Friday, November 26, 2010

November 26 -- better

Last night was horrific. Belligerent, abusive, bordering on hostile. Signs of dementia and hallucinations. Incapable of transferring from wheelchair to toilet.

This morning....clearly the pain has subsided enough for her to think straight. She actually went to the bathroom all by herself. I fell asleep on the couch in her room near the bathroom and the flushing of the toilet woke me. Then she did all her morning bathing and dressing with only a little assistance. Now she is exhausted--but I'll take that.

I believe I saw what lies ahead in the events of last night. If she continues to improve with regard to strength and will, perhaps her quality of life will be ok for a while. But I suspect the next time she "takes a turn" it will for the worse as they say.

Thursday, November 25, 2010

Thanksgiving - 2010...

(For those that once followed and may follow again: Buford passed away December 2009. That was the first day my heart broke. My best friend and soul mate unexpectedly passed away September 16, 2010. That was the second time in less than a year that my heart broke. And now we are most likely heading toward the third time...not sure if it will happen in the same calendar year but it really doesn't matter, does it?)

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Haven't posted in a year and half...frankly because I forgot I had the blog. I wish I could say there was better news to report but sadly things started to take a "turn" back in September 2010. The cancer has started progressing / advancing and well, here's what happened and where things stand with mom now:

She started to show signs of the cancer getting "smarter" and the Aromasin no longer being effective. The external primary lesion doubled in size almost overnight and a Pet-CT in October showed significant growth in the breast lesions and "activity" in the liver lesions. This was all discovered just before I moved my mother into my home because the external primary lesion on her breast began to bleed.

NYU was now too far away--everything had to be moved to Delaware. If she needed to undergo radiation then there was no way for NYU to be part of her world. Before being able to get anything set it was November and she ended up in the ER at the local hospital because I could not get the bleeding under control. While there we were put in touch with an oncologist and her first appointment was set up.

NYU started posturing with regard to releasing her records. I was in the middle of a professional pissing contest. NYU wanted DE to contact them--and they know it does NOT work that way. Fortunately the people in DE are more human that those in NYU (and I say that as a member of a family filled with doctors who are associated with NYU). Finally her records were received and she was seen by a very attentive and supportive oncologist.

Radiation was the next step and the appointment with the radiation oncologist was scheduled. All for naught as I had to call an ambulance to the house to take her to the hospital because again, the bleeding could not be stopped and this time it was very bad.

Time to add insult to injury: the bleeding was finally controlled but her O2 stats were in the mid-80's. BAD NEWS! So on November 18, 2010 my mother was admitted to Christiana Hospital. Her O2 never came back up without the aid of oxygen so she was plugged into the O2 system in her room. Next began the parade of doctors: oncologist, covering primary physician, covering surgeon...that's right, surgeon. There was no way to avoid it any longer.

At first it appeared as if they wanted to do a full mastectomy. Really?! To serve what purpose?? She's 86 years old, her breathing is compromised, she has had liver mets since diagnosis 2.5 years ago and the cancer has finally spread to her lymph nodes. Essentially she has been in Stage Iv for two and half years--median life expectancy for a woman HALF her age! Who are we kidding her? She would never survive the recovery and in all honesty, she's heading toward the final turn of the home stretch so can we PLEASE concentrate on quality of life and comfort?

I was heard...not sure by who, but I was heard. On Tuesday, November 23, 2010, my mother had a lumpectomy under local anesthesia. On Wednesday, November 24, 2010 my mother returned home to my house with a supply of oxygen the likes of which I have never seen. She is weak--from the surgery and from being in the hospital in a bed for 6 days. She is worn out, in mild pain, and I see a lack of willpower for the first time. She cannot transfer from the wheelchair to the toilet without assistance so I am going to need lots of help.

Me? I'm exhausted. I'm angry...ok, I've been angry for years (heck, my whole life). I have no patience to deal with this situation because I cannot "fix" it. I loathe her whining and constant asking for things---not things that she needs, but things to simply distract me from doing my work (which if I don't get done will not fare well for either of our futures). I know she just wants company. But if she would just once in her life ask for help it would be easier. That, of course, is not something she has ever been able to do so why I am hoping for the "old dog to learn a new trick" I have no idea.

Yes, it's like a mirror. And it is a valid argument for nature vs. nurture given the fact that I'm adopted. She has no patience--I have no patience. She cannot ask anyone for help--I most certainly cannot ask for help. "Damn it! Leave me alone! I can do this!!" (Um, no, I really can't but that is my make up, my personality, and these are perhaps two of the big life lessons I'm here to learn....wonder how I'm doing??)

So I do not really know what the road will bring...well, actually I do. I just don't know how long the road is nor how many potholes, hidden drives, and other obstacles are awaiting me. Regardless, it is going to be ugly and hard. And that is probably just skimming the surface.

