Friday, August 20, 2010

Amazing Gift

An amazing photographer offered to take pictures of the family for a slide show presentation at our benefit dinner tomorrow night. We had the pictures done on Tuesday night and I got a sneak peak at a few of them from her blog. I cried the first several times I looked at them. I think she did a wonderful job and I can't keep my eyes off of them. I keep coming back to look at them over and over again. Enjoy :)

Sneak Peek

Friday, July 16, 2010

Next Step

Will has decided to start chemo. He will be admitted to the hospital on Tuesday morning to start round 1. It is an in-patient regimen and should last 5 days. THank you for your prayers, we really need them right now. I have been posting a lot on the helping hands site instead of the blog, mostly because I don't have time to post 2 times. So if you are interested in the details, I would encourage you to go to THIS site. Hope everyone has a nice weekend. We will be showering Will with all the attention he can stand :)

Friday, July 09, 2010

Back From Houston

We got back from Houston late Wednesday night. The storm we drove through to get home was oddly appropriate for our moods. We got te Pet scan results that afternoon and it shows about a 20% growth in the tumors and new ones as well. I will write more when we have more information as to the what, when and where of Will's next step. We would appreciate your prayers for our family and especially for Will.

Saturday, July 03, 2010

Benefit Dinner and Silent Auction

Some friends of ours are organizing a benefit dinner and silent auction to help us raise money to continue Will's treatments. Insurance won't pay for any of it and it is quickly adding up! So, if any of you are interested in helping us get donations for the auction please let me know and I can email you the form. Or if you are on the Helping Hands site it is available there under the "Resources" tab. If you are not a member and want to keep up with updates about Will you can join that site. Just click HERE. The dinner will be on August 21st and it is going to be so fun! It will be a New Orleans theme with a DJ, jambalaya dinner and fun Mardi Gras decorations. We are so excited about it! Hope you all have a fun and safe weekend.

Monday, June 21, 2010

Birthday Party

Here are a few pictures from Liam's party. For some reason some of the pictures won't upload. I will try again later to get the rest up.



My Baby Is 3!!!






Liam turned 3 last Thursday. I can hardly believe it! He has grown so much this past year; in more ways than one. He is 36" tall and in the 17th percentile now and 28 pounds with all of his clothes on (and full of food from lunch) and in the 15th percentile now. Some of his accomplishments this year include: He can count to 20, recognize his upper and lower case letters, knows the sound of every letter, started writing letters and holding the pencil correctly, quick witted and soooooo funny! He loves to make all of us laugh, but especially his sisters. He is also very charming with the ladies. Everyone who meets him is amazed at how well he speaks and how great his vocabulary is. He loves to fish, sit on the back deck with his play gun and shoot at the ducks, play baseball, soccer and football and any other game he can think of with a ball. He is absolutely ALL boy and it is so fun. These pictures are from his actual birthday. We made his allergy free cupcakes that day while the girls were in VBS. If anyone wants the recipe let me know. They came out fabulous! I will post pictures from his party later.

Friday, May 21, 2010

Fishing






Here are some pictures I took of the kids with their fish. Each of them caught a fish with a little help from my mom. (Except for Emma who did the casting, catching and reeling all by herself!) Liam tantrum was because he wanted to stay outside and catch more fish. A daddy fish to be exact. He said that he had only caught a mommy fish and he wanted to catch a daddy one too! My mom was comforting him, but it soon turned into a flailing kicking, screaming fit on the ground. He had to be picked up and brought inside to time out to cool down. Either the boy REALLY likes to fish like his Uncle Chris, or he was in desperate need of a nap. Okay, maybe a little of both :)

Thursday, May 20, 2010

Big Girl

My Pagey is getting so stinkin' big I cried last night. She learned how to ride a two-wheeler this weekend thanks to her Poppy and her Daddy. And last night she lost her first tooth! This post will be dedicated to that.

She came running down the stairs last night about 8:30 all excited that she had pulled out her first tooth. We took some pictures and helped stop the bleeding, which was more than I thought it would be. Then she said she wanted to put it under her pillow for the tooth fairy. Here is where I need to insert some background information. Will and I both felt devestated as children when our parents told us that Santa Claus wasn't real. We felt like our parents lied to us and were really hurt be the experience. (I know it is odd that we both felt that way, most kids don't care.) So when we got married we decided that we would never lie to our children, not even about the littlest thing. So, we don't do Santa or the Easter Bunny. We simply focus our attention on the real reason for the holiday instead of the make believe. They still do all the things other kids do, like take pictures with Santa and do Easter egg hunts and things like that. But it is just for fun, they know the real meaning behind everything. I know a lot of people don't agree with that, but it was something we felt strongly about and both wanted to do for our family.

