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Our Rhabdomyosarcoma JourneyOne Family's Journey from Diagnosis to a hopefull cure of a 3 yr old's cancer story.
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One Family's Journey from Diagnosis to a hopefull cure of a 3 yr old's cancer story.
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Our Rhabdomyosarcoma Journey | cartwightsoftexas.blogspot.com Reviews
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One Family's Journey from Diagnosis to a hopefull cure of a 3 yr old's cancer story.
cartwightsoftexas.blogspot.com
Our Rhabdomyosarcoma Journey: Life gave us lemons and i wanted watermelon!
http://cartwightsoftexas.blogspot.com/2010/03/life-gave-us-lemons-and-i-wanted.html
One Family's Journey from Diagnosis to a hopefull cure of a 3 yr old's cancer story. Thursday, March 18, 2010. Life gave us lemons and i wanted watermelon! To me watermelon is joy, the happiness of summertime, contentment, that feeling after a long day of pure bliss and enjoyment of family. You know-like after a great 4 th. Of July weekend or just a nice weekend at the lake? Then came the lemons-June 1. I will never forget our ped's. Thanks Dr. S! He knew the battle we were facing. The giant lemon Go...
Our Rhabdomyosarcoma Journey: 1 yr ago and
http://cartwightsoftexas.blogspot.com/2010/06/1-yr-ago-and.html
One Family's Journey from Diagnosis to a hopefull cure of a 3 yr old's cancer story. Tuesday, June 1, 2010. 1 yr ago and. Sorry for the long break I took from posting, I’m back now. Disney World was AMAZING! 8203; Make-A-Wish (northtexas.wish.org) and Give Kids the World (www.gktw.org) made our trip full of memories we will never forget! Disney World was UNFORGETTABLE as well! Pictures to follow soon! How is Zach doing? Overall, my heart is so grateful for more time with Zach. I cherish each day ...
Our Rhabdomyosarcoma Journey: I hate Rhabdomyosarcoma
http://cartwightsoftexas.blogspot.com/2010/06/i-hate-rhabdomyosarcoma.html
One Family's Journey from Diagnosis to a hopefull cure of a 3 yr old's cancer story. Monday, June 28, 2010. Final pathology is still not back but I want to post what we know at this time. Thanks for your patience as we have been trying to get the best information we can about what is going on with Zach. It was all pretty shocking to us last Friday as to “what does this mean, they found cancer? We cannot know for sure if they got all the cancer or not. What now you ask? He guided us to move forward with t...
Our Rhabdomyosarcoma Journey: August 2012
http://cartwightsoftexas.blogspot.com/2012_08_01_archive.html
One Family's Journey from Diagnosis to a hopefull cure of a 3 yr old's cancer story. Friday, August 17, 2012. Two years post rhabdo. Still in remission. Still no more rhabdomyosarcoma. Two years this past June. Remission is not a perfect life. We still see Derm and urology. We also have a GI doctor as well as a endocrinologist! Our biggest issue is weight loss and wt gain. I can not keep wt on Zach for nothing! Fighing for other as often as we can. The cartwrights. Links to this post.
Our Rhabdomyosarcoma Journey: July 2010
http://cartwightsoftexas.blogspot.com/2010_07_01_archive.html
One Family's Journey from Diagnosis to a hopefull cure of a 3 yr old's cancer story. Wednesday, July 21, 2010. Our Mighty Mighty God! Please click the title and listen to this great song. Remeber when you think all is lost focus back on Him! He will never leave you or forsake you. Links to this post. Tuesday, July 20, 2010. Remission from Rhabdomysarcoma Rocks! We finally have pathology results back! We are very thankful to hear this is not classified as a relapse! Zach is now in remission. 8203; Please ...
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The Woodruff 4: September 2010
http://kwoodruff4.blogspot.com/2010_09_01_archive.html
Tuesday, September 14, 2010. Labor Day weekend and More! With summer coming to an end and school in full swing us Woodruff. Kids are settling in to a nice "fall" routine.but we couldn't let summer go away with out one last HORRAY. You know what, that is just what we did. Well first we grilled and hung out, then while the grown-ups where getting the fire going we all played in our yard. Here is Shane crawling around.he was having so much fun! Our favorite way to make them is with Peanut butter. Then she s...
The Hanway Family: May 2012
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This is our way of keeping everyone up to date on the happenings of our family of four. Wednesday, May 23, 2012. Sleep Study Results and ENT Follow-Up. Although Abby's done with chemo, we couldn't stay away from the hospital for long. Just two days after leaving, we had to head back for an ENT appointment to go over her sleep study results and determine the next steps that need to be taken to get rid of her trach. Posted by The Hanway Family. I have to agree. Dr Mian - Her Oncologist. Last chemo going in!
The Hanway Family: 18 Months
http://hanwayfamily.blogspot.com/2012/07/18-months.html
This is our way of keeping everyone up to date on the happenings of our family of four. Friday, July 27, 2012. It's hard to believe, but today marks 18 months since Abby was diagnosed with cancer. Her original treatment was only supposed to last 54 weeks, but she is still fighting. Given her odds, we are thrilled that she is still here and pray that she will beat them and be given many, many more years with us. To try to give you an idea of everything she's gone through. Bone Marrow Aspirate/Biopsy - 1.
