Happy to see him finally make an appearance. Can't wait to teach him some #PHP coding 🙂
Weather cleared up and was beautiful. Ton of people in good spirit here at Chelsea's Run #t
It's funny how some people react when they learn I had (ok technically have) cancer. You have people who in general don't mutter the word beyond a quiet whisper. Some people feel they are being insensitive if they discuss it; you're not by the way. Then there are the ones that want to tell you about every person they've known who has, had, or have died from cancer. Those conversations can get a little depressing.
But I digress because that is not the reason of this post. No, the reason for this quick little posting is to let my family and friends know that I am approaching 3 years of being "cancer free" and that in my appointment with my Oncologist today he informed me that my numbers where looking so good, I would not need to come back and see him for an entire year. On top of that, no more CAT scans.
All great news and I wanted to make sure to share it with everyone. I now return you back to your normal life already in progress.
Check it out, I am Radioactive again.
For those of you who follow my story, you might remember this is not this first time I've become radioactive but this time they gave me a cool card. This is so if I happen to set off a Geiger Counter (seriously). I totally want to go somewhere and set off a geiger counter. The key is in the timing, you have to say "What is that green ooze?" right before the alarm sounds. Where does a man have to go to set off a radiation leak alarm???
When I was going through treatment, the one place I would go when I had days off was Torrey Pines State Reserve and either walk the shore or hike to the edge of one of the cliffs. For my birthday today I decide to take my girls there and show them where their Dad would try and find his center.
Man March 1st already. Where does the time fly? Its been a long time since my last post and even longer since Ive talked about my cancer. Its not that Ive been avoiding the conversation, just hasnt been much to say. I do have a couple of updates now, nothing bad, just general updates.
So, if you recall one of my follow up treatments for the next several years is to have a CAT Scan and blood work done routinely every 3 months. The CT is not one of my favorite tests since they hook me up to this IV and pump something into me during the Scan. But hey, if that is the worse of it, I'm happy. Anyways, the first one was a big deal because it was the first time my body would have been normalized in months and the first opportunity to tell if chemo got all the cancer. I ended up doing that test at the beginning of January and everything came back normal; great news for me.
My oncologist introduced me to another of his patients, Paul, who was also diagnosed with testicular cancer only on a much more Lance Armstrong level than I. He actually has been back to a somewhat normal life for about 2 years I think. So weve been getting together for a beer about once a month and the good doctor has even joined us once. I asked the Good Doctor if I was in fact cured and the way he explained was that I am considered in remission for now. If I go the 3 (or so years) without the cancer coming back, then they kind of start saying I am cancer free. As an Oncologist, he rarely ever uses the term cured but from a more general public understanding I would be considered that.
I started playing baseball again which was a huge personal achievement for me. I do love playing baseball. Its still taking a lot of out me but Ive felt that had been happening more and more gradually over the years anyways. Probably has more to do with age than anything else. The girls and I have taken to walking to a local park pretty much every weekend which has been fun. Usually my sister, Theta, and I walk them there. I have taken to bringing a basketball with me and shooting around with her while the girls did their thing. It has been forever since I had picked up a basketball so that has been a lot of fun and one day I actually plan on getting good enough to beat my sister.
Thats about it for now. Take it easy.
Well on Monday it is. Thats right, for all those who have been following my progress online; my derailed life has jumped back on track. I have been very low key the past several weeks not posting since chemo ended because I didnt want to jinx things. Thank my lucky stars I'm not superstitious, knock on wood, but I had my tests last week and got the results this week. All my numbers look good and no new tumors, so I am released to return to work, which I will do on Monday.
Honestly, I dont know for sure if this means I am cancer free or just in remission but I do know I feel great, better than I have in months, and I am looking forward to getting back into shape. Although, I guess round is considered a shape.
Thats right I am done, at least for now. Finished my last treatment of my last cycle today. I wish that was it, I wish there was a switch that I got to flick that now made me better, but the truth of the matter is this last cycle has taken a lot out of me; one of my excuses for not posting anything in such a long time. But I am done with the treatment so now my body has as much time as it needs to bounce back, and trust me it has a lot of bouncing it needs to do. I see my doctor next week; I am really hoping I dont have to get jabbed with a needle but I am guessing there will be blood work involved, then its on to the scans and tests to make sure everyone is happy with the results. I am very happy I am done with treatment but its a very cautious type of joy. I need to hear the doctor say, Looking at the results we are good for now. I did learn that part of my life for the next 4 to 5 years will getting a CT scan of my chest, abdomen and pelvis every 3 months; which kind of sucks because they poke me and pump this chemical inside me that gives you the sensation that you are peeing yourself, a very weird feeling. But that is better than chemo so Im not going to complain; I can live with a poke every 3 months if I have to.
During my last treatment there was a lot of real talk about what happens if the cancer comes back and how it is common and it can still be beaten. It was something I didnt want to hear or think about but knew it had to be said. Honestly, this cancer is not something I can just put out of my mind. Its pretty much been my only focus for the past several months. The thought of it coming back is something I need to mentally prepare for and I honestly dont know how to do that right now. I assume it will come to me and I will learn how to deal with it just like Ive learned to deal with a lot of things I didnt think I would have to worry about, at least not at this age. Right now I am looking forward to dropping cancer down a few priorities in my life and having other things to deal with.
