my new normal life

A couple of weeks ago in my post ‘I had a bad day‘, I concluded with the following excerpts –

I was not having a happy day

This past Sunday, I had a bad day

In today’s post, I write the following –

July of last year in my post ‘Good‘, I wrote the following words –

I honestly feel many people don’t want to hear how others truly feel. 


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I think out of courtesy to others we ask; especially those that are dealing with a physical illness.  If I were to respond to the question differently and say “I feel very bad today, my body hurts and my bladder is burning and I am very tired.”, what would the response be?  I do not really know.  I doubt I would receive the same response as I do when responding with ‘I am good!”

Back when I wrote that post and up until recently, while in public I would pretend to be healthy, pretend to be happy, pretend to have fun and pretend to be normal.

Those days, they have changed.

I walk slower and usually am bent over – the lower back is always in pain and walking at times is difficult.

Yes, I have been out a little bit to explore the new surroundings in our new location.  I take pain medication with me ‘just in case’.

While exploring these new surroundings, I see the other people, the crowds of people who are normal, having fun and seeming healthy and happy.

I have a sense of bitterness, a sense of hatred because these people are normal and living a normal life.  These people are having fun and doing things, going about their lives and enjoying their day, each day.

After my exploring of new surroundings in our new location, after walking slower and usually bent over because the lower back is always in pain, I return home.  The event of the day, just the walking results in more pain, more pain medication, a bad mood and bitterness.

I don’t enjoy my days, there are very few days I enjoy – I am bitter.

This has become my new normal life.

(I wrote this post a couple of weeks ago, and to a certain point continue to have these feelings.  These feelings are negative and serve no good purpose.  My pain has increased and I am being tested.  I end this post with the following quote.)


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the importance of today

This month is full of national days.  Per, November National Days include –

November 1: National Vinegar Day

November 3: National Men Make Dinner Day (Must Cook. No BBQ Allowed!)

November 6: National Nachos Day

November 11: Veterans Day

November 18: Mickey Mouse Birthday

And there are national days that are related to our upcoming national holiday Thanksgiving which falls on November 24; these days include –

November 25: Black Friday

November 26: Small Business Saturday

November 28: Cyber Monday

If you are interested in viewing all the days of November National Days, click this National Day Calendar link to take you to their website.

There are some interesting and some important November National Days.  Thanksgiving has importance for me this year: I will write about this importance in upcoming posts.  I do have another day that I consider important in November – that day is today, November 4.

You may remember 3 weeks ago, my 2nd week of my 3rd cycle of chemotherapy was cancelled due to my low white blood count.  Last Friday, I met with my Oncologist Dr. D. prior to chemotherapy and it was decided the missed chemotherapy session would not be made up.  So, last Friday was the 1st week of my 4th and final cycle.

Today’s November National Day is not important to me – instead it is a November Personal Day for me.

Today I am receiving my last treatment of chemotherapy.

I recognize the importance of this day, but also keep in mind this journey is not over.  No, it is far from being over; there is much more to come to complete this journey, this chapter of my life.  In the immediately upcoming weeks prior to Thanksgiving, there will be additional doctor’s appointments, more tests, and further diagnoses.

But wait – before all those upcoming activities, I sit today in my last treatment of chemotherapy and reflect.  I reflect on these past 12 weeks, I reflect on cancer, I reflect on my life and I reflect on the upcoming holidays, I reflect on cancer and the significance it has on me.   It is in me in my life for a reason – I believe everything happens for a reason.  I may not know the reason for cancer in my life, but I feel I know how I can grow because of it.  Cancer is significant to me right now in my life, and because this blog is about my life – there are more posts about cancer and this journey that will come.

But there are other posts also, so for today, I want to conclude this post with words I wrote in August when I started chemotherapy.  In my post ‘those around me‘, I concluded with the following –

I sit, I wait, I watch, I ponder, I accept, I acknowledge and then I realize cancer does not discriminate.

There are black, white, young and old; a man wearing a dress shirt and tie, the stately woman and the tougher looking guy. Then there is the woman with the pink hair, the majestic woman needing a little extra help, the chatty lady next to me and the young man across from me.

Today I sit for hours taking in those around me.  Today I sit for hours viewing those near to me.  Today I sit for hours receiving chemotherapy amongst others; those around me.


Still unknowns

In my post ‘a no go!‘, I concluded with the following –

I will not have a chemotherapy treatment for 2 weeks and unsure at this time how this will affect my schedule.  You see next week would have been my week off and then followed by 2 final weeks of chemotherapy for my 4th and final cycle.  Now that I am not finishing the final week of my 3rd cycle I will not know when the 4th cycle will end.

You may remember I am making uncertain plans to travel back to Texas to spend with my family for Thanksgiving.  With this latest development in my treatment, these uncertain plans become closer to a certainty that the visit will not take place.

