Showing posts with label PSA test. Show all posts
Showing posts with label PSA test. Show all posts

Thursday, May 20, 2021

TODAY (5-20-2021)

Today was the first time we've had a face to face meeting with an Oncologist in over a year. It was a new (to us) Oncologist and he was pleasant and took his time answering our questions. I did a lot of talking because  my husband often forgets things, and well, I was nervous.

The Oncologist reminded us just how serious and aggressive my husband's prostate cancer was (as if WE didn't know!) but then he hit us with the GOOD news: Only one more year of chemo to go! After that, there will be close monitoring, and, ONLY if necessary, chemo.

Now, I know that doesn't sound like much, but add in the BEST NEWS EVER and it all makes sense. One word:

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REMISSION!!!!!

That's right! My husband's AGGRESSIVE Advanced Metastatic Prostate Cancer is in REMISSION! I know it doesn't mean cured, but remission is the very best we can ask or hope for, and it really is a miracle. 

The Lost Wife (Who feels less lost by the minute)


https://www.youtube.com/watch?v=mWvxORi2pc0
















Tuesday, November 26, 2019

So Much To Be Thankful For

Thanksgiving is in 2 days, and it's time to share the happy stuff. Yes there's much to be Thankful for, so let's get started.

In no particular order:

Here it is, TWO whole months since my accident, and I finally started PT today(!) My range of motion hasn't improved much, but here's hoping my PT exercises help. The good thing is that I manage most of my self care really well now, and I'm truly grateful that I have some independence now. I'm back to sleeping in bed with my husband (where I belong) even though getting in and out of bed is painful.

My husband is in his 7th week of radiation, and is scheduled to finish on or around December 17th. We can see our goal up ahead! It is still causing problems (nausea, vomiting, diarrhea, etc;)  but his Oncologist prescribed Lomotil for the diarrhea, so it's not as bad as it was.

We saw his Oncologist on Monday (11-18) last week, and we were happy to find out that his PSA level is down to 1.9! It was 120 in January, so it almost feels like a miracle.  In the meantime, his testosterone level is 18, and considering that it was over 500 not that long ago, we couldn't be happier. Apparently the chemo and radiation is doing what it's supposed to do.

I have also managed to keep my goal of attending the Friday night Dinners with my friends this month. It's nice to not feel so isolated. I even went overnight (Saturday to Sunday) with my friends and had sushi on Saturday night.

Maybe it doesn't seem like much, but I feel like a weight has been lifted off my shoulders. I even heard the words "Possible remission," and it makes me so very happy. From near death to near health, and I'm not as worried as I was.

BEST PART
For the first time in a long time, we're having Thanksgiving Dinner on Thanksgiving. My husband used to work on Thanksgiving, but since he's retired, we can do it like everyone else.

Happy Thanksgiving To ALL!


Thursday, August 22, 2019

Today's Oncology Visit


It was a mixed bag, and unfortunately, I'm not feeling very optimistic. It's coming up on the one year mark of dealing with this, and I guess I'm more discouraged than I care to admit. 

Nobody is interested in "Doom and gloom," and I'm just frustrated. Trying to be the best I can is hard today, but my mood is merely a reflection of the results we received.

My husband has a standing lab order for his Vitamin D levels, PSA, and Testosterone.  


Vitamin D is going up. It was too low before, so this is very good news.


Not so good news is that his PSA and testosterone numbers are going back up and they aren't sure why. His PSA at the beginning of the month was 2.6, and now it’s up to 4.7, and his Testosterone was 20, and now it’s up to 24.


There's a good chance they may have to start giving him the Casodex again if it starts going up more. It's discouraging and more than a little scary especially for me. My husband is taking this in stride, because his results have been so much worse, but he knows that I take all this to heart, and some days are more difficult emotionally for me.


His MRSA infection also came back, which means there might be a delay in other treatments until that goes away completely.

The Oncologist gave him a new prescription for a stronger antibiotic. Now we just have to wait and see if it works.