The Hanway Family: September 2012
http://hanwayfamily.blogspot.com/2012_09_01_archive.html
This is our way of keeping everyone up to date on the happenings of our family of four. Friday, September 28, 2012. Abby recently had her MRI to check on tumor progression and to see if her new chemo is working. Thankfully they showed a small decrease in tumor size. It is a very small decrease, but it is better than no change and definitely better than an increase in size. That means she will continue on the same chemo regimen for now. Posted by The Hanway Family. Sunday, September 9, 2012. I've been thi...
The Hanway Family: Last chemo?
http://hanwayfamily.blogspot.com/2013/01/last-chemo.html
This is our way of keeping everyone up to date on the happenings of our family of four. Saturday, January 12, 2013. Abby was admitted to the hospital on January 3rd for what was supposed to be her last chemo. We went in expecting the worst news we could imagine. Just a few days before Christmas, we found a mass of some sort inside her mouth in her right cheek. Her oncologist had told us to try not to worry about it, but who wouldn't? Posted by The Hanway Family. Prayer for you also.
The Hanway Family: November 2011
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This is our way of keeping everyone up to date on the happenings of our family of four. Tuesday, November 8, 2011. Abby had an appointment with her ENT last Thursday. We got some more information about what needs to be done in order for Abby to be decannulated. I'm allowing myself to dream about what life without a trach will be like again. It will be so nice to be able to leave Abby with someone other than Leonard and me. We could leave the house with just a diaper bag and feed bag, not the huge...This ...
The Hanway Family: October 2011
http://hanwayfamily.blogspot.com/2011_10_01_archive.html
This is our way of keeping everyone up to date on the happenings of our family of four. Sunday, October 9, 2011. Alexis had her 15th month check-up on Tuesday. She's a big girl at 32.25in (93%) and 25lb8oz (85%). Of course, her head is at the 25th percentile. My kids just have small heads. The pediatrician says that she is doing great and has an excellent vocabulary and she was a champ at her shots. Posted by The Hanway Family. Subscribe to: Posts (Atom). And Baby B Makes Three! View my complete profile.
The Hanway Family: April 2012
http://hanwayfamily.blogspot.com/2012_04_01_archive.html
This is our way of keeping everyone up to date on the happenings of our family of four. Sunday, April 15, 2012. No news is good news. May 11-15 will hopefully be her last chemo ever. Alexis continues to do great. She is growing like a weed and I can't believe how much she talks. She routinely puts together four and five word sentences. Most people can't believe that she won't even be two for another three months. To finish things off, here are a few recent pictures of the girls. Subscribe to: Posts (Atom).
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Trusting God no matter what: February 2010
http://trustinggodnomatterwhat.blogspot.com/2010_02_01_archive.html
Trusting God no matter what. 3 Year Old Nathan's Cancer Journey. Wednesday, February 24, 2010. Nathan has begun radiation! I can't tell you how amazed I am at this little boy. He's adapted to this new life so quickly. Today they asked if he wanted to ride in the bed down to radiation or in his stroller. Usually he's put to sleep before going to radiation but today he got to ride down awake, sitting up. He did fantastic! Lord thank you so much that Nathan has adapted so well to this new lifestyle! Thank y...
The Hanway Family: December 2012
http://hanwayfamily.blogspot.com/2012_12_01_archive.html
This is our way of keeping everyone up to date on the happenings of our family of four. Tuesday, December 4, 2012. Due to desats after her decannulation, Abby had another sleep study in October. Once again, it showed severe obstructive sleep apnea. For her age, she should have had an AHI of. We already have the Christmas tree up and Abby is so excited. Every morning when wakes up, she says "It's Christmas Time! I can't wait to see her face on Christmas morning. Posted by The Hanway Family.
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Cartwhisperer | The adventures of an ordinary guy looking for unordinary experiences
The adventures of an ordinary guy looking for unordinary experiences. May 12, 2015. May 12, 2015. Good news kids, your summer jam album dropped a week ago today but nobody told you. I’m here to clue you in. Acclaimed DJ and producer, RJD2. Teamed up with rapper, STS to create an awesome album – STS x RJD2. Continue reading →. May 1, 2015. I live near the Good Food Here. Food carts on 43rd and Belmont. One of my favorite carts to emerge for me here is the Fishbox. April 4, 2015. Continue reading →. There&...
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Our Rhabdomyosarcoma Journey
One Family's Journey from Diagnosis to a hopefull cure of a 3 yr old's cancer story. Sunday, April 27, 2014. Rhabdomyosarcoma does not have us. Zach is now four year cancer free! That is still amazing to me. We still see gastro and that is our main issue. We also now have an ortho doctor watching his hips and pelvis due to lack of growth due to radiation. Cancer does not hold us but we do hold many scars. Please find our caring bridge below. Thanks for always following us! Links to this post. I would nev...
USS SANTA MARIA*******SHIP OF TRUTH
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CartWills | A Family Embracing Autism
How Common Is Autism? In the Giles County, TN area or surrounding counties? This support group is a loving group of parents that support each other through happy and tough times. In the Giles County, TN area or surrounding counties? This group is just as the name says "Friends of" parents who have children with special needs. It is an informative group - bringing awareness to others. Autism Society of Tennessee. Innocence of a child. Autism, Hope and Faith. Apr 6, 2015 by. Feb 28, 2015 by. Feb 10, 2015 by.
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