0Mo6yc. Shop for a Cure.
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The Barquist Family: Mother's Day Tea
http://barquistfamily.blogspot.com/2015/05/mothers-day-tea.html
Keeping up with the Barquist family.one day at a time. Friday, May 8, 2015. One of my favorite things about Mother's Day are the special things they make and do at school. I was invited to a Mother's Day Tea for Colt's Kindergarten class. He drew this adorable picture of me. He also made me wind chime and a necklace. Then they put on a little production. It was so cute! Here are lots of pictures and videos. I forgot to get a picture of me and Colt together so we took a few selfies when we got back.
The Barquist Family: Post Dentist Treat
http://barquistfamily.blogspot.com/2015/05/post-dentist-treat.html
Keeping up with the Barquist family.one day at a time. Monday, May 18, 2015. The kids had a dental check up last week. I am not sure who dreads it more, me or them. Actually I do know. Me. I just cringe at the thought of the lecture I get when it comes to helping them brush their teeth. I fail miserably at this. But I will try to get better. This time we went two for four, which isn't so bad to me. Bo wasn't interested in the movie but he LOVED his frozen yogurt. Subscribe to: Post Comments (Atom).
The Barquist Family: Spontaneous Camping Trip - Day 1
http://barquistfamily.blogspot.com/2015/05/spontaneous-camping-trip-day-1.html
Keeping up with the Barquist family.one day at a time. Wednesday, May 20, 2015. Spontaneous Camping Trip - Day 1. Last Saturday we had a busy morning of baseball pictures, a baseball game and watching our cousin's soccer game. When we got back to the house at lunch time I was looking forward to the rest of the day where we had nothing planned. It didn't take too long for Brad to come up with an idea. What if we go camping? It took us a few hours to get packed up but we made it up to Denny Creek.
The Barquist Family: Slide
http://barquistfamily.blogspot.com/2015/05/slide.html
Keeping up with the Barquist family.one day at a time. Sunday, May 10, 2015. Ollie has been begging me to take him to the park with the big slides. It has been awhile since we have been there, but I finally took him, Darby and Bo. Subscribe to: Post Comments (Atom). First Slip N Slide of the Season. Spontaneous Camping - Day 2. Spontaneous Camping Trip - Day 1. Pre Mothers Day and Birthdays. Very blessed to be the wife and best friend to one awesome man and the mom to three boys and one girl.
Rydman Rumors: July 2015
http://rydmanfamily.blogspot.com/2015_07_01_archive.html
Thursday, July 30, 2015. We left work early on Thursday to pick up Rachel's new glasses. We got them fitted and then on the way to the car she said they weren't very comfortable. Hopefully they feel more comfortable for her soon. She wanted to pose with her glasses in the case for Mimi. I requested the special coating on these glasses, so I would see her eyes in the pictures I take. Rachel has beautiful blue/green eyes and half the time all I can see is the reflection off her glasses. The four kids playe...
Wishes for Rassie: January 2011
http://wishesforrassie.blogspot.com/2011_01_01_archive.html
On September 25, 2009, Rassie was diagnosed with Chronic Myelogenous Leukemia. His symptoms: Swollen Feet and bruising. We never exepected a diagnoses of Leukemia. The Doctors and we ourselves, are very optimistic about the treatments available. We know that we have a long road ahead of us and we hope that you will support us on our journey to recovery. Wednesday, January 26, 2011. I am just ready for this all to be over with! The 1st is Rassie mowing the grass back in October! Thursday, January 6, 2011.
Wishes for Rassie: Online Scentsy Party
http://wishesforrassie.blogspot.com/2012/10/online-scentsy-party.html
On September 25, 2009, Rassie was diagnosed with Chronic Myelogenous Leukemia. His symptoms: Swollen Feet and bruising. We never exepected a diagnoses of Leukemia. The Doctors and we ourselves, are very optimistic about the treatments available. We know that we have a long road ahead of us and we hope that you will support us on our journey to recovery. Monday, October 1, 2012. You can find our Scentsy Party by clicking the following link - Light the Night Walk 2012 - Team Rassie. Flameless, smokeless, a...
Wishes for Rassie: July 2013
http://wishesforrassie.blogspot.com/2013_07_01_archive.html
On September 25, 2009, Rassie was diagnosed with Chronic Myelogenous Leukemia. His symptoms: Swollen Feet and bruising. We never exepected a diagnoses of Leukemia. The Doctors and we ourselves, are very optimistic about the treatments available. We know that we have a long road ahead of us and we hope that you will support us on our journey to recovery. Tuesday, July 2, 2013. Subscribe to: Posts (Atom). Light The Night Walk. View my complete profile. Ph CML, is a slow-growing type of cancer of the blood ...
Wishes for Rassie: October 2012
http://wishesforrassie.blogspot.com/2012_10_01_archive.html
On September 25, 2009, Rassie was diagnosed with Chronic Myelogenous Leukemia. His symptoms: Swollen Feet and bruising. We never exepected a diagnoses of Leukemia. The Doctors and we ourselves, are very optimistic about the treatments available. We know that we have a long road ahead of us and we hope that you will support us on our journey to recovery. Tuesday, October 2, 2012. Help Support Team Rassie in LLS Light the Night Walk 2012. We really appreciate your generosity! Monday, October 1, 2012. Light...
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Monday, March 19, 2018. Strengthening churches as they execute the Great Commission. A Moment with Mike. Parenting in a Digital Age, Feb 18, 6 - 8:30 pm Westmoreland High School. Plenary session - The Challenge Before Us, Jason Gibson, Director The Babb Center. 5 Breakouts with practical training for your parents and grandparents. What do we do? How can we help our parents and kids? This conference will give you some answers! March 24 - 29. The Work—prepare for the public launch of. Parker and Jess have ...
Bledsoe Battle
Sharing thoughts on living with Chronic Myelogenous Leukemia (CML) in our family. Thursday, October 31, 2013. Tyler lives on in happy memories. On the anniversary of his birth, I find myself remembering Tyler in so many different ways. While some cause grief, many more cause smiles and laughter. I'm so very thankful to have had the years that I did with him and hope that each of you has happy memories of him today too. For a slideshow of photos of Tyler, visit http:/ youtu.be/ggeaw0Mo6yc. A few weeks ago...
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