So back to last night when Page said she wanted to put her tooth under her pillow I was taken aback. I didn't know what to do. She was SOOOO excited and full of joy. People have told us that we are depriving our children of fantasy and of being a child and those thoughts came rushing into my head. What if we are? Should I do it? She seems to think it is real, what could it hurt? So I got her a little bag to put her tooth in and she asked if she could write a note to the tooth fairy asking to keep her first tooth so she could show all of her friends at school. Once she was asleep I sprinkled glitter in a trail from her window sill to her bed and a little on her sheets. Replaced her note with one that said how proud of her "Flossy the tooth fairy" was for brushing her teeth so well. Then I put taped the tooth bag and the money to the card from Flossy and put it under her pillow.

Well first of all, the glitter in her bed was a bad idea. She got some in her eye when she woke up. She asked a few times if the tooth fairy had really come and I said yes. I lied to my daughter.
I took Emma to gymnastics and when I came back page had a few questions. She asked Will in the middle of a story if he had seen her come into the room last night. He thought she was talking about the tooth fairy, and said no. Then she asked if I was in bed when he woke up this morning. It was then that he realized where this conversation was going. She went on to say that she knew the tooth fairy wasn't real but that she pretended because other friends argue with her about it because she doesn't believe. He said to ask me about it when I got home and that we really just wanted her to enjoy the make believe with her.

When I got home she asked me why I tricked her. She knew the tooth fairy wasn't real and wanted to know why I would lie about it. Okay, stab me in the heart and make me cry again! I told her that she was so excited about it we wanted her to keep being that excited. She said she didn't like me tricking her and to please not do it again. I said that we could still keep doing the tooth fairy game even though she knew it was me and daddy. She said she didn't want to except one more time. Then she said that she wanted to put her tooth under her pillow but for us not to do anything. She wanted to see if the tooth fairy was real. I was kind of confused by that statement because she said that she knew we had tricked her bad that it wasn't real and then at the end of the conversation wanted to see if it was real.
Emma also had some issues this morning. She got on the floor and was examining the "fairy dust" for quite a while before asking me if it was true. I told her that I had heard that when Flossy dances in your room she leaves a trail of glitter. She asked me again and I lied and said yes, it was real. I could tell that she didn't believe me and I didn't know what to do. Man this sucks! I promised to never lie, my kids trusted me and then I lied and they felt betrayed. The exact thing I was trying to protect them from. Lesson learned, DO NOT LIE TO YOUR CHILDREN. They didn't care that it was pretend, they wanted to know the truth. I hate that I lied to them.

On a lighter note, here are some pictures.












Monday, May 17, 2010

Pain

Please pray for Will. He has been in unbearable pain for 3 days now. He thinks it is his kidneys, but we are not certain of that. His doctor won't call us back, after 3 messages have been left. He is getting on a plane shortly for a very important trip (and will return tomorrow evening) and is asking for everyone to please pray for him. God knows what the problem is and God can heal him, we need another miracle today!

Wednesday, May 05, 2010

Good News

We got some good news yesterday! DSRCT generally doubles or triples in size every 28 days. Will's tumors have not changed at all in the 6 weeks between scans. The doctor at MD Anderson was "very surprised" by the result of the latest PET scan. We are taking that as encouraging news and believing that God is doing a mighty work in his body! I smiled so much last night that my cheeks were hurting. Will said that was the best news he had been given in several months. We are so thankful for your prayers and ask that you please continue to beseech our Heavenly Father on Will's behalf.

We will be meeting with the local oncologist in Dallas on Tuesday to discuss these results and to talk to him about what we have been doing for the past few weeks that we want to continue. I will post in the near future about what alternative therapies we have been using to help with this battle. Anyway, thanks you again for all of your prayers and support - keep them coming!

Tuesday, April 27, 2010

Our First Day

We made it to Houston late last night exhausted, and yet unable to sleep. Will managed to get a few hours, but I was awake all night. I prayed and tossed and prayed some more and tossed some more, and you get the idea.

