Recap

I've been meaning to update sooner than this but I just haven't had the time and work on it so here it is. This week has had a lot of ups and downs. Last week we went to chemotherapy everyday from around 8:30am til anywhere between 1:30-3:30pm. It depended who our nurse was and how fast they felt they could run the fluids and the chemotherapy. On Monday thru thursday we went to the holland office, it was was nice that we are able to have our own room. On Friday theholland office is closed, so we headed out to Grand Rapids. It was a really amazing facility, with really beautiful layout and artwork. When we are there we are in our own little cubicle and are able to talk with people around us.
It was reallly interesting how people with cancer really bond when you in a place like the chemotherapy treatment facility. We had a nice older couple sitting next to us who was just diagnosed. We talked with them a bit and told our "story" and they shared their story. It was really nice.
Through the whole week Drew was really exhausted. Most days Drew would come home and go to the couch and feel pretty crappy. This weekend was by far the worst both with nausea and exhaustion. He has started to feel much better these last couple days, even been able to go into work and hang out on tuesday and Wednesday. Hopefully he will continue feeling good and able to get out and keep food down.
Thanks to everyone who has sent cards, messages, gift cards, and brought meals. We are eternally grateful to everyone who has been praying for us.

Sporting a new Look

Drew is officially sporting a new look. He decided that he wasnt going to wait for his hair to fall out, he was going to take matters into his own hands and cut his hair short now. We decided to go for a "Puck" look.  For those of you who don't watch Glee- here was our inspiration:

Before

During

After

Reality

Reality set in today when we walked up to Cancer and Hematology Center of West Michigan to get Drew's first dose of chemotherapy. We got to the building around 8:30am and luckily got a private room. Its a first come, first serve basis whether you get a private room or sit in the large "group" therapy room. Since we were going to be there for 8 ,we were really hoping for a private.
We arrived and our nurse for the day came in and took a look at Drew's new snazzy port and took off all the dressings. She was kind enough to put some numbing spray on the skin so it wasn't TOO bad putting the needle in place. She hooked Drew up to some fluid with different electrolytes to help protect his kidneys before she started the actual chemo, that lasted around 3 and a half hours. Then they gave him some medication to prevent nausea and to help relax him through the process. Then came the big guns. He is getting a triple threat of chemo drugs. Each drug took about an hour to infuse. After all that was in, he was disconnected and his port was flushed. He is able to keep the needle in place all week so he wont have to be continually poked and prodded. He's pretty excited about that.
From someone who barely takes a Tylenol, having 9 different fluids/medications in your body at one time is really crazy. He did pretty well through the treatment, he was a little tired from the relaxation medication. Right now he says he still is pretty tired and his stomach is a little "off" but overall doing pretty well.

Thanks again for everyone who is praying for us, we truly felt lifted up today.

Our "fancy" treatment room

Drew attacking cancer with full force!

Port Placement and Indiana

I'm back! Thanks to Lindsey for setting up the meal planner. We are so grateful for everyone who signed up.

This week has been crazy busy for Drew and I. It started with our Dr. appointment with the oncologist. I worked the next three nights and Drew even had the opportunity to go into work for a day. Then Thursday afternoon we headed back to Holland Hospital to have Drew's port placed.

He was in the procedure room for about 45 minutes and then went for a chest x-ray afterwards to make sure the placement was right. Everything went really well, and we were able to leave shortly after he ate something.  He is a little sore in his right chest/shoulder. After we left the hospital, we headed home and I packed up the car and we were on our way to Indianapolis.

We arrived in Indy late around 9:00pm and we were so blessed that my brother in law's parents live close to Indy and let us stay with them for the night. Thank you SO much Iversons!

 We woke up and headed to IU

It was a really beautiful campus and building. We waited for a while to see Dr. Foster. He was really personable and talked with us about what he thought was the best option for Drew. He agrees that chemo is the way to go. He confirmed everything the oncologist in Holland said. 3-4 rounds of chemo then we will have another CT scan  and lab work to see how the tumor in the abdomen responded. If it looks that the chemo did its job and the tumor is gone, that will be the end of it and we will just have check ups to make sure that is isn't going come back. BUT if there is still signs of the tumor, we will have to head back to IU and Dr. Foster will have to perform a surgery to remove the tumor. It was good to be able to talk with someone who has dealt with testicular cancer on a more regular basis and hear is opinions and confidence in the success rate of treatment.

