Showing posts with label cancer awareness. Show all posts
Showing posts with label cancer awareness. Show all posts

Thursday, February 20, 2014

Dates To Remember.



No, this is not an online site to find your mate or dish about your best/worst date.

I have always been fascinated by numbers and what they represent. Being a cancer patient and now a cancer survivor, the sheer volume of numbers can be overwhelming. But the numbers that stick out the most are the calendar type. They have an intrusive way of sticking in your mind––at least mine––because milestones are HUGE.

Yesterday, February 19, was one of those days. All day I kept thinking "why does today feel so different?" I checked all my blog posts. Nothing but a bad Valentine's Day post I wrote last year. No biggie. But as I began to look through past posts, I rediscovered that my first post on this site was July 19, 2008. And that I had a journal before––hand-written, not digital. Yep, let's go back in time.

My Sister-In-Law, Claudia, would have been 60 this year. She passed away from cancer 16 days after my diagnosis (the first cancer, head-and-neck) in August of 2007. Claudia loved life and her family. I know my Wife misses her every day. I miss her, too. That didn't come from my journal but after telling my Wife, "I keep feeling this is a monumental day somehow" she reminded me of Claudia's birthday (I have always thought it was February 18). "Oh yes, that's right, " I said. But I knew there was more to this day, as callous as that may sound.

February 19, 2008 was my first scan after all the treatments. It was a scan to see if the cancer was GONE completely. A little over 12 weeks after my last chemo treatment––I had finished 7 weeks of radiation, 5 times a week two weeks prior––I was going back in the tube. And it scared the shit outta me. I was a shell of my former self––both physically and mentally. I had already been back to work for almost two months and was struggling to perform. Fuck, I was struggling just to live every day.

Now I remember.


Tuesday, February 4, 2014

The Color Purple.

So today is World cancer Day, huh? (I don't put a cap on the "c" in cancer, ever. I don't want to give it that distinction).

Full disclosure: I am employed in the social media world. Any opinions expressed here are my own and do NOT reflect the opinions or practices of my current employer. The reason I write the above is because I'm a little conflicted on the efforts of some brands and their support of cancer research and prevention. Most notably, Chevy and their truck line's current Facebook posting https://www.facebook.com/ChevyTrucks which promises to give money and support to the fight against cancer. I'm also conflicted because I like their position which is "to make this cancer's last century" and the fact they are united with the American cancer Society.

The reason for my consternation is this: Purple Your Profile will receive the following info: your public profile and friend list. Uh, no thank you. Why? I'm afraid what they'll do with my profile and friend list. Meaning, will it clog up my FB friend's news feed and right rail with countless other "promotions"? What are they going to do with all that information? Are they going to help me pay my medical bills when cancer comes back? Do they really care about my story?

Yes, I'm a cynical bastard. Comes from learning about life mostly from the streets and 30+ years in a dog-eat-or-kill-your-dog business. I'm also very passionate about the prospects of having cancer become a disease in which the survival rate is as close to 100% as possible. Not just for me but for my Children, my Grandchildren and my soon-to-be Grandson who is arriving in this world in less than 30 days. So you won't see me "purple" my FB profile. I don't have anything against Chevy or the color purple.

I just try to fight every day without any commercial influence.


Wednesday, August 29, 2012

Hard To Believe

I have been putting off writing this post until I told my family.

No, not bad news. The best news. Ever. On August 23––which also happens to by my youngest Son's birthday––I had an appointment with my ENT, Dr. Patty Lee. Dr. Lee is my last stop before my annual CT scan, with contrast. A procedure that messes up my body completely and one that I don't look forward to at all. And since it has now been five years since I was diagnosed with head & neck cancer, this was a biggie. Could the 5 year remission landmark be that close? What if they find something? Am I strong enough––physically and mentally––to handle cancer if it is there?

My appointment was at 7:30am. And since Teresa was in Los Angeles, I was going alone. I also was alone at the pathologist when I found out I had cancer––this was starting to feel somewhat familiar so of course my mind started moving like a computer operating system. Too much data, too many windows open, too much distracting me from just concentrating on asking the right questions and see what my future may hold beyond today. And of course, I waited. And waited and waited.

As I sat in the exam chair, I thought of the time five years ago, with Teresa and my Dad sitting in the two chairs to my right. This was the appointment to tell me what my options were for treatment. And some other stuff that is now a blur. I thought about what would I do if I had to get that CT scan. And then thought "what if I am alright?" Yeah, both a good and scary thought. Why scary? I had grown to depend on these people to help save my life. They are my support system. And Dr. Lee has always been a straight shooter with me––some don't like that but I want to know the truth, in plain English and what do I have to do to survive.

A knock on the door happens and in walks Dr. Lee. She has my chart and starts talking to me about my unexpected scan in March. "What happened, why did you get a scan?" I almost said, "what, it's not written down in that 10lb file of mine?" But it was early in the morning and I just said, "I wasn't feeling great and I wanted to be sure it wasn't something serious. It had been going on for 4-5 weeks." She looked in my throat for about 3-4 minutes. Checked my ear and asked about my hearing––one of the side effects of the radiation is I have some hearing loss in my right era. (And I think this is the first time I've publicly admitted that). She then looks over the chart again, with special attention to the scan results. "You don't have to see me anymore." What? "Everything looks great. You're taking great care of your mouth and teeth. You hopefully won't ever have to see me again." I'm still in a little bit of shock. I AM cancer FREE and have reached the 5 year remission mark.

I still can't believe it.