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The Victory
Our beautiful Lindy, age 35, passed away peacefully surrounded by her family, September 14, 2012. Thank you for praying for her and our family during this incredibly difficult time. We celebrate Lindy’s homecoming and victory over her cancer battle, but we hurt so much.
A funeral service to honor Lindys faith and life will be held at 6:30 pm, Tuesday, September 18, 2012, at Haven Christian Reformed Church, 541 Alice Street, Zeeland. The Rev. Art Van Wolde and Rev. Scott Van Oostendorp will officiate. Visitation will be 12:00-2:00 and 6:00-8:00 pm, Monday, September 17, 2012 at the Yntema Funeral home, 251 S. State Street, Zeeland. Burial will be in Zeeland Cemetery.
Memorials may be made to the Ver Beek Children Education Fund (may be made at any Macatawa Bank).

She’s Winning The Battle
(Written by Dusty)
In the last few weeks we’ve seen a sharp decline in Lindy’s health. She’s been so fighting for so long, that I believe her body has just had enough. I like to think of her as winning the battle against her cancer since she’ll be free of it soon. Lindy’s Hospice nurse told us she thought she has about 4 weeks left based on what she’s seeing.
At the end of August, we were able to spend some time as a family at a beautiful cottage at Big Star (courtesy of Mike and Marci Baumann). I was able to speed Lindy around the lake on a Seadoo (thank you Jon and Denise Brown and Jodee and Eric DeWitt for the use of the Seadoos). We had fires and just watched the water together. The kids played in the sand and we pretended we were normal.

We are so appreciative of all the meals, gift cards, letters and prayers; so many of you have spent time and energy to help us. Those that take care of the laundry, the lawn, groceries; we could not do it without you. Everyone has been so kind to us. Thank you to Hospice of Holland for keeping Lindy comfortable during her final weeks.
Weve been crying a lot lately and sometimes the pain feels unbearable, but we are not without Hope. Our Hope is in Jesus Christ who will bring us all together again one day.
If you think cancer sucks, and want to join The Laps for Lindy Team (Susan G Komen Run/Walk on 9/22/2012), please click this link.
If you can’t make the walk/run, you can donate online in Lindy’s honor. Together, we can make sure no other families have to go through this.
Six Months
Since my last post I had another blood transfusion (last Friday) and thoracentesis (this past Monday).
I said to Dusty that ever since I went to the ER and spent a week in Spectrum a few months ago that things with my cancer have changed. For the worse. Yes the chemo is shrinking the spots we can see, but it’s clearly not helping with the fluid. The doctor who performed the procedure said I would probably have this every three to four weeks! Ouch! Having the fluid drained hurts.
Last Wednesday we met with Dr. VanderWoude. She thought it was going to be a routine visit until I dropped this question on her. “What’s my prognosis?” She sat down and explained to me and Dusty that I’m at the point where chemo, any chemo, is not going to give me more time. She said I can keep taking the chemo if it makes me feel like I’m “fighting”, but she said that if I choose to stop treatment it’s not giving up. I would be opting for a better quality of life. Chemo made me miserable. It was no way to live. Most of my time was spent sleeping or in bed. We left her office with a big decision to make. казино фурор
After an afternoon of ups and downs, prayers, thoughts, and questions, Dusty and I decided to stop the chemo. I’m done with the misery. Dr. VanderWoude estimates I have 6 months left (give or take).
We are now working with Hospice. I will meet my nurse tomorrow. Her name is Jane.
Please pray for our family as we work through this new phase of life and guide our children through it. Pray for the kids. Our family. Our parents. Our friends.
We’ve been blessed by so many. I will update my blog whenever anything exciting happens. I promise.
Thank you to everyone for bringing us meals, the gifts cards, and donations.
We will continue to have all communication go through Dani.
Please do not stop by unannounced. We just can’t deal with that right now.
Another One Wins the Race!
Our heartfelt sympathies go out to the Ellen VanOss family.
We had the privilege of meeting Ellen and Jack for dinner a while ago. Ellen and I had/have the same type of breast cancer. The beast known as Triple Negative. She was diagnosed seven months before me. She and Jack have two small kids. She won’t be forgotten.
In the words of Jack on 7/20/12:
A little before noon today Ellen crossed the finish line. She won the race and is in heaven right now receiving her prize. Well done good and faithful servant! She was a wonderful wife, mother, daughter, sister sister in-law and friend. She has taught us all so much about life, death and grace. She will be greatly missed.
I’ll post the arrangements when they are set. Thank you all for your prayers and encouragement.
My Thoracentesis last week went well. It wasn’t a fun procedure, but I’ve had worse. I would say having a halo screwed into my skull is worse than having a needle to numb and catheter put into my back for 15 minutes. They drained 900 ml from my right pleura. Afterwards felt a tad sore, but mostly better and able to breathe. Everyone at Spectrum was great.
I had my labs drawn this week and found out my white blood cell count is too low at 0.9. This means I should avoid large crowds, touching people, wash or sanitize my hands as much as possible and basically avoid contact with anything or anybody. Does anyone have a bubble I can live in until my count rises? My hemoglobin was at 9.4 or 9.6 (can’t remember). With my red and white cells working against me, I am VERY tired and could sleep all day. Yesterday I practically did. I have to pick and choose how I use my energy. I don’t like living this way.

