Showing posts with label shrinking tumor. Show all posts
Showing posts with label shrinking tumor. Show all posts

Saturday, April 14, 2012

I have to admit ....

When it comes to this blog, I am a procrastinator.  As I've explained before, I have this thing about talking about myself.  One excuse - I've never liked being the center of attention, and the other is I'm too critical of my writing that when I do write, I end up erasing, rewriting, re-erasing, so on and so forth.  I guess you could say I'm a self-defeater.  But then I guess I could also say that I'm not living up to my end of my adventure by blogging whatever experiences I've been experiencing.  So, here I am, once again, beginning my post with a disclaimer or excuse of why I'm a bad blogger.  
 (Love this little guy)  

Before I go on, I truly do have to apologize & thank all of you who have privately written, asking how I'm doing & offering wonderful words of encouragement.  I've not been a good friend.  I mean to respond back to you, it's just that time gets away from me.  I have good intentions, but I never know what to say because I don't want to come off as a chronic complainer, and I don't want to lie either. 

Many, many heartfelt thanks & my sincere apologies for being neglectful.  Just know, though, that you remembering me does lift my spirits, and I am very thankful for that. 

 
Good news for me ...
 
I had CT Scan recently to see if the cancer drug was working. It's been about 6 months since I began therapy, so I was pretty anxious to know what was up.  It was good to hear that the drug does seem to be working & it seems to be stopping it from running amok inside my body!  YAY! Wonderful news! 

A quick catch up ... 

The tumor in the right breast itself was the size of a baseball.  From this recent scan, the doctors can't tell how much of this 'baseball' has shrunk, or even what size it is today.  I can't help thinking that if I had better insurance or was flush with money we could do another scan to pin point it in more detail.  But, I only have Medicare, for which I am grateful.  I won't complain too loudly.

As a matter of fact, I can't write anything further until I plead with all of you to keep a vigilant eye on Congress.  Don't let them ruin Medicare or Social Security.  There's plenty of good information out there, just don't fall for propaganda.

From my earlier postings, you might remember how I didn't initially understand how far advanced my cancer is.  Funny how things work in your mind.  Some kind of denial, I suppose.  

When the doctor said it was incurable & that I'd have to take medication the rest of my life, I didn't think that was such a bad thing.  I suppose I wanted it to be like a really bad case of toe fungus or maybe like thyroid disease that would require years & years of oral medications.  You couldn't cure it, but you could manage it.

That's it in a nutshell.  That's what I thought back then.  You couldn't cure it, but you could manage it.

OMG!  A revelation!  That is how I thought of it!  This was a case similar to thyroid disease to be treated with a lifelong pill.  I just broke my own heart, because it's simply not true.
 
Last week, I learned from my oncologist that the breast cancer was spread throughout my body more than I initially realized.  It's in both lungs, well, hell, it seems to be everywhere, including in my bones.  But, the cancer medication is doing it's thing, & it's slowed the cancer progression - for which I am extremely grateful.  YAY!

BUT .... 

The drug is coming at a cost to my bones.  To quote a paper my doctor gave me: 
The spread of cancer cells from the primary tumor to the bones (bone metastasis) is a common complication.
The CT Scan showed many dark holes & splotches in my bones.  The doctor has said to be very careful in my daily life & to avoid bone stress, including using the stairs.

I've lost a quarter inch in height since last fall. <sigh>

Pain ....  

My joints are locking - under the arms, fingers & wrists joints, shoulders, hip, etc.  I explained to the doctor it's like someone pouring cement into my joints.  Ewww, what a horrible thought.  My hands are getting bad.  This past week, it's gotten to where lifting a regular size coffee cup with my right hand is almost impossible.  I wear arthritis gloves, & I also massage my hands with lotion, both seem to help a bit.

Because of hip pain, I wasn't getting much sleep, so about a month ago, the kids moved my recliner into my bedroom.  Now, the pain doesn't wake me, & I am sleeping much better.  I do miss curling up in bed, though. 

Besides the pain, are my infamous hot flashes.  

Oh, they are terrible.  I dread warm weather.  Then there's now the nausea.  Fleeting waves of nausea.  
Bisphosphonate Infusion Therapy

My Oncologist wants me to undergo Bisphosphonate Infusion Therapy to help rebuild the bone that is healing from the metastases.  The bones are weak, and have holes in them.  She mailed me info on this therapy; this is what it says:

Bisphosphonate Infusion Therapy is used to treat hypercalcemia, which occurs when cancer cells break down bone & release calcium into the bloodstream.  The spread of cancer cells from the primary tumor (breast) to the bones (bone metastasis) is a common complication.  Bisphosphonates targets cancer cells that have invaded the bone.  It stops these cancer cells from breaking down & weakening the bone & also prevents the abnormal bone growth, which occurs when cancer cells invade the bone.  These new areas of abnormal bone are weak, can break easily, and can cause pain for many patients.  Because it stops cancer cells from breaking down bone, less calcium from the bones goes into the blood stream & blood levels of calcium are prevented from getting too high (hypercalcemia).