Oh, and we're still waiting on insurance to approve the radiation.

So while we wait, I will grumble for a little while.








Thursday, August 8, 2019

Oncologist Appointment Results

I'm making this quick and dirty.

Good/bad news... 

The biopsy results from 2 weeks ago shows that the prostate cancer has metastasized (spread) to the pelvic lymph nodes. I mentioned it in my previous entry.

According to the Oncologist, this was expected, so please don't feel sad. The radiation can now get scheduled.

Numbers:
PSA  ("Normal" is 4, Goal is 0)
Early January: 120 
Early April: 98
Mid June: 4.1
Today: 2.6

Testosterone ("Normal" for a 62 y/o man is 200 Goal is <50)
Early April: 330 (Enviable by most men, bad for prostate cancer, because it feeds on testosterone)
Mid May: 500+ (initial side effect of Lupron even with the Casodex, this was surprising!)
Mid June: 25
Today: 20

Of note: Lupron destroys testosterone in the body, so estrogen takes over. There have been changes to my husband's body, notably, less body hair overall, and more scalp hair. I also noticed breast tissue development, and the Oncologist said it was normal.

For Comparison: The picture on the left was taken just over a year ago, and the one on the right today.



Notice the difference in body hair, chest, and weight.

So now there's more waiting.

Friday, July 5, 2019

Does "Absence Make The Heart Grow Fonder"

Or is it "Out of Sight, Out of mind?"

Either way, here I am. My husband's health has been all over the place.  The Lupron injection raised my husband's testosterone to over 500, so he continued on Casodex  until June 20th.

You know how sometimes life just floats along with no surprises and stays quiet, relatively speaking? Well, that had been life at home until mid-June, when all hell broke loose at once.

This blog was intended to talk about my husband's health, and my concerns, so I could stay calm, butso many other things happened too, so here I am, going a little crazy.

Let's stay with my husband first: Between May and June, he had a sonogram and biopsy of his pelvic lymph glands. Those results were inconclusive, so he needs another one.  Approval from insurance takes forever, so we're still waiting.  At his June appointment, we were given some very good news.  His PSA is down to 4.1 (4 is "normal" 0 is target) and his testosterone is down to 25 (50 was target) so apparently, his numbers are good. We just hope they stay that way.

Now me: Have you ever heard the phrase "Lead By Example?" Since June 14th, I've been working on a health project for myself, and it includes taking supplements, taking my blood sugar every morning, and a nutrition chart, including fluid intake. Each chart is for a week, and my blood sugar goal is <145 at least 5 days a week, and I've met that goal,other than the first week, which was rough, but I've never gone over 160. When my husband saw what I was doing, he started doing the same (taking his blood sugar) unfortunately, his numbers have been about 450+ most days, so he was prescribed insulin a few days ago.  We see his doctor later today.  Did I mention that I didn't sleep last night?

It seems like there's a lot of hurry up and wait when it comes to my husband's cancer, and that's why there's been no journal entries.

I nearly forgot! On June 17th, my ex-husband was hit by a car on his way to work. He was riding his bicycle, and the driver didn't stop. He called me to pick him up and I was shocked by all the blood. He was off work until this past Monday (July 1st) Just another part of all hell breaking loose.

Of Note:

Since receiving the Lupron injection, my husband has had a few more good days than before, although he still has sick days more than we would like.  I'm starting to theorize that his out of control diabetes has something to do with it. 

I think I'll go back to bed now.















Tuesday, April 2, 2019

A Pleasant Surprise

Note To Readers:

I purposely held off on writing this until now, because, well, yesterday was April Fool's Day, and some of what I'm about to share might seem unbelievable. I know that I had a few "jaw drop" moments.

Oncology Visit Report (4-1-19)

This was scheduled with the plan that the brain MRI and full body CT would have been done, and we could discuss results. As I mentioned in my last journal entry (https://alostwifesjourney.blogspot.com/2019/03/last-week-you-ask.html) a week ago, it wasn't happening anytime soon, and, in spite of my daily calls, it hasn't gotten any better.