Monday, May 4, 2009

Monthly Oncologist Appointment Today

Haven't written in a while because, well--Thank God but everything has been going well. I'm always nervous on these trip days to NYUCI just hoping and praying that she remains stable and that the blood markers continue dropping.

I'm been up to my eyeballs in medical problems with Buford, my oldest dog. So my attention and writing has been directed at that blog.

I'm worn out between all the worries of mom, the pup and the job. Hopefully today will be a good day.

Tuesday, December 16, 2008

Back on Track

Ok, cutting to it:

The PET-CT scan on 12/10 was finally compared to the original one from July and everyone is happy. While I did not speak to the doctor myself, and I am very careful with my mother's description of phone conversations, I believe she's in good shape. She said the doctor's nurse called and said the comparison showed good progress, and that Dr. Tiersten was very happy with the report.

I will call myself tomorrow to get as many details as I can but every time there has been "concerned" news they have called me and not my mother because they know I am the "go to person." Today they called her and I have to believe it was because it was only a good report.

More when I get details....

Sunday, December 14, 2008

Busy 2 months--waiting game

Never, ever assume things are moving along positively all the time. November's trip to the oncologist proved there are bumps in the road. Every month they take blood and check protein markers. Up until November the markers had been steadily decreasing. November: stabilization.

While stabilization is not a bad thing, it is not what the doctors want yet. So the PET-CT scan that was scheduled for January was moved up to December just to be "conservative." Needless to say, no matter how many times they tell me not to worry....I mean, come off it!

So on Friday, 12/12 we drove up to NY, mom had the PET-CT done and we came home. Monday we go back for the December appointment and a review of the scan. If they dare tell me they don't have the results I'll scream. The scan was done on the 2nd floor of the SAME building the oncologist is in. According to my cousin, a radiologist on the other side of the city, but who did all her medical schooling at NYU, they could have read the scan right there on the spot after it was done. So go on, I dare you tell me you don't have the results.

More Monday night---just hoping and praying we didn't take any steps backwards.

Tuesday, October 14, 2008

Today was a GREAT day!

Without going into the insane details of how one has to FIGHT with doctors, nurses, health care systems, etc., when faced with the health of a loved one, I'll sum the day up in a simple statement followed by a simple summary. I'm too relieved to bash the stupid people in the world right now (Diagnostic Imaging Associates in Delaware)--now you know whom I am referring to.

Doctor's appointment today: NYU Urology Associates with Dr. Stifelman
Purpose: followup appointment to July after a followup abdominal/pelvic CT w/contrast
Outcome: NOT KIDNEY CANCER!!!!!!

The PET-CT scan my mother took in July showed a mass on her right kidney. Given the breast cancer and the liver lesions which turned out to be metastases of the breast cancer led everyone to rightfully assume that the kidney mass was also a metastasis of the breast cancer. Since you cannot biopsy a kidney due to fear of spreading any cancer/disease it may contain, you take the negative position and assume the worse.

Last Monday's CT scan w/contrast did NOT light the kidney mass up like a Christmas tree as it did the other lesions--it showed nothing but a dense mass, indicating a benign cyst!!!!!!!

And that is that when it comes to the kidney worries--mom will have a 6-month CT scan w/contrast to confirm that it is indeed just a cyst and nothing more. One HUGE bullet dodged!

...someday I'll relay the story of DIA and their incompetence, but not tonight, too worn out!

Friday, September 19, 2008

September Doc Appointment Update

We've been in a bit of a holding pattern for the last month+ and will continue that way for another 3 weeks or so. This is a good thing!

About two weeks prior to this mom called to tell me the usual morning shower story but with a twist: she usually called to tell me the scab on her right nipple had fallen off in the shower and that once again she had some bleeding for a while. NOT THIS TIME! This time she called to say that it DIDN'T bleed! We were told that eventually this would happen but I never imagined it would happen after only 4 weeks on Arimidex. I said, "Well, until I am told otherwise I will take this as a terrific/positive sign. Scabs fall off when wounds heal."

On Monday, 9/15, I took mom to her first followup oncologist appointment at NYUCI with Dr. Tiersten. Mom was asked how she was feeling ("I feel fine!); what kind of side effects she was having from the Arimidex ("None!); etc. I explained about the scab and both the nurse and doctor concurred that all of this was great news. After a physical exam Dr. Tiersten said she thought mom was making great forward progress and that everything looked terrific. (Knock and everything and anything made of wood!)

We left to set up the October appointment and stop at Plembotomy for another blood test when Dr. Tiersten came up to me and said yet again, that she was very happy with how things looked. Being as superstitous as I am I said, "Thank you so much...now stop saying that!" She laughed and said, "Yes, yes!"

So now I have the delightful task of finding a day to take mom in for a CT scan (locally done) so that on October 14th her urologist can give us an update on the state of her kidney and then the next day Dr. Tiersten can let us know how things compare in the liver.

...and I have to remember to book a hotel room NOW or we'll be in trouble....

So, the last 6 weeks--a very good period of time.