Benefits:  reduces bone pain, slows down bone damage caused by cancer, lowers the risk of bone fractures, and reduces hypercalcemia.

Precautions 'before' therapy ....

Because of cases of osteonecrosis of the jaw - it can cause major problems with the jaw bone, it's strongly recommended that all dental work be done before hand.  This is serious.

When I read all this.  I cried.  For the first time, since diagnosed, I cried.  I cried out of fear.  I cried because I feel like the end is nearing for me.  The whole cancer thing is real.  So much for this idea: You couldn't cure it, but you could manage it. 

I have huge - mega huge - dental issues.  I need them all extracted.  My mouth causes me constant pain.  Because of my teeth, I can't have Bisphosphonate Therapy.  If I can't find a way to have dental work done, I'll just have to take my chances & not break any bones.

In the meantime, there are two dental schools in Michigan.  Both downstate.  Not sure if they'd do it for free, or a small fee.  And, I'm not sure if my hip can handle a compact car road trip, but I'm hoping something will turn up while my bones are still in the window of getting healed.

Radiation Therapy .....

The doc also told me she's going to start me on radiation therapy.  Don't know when, though.  She said it will hopefully save my breast.

Surgery ....

Remember how the surgeon said the tumor was too large & not safe to surgical remove?  I guess that's still the case.  No surgery is even hinted anymore.  At least not at this time.

Diabetes Type I ....

Not sure if I've even mentioned this to anyone, but last November I was diagnosed with Type I Diabetes.  This makes me so mad!

Proud mom ....

My son is getting married in September.  My baby!  He's marrying a very nice girl.  They are good for each other.  They complement & they challenge each other.  That is good.


Oh, how I love this Eagle Family.  I have two monitors hooked to my computer.  One is dedicated to the live streaming of mom, dad & their 3 little eaglets.  I laugh at them, worry about them, but one thing I know, mom & dad are old pros & their little babies are in good hands.  Watch them, they're good for your blood pressure.  You can follow them on Facebook, too, if you like.

I found this ....

... the other day, & it cheered me right up.  Merry Christmas - in a few months!


If you all made it with me to the end of this - thank you for your bravery!  I'm hoping I written with clarity, & I hope I didn't bore you. 
Seriously, you should check out the Decorah Eagles.

 

Thursday, December 15, 2011

Adventure Update ....

Although I have been a little motor-mouth the last couple of days, I've been remiss on keeping this blog up-to-date.  

Tumor 
The day before my last oncology appointment I wrote that I thought I had good news but I wanted confirmation from the doc.  It seemed that the cancer drug was working and that baseball size tumor was shrinking.  Good news!   My oncologist thought so too.  

The doc used her little measuring stick & it appeared smaller.  She cautioned that the tumor may have moved deeper inside.  There's no way of really knowing until the radiologist does his special ultrasound & pinpoints the marker he left inside my breast.  I think they plan on doing this 4-6 months after the start of the cancer drug treatment.  I'm nearing the end of the first  3 months.



Hot Flashes
I've been a little bit worried the drug isn't working as well because I don't seem to be having as many hot flashes.   But I am having other side effects.   I'm still trying to recover from a miserable cold & cough that hit me the week after Thanksgiving.   Funny, as I've been typing this, I've gotten 2 very hot hot flashes !  

 Diabetes
 In November I was shocked and unhappy to learn I am a diabetic.  Boy, if that isn't a life-style changer!  
 Medicine has changed over the years.  Remember the old Glucose Tolerance Test that seemed to take all day?  You fasted, drank a bottle of a sweet syrupy concoction, followed by blood levels drawn?   Nowadays they draw some blood & do a test called an Hb A1c Test.  This is a lab test that shows the average amount of sugar in your blood over 3 months.  That's a pretty cool. No muss, and no fuss.
  • Hemoglobin A1c test --
    • Normal: Less than 5.7%
    • Pre-diabetes: 5.7% - 6.4%
    • Diabetes: 6.5% or higher
The day this test was taken I measured at 6.8%.  It was about the same when I went to my first diabetes class.

I went to the first of my two classes to learn all about diabetes and how to live with it.  I thought the class was really interesting.  They brought in a dietitian who taught us how to read food labels, and how to count carbohydrates, and how many carbs we're allowed to eat.  We learned about the meters to measure our glucose levels, and what level parameters we should strive to stay within. 

