My Journey starts unsuspectingly by a routine annual physical by my general practitioner on October 19,2010. My diligent GP decided to order a CBC, Blood chemistry, urinalysis, etc. A week later the nurse called and said there were some elevations in my white blood cells. She said we'd need to re-test in a couple weeks. She then offered a copy of the blood work which I picked up soon thereafter. I have some background education in blood in my schooling as a Veterinary Technician. That being said, seeing the immature white blood cells on my results blew my mind. Since I didn't have any infections or fevers or even colds the elevation in my white blood count @ 16,800/uL was mind boggling. I started looking for answers on the web and I what I found over and over again was Leukemia. A day or so later, my GP saw me and tried to not upset me. She tried to be a voice of reason. My gut told me otherwise. I started taking more anxiety meds to deal with myself.
I went to a recommended hemotologist/oncologist and that day they did a bone marrow biopsy. About 2-3 weeks later ( November 19th, 2010) I was officially diagnosed with Chronic Myelogenous Leukemia. I don't remember much from that day at the Oncologist getting those results. I just know she told me we caught it super early, I won't lose my hair, I take a daily pill, and I won't die tomorrow. As anyone else that has faced cancer treatment of any kind knows, they suck blood from you regularly and often to monitor you. You see more doctors on a regular basis than you ever did in your life prior to this. You become a total germaphobe.
I started taking my chemotherapy pill (sprycel) on December 1st, 2010. I take this one pill daily for life until a CURE is found. My side effects have been minimal compared to what others people I know have to endure. I get skin rashes, headaches, heavier menstration, longer clotting time for cuts, I am more prone to infections, and occasionally I find new aches and pains that I blame on the meds. One year from my start date of my chemo I was in a cytological remission and I think a cytogenetic remission. I now am awaiting a Molecular remission.
Keep fighting girlfriend!
ReplyDeleteYou are an inspiration and I am so proud to be your aunt!
ReplyDeleteShelby,
ReplyDeleteHang in there you can do it!I found your blog searching for CML resources and would like to add it to our blog directory (link below) so that others dealing with CML can learn from your experiences. However, I wanted to get your permission first. Please contact me at nickv@navigatingcancer.com if you’d like me to add it to our directory.
Take Care,
Nick
https://www.navigatingcancer.com/explore/leukemia/blogs
Hi,
ReplyDeleteNice blog and story. I've had CML since 2003. I had to retire early from teaching as a result. Check out my blog if you wish :)
MaryCrocco.wordpress.com
I'll be following your blog. :). Take care.