We met with Dr. Ludwig this afternoon for our consultation. He wanted to run some more labs, do more x-rays and another PET scan. The good news is that we have that all scheduled this week and will be heading home this weekend! I am so happy about that :) Anyway, he told us that basically this type of sarcoma is very similar to Ewing's tumor and Wilm's tumor and the course of treatment is very similar to the way they treat those two types of cancer. It would be 5 straight days of 3 different types of chemo and then off 16 days for a 21 day cycle. Days 10-14 would be roughest days for him because of the white blood cell drop that would occur happens on those days. We could do the treatment in Dallas with the doctor we saw a couple of weeks ago.

He said that we would know if this treatment was going to work within the first 2 cycles. We would return to MD Anderson in 6 weeks to redo the scans to see if the tumors were responding to the chemo. This protocol is very hard on the kidneys and the heart. Both will be monitored 3x's a week to make sure they are still functioning properly. If either one starts to decline they would have to discontinue the regimen and start on plan B and if that doesn't work there is a third group of drugs they will try. If none of those work he would be considered for a clinical trial.

He is not a candidate for surgery, which is sometimes an option with this disease, because of the number of sites the tumors are.

The doctor says he has an 80% chance of living 1 year with treatment. After that he said that the average patient with this type of cancer only survive 2-3 years with treatment. I am crying as I type this because it is the first time a doctor has actually given us any kind of time line. We have read a lot online about how fast and horrible this disease is, but when you hear it face to face it is so hard to hear. I am holding on to God's healing power and trying not to put too much stake in what a doctor says. God alone numbers our days and knows exactly how long Will is going to be here with us. I am still hoping on 50 more years with him! With God all things are possible. I believe that with all of my heart and I will put my hope in Him.

Please continue to pray for peace as we wrestle with some very big decisions and wait to hear what God is directing us to do. NO one should have to make these sorts of decisions and my heart is breaking for our family and for every other family out there that has or is or is going to have to deal with this difficult diagnosis.

Monday, April 19, 2010

MD Anderson

We got our appointment at MD Anderson for the 27th of this month. We got our hotel reservations lined up today and my mom is coming in to watch the kids. I told them today about mommy and daddy leaving and I was able to not cry! I am so proud of myself. I pulled out a map and showed them where we were going and how long we would be there. They asked a few questions about whether or not this doctor was going to fix daddy and wanted to know why PawPaw couldn't come visit too. It was a hard conversation to have with them, but they handled it pretty well. I could tell that Page was a little upset by it because she didn't really eat much after that and kept asking if daddy was going to be better when we got home. Poor baby is really starting to sense the seriousness of the situation and my heart just aches for her and for Emma and Liam. But with God's grace and His abundant mercy I know we will get through this.

Wednesday, April 14, 2010

Please Pray!

We met with a sarcoma specialist yesterday in downtown Dallas. Our scheduled time was for 9:30. We saw the doctor at 12:00. No kidding. Then when he got there he had not looked at anything. He told us he would review everything in the morning and call MD Anderson and that we should call him back this afternoon at 4:00 to discuss things. I did call him, he has not returned my call. Neither has MD Anderson who said that everything was turned in on Monday to the review board and they had 24-48 hours to schedule the appointment. That meant today was 48 hours. They didn't call either.
I tried to do some research today to try and find some survivors of this disease. I was not successful. I spent most of the day crying about all these families losing their loved ones. I prayed that this is not Will's destiny. Our pastor's wife lost her battle with cancer today and went home to be with the Lord.
I am having a really bad day. Please pray!

Friday, April 09, 2010

Mayo CLinic

The Mayo Clinic gave us their pathology today. It is the same as the local pathologist - Desmoplastic Small Round Cell Tumor - DSRCT. So we now have 2 pathologists with the same diagnosis. I think we can call it official, unfortunately. More to come this weekend.

Thursday, April 08, 2010

Diagnosed

We got a diagnosis today. I am not going to write much tonight, because I am exhausted and feel like I would just be really negative if I tried to sort through my feelings right now. I will post more this weekend, but for now you can follow this link to read about Desmoplastic Small Round Cell Tumor:
http://http://en.wikipedia.org/wiki/Desmoplastic_small_round_cell_tumor
We continue to ask for your prayers right now.

