- dry lips
- dry skin
- dry nasal passage
- diarrhea at times
- constipation at times
- swelling in her arms, hands, feet, and legs
- metal taste in her mouth
- cold sores
- loss of hair
- soreness in her chest and arms, particularly after her Nulastin injection that increases creation of her white blood cells
- urinary tract infection (just one so far)
- dizziness
- blurry eyes
- restlessness and fatigue (at the same time!)
- inability to focus on things
- lack of memory
- sad moods (occasionally)
- hot and cold flashes (especially at night)
- sleeplessness at night
- lack of appetite (at times)
- nausea (only once for a straight hour)
- fluid retention (for a few days after chemo)
- sensitivity to the sun (got a sunburn after just a few minutes)
- unhealed wound where the port was put in her chest
- constant cough and weird voice because of damage to vocal cords during surgery
Here are the things that bring Cathi comfort (to sort of counter-balance the negative symptoms):
- Wearing a soft turban-like hat at night to keep her head warm
- warm, long showers
- back rubs from her wonderful husband
- lots of soft pillows and blankets
- staying indoors out of the sun (which comes naturally to her anyway!)
- Tylenol, Tums, Imodium and Colace...some of her over-the-counter medicines of choice
- the two anti-nausea drugs Compazine and Kytril (they work miracles to prevent nausea for the first 6 days after chemo)
- medicated lip balm (given as a gift from a friend who recently finished chemo)
- Ativan (a drug she takes the first week after chemo that helps her to sleep at night)
Although you will rarely hear Cathi complain about this whole experience (and more likely hear her make light of it), this is NOT the easiest thing in the world. The effects of the chemo are much more than physical. Cathi explains that because the drugs affect her concentration and cause restlessness and fatigue at the same time...and because the treatment spans so many weeks, it's really easy to slip into irrational thinking and forget that it will end. Fortunately, the timing of the worst effects have been fairly routine. She gets her chemo on a Tuesday and will be fine Tuesday and Wednesday. Somewhere around Thursday, the worst will start kicking in and she'll suffer through until Saturday when she starts feeling a little better.
The good news is that she is on the downhill side of this. By August, the chemo will be done and she will start on a 5-year regimen of hormone therapy, which will be another fun adventure (but nothing like what she has been enduring).
I'll end with another list...things I (we) have gained as a result of this experience...
- new friendships
- stronger old friendships
- Food (I think of the many meals we've received as some of the "perks" of cancer and I'm sad at the thoughts of these ending someday!)
- hugs from strangers
- flowers
- greater sense of family
- learning what the power of faith means and learning to rely upon it
- courage
- perspective
- an appreciation for Cathi's beautiful eyes
- humility
- awareness of little things
- greater love of nature
- greater love of good music
- enthusiasm for life
- learning not to sweat the dumb stuff
- flexibility
- expressiveness
- general, stronger connection with people
- chance to prove my love to Cathi
- new appreciation for her
- new dependence upon the Lord
- gratitude
Thanks to all of you who continue to pray for Cathi and serve our family in so many ways. We are very blessed!
We love you folks and continue to follow your journey of faith and courage and hope. And our prayers follow you as well. - Laurelle and Grant
ReplyDeleteSounds like you guys are really managing well in spite of it all. August needs to hurry up and get here! :) Has Cathi tried Abreva for the cold sores? That's my go-to med to stuff with those. ugh!
ReplyDeleteLOVE to you guys! Keep kicking cancer's butt!!!
Love your sharing. We wish you all the best. Happy you are dear friends!
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