I was supposed to start the next cycle of Chemo on Monday, two days ago, but unfortunately it did not happen. My white blood cell count was too low so I needed an injection of medicine to get the count up. I was told that the common side effect of this drug is that your bones ache. This sounded quite odd to me until I had a sudden pain Monday afternoon that felt like I had thrown my back out! After thinking very hard to come up with what I might of done it dawned on me that this was the side effect. No worries!
The white cells were up sufficiently on Tuesday to start the normal treatment. So we had the marathon first day session yesterday and got home around 7:00. While we were gone Aunt Shannon and Uncle Devin, along with partners Ellana and Ben respectively, took part in a gingerbread house making contest. Bennett got a better offer part way through the contest and went to play with his buddy across the street. Needless to say the work suffered and Shannon and Ellana were declared the unanimous winners.
Thanks to Aunt Shannon and Uncle Devin for coming in to help out!
Here is a picture from Chemo (just getting a little work done):
If you can not tell I do have a nice Sun King Brewing stocking hat on, thanks to my friend Mike for keeping my bald head warm.
I did have a little nausea last night but I did not let that stop me from having Taco Tuesday when we got home. Right now I am sitting here getting my second chemo treatment of the second cycle. Feeling great right now, just a little tired. One more treatment to go tomorrow.
Hope you are well and I will talk to you soon.
I am fighting Adult Recurrent Wilms' Tumor and this is a chronicle of that fight. If you would like to reach me directly please e-mail jdmorse78@gmail.com.
Wednesday, December 18, 2013
Friday, December 13, 2013
No More Hair
After a number of days cleaning the hair I was leaving all over the house I decided it was time to get rid of it. Bennett has actually been looking forward to this because he was told he could finally get the mohawk he has been wanting:
Ellana told me "you look like you are going to steel something!" She was not a fan of the mohawk.
Here is the final product:
All for now, everyone have a great weekend!
Ellana told me "you look like you are going to steel something!" She was not a fan of the mohawk.
Here is the final product:
All for now, everyone have a great weekend!
Monday, December 9, 2013
My First Blog Post..... I know it is shocking, try not to faint
The family on 2013 Spring Break |
Those of you that know me well may be saying “Jason Morse is
writing a blog you have to be #@%^&*$# kidding me.” This is not an easy
thing for me to do. I do not enjoy talking about myself. However, I know people
want to be kept up to date on what is happening in my fight with cancer so I am
going to try and update this as often as I can. Please forgive me if I veer off
into my personal reflections on the impact of this disease on myself and my
family (which I intend to do from time to time). If nothing else I think this
has given me a unique perspective and I would like to share that perspective
with you. Who am I kidding if you don’t like it sorry about your luck!
I am 37 years old and live in Westfield, Indiana with my
wife Sandi, daughter Ellana (6), and son Bennett (8). I was diagnosed with
extensive stage Small Cell Lung Cancer on November 20th, 2013. There
were no symptoms until approximately 4 weeks before I was diagnosed. This
cancer is typically associated with smoking or exposure to other environmental factors
(asbestos being one). Neither of these fit my situation which makes the diagnoses
very rare. The normal course of
treatment is a combination of two chemotherapy drugs given for three days followed
by three weeks off. This is referred to as a cycle. I started my first cycle on
November 25th. I am fortunate to be involved in a clinical trial
that adds a immunotherapy drug to the regimen. My next cycle of chemo will begin on
Dec. 16th.
Currently, there is no known cure for extensive stage Small
Cell Lung Cancer. The treatment above has shown temporary success in fighting
the disease. The clinical trial drug has been used to fight another form of
cancer with added success so we are hopeful it will do the same for me.
Today.....I feel great. My activities are limited in very few
ways. I am trying to eat better and sleep a little more. Sandi is trying her
best to turn me into a vegetarian but that is going to be a difficult task! I
am trying to avoid being around sick people as my immune system is not up to
the task of fighting any other illnesses. My hair is officially falling out as
of today. Fortunately, as a retired competitive swimmer, I have been bald in
the past so at least I know what is in store for me!
I will fight this cancer to the end and am hoping for a
miracle. We appreciate everyone’s well wishes and offers of help. At this point
Sandi and I have more offers of help than we have things for people to do. It
is great to know that we have such fantastic friends and family. I love you all
very much and thank you.
That is all for now. First blog post complete! Please feel
free to post any comments or questions and I will try to respond to all of
them. I am leaving this blog open for anyone to read so share this with anyone
who might get something out of it. Add your e-mail at the top of the page and you
will be notified when I add posts. Thanks for reading.
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