Wednesday, April 07, 2010

No More Information Yet

I wanted to let all of you know that we are still waiting. We have no more information yet. In fact, we have been told that it will be Friday at the earliest that the pathology is expected back. We were also warned not to get our hopes up about Friday and to plan on it coming in some time next week. We are frustrated by how long this is taking, but we are also trusting that God's timing in way better than our timing. And we continue to put our trust in Him and rest in the fact that He is in control. So, while we are praying and hoping that things would move more quickly, we will continue to wait.

In the meantime, we have hired a cancer coach. He is helping us sort through all the alternative medices for cancer. If the medical community isn't going to do anything right now, we certainly are going to do our best! We are doing a sugarfree, alkaline diet and trying a few supplements that he has recommended. We are reading a ton and doing lots of research about doctors, hospitals, alternative treatments and regular treatments.

Thank you all again for your prayers. We believe so much in the power of prayer and are blessed that we have so many people around the country praying for our family. We are also praying that God would bless each of you for you faithfullness in standing with us in prayer. We really do appreciate it so much. We serve a mighty God and we put our hope in Him!

A friend of ours from church has started a website for us. I will be able to post what needs we have on the site and will post updates on their as well. It is: http://www.lotsahelpinghands.com/c/624545 It will ask how you know our family when you sign in, please just put a brief sentence so that she can add you as a member quickly. (Otherwise, she will send you an email back asking ow you know us.)

Friday, April 02, 2010

Crying

Liam and Emma were playing on the sofa this morning, having a little pretend tea party just between the two of them. It was adorable and sweet and oh, so funny! I was sitting across the room from them just watching them play together. Liam scooted to the edge of the sofa to reach for something and fell off. Head first onto the wood floor. I couldn't get there fast enough to catch him. He started screaming immediately and all I could do was scoop him up into my arms and hold him. I held him tightly and rocked him back and forth just kissing his head and letting him cry. Then I heard in a sweet soft voice "this is what I am doing to you." I started crying myself as I realized the tenderness and the love that my Father in heaven is pouring out onto me as I cry out to him. It hurts, but more than anything else it is just plain scary. The thing is, He knows, and He is there holding me, rocking me and kissing my head while I cry out in pain. And just like Liam finally stopped crying and looked up at me to tell me he was okay, I know I will get to the same point with my heavenly Father. And I know that He will kiss me, and hold me until I get there, without ever letting go. What an amazing God we serve, let us never forget how great his mercies are!

Wednesday, March 31, 2010

Still Waiting . . . Seriously!

Today did not go exactly as planned. We were told last week by Dr. S that we would know something at this appointment and would be moving forward with the treatment plan. That did not happen. I got a call at 3:00 today, and our appointment was scheduled for 3:30, from Dr. S's nurse to let me know that the results of the biopsy were not in and we needed to reschedule our appointment for next Tuesday. I sat there for a minute not really knowing what to say. Then the tears started coming. I could not keep them in. I kept apologizing to the nurse for crying and telling her that I was not angry with her, but that this whole situation was so ridiculous and I was mad. I was really mad. I did not want to wait another week to get answers. I was sick of every single diagnosis being wrong and was beginning to wonder if anyone knew what the heck they were doing. I told her that I wanted to meet with Dr. Stone anyway, at least to discuss the results of the blood work and the CT scans. She was not happy. We arrived for our appointment anyway. Dr. S walked in and said "what are you doing here? Didn't you talk to my nurse?" I cried a lot at the appointment. I think I had just built up in my mind that we just needed to get to Wednesday. We could move on and start doing something once we got to Wednesday. And now that it was here, we can't move on.

So we discussed the results that we did have, just for our curiosity. The blood work that was done on Thursday of last week was a marker test. Different cancers have different markers and we could see which markers showed up on the tests. Well, the only one that showed up was for breast cancer. Dr. S said this is not breast cancer. So, the blood work was of no help in getting a diagnosis. The CT scan gave a definite number of tumors and the sizes of each one, but again, does not help with the diagnosis. And finally, the pathology on the biopsy was not in yet and that would be what we needed to determine whether it was an unknown primary or a specific cancer since nothing else was giving us a diagnosis.

Well, while we were in the office, saying our goodbyes, Will's cell phone rang. It was the ENT that did the biopsy saying that the pathologist had called him and said the tissue actually looked like sarcoma instead of carcinoma, and he was sending it off to MD Anderson and the Mayo clinic. (They said that it was carcinoma from the fine needle aspiration he did a couple of weeks ago.) It would be another week before we got the results in. So we wait. We are still waiting. We are tired and frustrated, and yet still hopeful. We ask that you continue to pray for us and with us as we continue to wait.

