Posts by Emily the Mom-cologist

Our Journey by the Numbers

»Posted by on Sep 13, 2012 in Updates | 5 comments

I’ve been pondering the magnitude of medical care Ethan has received thus far. I’m a numbers person by nature so it was therapeutic for me to compile the data. It’s probably missing some things but this is the treatment Ethan received during the 223 days of frontline therapy: 3 bone marrow aspirations 23 nights spent in the hospital 154 doses of oral chemotherapy 12 doses of intrathecal chemotherapy (in the spine) 58 doses of IV chemotherapy 80+ lab draws 14 procedures under anesthesia 5 transfusions of packed red blood cells 1 transfusion of platelets 3 x-rays and 1 echocardiogram hundreds of doses of supportive medications such as: bactrim, zofran, reglan, benadryl, omeprazole, ranitidine, oxycodone, oseltamivir, miralax, etc. Truly...

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Moving On

»Posted by on Sep 5, 2012 in Updates | 0 comments

We are one week from the end of frontline therapy. Leukemia treatment works like this: 6-8 months of frontline (intense) chemotherapy followed by 3 years of maintenance chemotherapy. Frontline therapy consists of a lot of IV and spinal chemo: anywhere from 1 to 5 days a week, every week. Maintenance chemo consists of spinal chemo once every three months, IV chemo once a month and oral chemo given daily at home. So basically for the next three years 90% of the responsibility for maintaining my sons remission falls to me. No pressure. I will be relieved to get our clinic visits down to once per month. But if I’m being honest I’m weary of chemo. So much chemo for so long. I feel like three years is stretching before me like the giant dead marshes in The...

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Vacation

»Posted by on Jun 22, 2012 in Updates | 0 comments

Vacation

Some of the best news that we’ve had in a while: Ethan gets to go with us on vacation to North Carolina! He went through the first three hospital stays for high-dose methotrexate with flying colors and blood counts are great so his oncologist gave him “time off for good behavior”. Not only that but we will be heading into the last phase of intensive chemotherapy in the 2nd week of July. Can you see that awesome light at the end of the tunnel?! I will try to blog some awesome pictures of us at the beach. We are really looking forward to connecting with our extended family.

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Vote for us! – UPDATE

»Posted by on Jun 11, 2012 in Updates | 1 comment

Vote for us! – UPDATE

The contest is over! We ended public voting in first place with over 1,000 votes. Thank you to all of our friends and family who voted. Unfortunately, Tracy didn’t pick me as the winner but did give us a very sweet mention on her website. When I told Ethan we didn’t win, he climbed on my lap with a big smile and said “I’m still happy” while giving me hugs and kisses. He is a shining example of an unbreakable spirit! He gives me so much inspiration and motivation to do my best. I’ve entered to win a week long detox retreat with a celebrity trainer and I need your vote! I’ve been doing Tracy Anderson’s Metamorphosis program for a year now. When Ethan was first diagnosed with leukemia I spent a lot of time just...

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Seven

»Posted by on Jun 3, 2012 in Updates | 2 comments

Today Ethan turned seven. To be honest, there were a few times this year when I wasn’t sure if we were going to be celebrating on this day. How easily fear and doubt creep in…. but here we are and we have so much to be thankful for. It’s been four months since his diagnosis and we are more than halfway through his intensive chemotherapy. Ethan is doing so well. Physically, mentally, emotionally and spiritually he has exceeded all of our expectations. He is a joy to everyone we meet and I am so proud of him. The day he was born was a pivotal day in my life and I thought I would share the story with you as a celebration of what God began…. The Story of Ethan Gabriel’s Birth His due date was May 23rd, 2005 and I went into labor twice....

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