Thank God for Dusty. He takes the kids to the pool nearly every night. If he needs to run an errand, they all go along with him. One night I was putting Max to bed and I said “You have a really great dad”. He said “Yeah he takes us places with him. I love him”. So sweet.
Next week is chemo. Please pray with me that my WBC and Hemoglobin are at a safe level so I can receive chemo. That my fluid does not accumulate. That my pain will lessen. For my family. For our support system – we would be lost without them.
Thank God for doctors, family, friends, insurance, jobs, and things that make you smile.
All in a week
My blood transfusion I had last Friday gave me a boost. I went from 7.6 to 9.0. Still low, but I’ll take it. The bottom of normal is 12. All in all, my energy has improved slightly. I thank God for that. The color in my face returned a bit. I don’t look as creepy as I used to.
Wednesday I had another round of chemo. It went fine.
Today I woke up looking like I was punched in the nose. No bruising, just a puffy nose bridge and eyes. I have no idea what that’s from, but I’m too tired to care.
Later today, Dusty and Brooklyn are taking me to Lemmen-Holton Cancer Pavilion to have a Thoracentesis. This is to drain the fluid from the space between my lungs and my chest wall. I’ve been told they do this “all the time” and “they’re really good at it”, but I’m still nervous. Any prayers you could provide today around 12 noon or 1 o’clock would be greatly appreciated. Please pray my lungs and/or no other major organs are accidentally punctured.
We thank everyone for their kindness. Whether it’s taking care of our kids, prayers, cards of encouragement, meals, gift cards, etc. It’s all so uplifting.
Thank you for walking through the desert with us. Cheering us on. Reminding us that you’re in our corner.
We are to pray in times of adversity, lest we become faithless and unbelieving.
We are to pray in times of prosperity, lest we become boastful and proud.
We are to pray in times of danger, lest we become fearful and doubting.
We are to pray in times of security, lest we become self-sufficient.
-From one of my daily devotion books Hope for Each Day by Billy Graham
ixna on the loodba ansfusiontra
After waiting three hours at the hospital for my blood transfusion yesterday I was sent home. Without a transfusion. I have antibodies in my blood. You may be asking “what” “why” “where did those come from” “never heard of it”.
After I gave birth to Max and Samantha I was anemic and had a blood transfusion. I remember towards the end of the second pint feeling “not right”. Me being me decided not to make a big deal of it and brush it off. Apparently that feeling of “not right” was my body having a reaction to the transfusion. I was building antibodies against the donor’s blood. OF COURSE I WAS! WHY WOULDN’T I BE!
Yesterday my nurse said I’m “special”. I’m going to take that as a positive and go with it. From here on out, whenever I need a transfusion I have to go in for labs, go home and wait for the hospital to call me.
Meanwhile, my special blood is driven to a place in Lansing where very smart people try to match it with a donors blood. I imagine once they think they have a match, my special blood and it’s new friend go through rigorous tests and exercises and questioning. If they are considered a true match, someone is called and they come with their Prius (again, just imaging) and drive my special blood in a cooler on an ice back to Zeeland where they give my special blood special treatment until my special self arrives for it.
When I get the phone call, I come and get the transfusion.
So today I go back to get my special transfusion. So tired.
so tired
I’m writing this on my kindle fire so once again bear with me. I’m going to have spelling and grammatical errors.Thank you for your prayers since my last post. We met with Dr. Schott at u of m on Tuesday. The Ct scan I had last week hasn’t been read by a radiologist yet. Dr. Schott could see that the chemo is working. The spots in my lungs are shrinking! Praise God for hearing prayers.Dr. Schott could also see that I have more fluid in my lungs compared to a few weeks ago. This explains my pain and breathing difficulties.My hemoglobin also dropped to 7.6. This brings me back to the spelling and grammatical errors. I’m sitting in the hospital waiting to get a blood transfusion.The next step will be to decide if we are going to tap my lung to drain the fluid. I’m so glad I have doctors I can trust with those decisions.I’m tired. Of everything. In every way. Sorry I have no light hearted humor today. I’m just too tired. So tired!



