update July 2014

Not much to report I get my port flushed every 4 weeks and that's about all we do any more. say hi to the DR and yeah I'm still here, breathing and walking.

I've been busy training and showing dogs. 

the end of May 2014, Amber, Keep-Her and I took two weeks and went to Arkansas cause we could, We went to the diamond mines, and the off to Grace Land, and Beal Street, went to a ton of museums.  we'd see a "brown sign" (some historical place) and follow it to see where it lead to and what all we could see.  we we got home I place Shadow with a lovely family as he was not working out as a service dog for me. so now I have Mr Cotton (9 months old) (named for all the cotton gins and cotton we played with while back east)

March 2014 Update where has the time gone?

Over the holidays I came down with the horrid “Crud” that was going around and it knocked me for a real loop.  The dogs and I are now up to walking about 2.5 miles a day, since that was a major setback for me. It took a lot out of me. Since I only see the DR about once every two months while we wait for me to recover from that, not much to report here on the blog.

 I’m back to training my dogs and showing them again. So as the weather warms up we’ll continue our walking and push it as my strength rebuilds again and hopefully we’ll be back to at least 5 miles a day by summer. So I’m doing well, better than the DR have expected. They tell me whatever it is I’m doing keep it up.

I just celebrated my  birthday which I share with my Daughter Roxanne McKay, and a very close birthday (next day) with my Granddaughter Brookelin McKay, over this past weekend. It was a big one for Brookelin as she is now 18 (WOWzer!! Where has the time gone).

12 December 2013 update

Well the blood count has not recovered enough from the hit it took with the Halloween dose of Chemo. So we have decided to take a break until after the New Year to see if they have recovered or not. I feel fine, but it sure explains why I tire  so easily these days.


I'm still attempting to walk only 10,000 steps (which is about 4-5miles) a day with the dogs. it gives us something to do.  Nothing much else going on here, getting ready for Christmas with the family.

Thursday 21 November 2013

So the fun begins again. Not much else to report

Thursday 31 October 2013 Happy Halloween

I’m Sad to say that after a 22 year long relationship I have had to change Oncologist. Since Dr R, was transferred to a clinic 1.5 hours away.

It appears from my latest CT Scan that my cancer has decided to work on the “other” spots that have been dormant so far, and that I’m going to need to be seeing an Oncologist on a more regular basis, I/we have decided that the 1.5 hour drive to visit with Dr R. (since his move) is going to be a bit much.  I am also most likely going to have to have intravenous Chemo infusion again and that would be done up here. 

well we've met with the new DR, Dr B. she's really nice. she doesn't sugar coat anything. she's blunt and to the point, but she's not rude----make sense. She shoots from the hip very straight forward with her answers.

It was decided that I would start with drug #7 today and see how that one works or doesn't.  It's a 3 hour infusion once every 3 weeks. fun and games NOT!

The view from my infusion chair today.

12 Sept 2013 - 17 Oct 2013

I am remiss in that I have not been keeping my blog updated well at all. My last Dr appointment was 12 September 2013 at that time Dr R ordered blood test and a CT Scan to see where we were.

On Thursday 10 October 2013 I had my CT Scan done. I received an email with some not so good news.  The current drug is no longer working, and Dr R is recommending another IV medication. Said that he would call me in a day or two.

Well a week later, DR finally called back and we are going to start the new drug, #7 next Thursday 24 Oct 2013 that is if we can fit in on the clinics schedule. this one is only done once every 3 weeks.

Thursday 11 July 2013

I had my follow-up appointment today Thursday 11 July 2013, with Dr R.  As I expected he didn’t have any more/different information than he did last time.  This drug appears to be working its magic still and the tumors continue to remain status quo.  For which I am very thankful as I’ve been quite ill this past month with the “Crud”.  I had it all; some people only get one of these symptoms, not me I got to do them all, the upper respiratory, nausea vomiting and the runs, along with the fever.  I’m finally down to the annoying nagging cough that seems to linger on forever with the junk.  In the pass when I’ve gotten ill the tumor has taken that as a sign to grow again----this time it’s behaving.

Asked me if I was still walking and I told him, no, just staying close to home and the bathroom. He just laughed at me and told me my lungs were clear and that I definitely sounded like I was on the mend.  YEAH!!! I can hardly wait. But I do hope to start back to walking next week. I’m finally feeling better, and not as friendly with the “ivory throne”, and able to stay away from it for longer periods of time.  

I see him again in two months.