This sure wasn't in my plan, but it is my journey! To follow my story be sure to go to my first post as I am attempting to write this blog chronologically. Blog Archives are on the lower right hand side of the blog.
Thursday, February 9, 2017
Six Year Cancer-versary!
I admit that it has been a roller coaster of a ride, with many ups and downs, but I am happy to report, that I am still here; enjoying life, family and friends.
Looking back on my journey I realize how far I have come, and am so grateful for the medical advances that have kept me alive.
I find it ironic that I am in Palm Springs, as I now live in Boise, Idaho, on the day, in the same town that I was diagnosed. It is bittersweet. Joe and I are staying at the same resort that we came to, on Valentine's Day, when I was released from the hospital.
As far as, how I am "doing" now, I can tell you that last year was my very best year since diagnosis. All of my PCR's were below the magical .0 number and my side effects were minimal. I still deal with the typical nerve and bone pain, fatigue, headaches and nausea, but they were more of a nuisance this year, than debilitating.
I also still deal with pleural effusion from the Sprycel, but have found that a thorocentesis does wonders!
Living life with cancer is definitely an inconvenience; we spend much of our "vacation" time traveling to see my oncologist, having blood drawn and scans taken, but I just accept that this is part of the deal, in keeping me alive.
There is a small amount of stress, every three months, waiting for test results, but that is a small price to pay for the privilege of being around to enjoy my life.
Tonight I will spend with my youngest son and tomorrow morning we will travel to see my middle son, and his family. The joy that my grandchildren bring to my heart is like no other and I feel blessed to still be alive!
Reach out to others for support and be kind to yourself; accept your new normal and learn to roll with the punches.
And remember, that someday, there may actually be a cure for chronic mylogenous leukemia! I intend to be here when it happens!
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Michele, I cannot be happier for you than I am. You have set a standard for so many of us of follow, to emulate, to pass on to others. You never lost hope nor faith, you chose to deal with it all, to have taken it head on. God bless you my friend. Stay well, stay happy, and come to see it one day beat. Much love to you always,ReplyDelete
What a wonderful, refreshing outlook you have! God Bless you on your life journey!ReplyDelete
Your CML Sister in NH,
Michele, what a beautifully uplifting post. I commend you for your spirit and fight. JeanneReplyDelete