So the plan is to start chemo at 8:45am on Monday for 8 hours each day this week and then two weeks of shorter visit once a week and the cycle will repeat 3-4 times depending on how the doctor feels he is doing.

After the appointment we headed to a little area called Broad Ripple and sat down for a lunch. Afterwards, we headed to a  park on the way home called Holliday Park. We did a little hiking through the woods and took a couple pictures :) 

It was a BEAUTIFUL day for a walk in the woods

There was a large piece of "ruins" in the middle of the park

Random statue in the park

Drew's Statue

My Statue



More of the ruins





Thanks:

To all those who have sent the message, calls, and letters.

To the girls at work who have been so amazing at switching and covering shifts for me!

YOU ARE THE BEST!

To all those who are praying for us, we can feel the love.

To all those who have signed up to bring meals.

Verses

 In his hand is the life of every creature and the breath of all mankind (Job 12:10)

But they that wait upon the Load shall renew their strength: they shall mount up with Wings as Eagles: they shall run and not be weary they shall walk and not be faint. (Isaiah 40:31)

Have I not commanded you? Be Strong and Courageous. Do not be terrified. Do not be discouraged, for the Lord your God will be with you whereever you go (Joshua 1:9)

Finally, be strong in the Lord, and in the strength of his might. (Ephesians 6:10)

My soul is weary with sorrow: strengthen me according to your word.(Psalms 119:28)

.

Prayers:

for minimal side effects from the chemo

for the chemo to do its job and the tumor will shrink completely

for strength and patience

for our family and friends who have been so amazing and supportive



Meal update

I knew someone was smarter than me who could help us out!!! :)

To sign up to bring a meal, please go to http:/www.takethemameal.com and enter Durham for the last name and "food" for the password. This will show you the schedule and allow you to sign up right there! :)

Thanks again for your willingness to help!

Hijacked and Help!

Hello all!

This is Jay's biggest sis Lindsey here! I've hijacked Jamie and Drews Blog to ask for some help.

The treatment phase of this journey is quickly drawing near and as a family, we really believe that Drews energy is best used in focusing on healing his body and Jamie's energy is best used in nursing Drew back to health. Taking meal planning, cooking and shopping off their plate is just one way we can help them direct their energies where they are most needed! We would love to be able to provide Jay and Drew meals during the time while Drew is undergoing treatment.

As it stands, Chemo will start Monday, with an intense week (5days, 8 hrs a day) and then two lesser intensity weeks. Our goal is to provide 3 meals during the intense week (mon, wed, fri), and two meals in the lesser intensity weeks (tues, thurs).

My goal is to try to get a sign up "thing" right here on the blog, but being I'm not a computer guru, that may take some work (let me know if you can help me here!)...but as for now, if you are interested in helping out, you can contact me by e-mail  hoogielj@Hotmail.com with "durham meal" in the subject line so i know its not junk :) Also in your e-mail please include a phone number so we can contact you if needs be.

If for some reason the treament plan changes or their needs change, we will contact those who sign up as soon as we know what the updated plan will require. 

Thanks again for all the support you all have been giving Jamie and Drew! We love you all for it!

Moving Fast...

We met with the Medical Oncologist today and we are now moving at warp speed. We sat and talked with the physician for a while then we were brought into the "treatment area" where the chemo would be administered. A financial coordinator came and met with us and went over insurance information, then a nurse came in with is and talked with us about They do it over a 3 week cycle. The first week is the toughest week and we will have to be there at 8:00am and stay for 8 hours, Monday thru Friday. The next week it would only be a one hour visit and same with the third week. That whole cycle would be repeated 3-4 times. Drew is having a port placed on Thursday at Holland Hospital, which will make administering the chemo alot easier and safer. We would start the chemo next monday the 18th, all depending on what they say at IU on Friday.
 We are still planning on going down to Indiana University on Thursday night to have their opinion. If they say that Chemo is the best route then we will start immediately. There still is the chance that they might say surgery is the better option to start with then we can still cancel the chemo and move on from there. He would most likely still have to have chemo after the surgery and is why they feel like they can put in the port. 
Im writing this very quickly before I have to go to work, so i apologize if i missed anything or anything is spelled wrong:)