Guess who came up with this title?? I had my first dose of my new IV chemo drug today. It is called Doxil for short. The real named is too long for me to remember. They first drew lots of tubes of blood, then gave me oral Benadryl, IV steroid and then the red colored drug. It looks like a strawberry daiquiri that I should drink rather than have it infused. The drug comes all pakaged up in a huge box of ice with just a small box inside that is the drug they mix up. I am feeling fine tonight after the treatment, but I must admit I am a bit shocked at the restrictions I now have to follow to avoid the bad side effects of this drug. PPE (Palmar-plantar erythrodysesthesia), commonly called hand-foot syndrome. It is skin reaction that sometimes occurs as a side effect of Doxil. It ususally appears on the palms of the hands and the soles of the feet, but may develop anywhere on the body where clothes are tight or where friction, rubbing or sweating occurs. This reaction may cause the skin in these areas to become red, swollen, itchy or painful.
Soooooooooo, I can't have anything hot, (like my morning coffee). I can't have a hot shower, boo hoo. No direct sunlight, so no floating on the pond for me this summer. I have to wear loose clothing, can't take things out of the oven. I can't do dishes with hot water. I can't chop hard foods such as raw vegetables, I can't lean on my elbows and on and on and on. I now get to enjoy frozen frappachinos and lots of iced drinks. They gave my these flat ice packs that my meds came in and twice a day for 15 minutes, I have to ice the palms of my hands and soles of my feet. I did that a minute ago watching the Tiger Game.
I was a bit shocked when they handed me my schedule and it goes up to next February!! IV chemo once a month and then a sub Q shot every week for three weeks and one week off. Lots of Chest x-rays and CT-scans to see if the drugs are working.
So if you see my with my new large sun hat that I got for Mother's Day, you will know why. I had a wonderful field trip last week with my two friends, Jackie and Deb and my sister-in-law Nancy. We did so much in two days!!! Saw the Tigers win last Tues. night, we were so shocked when the bat boy came over to us from the field and threw all four of us a pink Tiger baseball. The fans around us were going nuts. I figured after about the second ball that it was a set up. My wonderful brother Jim had bought them and had him throw them out to us. Thanks again Jim for a great night!! We went to Greek Town for fresh Baklava, rode the People mover, had a tour of the Pewabic Pottery Studio, Hitsville (the beginning of Motown, saw the Heidelburg project ( an neighborhood where they make art out of junk), had dessert and coffee at The Wittney House (and amazing old manion) had a wonderful lunch at Colors, a restruant that teaches locals a trade to serve and cook, using local produce. Dinner was happy hour at the Westin, which was the old Book-Cadillac Hotel, and many more sights......Detroit has lots to offer for those who haven't been there for a while, you should give it a try. We only ran into very friendly locals. Nancy has a new name by the way, "Baby Girl".
I don't always have a lot of energy and I was sure tired after our busy two days. My body didn't know what hit it. We are looking forward to up north this weekend. Stan's parents and his aunt Merle will be coming, along with Ross and Rumy. Mieke and Aaron get my new grandpuppy this weekend, so they will be a little busy with their new addition. I wish you all a wonderful Memorial Day.
I thank you all for the love and prayers that continue for us. I am trying to enjoy everyday to the fullest and like my friend Dave, eating my dessert first if I want. I am so thankful that Dave B. is doing better with the PICC line and IV fluids. We love you Dave and pray for you constantly. Prayers also for Dave's son-in-law and my friend Kent who also has a reoccurence of his cancer and back on chemo. Kent, I miss our talks when we were in having our surgeries at the same time. Hang in there buddy!!! Prayers also for my friend and PEO sister's husband David V. who is also battling cancer. Hope you are feeling better. There are way too many people in this cancer club as I know all of you who read this know all too well.
Watching the news about the tornado in Oklahoma, can't imagine how those people feel. My heart and prayers goes out to them as well.
You are a brave lady! It was so great to see you yesterday and you just looked beautiful. You certainly have my prayers and those of all your P.E.O. Sisters.
ReplyDeleteLove you, Jeanne
Hi Deb,
ReplyDeleteGood to see you yesterday. You are handling all the complexities of the medication world so beautifully and with a positive attitude ....and finding alternatives from hot to cold. As they say, attitude is everything. You have it and it will see you through!
Hugs, Terri H.
Hi Deb,
ReplyDeleteYou DO have the best attitude about all these changes you must endure. Dave's doctor "mentioned" this hand/foot syndrome too for chemo they might try on him. Of course he never really said all this would entail. Wow, I am not so sure Dave will have the same good attitude. He is always cold and I think the thought of all this "coldness" will make him very miserable.
Thank you for your endurance. We LOVE having you THIS side of heaven. Thank you, Jesus.
In His love,
Linda Breen
Hi Deb! I just got caught up on your blog, was wondering how you were doing and what was happing! I met your friend, Karen this past week! I have been praying for you, hoping this new drug will do it's job on the cancer and not on you :) Sounds like you are busy as usual! Thanks for the update and keep your chin up! You always seem to be upbeat, thankful for that! I'll keep lifting you up..... hugs and love, mary leeuw
ReplyDelete