Wednesday, April 23, 2008

Chemo #4 and Some Really Great News

Susan about to board Doug's car, pumped and ready for her chemo. Go and get some, Susan!




It’s been March since I attended one of Susan’s chemos. The last time I went I was pushing Susan in a wheelchair trying to maneuver her in the elevators, around people and corners. This morning she strolled from the car to the doctor’s office using a walker. But once she was signed in, she got up with ease from her chair to the receptionist desk and back, into the examination room, and finally to the party room without it. I was amazed to see such a change in her in this setting.

The nurses took her blood for testing. I had no doubts whatsoever that today would be chemo day. Susan always has her doubts each time she goes, or at least, carries with her the possibility that it could be delayed. I didn’t have any doubts today. I could tell by the color of her face and her eyes that her numbers were right.

Sure enough, the nurse’s assistant read the numbers to us:

Her hemoglobin was 9.2. The last reading was 8.7.
Her platelets were at 198. The last reading was 139.
Her white blood cells were at 7.4. The last time she was tested she was 1.3.

Dr. Nguyen came into the room saying “Wow, did you see these numbers?”

Did you read that right? We got ourselves a “wow” from this very reserved oncologist. Not only a “wow” but a laugh of astonishment and a big smile from him that surprised even me. I’ve heard that he can smile. I’ve seen him grin when Susan cracked a joke. But a smile from him was like a blue ribbon for the finest tasting pecan pie – it was a reward duly earned after so much went into making it happen. I was amazed to see it myself. To say he was pleased with her results wouldn’t do the moment justice.

He patted me on the shoulder said laughingly and said, “she’s doing great.”

He proceeded to examine Susan and announced that that she wouldn’t need a blood transfusion tomorrow; which it was routine for Susan to go for chemos on Wednesdays and blood transfusions on Thursdays. Not this time. She’ll still need her mother to give her shots to keep her red and white blood cells, but extra pints of blood won’t be necessary.

He’s also changing her chemo to two different types. She’ll endure less of the negative side-effects and the medicines will focus on the cancer cells themselves, and not healthy ones. This is so promising. This is the chemo he’s been waiting to use, but was waiting for her white blood cells to be at the level they are now in order to that. In a couple of months he’ll consider giving her a pet scan. Now it wasn’t necessary since it was evident that Susan’s responding well to the treatment.

Upon leaving, he said in passing to us “she’s getting better and better every day.” Which surprised me; his comments paralleled Susan’s anthem of “I’m getting stronger and stronger every day.” I have no doubts in Susan’s commitment to beat this thing.


We proceeded to the party room and Susan received her chemo. She was in good spirits. She drank pomegranate and Fritos.

I stand beside Susan as she receives her chemo. If someone had offered me a donut my smile would have been wider. But no, nobody did. So this is all you get.

The nurses give Susan a thumbs up. They are great people. I hope the doctors give them raises soon. They deserve them.
After we returned, I went to work and Susan and her parents went to Le Madelaine for lunch. This was her first sit down meal at a restaurant. And in spite of the awkward stares and the encouraging smiles, Susan didn’t feel self-conscious about her appearance – and no reason that she should have. She’s beautiful and quite powerful.



Susan and Kay eating Le Madelaine's foo-foo grub.

I do have to admit, the restaurant's pastries do look good from here. I doubt anybody will bring me anything.
Here's Susan and Doug completely replete from a good meal. And look, Susan's bringing me a big bag of nothing.
All of this good news and Susan's apparent recovery goes to show you that your prayers and wishful thinking has the power to subdue the monster who is obviously failing to bring down Susan, and they have the power to make a reserved oncologist smile, too. Please keep it up.

Thank you all.

Ray





7 comments:

Kaylee said...

YAHOO!!! GOD IS SO GREAT! What thrilling news! Ray, I can tell you are happy as your very dry wit is out and about on the blog tonight....no plain shipley cake donut for Ray?? :( !!! You are too funny! ANyway, we are keeping on keeping on praying for Sue and God's miracles and SUe you keep up the GREAT attitude and intenstinal fortidude necessary to beat this, cuz YOU WILL!! What a great day and great news!! Thanks for the great job on the blog Ray!! I can't wait to see what happens in 4-5 days when this chemo makes it's way through Sue, will she be doing cartwheels??

XOXO Kaylee, Mike, Ashlee & Alex

Anonymous said...

Wow!! What great news and what a great day you had Sue. I do believe in the power of prayer and there are so many that are praying for you Sue. I know that you will keep on getting stronger and being able to get out more. You have sure come a long way these last few months. The pics were so nice to see. Have a great day tomorrow and keep on keeping on. Our prayers will continue. Thanks for the blog Ray. Nice you could go with her to hear all the good news of the day. You are sure radiating Sue with your smile and great color. We love you and think and pray for you often.

Pat

Anonymous said...

Ray made it sound so fun. I want to go to a party room, have some Pom and Fritos, then eat at La Madeline's too! Is it true that what happens in the party room stays in the party room?

All that aside, that is really great news!!! Halfway through this ordeal and you are not only strong, but doing so well you get to upgrade your type of treatment? Awesome!

Get your rest and keep up your strength! Take care!

Anonymous said...

Oh thank the lord for such great news! Susie, you continue to overwhelm me with your fantastic attitude and beautiful smile. Dr Nguyen - thanks to you too for all that you've done for Susie - please keep it up. Thanks to Ray and Kaylee for letting us know exactly what to pray for - it's obviously working! Have a great day and stay strong. Love ya.
G

Anonymous said...

What a thrilling day!! Thanks for the update. We're so glad to hear things are going so well, and that you were able to celebrate this victory with a special lunch out! Keep that lovely smile on your face! Thanks for keeping us updated Ray!

Love you,
KT

Anonymous said...

I was soooo elated to read Ray's infomative and Witty comments and get THE GOOD NEWS that Sue's chemo has been doing its job and God has been good to all of us and hearing our prayers on Sue's and her families' behalf too. We truly have a loving, caring and a God who heals and answers our prayers. Sue, you are fantastic and doing sooo well. Hang on to THE FINNISH SISU ALONG WITH YOUR MOM. YOUR DAD MAY POSSESS A BIT OF IT TOO. Remember Jesus Loves You and so do I. God bless you all, Auntie Helen Kaylee, you and your family deserve a special thanks too.

Anonymous said...

GOOD MORNING, I was so HAPPY to read the latest blogs and to see that Sue is doing soooo well. Praise and thank the Lord that Sue's doctors, caregivers, hubby and family are all doing thir bit to help Sue fight the THE BIG C. But most importantly, Sue, is not letting her defenses down, and is fighting this beast with her postive attitude and her faith and trust in our healing and loving Lord. Lotza love and prayers to each of you on Sue's PRAYER AND CAREGIVERS TEAM. YOU'RE THE GREATEST. MAY GOD'S PEACE BE WITH YOU AND YOURS, AUNTIE HELEN I enjoy the blogs as is such a good way to keep in touch with what's happening on a day to day basis.