Posted in angels, cancer, Florida

Florida Cancer Specialists

This will be my last post about the dreaded “C” word until I can post a big YEAH about being cancer free, which should be sometime in the spring.

For now, I am done with my chemo treatments. Radiation is next. Before I enter into the next phase of my recovery, I must do a huge shout-out to the staff at the Napa Ridge Florida Cancer Specialists in Naples, Florida where I received my chemotherapy. These people are phenomenal. Not only do they give excellent physical care, being so sensitive to their patient’s discomfort, but they also offer immeasurable emotional support. Some days I went in feeling optimistic and they shared my joy. Other times I came in depressed or emotional when I couldn’t even pin-point the problem. They were there for me every step of the way. Every single person in that treatment center is truly an angel. From the front desk staff to the phlebotomists, to the nurses in the treatment rooms, and of, course, the doctors, I could not have had better care. All I can say to them, is Thank you, Thank you, Thank you. I truly believe I owe my life to you. Thanks to you and the multitudes of prayers that went out from family and friends, I am confident in saying that I am on the way to being a cancer survivor.

To other cancer patients in my area, I am sure there are situations where you need to make the trek across the state, or perhaps even across to country, to places like The Moffit Center in Tampa or The Sylvestor Center in Miami, but I can honestly say, I believe most cancer patients in the Naples area can feel confident going to Florida Cancer Specialists. Even during Hurricane Ian, when no one had electricity, they moved us around to different locations that had power to make sure each and every patient received the care they needed. If you live in the area and are struggling with where to go to get the best care, ask your doctor about Florida Cancer Specialists. You may not need to go any further than your backyard.

Posted in Brave, cancer, challenge, determination, family

2/3rd through

Chemo treatment #4 was this past Tuesday. Even I am surprised at how well I am doing. The first day or two after treatment is a breeze. By day three, the neuropathy starts kicking in. It baffles me what parts of my body have a reaction. Why not my arms, or my back? Who knows. The neuropathy is only in my legs, especially my knees, making me feel wobbly and unsteady on my feet. Reluctantly, I secured a walker to use around the house when I am too wobbly. But with our condo being so small, most of the time I can walk holding on to chairs or tables. Doesn’t do much for my ego to look at a walker. Makes me feel old.

Next steps are two more chemo treatments before 18 radiation treatments. I spoke with Dr. Sam, my surgical oncologist last week and asked about guarantees. Of course, he can give none. But he did say that they would do another pet scan after the last radiation to compare it to the original one after the surgery. If that is clear, then I can cautiously say I am cancer free. The bigger test is 6 months after that (so around November 2023.) If cancer has not come back by then, I am pretty home-free for the rest of my normal life expectancy.

Most of my fears are gone. That is HUGE. Remember how terrified I was? Other than the unknown of the radiation, I now know what to expect with the chemo. I am stronger and braver than I was when this started. Can you believe that was over four months ago? (Surgery was in July) I am curious about when and what my hair will look like when it grows back in. I have hears that it could be any color or texture and completely different from what I had before. A new me???

People do love my wig and most do not even know it is fake. In fact, my nurse double-questioned what chemo I was taking because “you shouldn’t have any hair.” I don’t – I just have a really good wig. Life goes on.

I am eternally grateful for my wonderful family that takes turns coming each “treatment week” to make sure I am not alone while Tai is at work. And what a great opportunity to spend time with my kids. First was Candy from Ohio, second was Amy from Virginia. Then Dru and Cybil from Colorado. This week was Terri’s turn from Miami. Eliana will be here the week of my Dec. 6 treatment from Virginia and then Terri will be back for the last one after Christmas. I have the best hubby in the world too, who takes over all the stuff I would normally do around the house, like the cats, the laundry, vacuuming, etc. I am blessed beyond reason.

I would love to hear how other people are dealing with cancer or any other infirmity. Helping each other to cope is 90% of the battle. We need the village. Feel free to share.

I hope to get back to more writing soon. I have not done much since all this began. Now that I am more confident that I will have a future, it is time to get back to my stories and helping others get published. I have not given up my business, Simon Publishing LLC, so if you need help publishing that book, let me know. I am here for you.

Happy Thanksgiving. We all have a lot to be thankful for.

