by Jeff Meckstroth, as Kara Mayer Robinson said
I'm a 62-year-old firefighter Retired. I live in Piquá, Oh, with my wife, Rhonda. In 2015, I was diagnosed with non-small-cell lung cancer, or NSCLC.
Getting a diagnostics was a delayed process. He began in an annual physicist with my family's doctor. It happened to mention that he had a persistent and non-productive cough. This simple cough discussion led to a test battery. Ultimately, in 2015, I received a diagnosis of stage IV NSCLC.
The diagnosis was a complete shock for our family as well as our community medical team. No one believed that it was possible for a healthy adult male with a simple cough and no tobacco use history to have stage IV NSCLC.
Along with Rhonda, I felt emotionally broken. Imagine the sensation of drowning while trying to understand a foreign language - and then be responsible for making immediate decisions that your life depends.
I went to a community oncologist, who received a recommendation from an NSCLC specialist to perform comprehensive biomarker tests in my fabric and my blood. This gave us a detailed analysis of my cancer and my treatment choices. It was invaluable information.
I think it is vital for each medical professional that treats this disease conducting biomarker tests. It can make all the difference in living with the disease.
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My disease has metastasis, or spread, to my bones, so I also had five rounds of radiation. Every 3 months I have laboratory work, a computed tomography of my chest, abdomen and pelvis, and a cerebral magnetic resonance. Periodically, I get an injection to strengthen my bones. I also have a bone sweep.
Both Rhond and I had to develop coping skills to manage life with NSCLC. They include counseling, living at the moment - because future thoughts are unaccept - and finding gratitude and joy every day.
For Rhonda, Education and Advocacy for NSCLC families is an important way to do this. As a lawyer, she advocates the voice of the caregiver and helps people who are newly diagnosed. It also directs education and awareness for appropriate testing and treatments. She spends time every day defending and helping other families surfing on this journey. She firmly believes that helps her deal with diagnosis.
One of the biggest changes we made was our mentality to die from living with NSCLC. We know the reality of this diagnosis, but it was not helpful to live in a constant state of thinking about death and housing on the negative aspects of everything we lose. Instead, we find gratitude for what we still have.Among the downs of the trip, we work hard to live a normal life. I remember a particular day that changed everything. I told Rhonda: "If I did not have NSCLC, I'd buy a new combination."
We decided to buy it anyway. Now when we arrived on new life choices, we make a conscious decision to "buy the combination", despite having cancer. It has been a game exchanger to survive the roller coaster tour.