Thanks again to everyone who has stuck by my side and my familys while we went through this. I will never be able to repay the love and affection that was showered upon us; it will never be forgotten. The posts are going to slow down, I will let everyone know the results from all my tests to really put some closure on this. When I get running full steam again, I might start posting general crap again like I did before and will try to keep including helpful geek tips to all my friends and family.
Thanks again for being here for me.
Well, I started my 3rd and final cycle of chemo today and we are in the home stretch. I am on my full week this week, which means everyday for 5 days then its only a matter of 2 more quick treatments and I am done, hopefully. There will probably be some more testing when all the treatments are done to figure out if I am indeed good for now but I have no reason to think I wont be. My blood work came back good today and everything is low but thats to be expected. I am really getting excited about moving back to normal everyday life. I miss my friends, I miss playing baseball, I miss playing with Emily and Alyssa, I miss work (if you can believe it), I miss feeling good, and I miss my hair, what little I had. Im looking forward to missing the doctors and nurses (as wonderful as they are) and more importantly I am really looking forward to not getting jabbed by a needle every couple of days. I am trying not to get too far ahead of myself; there is still a lot that needs to get done but damn, I cant help but think about normal life again. I hope posting my progress here has helped everyone keep up to date about how I am doing but I am looking forward to not talking about it every day.
Continue reading 15 down 6 to go
In the morning, fever all through the night! You know how the song goes, and that's what landed me back in the hospital. No, not my singing but a fever. In all honesty, I was probably no sicker than your normal person with the flu but because of my condition, red flags went flying up all over the place. I had been feeling bad and getting progressively worse everyday starting about a week ago. Then Saturday night I got a fever and the chills. Funny how you get those two things together, physically you body temp is too high but you feel like you are freezing. Bek called the doc, the doc sent me to the emergency room, and that was all they wrote.
I tell ya, the one thing I can't complain about is the level of care I am getting. At every turn the Scripts Health Care System and all the doctors seem to really go above and beyond to make sure they are covering all the bases with me and giving me the best care there is. Now again, if I didn't have cancer, I'm sure it would have been one of those normal situations where they would have given me some antibiotics, and told me to drink plenty of fluids and get lots of rest; but I do have cancer and these guys where pretty hell bent on figuring out what was causing the fever. I ended up staying in the hospital Saturday night and Sunday night, getting x-rayed, CAT scanned (twice), and having an entire battery of tests. Although, I still can't figure out why 4:30 AM seems to be the best time of day to weigh me and draw blood; that just seems mean. It took a lot of talking to finally convince them to let me go home late Monday. They never really figured out conclusively what was causing the fever, but since I had a normal temperature all day Monday and didn't get the chills, they decided I could go home.
Not only did they let me come home but they also let me stay on schedule with my chemo treatments instead of delaying them. This is real nice being how I am so close to done. I would hate to have to tack on another week to that. So I am feeling better and we are back on track with treatment.
Or is it, two steps forward, one step back. Progress is being made but we've had some setbacks. Eric was admitted to Scripps Green last night with fever and chills. They know he must have an infection somewhere but at this point, they don't know where. They've run labs and did a CT scan and ultrasound. He'll be there until tomorrow at least. I'll keep everyone updated as much as I can. Bek
One more treatment and Im finished with Cycle2 and moving on to Cycle3 and hopefully my final Cycle. Heard a lot of the phrase cumulative effects this past week. My full week hit me a little harder than Cycle1 and over the weekend I was probably physically lower feeling than I have been since my actual surgeries. Hair loss is fun and spreading 🙂 and I have a lovely rash that now makes it so I dont only feel like a sick heroin addict but I kind of look like one too. Its a nice rounded look. Bruises, punctures, and red little dots litter my arm which struggles to hold on it its hair. One little fact that is always fun to show people is how the chemo burns the blood vessels and leaves the dull browns streaks on my arm. Hey, I told you guys I would be honest and let you know what I was going through, for better or worse.
Today was a better day although I did have to get my nasty treatment today and that usually hits me the next day or so. Besides that everything is moving along. As nice as it was to have a free week a couple of weeks ago, I really want to get into Cycle3 and get it done. So lets hope there is nothing to slow down that process.
My Dad is doing much better. He got his staples out and is moving around more, which is great to hear. Beks Dad in Alabama is still OK. Which was nice to hear. Besides that everything is moving on. Girls are doing great in school and enjoying their new teachers.
Oh and one more thing, turns out one of my nieces decided to tie the knot. Kristine got married to a young gentleman today and she is now Kristine Harvard. I felt bad her Mom (my sister) was out here taking care of me while this was happening but I guess it couldnt be avoided. You know young people when they are in love there is no reasoning with them. I believe the ceremony was a simple Justice of the Peace type of thing with a full wedding to follow.
Not much to talk about really just wanted to let everyone know how its going. It's mid-week and the long chemo days are starting to wear on me. But this is typical. I was feeling so good over this past weekend but I knew it couldn't last.
My Dad seems to be doing well. Healing can be a long process. Bek's Dad seems to have dodged the major wrath of the latest hurricane down in the south. He said there was a lot of wind but everything held together. Happy to hear that.
Thanks for all the emails and keep them coming. There is nothing nice than coming home from a day of chemo and reading emails or comments on the website, it is a real pick me up.