Friday, September 13, 2013

Joys of Summer with Heavy Doses of Dread

It has been a good summer.  Weather has not been great but no chemo.  Still on a rest from carboplatin after having a severe reaction in June.  Making sure to find joy in every day.  Sure is tough especially with my Dad suffering with pancreatic cancer.  He has deteriorated quite a lot and my Mother is still able to provide care at home.  I don't know for how long.  She is adamant that she will keep him there as long as possible.

Dad has just finished 2 weeks of radiation.  Radiation is used to alleviate pain, it is not used for treatment in his case.  There is no treatment for him and the inevitable will occur within 6 months to a year, at best.  The family has come to accept the seriousness of the situation and we try to spend as much time together as possible.  It is a time to make my Dad as comfortable as possible and make his remaining life as pleasant as possible.  It has been very tough for my Mother as you can imagine.

Franca came for a visit in July and we had a lovely time.  During her visit we celebrated Corina's graduation from Conestoga College.  She is a Health Administrator and is working at Stratford Hospital in Patient Registration until her contract is finished.  Tough to find those permanent full time positions!  She will persevere!

Corina's Graduation Day

Graduation
Corina's Graduation Party in July
Franca making herself useful






















This past summer we were able to get my Mom and Dad to Pat's cottage for a couple of great weekends.

Mom at the helm
Dad enjoying the cruise

Viewing the Sunset at Cordova Lake









































Dylan is at Mohawk College and has just started his program in Applied Music.  We miss him but we hear from him via texts all the time.  I wish I could see him doing the laundry!  :)

As for me....  I have been having some pain in my abdomen which means the cancer is making itself be known.  CA 125 is up to 386 which is up from 40 a couple of months ago.  It never was gone but it was quiet in a sense.  It gave me the time to relax and enjoy the summer without dealing with chemo side effects.  But now I must begin chemo again.

I have been scheduled for the 1st infusion for Monday, September 16th  in the chemo lounge.  Should only take a couple of hours and I will do this every 4 weeks perhaps for 8 treatments.  This time around we are going with pegylated liposomal DOXOrubicin or Doxil for short.

Wish me luck.  I will post my experience with this drug.

Enjoy the weekend!

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