Thursday, April 25, 2013

Thursday, April 25, 2013

Wow - it's hard to believe April is almost over.  What a crazy month. 

Sorry for the late update but things have been hectic and I've been out of town.  I had a CT scan on April 9 showing STABLE.  It's funny where before I would have been frustrated with the word stable in regards to anything else; it actually has become a favorite word in my world.  Don't get me wrong, I'd love to hear improved, but stable will work.

Same old BS when going for the CT scan.  You would think that after three years and many, many scans that they would get things right especially at a world class hospital.  But no I still had to argue with the tech who insisted that my orders state I needed to take the oral contrast.  It wouldn't be so bad but I have made a habit of checking the day before to make sure the orders are correct only to walk in at 6:45AM and be told the opposite.  I have to give the tech credit though in this case, after telling him to scan down the order and look at the notes he did come back to me with a printed copy to show me that indeed it said NO ORAL CONTRAST,  Seems the Radiologist can't read.  But lets focus on the results - STABLE.  That's what gets me through.

Wednesday was a doctor appointment and chemo.  After a while you can tell when something is going on and as usual my radar was working.  First saw the Fellow who asked a bunch of questions (why isn't all this in the computer so they stop asking the same questions every three weeks???   It's not like it's been a year since I was last seen).  I got a lecture on my non-healthy eating habits.  You would think she would understand that after working 9+ hours a day I just don't feel like cooking when I get home.  Then the nurse came in and I could usually read her like a book.  I knew something was brewing.  Sure enough my doctor came in and said she couldn't give me any more chemo until I saw a Pulmonary Specialist because my lungs showed having opacities (cloudiness).  I almost hit the roof thinking that I have been sitting and waiting all this time only to be told I wouldn't have a treatment.  Luckily she clarified and said I could have the treatment that day but no more until she  (covered her butt) talked to a Lung Specialist.   So of course the next open appointment with a spcialist is May 8 at 8:00AM (three weeks later).  Problem is that I have chemo that day at 2:30 and there was no way I'm going to be at the hospital at 8AM and wait around until 2:30 for chemo.  I usually don't get out of chemo until 6PM so that's 10 hours of sitting around.  Supposedly they are trying to get the appointment for an earlier date but I have half a mind to start calling on  my own to see if anything is available.  They have over 15 Pulmonary Specialist.  You would think one would be available!   You could see my frustration!  I really believe part of the problem is that most of my doctors patients are on disability and have all the free time in the world.  They forget that those who work really need to be at work and not sitting at a hospital wasting time!   Well, hopefully we can get this resolved in the next few days.

Through all of this I still have managed to keep my blood pressure in check:



Otherwise I feel great except for a slight head cold and cough.   I just can't wait for the warmer weather so I'm not so cold all the time.

I'll try to update you all in a more timely manner.  Until then keep a smile and your face and a positive attitude!

Wearing my waterproof dancin' shoes!

Keep on Dancin"

Tuesday, April 2, 2013

Tuesday, April 2, 2013

Sorry I have been out of touch for the past several weeks but there really hasn't been much to write about (which I guess is a good thing). 

Chemo last week was pretty typical.   I did get a new nurse who learned a valuable lesson from our time together.  Although I have tried not to interfere with how they insert the IV needle, let's face it after three years I'm pretty much aware of what's going to work and what's not.  So when he laid down the IV kit and I noticed he had a blue (22 gauge) instead of a yellow (24 gauge).  Experience tells me that due to the fact that my veins are small that a yellow works much better then a blue because they are able to advance it into my vein without it breaking through.  So I mentioned to him that I usually have a 24g but it was his call what to use (see I'm getting better at letting them do their jobs).  He decided to use the 22g and proceeded to insert it and advance it right through my vein.  Second try was with a 24g with no problem except now I have a huge black and blue mark where I bled out under the skin.   To his credit when all was said and done he did tell me he should have listened to me since I knew better having gone through this so many times.   Lesson Learned in this scenario is as a patient speak up and be a part of the team instead of a bystander.  As a health care professional listen to your patients as they have valuable information to share.

The only other thing on the horizon is a CT Scan scheduled for April 16.  It will be 12 weeks since my last and I'm feeling a little nervous.  I know how quickly things could change and how imperative it is to catch it quickly.  Fingers crossed for good results.  As I always say when I'm asked how I'm doing "you're only as good as your last CT Scan".  Not being negative but stating a fact.

Otherwise I'm just tired and cold as usual.  I can't seem to shake this head cold and stomach virus that's been going around.

Waiting until I can put on my dancin' flip flops.

Keep on Dancin"