Friday, March 26, 2010

More Tests

We met with the oncologist, Dr. S, yesterday. He is actually a friend of one of Liam's teacher's at the Mother's Day Out! God has such a way of putting us on directly the right path that it makes me smile in the midst of this storm. Anyway, Dr. S looked at all of the tests we have done already and actually pulled up the PET scan in the office so that we could see it as well. He really thinks that we should do a few more tests to try to pin down a diagnosis. Will did lots of blood work yesterday and Dr. S got us a CT scan today!!! (We are leaving right after I finish typing this.) It will be 2 CT's actually, one of the chest and one of the abdomen. Then on Monday Will is going in to have the lymph node in his neck completely biopsied so that they will have a large tissue sample to work with. Dr. S believes that all of the tests will be back by Wednesday and scheduled us for an appointment on Wednesday afternoon. He said that if we don't have a definitive diagnosis by then, we will have to go with carcinoma of unknown primary. So, we will know things by Wednesday and will update all of you then. (It may be Thursday before I can do that.)

Thanks so much for the love and support we have received. Please continue to pray for peace and for wisdom for the doctors. There have been a few comments to Will and myself that have been anything but encouraging. I just ask that during this time, you please keep those comments to yourself and simply pray for us. We are dealing with very traumatic news right now and are handling it the best way we can.

Tuesday, March 23, 2010

It is, it isn't . . .

Wow! What a week it has been. Thank you all for your kind words and your prayers for our family. We have really felt the presence of the Lord this week. And while the waiting and testing process is so hard, we have found strength in Him and He has filled us with great peace. The Lord is hearing our prayers and we are so blessed by all of you!

I want to document this process so that when we get through this I will be able to look back and see all the amazing things God has done and not just remember the sleepless nights and the chronic worry this has brought to us. So if you all would bear with me, this first post might be a little lengthy, so skip on down to the bottom if all you care about is the result of the colonoscopy.

Will found a lump in his neck in a lymph node just about the clavicle. It was hard, but did not bother him. He pushed on it and wondered about it for a while, but hoped it would disappear. When it didn't go away he called his general practitioner, Dr. J, and scheduled an appointment. A week and a half later he was sitting in the Dr. J's. He said that he honestly didn't know what it was and that we should schedule a CT scan of the neck. He thought for sure it was not in a lymph node, however. By this time, the lump was growing daily and it was actually starting to cause some pain for Will. The result of the CT was a mass about 5 cm large with suspicious edges. We were then referred to an Ear, Nose and Throat specialist.

A week after that, we were sitting in the ENT's office, Dr. M, told us that 9 out of 10 times this is just an infection and antibiotics would do the trick. Well, after a week on antibiotics there was no change. Dr. M said it was time to do a fine needle aspiration. It was done in the office and was pretty quick. His opinion was that if it was anything, it was probably lymphoma. We braced ourselves for that and did a little research about that type of cancer. A few days later we got a call that the pathology on the FNA was back and it was not lymphoma. Dr. M told us that based on the pathology of the cells we were probably looking at thyroid cancer or lung cancer. (Seeing as Will still runs 50 miles a week and has never been a smoker, he put his wager on thyroid cancer. Again, fairly easy to treat in the world of cancer.) But the pathologist could not come up with a definitive answer on that. He would need a few more days to try to pinpoint exactly what kind we were looking at. The results, 4 days later, were still inconclusive. It was positive for metastatic carcinoma of the neck with unknown origin, non small, non squamous with papillary characteristics. We were on the move again.

We were referred to an oncologist and a radiation oncologist from there. The radiation oncologist had the first available appointment, so we went there to see Dr. G. Our appointment was on a Tuesday. Dr. G's assessment was that a full body PET scan was needed next to determine if we could find the source of this cancer. He explained to us that there are certain characteristics that each type of cancer will have, like different flavors of ice cream. He used the analogy of ice cream so much that I thought about asking him to stop referring to my husband's cancer as ice cream. He was also very offensive in his speech. I left his office feeling like I needed a bath. Although he did a great job of explaining every aspect of the information we had so far, I was ready to get out of there and go schedule the PET scan. To me, it should have been done that day, but sadly he said we needed to schedule it.