Posted in cancer, challenge, family

Mirror, mirror on the wall…

Chemo Treatment number three. Done. Exhausted, but that is all the side effects so far on day three. What I really want to talk about is this damn mirror. Most of the day, I do not see myself. I go about the day with a beanie on my bald head to keep it from being cold, and often forget all about it. Or I put a hat or wig on to go out. All fine.

But it’s this damn mirror. every time I walk past it, I am shocked again at what I see. It screams “YOU’VE GOT CANCER.” at me in bold letters. And it all comes rushing back to me. Will I ever be cancer free? Will all of this really work? Will I ever get my strength and comprehension back? It feels like such a long journey to the middle of May until all my treatments are done. And I am so tired. And these stupid mirrors, remind me all the time.

I never thought I was vain enough that this would bother me. And I still don’t think it has anything to do with, do I look pretty. Hell, at my age, who is pretty? No, it is the reminder of my condition that shouts at me. It taunts me with: you know this is not going to work, it’s going to come back, why are you filling your body with poison? So I fight these thoughts, try to push them out of my mind. And I succeed for a while — until the next time I pass a mirror.

My son and daughter-in-law are here this week to watch over me. They are wonderful. Not that I need anything done for me, but it is nice to be waited on (even more than Tai already does) and to have their company. I am grateful I am not really sick and they had to do a lot for me. This is better. Maybe this is my silver lining. That I get to spend time with my kids which would probably never happen otherwise. So I will take that for a win.

Yes, this is how I feel today. But I am still breathing and kicking. So don’t give up on me and I will try not to give up on myself.

Posted in cancer, challenge, family, Florida, Hurricane, writers

Looking forward to better days

I had my second chemo treatment this week. So different from the first one. No tears, no trauma. Going in knowing what to expect makes a huge difference. Side effects have been almost non-existent. I have a little nausea, some headaches that come and go and I am feeling really tired. Even putting out this blog post is a challenge. But mentally, I am much better and feeling more optimistic than my last post. My daughter Amy is here to take care of me this week. I am so blessed to have family. Perhaps my optimism has something to do with following a major Hurricane. I find it hard to feel sorry for myself when I have a roof over my head, electricity, and water when some people have nothing. It is all relative, isn’t it?

Hurricane Ian roared through here, bringing massive damage to homes, businesses and cars throughout southwest Florida. We were spared any of that. From the safety of our little condo, we were untouched. Only a few inches of water on the parking lot that quickly disseminated. Too many people were not so lucky. Fort Myers Beach is a disaster. So are Sanibel Island, North Port and Port Charlotte. Isles of Capri is almost directly across the street from us and they suffered a lot of damage.

But, back to me. I lost all my hair this week. In less than a week, I went from a full head of hair to really thin and bald spots. When it started to fall out, I was obsessed with running my hands through it to see how much hair would be in my hands. I couldn’t seem to stop, which I am sure hastened the demise of it. When the bald spots started, I knew it was time to shave it all off. And yes, I cried through the whole head shaving. But now that it is done, I no longer have anxiety about it. I bought a lot of cute hats and have a wonderful wig. I noticed one thing. My head is always cold without hair. In the house, the A/C blows right on it. I need to wear a cap at all times. We found some nice soft skull caps that keep me cozy and they also fit under my hats to protect my gentle scalp. Most of the hats are bucket hats, but I also have a baseball cap I wear with a fake ponytail which is kind of fun. And the wig looks just like my real hair. So I am in good shape. You wouldn’t even know I am bald as a billiard ball under that.

Since my treatments are every three weeks, I will try to always post after each treatment and keep you in the loop.

For other cancer survivors, I would love to hear how you are coping with this. Are there tricks to the trade that help or hinder your progress?

Posted in Brave, cancer, Daughters, family, health, Strong, writers

Brave, Strong, Smart, Believe

This quote really touched me. I have been feeling anything but brave, strong or smart. In fact, I was wallowing in my fears. Regardless of all the platitudes and words of encouragement everyone has given me, I was being consumed by fear.