I've been feeling awfully burdened (https://alostwifesjourney.blogspot.com/2019/03/some-nights-are-like-this.html) by all this. I mean, I'm human, and nothing at all like the "Superwoman" I often portray in public. I frequently find myself grasping for invisible lifelines that just aren't coming, and it's exhausting. I realize I'm frequently exhausted. The insomnia coupled by the constant worry has had an effect on me.  This appointment turned out to be an answer to my prayers (and probably the prayers of others) We were handed a "lifeline" and the both of us are taking it for all it's worth.

The first thing on our personal agenda was getting the Social Security disability papers filled out and signed. We were pleasantly surprised to find out that my Husband is eligible for disabled parking as well. His energy level is so low, and even getting out of bed is hard for him. When the Oncologist told us and offered to do the paperwork, it put a smile of relief on my Husband's face. Really, he rarely complains, but it's been a rapid downhill slide over the past few months.  I see it, and it scares me. 

No, the paperwork wasn't the lifeline, neither was the parking permit.

The next thing on our agenda was to have the Oncologist look at a rather large abcess that mysteriously appeared last week.  He diagnosed it as MRSA, and prescribed a very strong antibiotic.  Unfortunately, combined with my Husband's blood pressure medication, it has a side effect of elevated potassium levels, so he will have to restrict his intake of potassium.  Unfortunately, I learned in recent months what effects elevated potassium has on a person, because it caused a dear friend to wind up in the ICU not that long ago. I will have to be hypervigilant for the next two weeks.

After that, we discussed the blood test results from 2 weeks ago (pre-treatment). This is where it all gets interesting: Apparently, my husband's Vitamin D levels are extremely low.  His result was 11. Normal is at least 30. It adds to the normal fatigue of cancer, adds to depression, and contributes to his pain levels.  It was definitely a lightbulb moment. It was decided that he would take a high dose Vitamin D supplement once a week. Since it's a special order, it will take a day or so for the pharmacy to get it.

Next was Testosterone levels.  My Husband is 62, and most men his age have a level of 200. In other words, decreased testosterone levels are common, and since prostate cancer is related to increased testosterone levels, he was placed on anti-androgen (anti-testosterone) medication.  His level came out as 330. Another AHA! moment. Most men his age would be envious. Except, that's why his cancer is so aggressive.

Finally, (and this was the biggest "jaw drop" moment, and much-needed lifeline) we were given the PSA levels. In January, they were 120. As mentioned before, normal is 4, and since my husband had received NO TREATMENT until his last appointment, there was a concern that the levels would be drastically higher, and the higher the levels, the less "time" there is for him to get life-saving treatments. "Time" is our only hope right now. The lack of "time" is my obsession, my worry, the thing that keeps me up at night, the reason for my tears and frequent feelings of hopelessness. He saved the best for last.  My Husband's PSA level was 98!  Yes!!! 98! 

My question and my Husband's question (and probably yours too) was How???!!! The human body is amazing, and PSA levels will fluctuate some. That's what happened in this case, and it buys us a little more time. I'll take it!

Future Plans

We were told to not worry about changing the MRI and CT scan to a sooner date, the next Oncology appointment is Tax Day (4-15) and the results will be in by then. We understand that just because the PSA levels have lowered it doesn't guarantee that there hasn't been a bigger spread of the cancer, so we're still hoping for the best, but we're also working on a bucket list.

The Casodex (anti-androgen medication) will continue, but the next visit will mark the beginning of the Lupron injections, which will eventually replace the Casodex completely.

We still have so much to do, but the fact that the Oncologist is being transparent with us, and explains everything, it makes this much easier for us. 

Maybe we can breathe, and for the first time in a while, the waiting isn't quite as scary.

https://www.youtube.com/watch?v=B3blT1IRafU

Tuesday, March 26, 2019

Last Week, You Ask?