I remember standing at the counter trying to hold back tears while we waited to find out when that was going to be scheduled for. The following Monday was the first available. I couldn't control it; I started crying and begged him to fit us in earlier than that. I told him that my heart could not handle another weekend of not knowing. He told me that the PET machine had been broken for 2 days and that the guy who ran it was off on Wednesday. So all the patients from Mon., Tues., and Wed. had to be fit in the last two days of the week along with the ones that were already scheduled for those days. There was nothing we could do. He was sorry. We walked back to the van and Will just reassured me that God knew when we needed the scan. That God was in control and that we had to trust in His timing right now. On the drive home Will's cell phone rang. It was the guy who schedules the PET scans. He had a cancellation on Thursday morning right after we walked out the door. I nearly peed my pants I was so excited. Will looked at me and smiled "God is in control of this, not us."

We went to a prayer meeting that night with our pastor and his wife, who has been battling Stage IV breast cancer for 6 1/2 years. We had a wonderful night of worship and then Will, and many others, got prayed for. He actually fell to the floor and started shaking. He said afterwards that it was like a bolt of electricity running through his body. He felt the Holy Spirit like he had never before and was glowing the rest of the night. The woman praying for him said that she could feel such heat coming out of his body, that it felt like fire. By the way, the woman praying for him is a woman that we have known for years; she loves the Lord with all of her heart.

I prepared myself to not get the results of the scan until the next day and possibly even over the weekend. But on Thursday morning, not 2 hours after the PET scan we got a phone call from the doctor. He was leaving for the day and had not gotten Will's results so he went to the lab to look at them himself. I felt like this was great favor given to us by God for the doctor to do that. Unfortunately the news was not good. He told us that there were lesions on the colon and the liver. He said that he was going to get a colonoscopy scheduled as quickly as possible, and that it looked like we were dealing with colon cancer. I cried my eyes out. One of those cries that comes from so far within you have no idea where it is coming from. Will had tears in his eyes, but decided to go to work to keep busy and not think about it. I could barely breathe. I felt a tightness around my chest that I can only liken to a snake wrapping me up in it's coils and squeezing me to death. It was that bad. I called a dear friend of mine to come over and help with the kids. I just didn't think I could do it. Of course she came right away and stayed with me until Will got home that afternoon.

I did a search on the Internet about colon cancer after Will left for work. Based on the fact that it was in his lymph nodes and in his liver everything I could find said that it was Stage IV; likelihood of survival very low. I just freaked out. I sent out an email to everyone I knew saying that Will had Stage IV colon cancer and to please pray. We were devastated, but continued to seek the Lord for a miracle and for strength and peace. The phones started ringing off the hook, emails were coming in faster than I could read them. The love and support from our friends and family was truly overwhelming. While it was wonderful, quite frankly it exhausted me. I felt like a zombie by the time I got to bed that night.

But I kept turning to the verse in Jeremiah 29: 11 " For I know the plans I have for you, declares the Lord, plans to prosper you and not to harm you, plans to give you hope and a future." If you continue to read past verse 11 it says that we are to call upon His name and pray to Him and He will listen. If we seek Him with all of our heart we will find Him and He will bring us back from captivity. This was what I am holding on to. This is a promise from the Almighty God, our Father, seated in Heaven and enthroned on high! I will call upon His name and pray. I will hold onto this hope and it will give me strength. Because nothing earthly is going to do that. Every appointment we have been to is worse news than the one before. Even the colorectal surgeon looked at us and said "wow, you guys haven't heard anything good in a while!" It is true, but we are choosing to put our faith and our hope in Him, not in the doctors.

The colorectal surgeon, Dr. B, brought us into his office yesterday and gave us even more horrible news than we got from the phone call from Dr. G. He said that Will's entire abdominal cavity and pelvic cavity were full of lesions. He said that it was covering the lymph nodes surrounding the colon, on the liver, on the spleen, and going up the lymph nodes towards his neck. It was everywhere. He said that unless he found something obstructing the colon, he was not going to do surgery. He didn't think we had that kind of time to wait for Will to heal from surgery before starting chemo. I have to tell you, it took my breath away. I tried to breathe, but I just started crying. He asked me if I was okay and, through blowing my nose and wiping tears from my face I said "NO! I am not okay. I have 3 small children at home; I need him here with me and no one is moving fast enough." He was very kind about my losing my temper, but none-the-less, couldn't promise us anything other than he would do his best to get our answers as quickly as possible from the colonoscopy. We left his office and bought Miralax, Gatorade and Dulcolax. We went down the self check-out lane :)

