Tuesday, January 15, 2008

Catch Up Time...Day 56 - (Tues)

Guess it's about time I update the blog for mom and bring everyone up to speed. My apologies to so many of you who have been faithfully checking for updates...

This past week was a rough one. Mom had numerous struggles - her fever fluctuating up and down, vomiting, weakness, exhaustion - but as always, rarely a complaint.

Today mom, dad and I went to the Juravinski Clinic for the usual bi-weekly blood work and appointment with the oncologist. 2 weeks ago was mom's 4th and final treatment of AC (the 1st chemo cocktail). She is now halfway through her chemo treatments! At this point things appear to be progressing as expected so they will begin a new chemo drug tomorrow - Taxol. It will consist of 4 more treatments, given every other week. This means Feb 27th should be her last and final chemotherapy treatment!

With Taxol comes the possibility of new side effects. The doctors do not know how each person will react and so it's always an "unknown". However, we've been informed of the possibilities which may include an allergic reaction, musculoskeletal pain and sensory nerve damage which could cause permanent numbness/tingling in her hands and feet...not to mention a continued increase of weakness and fatigue. Because of the possibility of an allergic reaction, mom has to begin taking medication the day before chemo and continue it until the day after chemo. They will also give her additional medication the day of her treatment to help prevent a reaction. Tomorrow, being her first day to receive Taxol, they will keep a close eye on her to make sure she does not have a reaction. She has to be at the Juravinski clinic by 9:00AM and once the treatment begins, the process will be a minimum of 5 hours.

Please be praying that there will be no allergic reactions to Taxol and that the extreme side effects (ie pain and nerve damage) will not affect her in any way. Also pray for my dad while he tries to entertain himself at the clinic for 5 hours or more!! (any one who knows dad knows how easy that will be - haha) :-)

Once again, thank you for the wonderful support, prayers and many things so many of you have done for mom/dad and our family! We thank God for all of you and speak His MANY blessings over you and your families!

Andrea

6 comments:

Valorosa said...

Thank you our good and loving and kind Father for your protective covering over Joy ... pour into her the positive disease killing elements of this new treatment and hold back the negative effects to the healthy tissues in her body. We are asking for NO permanent or lingering side effects from this treatment. Hold her up and strengthen her in the precious and almighty name of Jesus Christ.

Amen

Will be thinking of you all today.

Wendy

Valorosa said...
This comment has been removed by the author.
Eva said...

hi Joy my thoughts are with you and Scott as you were always there for use when needed now it is our turn.
I will pray that you don't have any lingering side effects from this round of treatment and that he gives you the strength through it
love Eva

lyn said...

Praying always.....

Anonymous said...

Hi Joy,
the song
"One day at a time, sweet Jesus" comes to mind!
4 more treatments.
......every day behind, is a day towards being finished!!
I know that you are clinging to Him.....
Great is His Faithfulness....
He gives strength for today,
and bright hope for tomorrow!!
Hang on!!
love ya
Ingrid

Anonymous said...

Hi Joy,
A day in the life of Joy is such a blessing. It stresses taking life 1 day at a time.God is in control as you have cast all your cares upon Him.
Praying for you as you face surgery.We will put you on our church prayer chain.Love and prayers,Aimo & Irene