Making The Struggle Worth The Hassle...


I'm not made for emotional pain and heartache. It destroys me to the core. The situation with my Husband's prostate cancer has all but destroyed me in so many ways, yet I still come out fighting. Fighting for him, because when it all comes down to the basics, he is MY HusbandMINE!!! and there isn't a single person on earth who will feel his loss as much as me, or even the same way that I would. Keeping him alive and feeling well is my number one priority. I might destroy myself in the process, but as long as he is alive and feeling well, I win. I would gladly sacrifice my life for him, and these aren't just words on a page or a computer document. I mean it, and unless you've seen me, the whole me, you have no idea just how strongly I feel that.

Now, before I go off on a tangent, One of the final things the original GP did was refer my Husband to an Oncologist. This wasn't just an Oncologist, but one of the best and highest rated in the area, but we didn't know that. All we knew was that this Oncologist was local, and he had a funny name. The appointment was on Monday last week (3-18), and after all the stress, we didn't have very high hopes. The pile of paperwork they handed to my Husband was more than he's ever filled out before. When he was called in, we went into a nice exam room and waited. My emotions have been all over the place, and my husband has been guarded in showing his since the last breakdown in tears over a month ago, and this Oncologist with the funny name put us both at ease, and he listened. Being heard is the one thing that was lacking with our original GP, and I've had it with false reassurances. I want the truth, my Husband wants the truth, and both of us want to do whatever we can so my Husband lives as long as possible, and stays feeling well.

The Bad News:


I'm not a fool. I spent years caring for people who were close to death, and I've seen more than my share of people dying, so when the Oncologist said that if my husband went untreated, he could expect to live "maybe a year." I wasn't surprised. I kind of expected it. After all, my Husband had advanced aggressive metastatic prostate cancer that is in his lymph system.

The Good News:


The Oncologist said that the first line of defense was prescribing an anti-androgen medication that would reduce the testosterone in my Husband's body, because prostate cancer feeds on testosterone. Casodex taken once a day decreases testosterone production.

The Treatment Plan:


According to the Oncologist, Casodex will often stop the prostate cancer in its tracks. Lupron injections will be used as well, but sometimes Lupron will actually increase the testosterone levels at first, which is why they start with Casodex. Another side effect is that his hair on his head might even grow! (yummy long hair!) That made me smile, because I love my Husband's long hair, and I was afraid it might fall out. Apparently not with the starting treatments.

Tests Ordered:


1. Blood tests for PSA and Testosterone as a start, because there's a good chance that those have both increased, and the goal is to get the PSA to 0 (zero) This will be done on a regular basis.

2. Full body CT scan to find out how much the cancer has metastasized. Ordered as URGENT but we're still waiting on insurance to approve the test.

3. Brain MRI to determine if the cancer has metastasized to the brain. Ordered as URGENT but we're still waiting on insurance to approve the test.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

The NEW GP:


Strangely enough, my Husband's new GP also has a funny last name, and when I tell people they laugh, because one is the opposite of the other.

Negative Things:


Parking is difficult to find. We also had to wait in the waiting room for about an hour, and then another hour in the exam room.

Positive Things:


When the doctor came in, he was thorough. In fact, he spent over an hour talking and asking important questions, including about the prostate cancer. He ordered a full panel of blood tests for my husband including blood sugar, A1C, liver function and kidney function, plus a few others I can't remember. He was definitely worth the wait.

How We Feel:


We finally feel like our concerns are being taken seriously. We're feeling much more positive and good because both the Oncologist and GP are actively listening and involved, and not leaving us in the dark. Yes, this is an uphill battle, and I've been under extreme stress, and it has affected my general health, but I know it will get better. My husband is slowly starting to talk about things, and I think that our relationship will only improve. No longer feeling helpless, I'm speaking up, and (finally!) my husband is too. We also jointly decided that appointments are to be made in the early afternoon.

Still, we wait, but no longer passively.