Thanksgiving with my family – it may be a no go!

In today’s post I write the following –

This is my scheduled week off from chemotherapy and next week will be considered the 2nd week of my 3rd cycle since last week it was cancelled.  Friday of next week I will meet with my Oncologist Dr. D. prior to my chemotherapy treatment and should know how the delay of last week’s treatment will affect the upcoming schedule.  I am unsure if eventually I will have 3 weeks in a row of chemotherapy or if the regular schedule will take place and therefore pushing my original end date by a week.

If the original end date is pushed back by a week, this will certainly affect my trip to Texas for Thanksgiving.  My original end date is November 3rd and pushing a week later will be November 11th.  With Thanksgiving less than 2 weeks later, it is difficult to determine if my body will be able to handle the travel.  The concern I have is whether my white blood count will be back to a normal count as I certainly do not want to expose myself to possible infections when traveling, especially on a plane.

Also sometime during the month of November I will receive imaging tests that will determine the future of my healthcare with regards to my cancer.

The only important happening this past week is Gary and I moved the RV back to our original location on the Pensacola Naval Air Station.  We will now live here at the RV park on the Naval Air Station for the next 3 months.  We wanted to be at this location for specific upcoming events such as the holidays and other possible activities.  Once the 3 months is over, a determination will take place where the next location will be as this is dependent on my health concerns.

Still unknowns at this time and as they reveal themselves the future will become clearer.


Why would I watch it?

In my post ‘Bacon Grease‘, I wrote the following –

One interesting side effect of the chemotherapy is a couple of days after my treatment, my hands feel greasy; not oily but greasy.


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They have the feeling of me taking them and rubbing bacon grease all over them, greasy bacon grease.  Very strange feeling and I constantly wash them thinking the ‘grease’ will be removed, but to no avail.

In today’s post, I write the following –

I received many comments about that post, and certainly appreciate each and every one of them.  One of those comments came from Clare over at Around ZuZu’s Barn.  If you are unfamiliar with her blog, I encourage you go visit her – she is dear to me.

Clare and I exchanged a couple of comments, that went like this –

Clare –

Terry, Did you watch “Stand Up to Cancer” Saturday night? It was filled with stories of people who had chemo and are cancer free or in remission. Chemo is one of the most difficult of treatments, i think. It must be an interminable time for you and so a week’s vacation is a joy in itself. I think about you often and send good wishes off to you in Florida as you deal with cancer and become settled in your new life style. Clare

Me –

Clare, I did watch “Stand Up to Cancer” and I was emotional the whole time watching. Thank you for your thoughts and wishes and yes, back to chemo this coming week. Happy Sunday!

Clare –

Me, too. But you saw how much hope there is for all of us and that must have made you smile through the tears..

Me –

Yes, absolutely!


Prior to today I would have never watched this show.  Why would I watch it?  Cancer has nothing to do with me and therefore the show would be boring and a waste of my time.  That day I expressed to Gary I would like to watch it, and he agreed.  As indicated in my above comment to Clare, I was emotional the whole time watching.  I felt sorrow for others and myself that we are dealing with cancer and having to deal with it in a not so pleasant method.  I felt joy and happiness, that advances are taking place and people are recovering from their cancer and living wonderful lives.  I felt heartache for those families and friends who lost a loved one to cancer.

There is no reason for me to watch this show in the past.  Why would I watch it?  In the past I did not have cancer and I have no immediately family member who has had cancer, why would I be interested?  Today cancer is me and I watched the show with many moments of tears coming from my eyes.  As I sat there watching, I wondered if any of my family were watching?  I assume they never watched this type of show in the past, why would they watch?

Times have changed and now I have cancer – I hope there were a few family members that watched this show.  Not because of me, but because of others; the progress being made and those stories that touched my heart.


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Thoughts, Feelings; moving forward

In my post ‘The number 12‘, I concluded with the following –

Chemotherapy will begin this Thursday and continue for the next 12 weeks. . . I will keep positive thoughts and faith to create a positive outcome.

In today’s post, I conclude with the following –

Yesterday was the first day of my chemotherapy treatment.  Thoughts, Feelings; moving forward –

Stage 4

In my post ‘The roadmap to remove cancer‘, I wrote the following –

Dr. P. desires a roadmap before we can proceed with making a decision for the immediate future selection.  This roadmap starts with a chest, abdominal and pelvic CT Scan with contrast; then will be followed by a surgical procedure.  The CT Scan took place this past Wednesday and the surgical procedure should take place next week.  I have an appointment with Dr. P. this morning to discuss the results of the CT Scan.