Well, I made it through my first chemotherapy treatment on Tuesday. And yes, I was a blubbering mess through the labs, the consult with the nurse practitioner, the insertion of the needle into the port, and even up until the first med was pumped through. But eventually, things calmed down (most likely in part by the Benadryl), but I realized I was not in pain. Nothing terrible was happening to me. I just sat there and let the meds do their thing for five hours. Bottom line is, I made it.

I went in and out of some pretty weird dreams, but they were not scary, just odd. And when I got home I was super tired. And so glad to have my oldest daughter Candy, here from Ohio to look after me so Tai could work this week.

Today is now Thursday. My symptoms have been extremely mind. A tiny bit of nausea that is quickly remedied with a pill on my tongue. I’ve had some slight stomach cramping and a little tingling feelings in parts of my body, but very mild. Nothing I can’t live with. Much better than I expected. Today we went out shopping, and although I was tired when I got home, it was good to get out. So far, no hair loss (one of the things I am dreading most). Supposedly that could start as soon as next week.

What I really want to convey here is I made it through the first treatment. I AM now braver and stronger and smarter than I was on Monday. Now I know what to expect when I walk through that door to the treatment room. I doubt there will be any more tears, at least not over that.

I am still fearful of the side effects that will happen with more treatments. But I don’t think I am terrified anymore, and that is a huge step forward. In fact, I don’t think I have cried since yesterday. And that was very brief and private. I am making it through.

If you are going through something like this, whether it is cancer or something completely different and not feeling brave, strong, or smart, hold on. It will come. I can’t promise you when, but together, we will make it through to the other side.

Feel free to share your thoughts and what you are going through too. Let’s do this together.

Posted in cancer, family, writers

Wonder Woman – my ass

Am I handing this well? God no. What happened to “I am Woman, I am strong?”

I am weak, a basket case, crying every single day. Now when someone says to me, “You are strong, you’ll get through this,” I want to throw something at their head.

I do not FEEL strong. I am crumbling inside. I remember once when I said those words to one of my daughters. “You are strong, honey, you’ll get through this.” And her answer was just like mine, “I don’t feel strong.” What she was really saying was, I NEED YOU to be strong for me. Now I get it. Sorry, honey.

Thank God for husbands like mine. He is gold. As calming as Dr. Sam is, Tai is my rock. His arms don’t stop the tears, in fact, they seem to open the floodgates even more. But they are the only place I want to be. Last night I woke him up at 3 a.m. because I was having a panic attack. My mind was all over the place. I didn’t want to do this. (the chemo) . What was I thinking agreeing to put 5 hours worth of poison in my body? It reminded me of old-time doctoring with leaches or bleeding. He held me and comforted me until I was calmer. I can’t promise him I won’t put him through it again.

I am also blessed with a loving, supportive family. My children are amazing. My brothers and sister-in-laws are fabulous. We are a big family. And I love every one of them.

So, now we are almost at the beginning of the end of my journey. The Chemo. First treatment in 3 days. I hope I have the strength to walk through the door. I had this “thing” inserted under my skin called a port. It is supposed to be where all my blood draws and chemo treatment will happen.

I’ll admit. I am afraid. I am afraid of all it. The chemo, the radiation, losing my hair (I know that is frivolous, but I still feel it), of being sick, of not being able to do the things I love. To die. Yes, it could happen. There are no guarantees.

For the first time in my life, I find myself saying “I just can’t” to just about everything. No, I can’t go to the office. No, I can’t meet my friends for lunch. No, I can’t work on your book. No, I can’t write a single legible sentence in my own novel. I can’t. I can’t. I can’t. I needed to stop that.

I have learned one thing. It is okay to lean on others. It is okay NOT to be strong. It is okay to cry. My yogi-daughter told me I needed a positive mantra, to repeat over and over, especially when I am in my quiet zone first thing in the morning. She helped me to recall I already HAVE a mantra. I just did not know it was called that. It is a Bible verse I have used when things got tough before (and they have) since 1972.

It is Romans 8:28 Everything works together for good for those that love and serve the Lord.” EVERYTHING – even cancer.

So every morning, I repeat that, do a deep inhale, hold it for 5 seconds an do a slow exhale. And I repeat that a minimum of five times. I am calmer.

I think I am ready to face the future. Do you have a mantra? What gets you through the hard times. Share them with us if you can.