So that brings us to today. A sweet friend of ours picked up the kids to take them to their Mother's Day Out program and brought us dinner for at least a week! We left for check in at the hospital. Pastor John, Will's mom and I were all there. The procedure took about 30 minutes during which time I had the unmistakable urge to vomit. The kind of sensation you get when you are in your first trimester of pregnancy and you feel like any little thing will set it off. It was a long 30 minutes! Dr. B said that he saw nothing of significance and that he found only one small polyp and he did not believe it was cancerous. He said that he could feel a mass in the pelvis pushing down on the colon, but nothing inside the colon itself. While the excitement of it not being colon cancer should have given me reason to celebrate, I couldn't help but worry about what that meant. He has no idea where the cancer is coming from and we may have to classify it as unknown primary.

Dr. B said that Dr. S, the oncologist that we are meeting with in two days, knows the steps to take at this point. There are other tests that we could run, but Dr. S is the expert and he would tell us how we should proceed from here. He kept telling Will he had to focus all of his energy on beating this cancer and even went as far as to say that if he beat this cancer he would do another colonoscopy in 5 years. That floored me, just the simple word "if" can do more damage to your heart than a thousand other words. My natural mind wants to keep thinking about that simple little word and how that would change our lives forever, but I choose not to. I am going to meditate on God's words and God's promises to me and to Will and to our family, because I believe that is what he wants me to do and to be quite honest, I don't think my little broken heart could take thinking about that word right now. I believe that words are very powerful and should be used with extreme caution. I want to speak life giving words now and always; and that word is definitely not life giving.

I have another post that I can't wait to pull up on all the crazy books and emails and phone calls I have gotten over the past few weeks. It really will lighten things up around here. Not to mention the tons of pictures of the kids that I need to get up. Oh well, I am exhausted and need to get some sleep tonight.

Thursday, March 18, 2010

Update on Will

We got the results of Will's PET scan this afternoon. They found more spots on his colon and liver. We have a colonoscopy scheduled for Tuesday and will move forward from there. Please continue to pray for a miracle! We are completely stunned by this news, but The Great Physician is not. He knows exactly what is going on and that alone brings peace during the storm.

Friday, March 12, 2010

Bad News


There are a lot of reason I have been absent from blogging for a while. First of all we took a trip to Baton Rouge to spend a week with Will's grandmother. She has advance stage Alzheimer's and is dying of cancer right now. I don't know all of the details of her condition, but we felt it important to see her one more time. The picture is of Will and his grandmother. She kept hugging him and kissing his face. I snapped this picture just after she wrapped her arms around him and told him he was getting so tall :) It was a very special time and I am so glad we will have those memories after she is gone. I have a ton of pictures from the trip that I will post at another time.


The second of which was getting 2 puppies; both of which came to use infested with worms and then contracted Parvo virus. It was horrible, disgusting and very expensive! They are bothe doing very well - outside of my house - and eating like starved horses!


But here is the kicker. Prepare yourself, it was so unexpected we have been knocked down and dumbfounded ourselves. Will found a lump in his neck about a month ago. He went to the general practitioner and he scheduled a head and neck CT scan. The CT scan showed the mass was "suspicious" so Will was sent to an ENT. This doctor said it was probably an infection and put him on antibiotics. The antibiotics did not work so he did a needle aspiration. We got the results of the aspiration and it is cancer. We are still waiting for the pathology report to give us the specific type of cancer. Right now we know that it is not lymphoma and that the mass in his neck is metastisized from somewhere else in his body. We don't know where and we don't know how many more masses there may or may not be. Will is having a lot of pain in his shoulder and in his neck. He is tired all the time, but dealing with things well.


We are asking for your prayers right now. Things don't seem to be happening as quickly as I think they should, but I know that my timing is not HIS timing and so I am choosing not to stress out about it. It is a choice, because everything inside of me wants to scream out loud that things need to happen now regardless of the weekend and spring break. Will wants to have a ton of fun with the kids this weekend and to spend quality time with each child before the insanity of appointments, decisions and treatments begin. He is such a wonderful father, I am just so broken that this is happening to him, and to our family.