Yesterday was kind of a mixed bag.  When I got there I had to  go to the main desk and register that I had arrived.  Because of my  problems with the RN last time for the lab work, I told the woman at the  desk that I did not want the same RN I had last infusion.  She asked me  who it was and why.  I didn't remember her name but described her and  she knew who it was.  I told her that the main problem arose because she  would not listen to me.  I know ME better than anyone else and when I  say I have to be inclined for access to the port, it just makes  everything go smoothly.  Instead, she 'knew' better than I and,  therefore, the procedure took 1 1/4 HOURS!!!!!  The registrar said  Joanna wasn't there today (they rotate) but she would note it on my chart.  I then went out in the hall to sit and wait.  Within just a few  minutes, Maureen called my name.  From the time I got up, walked into  the cubicle, explained the procedure for being inclined, she said, "Yes,  I have accessed you before."  She inclined me - got the access, drew  the blood she needed, capped the tube for infusion.  I was back sitting  in the hall no more than 5 minutes later!!!   Hurrah.  I told her she  had lowered my BP by 10 points!  I also asked her how long she had been  an RN (5+ years) and where she had trained.  She said CT!  I asked where  and she said Fairfield.  I told her I had lived in Newtown for 20 years  and that my best friend was living in Fairfield.  We had a good laugh.
Everything is good from the blood work and physical exam.  However I  had some difficulties with the infusion.  I had told the Dr. that I had  again had the restless leg syndrome with the previous infusion so he  ordered Ativan.  It was given through the port, immediately followed by  the Benedryl.  Unfortunately, I was both groggy and had RLS and just  couldn't relax.  I would start to drift off but then would be restless and  just couldn't relax.  I finally got another 1/2 mg of Ativan but that  just didn't take care of it.  I finally asked if I could go lie down on a  bed, instead of reclining in a chair.  That helped a little and I did  doze but couldn't quiet the RLS.  That, unfortunately lasted about 2/3  of the infusion.  I finally was able to have the lights on and could sit  up without discomfort.  Dave said I was a lot more fun!!!  I walked  like a drunken sailor!
I will gladly suffer those side effects if that's the worst I have  during the infusion, but I do think I need the 1 mg of Ativan before the  benedryl  and time in between those two drugs.  Because they feed all  the infusion chemo through saline, I spent last night peeing every 1 1/2  - 2 hours all night!  So I didn't get a particularly good night's sleep  when I was really exhausted.  Tonight will be better, I am sure.
The fact that I have only ONE MORE TO GO encourages me to finish it  out.  I had already decided that unless cancer showed up in one of the  test or exams, I would finish the chemo regime regardless, this was an  easy decision to make.  In fact, if cancer showed up while I am on this trial, I will be booted out of it.  Obviously, it would not have been working.
I sort of expect the same fatigue and lethargy to become the routine  this next week.  I will just rest and sleep when I need to.  Not a  problem.
I also screwed up the courage to ask the Dr. of the four  from this area, how many have been able to continue the trial.  He said  I was the only one.  The other three came into the trial with cancer  present and it progressed, which means the chemo was not working.  With  that, they are automatically out of the trial, unfortunately.  When he  comes in to have the consultation and do the physical exam, he is much  more personable with me.  Now I know why.  I guess I am his start  patient.  I am sorry the other three have had to withdraw and I wish  them well, although I don't expect they are having an easy time of it.
I feel fine today.  Last time it was Sunday before I felt the side  effects.  Regarding the RA, something is working very well. With the 1st  infusion, I was free of RA symptoms for about 5 days; 2nd fusion, about  10 days; 3rd infusion, 2 full weeks; 4th infusion the full three  weeks.  I have no symptoms today so that is continuing.  I asked them if  they knew which drug it was that was doing the magic.  They don't know  but are anxious to follow me.  We're all hoping it is the Avastin, which  is the biologic I will continue after the 6th infusion.  I am the only  one who will initially know if that is the one working.  Keep your  fingers crossed.
That's it for today.  Thanks for your terrifically good thoughts.
 
 
Well, Betsy. I feel like I've spent some time with you after reading your thoughts in this blog. I'm looking forward to your post describing your FINAL infusion. I'm so glad you have such a wonderful family to support you during this very difficult time.
ReplyDeleteI'm sending you a hug from Houston.
Love,
Nancy (Howard)
Great post Betsy, So good to hear that you are the (star) Makes it all worth while. Not sure if you heard that Vicki had a PETscan on Monday and her cancer IS GONE Its like miracle. She has her appointment with her doc this morning and will see the scans for herself, She is in disbelief..... She will have her 3rd chemo today and the plan now is for 6 instead of 8. So hope this good news continues... Plus the good results for you too. You are in my prayers. Shirley (spfargo)
ReplyDeletesorry about the anonymous, only way I could get it to post... so have a giggle
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