welcome

(photo of my sister's backyard fence...all photos are thru my lens)

This is just a way to express my thoughts as I walk this path and journey through as a breast canSURVIVOR.

Make cancer mad, just piss it off by misspelling it..... like "canzer"

In remission ~ December 2012

Invasive Moderately Differentiated Ductal Carcinoma T1cN0M0 Stage 1

Estrogen receptor-positive cancer - Here is how it began



Showing posts with label Oncotype DX. Show all posts
Showing posts with label Oncotype DX. Show all posts

Thursday, January 26, 2012

Oncotype DX Revisited

Blue Ridge Parkway
During my follow-up appointment with Doc Esther, I mentioned that the surgeon had ordered the Oncotype DX test. (see post "The Day After - Jan 13") I had agreed to the test in a phone call with the agency and asked Doc if the results would make a difference in my treatments.  She said that I tested positive for all 3 areas that matter and the test would not provide anything new.  Doc recommended cancelling the order.  Okay, so it cost $4,100 ... I have no problems cancelling if the information is redundant.  Even tho they said I qualified for financial aid, I didn't have that in writing.  Makes me leary ~

I called to first find out if the test was already completed and therefore too late to cancel.  It would be complete within 24 hours and if I wanted to cancel it, my oncologist had to make the call.  Well, I'm the one who has to pay for it, why can't I be the one to cancel it? 

This morning, the Doc's office took care of it.  THANKFULLY.

Lesson learned - remember that there is a WHOLE lot of people on your "team".  Make sure the right hand knows what the left hand is doing.  It didn't dawn on me that my surgeon ordered a test to decide what the best treatment is .... get it?  The medical oncologist is the one who decides the treatment.  Light bulb!

All's well that ends well ~

PS  I feel good today.  :)

Monday, January 23, 2012

First Follow-up Post Chemo & Hospital Stay

Very long day....but now that I am finally settled in my hospital bed (10:25pm), I'll try to recount the events of today.

My appointment with Doc Esther was at 1pm today.  My blood count (napir) was great and I got the opportunity to ask her a lot of questions.

First on the list was my port and the fact that I had deep blue veins showing through my skin.  It was still tender and sore.  Once she examined me, she decided to have an ultrasound done to check for blood clots.  Her assistant got it set up for 4:00 today and the work order said "Hold patient".  So, I wasn't going anywhere until the test was read and my doctor reviewed it.  So, I waited in the waiting room (good name to call the room) until I got antsy around 5:20p and asked them if I could go home.  The receptionist said my doctor is calling me on the hallway phone.  Doc Esther said that there were blood clots and that she wanted me to report to admitting in the main hospital.  Whaaa???? I wasn't ready for that! No overnight bag....what about my car?.....what about my husband?  (you should call him, she said).....my head is swimming (I know that, dear, but you just need to go to the admitting desk and they will take care of you).

I called Matt to tell him and he quickly made arrangements to get to the hospital.  Jasmine was with him as she was coming over for dinner tonight.  My brother-in-law dropped them off at the hospital so Matt could take my car back home (good thinking sis).  They arrived while I was still in the lobby waiting for my transportation.  We decided to get dinner at the cafe since I would be missing the dinner hour on the floor.  Salad was great ~

While we waited, Doc Esther walked by, saw me, and stopped to explain further what was going to happen.  Cumadine takes too long to take effect in the body, so in the meantime, I am to get shots of Lovenox in my belly. They have kits and will teach us how to self administer twice a day in the belly for five days.  Wow, what a turn of events!

So, I finally got settled in.  Family has gone home. Meds have been given. Shot has been given. Now, I've just settled back with the laptop that mom & Tommy got and listening to the constant beep in the hallway. 

The pharmacist will be here in the morning to show us how to administer the shot.  After that, I should be able to go home. 

I did call the doctor's office Friday about the port, but was told it was normal.  I mentioned that I didn't want to call and bug and Doc said "you have to be a bitch. you have to nag"  So, next time, I'm going to press harder because I did know something was "off" in my body. 

Some of the other questions:

1) pH balance and vitamin supplements (specially Vitamin D): Doc wasn't very keen on either ideas.  She said the kidneys already did a fabulous job of balancing the body.  If I drink milk, then I am probably getting enough Vit D.  Always room for better food intake and I know I need to do better in this area. Feedback?

2) Talked about the bone-crushing effects and the neuropathy. Doc said that each chemo treatment would have a different level of pain and symptoms each time.  She agreed to change my pain meds. (relief)

3) Talked about chemo and radiation treatment....staying on course? or any changes?  5 more treatments, plus 11 more for the Herceptin.  Then radiation.  Any chance we can cancel the radiation? "not a chance, there would be a 40% chance of canzer coming  back if we don't". hmmmmm

My notes are out in the car,  but this is what I remember so far.

My night nurse, Ashley, has been great.  She is personable and told me about her mother's experience (6 years survivor and doing well).  Her brother is studying pharmaceuticals in Germany and you can tell how proud she is of him.

Backyard
Getting tired, so I'll sign off for now.  I'll certainly keep you posted!
Sleep well ~

Friday, January 13, 2012

The Day After - January 13

I'm not superstitious (don't tell grandpa). So, today is just another day.  Woke up to a whole lot of snow.  First heavy one since winter started. 

Slept on/off last night, kinda tired today.  Had a bowl of cheerios (good) and a cup of coffee (not so good).  Note to self, no coffee after chemo.  Took all required meds this morning...fighting off nausea.

Called Radiology today about my stitches.  Suppose to get them removed 7-10 days, today is Day 8.  She told me to stay home because of the weather and that Monday would be just fine.  Happen to have Monday off work, so that is fantastic. 

In the meantime, Matt was busy snowblowing.  He wanted to keep up with it anyway. 

Got a call today regarding a test of gene patterns called Oncotype DX.  There is still research to show if this test is beneficial, but I think anything that we can do to help others is worth it.  After talking about costs ($4,100) and I qualify for financial support bringing the total to ($0), I said yes. 

Ordered my hats & scarves today.  Should be here in 2-3 days (I hope).

Gonna bundle up and go rest today.  May God keep you safe and comfort you always.