In today’s post, I write the following –

Last Friday I met with urologist Dr. P. at which time he inserted a scope within me to view my bladder and the cancer that is growing within it.  After the procedure we discussed the results of my CT Scan performed earlier in the week.  Dr. P. informed me that the cancer had spread into my abdominal lymph nodes.  There are also multiple lung nodules that need to be further investigated.  Dr. P. recommends I be referred to an oncologist for chemotherapy prior to my next surgery.  The success rate of stopping the cancer from spreading by having the chemotherapy before the surgery is quite high.  Dr. P. also is recommending I have a PET Scan to help identify the lung nodules.

I currently am seeing Dr. P. at the Naval Air Station Pensacola hospital.  The PET Scan and the Oncologist I will see will be located at a hospital outside the naval base.  The PET Scan is not performed at the naval base hospital as well as oncology services.  Dr. P. is associated with this outside hospital as well and this will be where my future surgery will take place.

Yesterday, I met with my new oncologist Dr. D. and we discussed my health history and the current condition regarding my cancer.  Upon reviewing my recent CT scan and the related information from Dr. P., she indicated to me my cancer is stage 4.

Google Results –

Patients with stage IV bladder cancer have cancer that has extended through the bladder wall and invaded the pelvic and/or abdominal wall and/or has lymph node involvement and/or spread to distant sites. Stage IV bladder cancer is also referred to as “metastatic” bladder cancer.

Thursday of next week I will begin chemotherapy for my cancer that will last for 12 weeks.  Depending on the results of the chemotherapy will depend on what will take place next with regards to my treatment.

In order to avoid making this a long drawn out post full of details about the possibilities of outcomes regarding my treatment; I will plan to write another post next week about what those possibilities are.

The next 12 weeks will involve some powerful drugs being injected into my body to fight cancer.

I will have tough days ahead of me.

I will have days I will be very tired.

And I will have days I will be very inspired.

For this post I end with this quote –


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The roadmap to remove cancer

In my post ‘5 days, and more‘, I wrote the following –

We are starting our 5th full day here in Pensacola, Florida.  Today is an important day in that I have my first doctor’s appointment here.  My appointment is with my Primary Care Manager at which time a referral will be submitted for a urologist visit; hopefully sometime within a week.  Several weeks ago, I faxed a portion of my medical records from my previous urologist Dr. F. in Dallas; I wanted the Primary Care Manager here to be aware of my situation.  My hope is this would place an emphasis on the importance of receiving a referral as soon as possible.  The completed medical records will be delivered today.

In today’s post, I write the following –

My first visit with my Primary Care Manager and Naval Hospital of Pensacola were excellent.  I felt very comfortable with my new Primary Care Manager and his urgency to meet my needs were outstanding.  The visit involved him learning about the history of my cancer, prescribing medications for my pain and ordering lab work and chest X-ray. He proceeded with the instant referral for me to see the in-hospital urologist.  I was amazed with the speed at which this process took place: initially this could take up to a week.  Following the visit with my Primary Care Manager I had the opportunity to visit with my new urologist Dr. P.

I am absolutely totally pleased with Dr. P. and I feel extremely comfortable in his excellent expertise from this point on with regards to my care.  We spoke about my history of cancer and surgeries for this past year and he discussed the future options available.  Before a future option is decided, other activities must first take place.

Dr. P. desires a roadmap before we can proceed with making a decision for the immediate future selection.  This roadmap starts with a chest, abdominal and pelvic CT Scan with contrast; then will be followed by a surgical procedure.  The CT Scan took place this past Wednesday and the surgical procedure should take place next week.  I have an appointment with Dr. P. this morning to discuss the results of the CT Scan.

The surgical procedure next week requires that I be placed under general anesthesia at which time Dr. P. will use a scope to view my urinary tract system to determine if the cancer is in other areas besides the bladder.  Upon this procedure Dr. P. and I will discuss my options in greater detail and make a decision for my next major surgery.  He has indicated the surgery will most likely be scheduled for late this month or early next month.  Also depending on the results of the CT Scan and surgical procedure; the possibility of Chemo Therapy may be required.

Gary and I are extremely pleased with the response from the Naval Air Station Hospital and my new doctors.  I feel very comfortable with our new living location, my new doctors and the possibilities for the future.

Me (2)


Rain, Rain, Bring on the Rain

I am in Pensacola, Florida for a little over a week now –

I have seen more rain than sun –

Here is the forecast for the next 10 days –


In the coming days there is more rain than sun –

I am feeling better due to medication I am taking for pain and discomfort –

The constant rain and gloomy weather makes it difficult to smile and be happy –

I will remain optimistic and upbeat, because this is what will help me through the storm taking place in my life at this time –

So bring on the rain –

This too shall pass –

From the website article Top 10 Country Songs About Rain lists this song as # 6 –

“Bring on the Rain”

Jo Dee Messina and Tim McGraw

We’ve all been at the end of our rope, ready to just give up, and a literal storm on a dark day can be just enough to push someone over the edge — but Messina, with help from her producer and friend Tim McGraw, reminds us that it’s just a little water, and we’re thirsty anyway. This defiant anthem preaches taking things one day at a time and remembering that this, too, shall pass.

