Thursday, July 3, 2008

So...What is It?

We awoke yesterday morning with mixed anticipation of what the day might bring. Excited to finally be meeting with an oncologist, but with lumps in our throats as to what he may have to say. We knew nothing at this point could be definitive as Dave would first have to have the results of his full node biopsy. This too, was yesterday following our appointment with Dr. Kuebler.

I apologize if this post gets lengthy, but I want to give you all we know.

Dr. Kuebler explained to us that based upon the pathology report Dave has Follicular B-cell Lymphoma. However, this could change after the full node biopsy is analyzed. He described two types of lymphoma to us; favorable and unfavorable. As we listened to him describe these terms, we quickly realized they are a bit misleading. Follicular Lymphoma is a "favorable" cancer. Favorable basically means it is a chronic cancer that can never be cured...sounds like something you would describe as "favorable", huh? The reason it is put in this category is because it has a longer life expectancy than "unfavorable". Many people live for many, many years before they every show symptoms or even need treatment. Dave, fortunately, has no symptoms. In truth, we would have probably never gone to the doctor if he didn't have such a long family history of Lymphoma.

"Unfavorable" means it is an extremely aggressive form of Lymphoma with a much higher fatality rate if untreated. However, if treated it is curable.

So...going on the doctor's gut feeling of Follicuar Lymphoma, we began to talk about course of action. This is the most difficult part for me to wrap my mind around. There are four stages of Lymphoma. We know that Dave is at least in Stage Two as he has swollen nodes in more than one area. (neck, chest, and under his arms) Dr. Kuebler explained that by the time most patients are diagnosed with Lymphoma they are in Stage Four. However, Dave is also the youngest Follicular Lymphoma patient this doctor has ever seen and he is suppose to be "Nationally Renowned". We will not know his stage until we have a full body PetScan. (July 16th) He will also have a Bone Marrow biopsy this day.

Of course in my mind, at this point, I'm thinking...okay, let's get started. I realize it's not curable, but you need to fix my husband within the next 73 days because that's when this baby is coming! Dr. Kuebler thinks a little differently than I do apparently. He likes the "Wait and See" approach. This is a little confusing to me, but he tries to make me understand. Because this cancer is so slow-growing, he says they don't want to start chemo. Follicular Lymphoma does respond well to chemo, but always comes back. Remember it's not curable. Each remission gets shorter and shorter. So if they started chemo tomorrow, Dave may go into remission for 7 years. But in 7 years, when the cancer returns, he would have to do chemo again. This time the remission may only last 4 years. You get the idea...once you do chemo, the remission clock starts ticking.

If Dave has no symptoms and a good quality of life, there is no point in treating the cancer right now. I told you it's tough to wrap your mind around, didn't I?

Now we sit and wait for the "official" diagnosis to come back based on the full node biopsy. This should be Monday, July 7th. We are, of course, getting second opinion, next Friday with Dr. Kristi Blum at The James. We'll see what she has to say.

We know you have each been thinking and praying for us and we really do feel your love and support. Today was the first day that when I woke up Dave's cancer wasn't the first thing that popped in my mind. Maybe the second, but it's a start, right? :)

I do want to share with you the most touching part of yesterday's appointment. At one point, I asked the doctor..."Is Dave going to see this baby be born?" The doctor, very assertively looked back and both Dave and I and responded, " I whole-heartedly believe Dave is going to be around to pay Marshall's first college tuition bill." The power of words...are truly amazing!

10 comments:

Danielle said...

Thank you for the update! My heart and prayers go out to you all. Just so you know, Ella and I have added Dave and your family to our prayer list at bedtime. We love you all and will continue to keep positive thoughts. Keep your chins up and take good care!

Anonymous said...

Thanks for the update! You know you are in our prayers - glad to hear that the meeting went well and Dave is still stuck with the tuition bill. :)

Take care of each other and we'll see you soon!

Bonnie said...

Promising and very encouraging! You 2 are so strong and shall become 3 strong shortly. Your love for each other and God will hold and comfort you! I added you to the prayer list with my church family and given them the blog to add encouragement to you. (Plain City United Methodist Church/ PCUMC) I love you both and know God has much in store for you. And Dave don’t think you are getting out of ANY of the kid bills…diapers, formula, cars, college… and the infinite list of others….You are just getting started Buster!

“Father God, I lift Dave and Mandy up during this very stressful time. Cover them with the veil of your love and give them the peace beyond understanding. Put them in touch with the right doctors to carry your healing touch. Watch over baby Marshall and Mandy through the final stages of this pregnancy until we meet him in Your time. Father, thank you for always being a God of Love that brings people together in times of need and hear the prayers for this lovely family. In Jesus name we pray AMEN.

Anonymous said...

I have been thinking about you both and wondering what you had found out. I know that you two are awesome people and you will have many prayers over the years to come. It all does sound so confusing for you guys but your explanation was amazing for us common folks to understand. Keep us posted and let us know if there is anything that we can ever do to help in ANY way at all. Love and lots of prayers for you both!!

Kelly said...

Hi Dave and Mandy,
Know that you are in our thoughts and prayers. We have an amazing group of ladies who are prayer warriors at our church and I have added you both and baby Marshall to our prayers. Thanks so much for the blog, it will help to keep us informed. Know we will keep in close touch. We send lots of hugs.
Kelly

Anonymous said...

At least its a good and reassuring starting point You are always in our thoughts and prayers.

Anonymous said...

I know I am not alone when I say that I have thought about you guys every single day. Stay strong and when you are having a tough time, just know that you are loved by people that can and will be strong for you...

Anonymous said...

Thanks for the update. The blog is wonderful and what great therapy for you guys. I am thinking about you guys every day and I cannot wait to see you both soon and give you a giant bear hug!!! Keep strong and reach out if you need anything! Love ya both!
Alison

Unknown said...

Having just traveled this road, my heart and prayers are with you both.

Expect those miracles; God is good all the time

--c.

Marsh said...

Dave and Mandy...

My name is Marsh Williams and my wife and I have just spent a year living in the shoes which you now find yourself.

Nine months after my diagnosis I find myself realizing that after the initial shock, it has been one of the geatest gifts I've ever been given.

We will pray daily for the three of you and if there is anything else we can do to support you through this adventure please let us know or tell Paul and we'll be there in a heartbeat.

The blog is wonderful and over time you will find it incredibly liberating...

God's peace to you.

MW