Infusion #3 and #4


My last two infusions of the “nasty” chemo are gone and done!  Number 4 really hit me harder than the first three, which was expected since chemo is cumulative.  I was much more nauseous and way more tired for the week following treatment, but my energy levels are back up and I can pretty much eat what I want without any unintended consequences.  Also, the one thing they don’t really emphasize is the extent of constipation you experience due to chemo.  Forgive me for diving into bodily functions, but at this point I need to invest in some laxative companies on behalf of all cancer patients.  They single handily can keep those companies in business.

My husband and I have a trip to Florida for a wedding for some really good friends and I was beyond nervous that the Oncologist would ex-nay my travel but luckily, I was given the all clear and even given an extra week break between infusion #4 and #5! 

Not much more to report.  I am excited to be starting the “easier” chemo, because it should mean a huge decrease in negative side effects.  The only downside being that I have to receive the treatment, every week, for 12 weeks which takes me into the new year.  I was hoping to be done by the end of December but with the Florida trip, Thanksgiving, and Christmas holidays, I have to adjust my schedule to when the hospital and oncologist are available. 

I continue to be positively overwhelmed with prayers, gifts, and frequent check-ins from loved ones, friends, and family.  Some who I see on a regular basis, some I haven’t talked to in years, and some distant family members I have never even personally met.  I am so thankful for every one of you all and pray that the love and caring you have shown me and my family will be bestowed upon you in return.

Until next time. . .

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