Average, Ordinary & Boring

In my very first post ‘Hello world, this is my blog‘, I wrote the following –

This is my very first post. What should I write that may be of interest to others?  Not much and then again maybe I do have many things I can write about.  I am an ordinary person, just like many others who live ordinary lives and do ordinary things.  I have many opinions about the everyday stuff, some important and some not so important.


On my ‘About Me’ page, I wrote the following –

Most of us have average lives, filled with disappointments and failures and through life we have issues to deal with due to events and other people and with ourselves. So, what makes my life more special than others? Well nothing really. The difference is this is my life that I am writing about.


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In today’s post, I write the following –

I received a comment about 9 months ago on my ‘About Me’ page, that included the following –

I am 59, a stage 4 Cancer survivor who is blogging because it’s something I have always wanted to do, I enjoy writing and like yourself maybe my words about my life can help others. I have not led a boring life ( Cancer is my exciting life trophy) and don’t know many people who have and your short “bio” does not insinuate you have had a boring life either. What made you say that?

Here was my response to that comment –

Hi, thanks for stopping by and visiting my blog. First of all, congratulations for being a cancer survivor. In my ‘About’, when I refer to boring, I really am referring to ‘tedious’, ‘tiresome’, ‘well-worn’, etc. In my many years of therapy, which included years of group therapy, I realized there are many of us that are the same; experiencing issues and sufferings in our lives that can be tedious and tiresome at times. I read your blog as I read many other blogs from WordPress ‘The Daily Post’ and other sources. I enjoy reading other blogger’s posts, because I can learn something from other people – as I hope they can learn something from me.

In my post ‘How will my story be written?‘, I wrote the following –

I continue to believe I am no different from you and others in this world.  Sure we have different lives, different locations and different people in our lives, but we truly are not different.  Our lives are filled with disappointments and failures as well as successes and wins.  I still believe we have average lives; average is not a bad word, it is a midway between good and evil, high and low, happy and sad.


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In today’s post, I conclude with the following –

Remember this blog is about me and my life.  I have experienced many ups & downs, bad things & good things, let-downs & achievements.  I still consider my life boring, why?  I will never will be president of the United States and I will never be an astronaut and I will never find the cure to cancer.  That makes me average, ordinary and my life boring – and that is okay with me.

18 days and counting!

In 18 days, we will say goodbye to our home of almost 14 years.


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In my post ‘Exciting times ahead‘, I wrote the following –

Let’s get caught up on the other important events taking place.  The house appraisal was completed a little over a week ago and the results were all good.  The home sale continues to proceed without issues and we are still on the calendar to close on August 2nd.  Gary and I continue to downsize possessions while we also have administrative duties taking place such as updating address on all our accounts.  In 2 weeks a PODS container will be delivered and parked in our driveway.  The PODS container will be packed with items and possessions we are keeping for our future home.  Once the PODS container is filled, it will be picked up and stored locally here in the Dallas area until we are ready for it.


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In today’s post, I write the following –

The PODS container was delivered yesterday.  Items we are keeping and storing are now starting to make their way into the container.  Much downsizing has taken place over the past year and a little more to go with regards to ridding of un-needed items.  Tomorrow we are having an Estate Sale and hope to downsize considerably more items.  The PODS container will be sitting in our driveway for 2 weeks at which time it will be picked up and stored.

Last week Gary and I had the pleasure of meeting one of the future owners of our home.  The future home owners had an appointment to have painters come to the house for an estimate.  The future owners will be repainting several rooms in the interior and needed access to the home.  Gary and I decided to stay and we met the wife/mom of the family that will be moving in shortly.  She is extremely excited about moving in and loves this home very much.  Gary and I know, when we leave our home, it will be a home for a vibrant young couple with very young children.  We are happy.


My final appointment with my urologist Dr. F. was last week at which time I received all my medical records for my next doctors.  When we leave Dallas on August 2nd, we will make our may to Pensacola Florida the location of my next surgery.  My new primary care manager is selected and appointment scheduled for August 8th.  Because Gary is a military veteran and I am his spouse I have access to the healthcare system at the Naval Air Station Pensacola.  Once the primary care manager appointment is complete, a referral will be submitted then an appointment will be scheduled with the urologist at the Naval Air Station medical facility.  Once the urologist consultation takes place, we will proceed with the best course of action to take care of my bladder cancer.

The days are coming and going and many activities continue to take place.  This chapter will soon be over and the next one will begin.

18 days and counting!