Before the chemo started, Amy cut her hair short in hopes that when it started falling out, it wouldn't be quite so icky.
Despite the short-haired efforts, hair-loss was still pretty icky... especially when her son, while at a birthday party at California Pizza Kitchen, grabbed a clump of it right off her head to show off to the people at the party! After that, she gave in and asked Anne to shave her head. She debutted the cancer-chic look at the Twilight Town Trek.
And here is the best reason for her fight...2 lovely children who love their mama!
To keep you all in the loop as to how she's coping, I am copying in her latest email update. She's due for another one soon since this one is already 3 weeks old (hint, hint Amy!).
Well, hello to all.... Since my 3rd round of chemo was on Thursday July 1st and it is now July 7th, I bet you can figure out I didn't have the greatest reaction with my latest chemotherapy. The nausea is still an everyday battle-the patch I wear on my arm is helping, but it's worse than morning sickness, and now the fatigue has set in. My normal fast paced walk is now just a slow crawl- I actually had to have Aden hold my hand to keep my pace up while at the mall looking for big girl beds for Cerys!
For 4 days I slept probably 18 hours a day- which to many of you hard working people sounds like heaven- but for me, it caused my back to slip out and now I can't walk standing straight up! So I'm BALD, BENT over at the waist and shuffling my feet to walk- I look like a 90 year old man!!! I've been to the chiropractor (keep adding up those medical bills!) the past 3 days in a row, but the back is in alignment. Now i'm just dealing with muscle spasms from being in bed so much....gee, the days that I dreamed of staying in bed for the whole day are no longer - I miss being me.
I did take my kids to the pool- because they were really wanting mommy time (Cerys) and Aden wanted to play with the boys. Even though I kept my bald head covered and was sitting in the full shade with only my legs in the water, I had some British man come up to me and ask me about my cancer treatment, and why with my port and the patch, was I not covered up due to the hypersensitivity issues of the chemotherapy? He also asked me if the man playing with Aden and the other boys was my husband (i wonder now if he was hitting on me-naahhh) which it wasn't, Lane was working. I wanted to tell him to mind his own business, but instead I told him sometimes I have to be a mom first and put the cancer treatments on the back burner.
I only have one more treatment of the nauseous cocktail of cytoxin and adrinomy (spelling is now gone)....that will be on the 17th. On the 29th, I"ll start the taxol chemo treatment of which the side effects include muscle and bone pain, neuropathy (numbness) of fingers and toes and metal like tastes/food. I just hope the nausea really does subside....
Hope you all had fun on the 4th of July- our kids really liked setting off fireworks with Lane and hanging out with the grandparents. I was just so thankful for their help and some awesome Omaha steakburgers from the Hawkins and Mabb families!!! You guys rock!
I am starting to wear my wig a little more- just realized I don't have a picture of me in it yet- I'll add that next time! Love you all- sorry to bitch and moan about me- so please email or call and inform me and distract me with fun things (or even bad things) from your lives to keep me sane!
love again- amy
Keep fighting, Amy. We all love you!! And happy birthday!