My next class is next Tuesday.  I'm looking forward to it.  My meter is in the mail & should be here any day.  Oh, boy, a new toy!  

Diet
Because of the cancer, I had already changed my diet.  The family & I agreed that all of us would benefit in eating smart and balanced foods.  We had a sit-down meeting about how we were going to do this, and that it would be a family affair.  
Before learning I am a diabetic, I had solace that I could cheat every now and then.  Now, however, that's not even an option, & that ticked me off.  Anyone who knows me knows how much I love potatoes.  I can't live without potatoes, & I refuse to go without potatoes!  Luckily for me, I can still eat potato, just not in the quantities I think I deserve!  LOL
 Family
The kids have told me they want to do all they can to help me stay alive.  Those are wonderful words to hear.  I admit I wonder about what next Christmas might or might not be like.  Makes me sad, not that I'm afraid of dying, I don't think I am.  It's just that I don't want to die.  Anyway, I'll do what I personally can do, pray the meds will continue to work & shrink that dang tumor & keep the cancer from spreading beyond the breast & lungs. 

This afternoon I have an appointment w/ the GYN to set me up for a biopsy.  Been having sporadic post-menopausal bleeding, so doc wants to rule out cancer.  The GYN I'm seeing is my oncologists' GYN.  That's reassuring, I think.
Well, that's it for now.  Hope I wrote this well enough where it's understandable.  Ol' motor-mouth me, eh?

Saturday, November 12, 2011

Hot Flashes ...

Where to start?   My last post I was looking forward to my Oncologist appointment because I wanted the doc to agree that my baseball size tumor was shrinking.

But first things first, since beginning my cancer medication (9/27), I've been having a lot of very hot hot flashes.   And, boy, they are sizzling hot.  When I told the doc, she clapped her hands, and with a big smile told me that it means it is working!  YAY!

Anyway, about the shrinking tumor.  The doc reminded me that I had a good deal of swelling from the biopsy when she initially measured it, so while it does seem to be shrinking, she can't confirm it.  I haven't noticed any major shrinking since that last appointment.

The cancer has not spread into my bones, but osteoporosis did appear on the Bone Density test.  That explains why I'm nearly a full 2 inches shorter & why the kitchen cabinets are built higher than they use to be.

Since that last appointment I've had a dildo looking Endo-vaginal Ultrasound.  Oh, boy, that  was a dignity teaser.   It all looked good, but since I've been having post-menopausal bleeding, my Oncologist wants a consult with a GYN.   

Well, it's about 5:30  in the morning, and I ought to be in bed.   There's more to write about, I suppose, but this is it for now.

Tuesday, October 25, 2011

I am such a bad blogger ...

First things first:  Two months until Christmas!  Ho! Ho! Ho!

The whole idea of blogging is to write at least a few lines on a regular basis.  I get it; and even knowing this, I've been a bad, bad blogger.

There aren't any excuses to explain it away.  I think I already mentioned that I don't like to be the center of attention - which might make anyone ask why in the world I chose to blog? 

Good question.  Really, good question.  While I think some of it has to do with that, the other is I am in such a quandary.  I don't know where I am in life, and that confuses & puzzles me.  Everything just seems to be scattered.  I don't know how to explain it.  I don't think it's suppose to be explainable.  How can you make sense on anything that has so many open-ended questions?
 
Someone sent me a link to a breast cancer website, & I realize it was sent to me with good intentions; it ended up depressing me.  You  decide .   I have not read it.  I don't want to read it.

I meet with my oncologist tomorrow afternoon.  We scheduled my Vampire day at hematology just before the doctor's appointment.  Tomorrow I should learn about the bone density scan & see if the tumor is shrinking (I think it is).  I have a lot of questions.  I really like this doctor, & as much as I hate going to the doctor's, I'm looking forward to this visit.

I've been taking my cancer drug 29 days now.  I think the tumor is shrinking.  The tumor just may have moved around a little or maybe it's my imagination, but I am sure hoping to learn it is a little smaller.  Wouldn't that be great?  The biggest side effect I have with this drug so far, is the hot flashes.  I actually feel as if I'm sitting next to a furnace.  I do itch, and I've lost head hair, though my hair was thinning even before taking this drug.  But it does seem as if I'm losing more than I was before.  Who knows?  The hot flashes will come in handy this winter.

I have to hand it to my son.  He is with me for each of my appointments.  I am thankful for his support, but I worry about becoming a burden.  I have to eat before they Vampire my blood, so we'll have brunch out at the Cracker Barrel.  I'm hoping for pancakes & bacon. Mmmm ....