Tuesday, July 26, 2011

Halfway Through Chemo!!!

I have another round of chemo done and I'm halfway through! I have 6 rounds to do and 3 behind me. I can't really say they have been easier or harder they've just been more chemo. :(

I learned something interesting this time. I usually get bad bone pain in the form of a nasty headache two days after chemo. The nurse told me to take Claritin for the bone pain. She couldn't explain why it worked only that she had heard it worked. She was right! I took Claritin Friday night and Saturday morning I work up with no headache. I still had the queasiness that goes along with chemo but the actual pain was greatly reduced.

I did have a moment of "can I go through this for three more treatments?" The nausea and generally feeling poorly had all caught up with me but then I don't like having a cold for more than 3 days! I decided I needed a nap and (as Jessie says) "a do over". That nap made all the difference. Never underestimate the power of a nap.

In summary, chemo on Thursday, queasy and achy Friday, Saturday, and Sunday then back to work on Monday. It doesn't get easier but it doesn't seem to get any worse either. It's just chemo!

Next chem (#4) will be August 11th.

Sunday, July 17, 2011

Latest Update

I haven't done any updating recently because I've been back at work! After my first chemo I was out for the next 7 days. Following the last chemo treatment I was able to go back after 6 days. I've found that going back to work gets helps me to recover faster. I think it's having a routine and physically moving more helps me get my strength back sooner.

My next chemo will be on Thursday, July 21st and I'm ready. This one will get me to the halfway point - three down and three to go! I know now when I will have good and bad days and I can plan accordingly. Oddly enough, the day after chemo I usually feel pretty good, tired but good. It's two days after treatment that the side effects start in. Three and four days after chemo are usually the hardest. I would describe it as having a bad case of the flu for two days. Someone asked me the other day if I was just not telling her how bad I really feel! It's true, I really only have a couple of days of feel poorly and two to three days of being tired and worn out. I think chemotherapy treatment has come a long way!

I was in Las Vegas from June 24-29 for the National HR Convention. I had been planning to go to that conference for months and NOTHING was going to stop me! It was a great convention and my energy level was very good. We had some late nights so there were a few mornings where I wasn't up too early but don't think I had any chemo effects the entire time I was there.

I have lost all of my hair now. Once it started coming out it all came out. I have a few areas of hair stubble but it's pretty limited! I picked up my second wig last weekend. I like it more than the first, shorter wig! The new one looks very much like my old hair. Many people have been fooled by the wig and think it's my own hair - that's how good it is! Again, I'm very grateful to my co-workers at Peregrine who provided the funds for me to buy these two wonderful wigs. Being able to wear a wig helps me to feel a little more "normal".

I'll provide another update after my next chemo!

I

Sunday, July 10, 2011

Chemo - 2 Down / 4 To Go!

I've gotten a little behind on my blog but I do appreciate all of you who called to get updates on how I am doing!

I had my first chemo on June 6th. Because I have drug allergies I was instructed to take steroids the day before chemo to prevent any negative reaction. The morning of chemo I woke up at 3 a.m. and was ready to take on the world! I had an overwhelming urge to clean the kitchen floor, the mirrors in the bathrooms, and vacuum. Wow! Steroids are amazing! Once I got to chemo my energy turned to nervous anxiety.

I had a nice comfortable recliner to relax in while getting the chemo cocktail. My friend Jessie came along for entertainment AND she gives a great foot massage. The chemo treatment took about 4 hours.

After the first treatment I got terrible heartburn. Every attempt to sleep was met with more heartburn. I've since learned that Zantac and Maalox will calm the heartburn. Following treatment number 2 I was ready for the heartburn and took care of it very quickly. The biggest problem last time was not drinking enough water. About 2-3 days after treatment everything tastes bad including water. I've tried a little lemon or lime juice but I have to be careful with that or the heartburn comes back.

The next chemotherapy is July 21st. I'll work on perfecting my treatment of the side effects.