Skip to main content

.hats, hats, hats.

“Bless the Lord, and forget not all his benefits.” Psalm 103



(the hats Jack has been given so far)


There are certain ages that are optimal if someone is going to get cancer and undergo chemo, and Jack’s age is one of those. We are very grateful for this, and thank God that if he was to get cancer during his life that he got cancer when he did.


Since he is so young, he also has the added benefit of most likely not remembering the early and most intense phases of his treatment, and will hopefully be able to look back on his childhood without having needle pokes, chemotherapy rounds and no hair in the forefront of his mind! We are so grateful for this. I am consistently amazed at all he endures with little to no complaint.


However, we do want him to remember some things about this trial we are walking through. One of the things we do want him to remember though is the faithfulness of God to him through this time. I wouldn’t want him to be unaware of how people prayed for him, supported him, and how God sustained him throughout. It has truly been amazing and humbling to be carried by so many. We want him to see this multitude as an extension of the love of God for him and God's church in action. One of our friends suggested an idea to achieve this that Tali and I loved and wanted to do.


So here it is: we want people to send Jack hats. That’s right, hats.


This idea has a threefold purpose. One, is so that Jack can have a collection of hats to choose from once he loses his hair (which will probably happen in the next few months). Two, and most importantly, we want to have a physical reminder of God’s love for him, specifically through people that have prayed for him. We figured a tangible thing like a hat would be a great way for him to see the love of God in a very real way. Finally, we figured down the road we could donate these hats to leukemic societies for other little boys with cancer so they can benefit to (we will probably keep the teams we actually like though!).


You must know that there is absolutely not pressure to do this; we are overwhelmed simply to have people praying for us at all! We could not ask for a better gift from anyone than this. Your love and prayers for us will not be lessened in value in any way if you do not send a hat. We hope you hear that and know we are grateful beyond words for the lavish outpouring already demonstrated on our little family.


If you would like to participate, here are a couple ideas we had:


- The hats could be from whatever sport team you want (college teams would be ideal because they’re generally state schools and easily represent a location, but seriously, we’re not picky!), and we were thinking it would be great to be a team in your area so that Jack can see people are praying for him all over country.


- Feel free to send one on behalf of multiple families or people, this would also help in not getting 10 hats from the same team, and save money!


- You could write on the underside of the bill who it’s from, but it would probably good to not make this too obvious (ie. small letters in a corner), because we’ll eventually give them to other kids.


If this is something you’d like to do, email Tali (tkauflin@gmail.com) or me (jkauflin@gmail.com) and we’ll send you our address.


Thank you to everyone who is praying for our little boy, God is definitely hearing and blessing our prayers in so many ways!


Gratefully,

Jordan

Comments

Hilary said…
GREAT idea! We will for sure be adding to Jacker's hat collection soon :).
Jordan Family said…
Go Longhorns!!! Whoohoo! ;)
Anonymous said…
I just sent this to a few contacts in sports & entertainment. Bless you and Jack through this ordeal. My nephew is 6 and I don't know how I would feel if it were him, but I would want the love and support of everyone we knew, and didn't know.

P.S. Jeremiah 29: 11-13 may help you like it does me.

Popular posts from this blog

Diagnosis and Grace

Friends- "God is our refuge and strength, a very present help in trouble" Psalm46:1 Much has happened since I last wrote only 2 short days ago. We found out much later that night a new diagnosis, that our sweet boy has leukemia . We were not completely shocked but we were certainly shaken. After I posted about what was going on at Shady Grove, and we waited a bit more for some results, and we were informed that we needed to take Jack to Children's Hospital in DC for further testing with specialists. This raised our concern level quite high as you can imagine, that even with a snow storm coming, we were needing to make this trip. I began to google the combination of things they had found in the tests done on our little boy (swollen spleen, low platelet count , swollen lymph nodes) and came up options that were NOT Lyme disease, although a few of these symptoms did also look like Lyme. As a result of the google quest, I came across some concerning outcomes, one of the most...

.coming home.

Well, the past 24 hours have changed things again for us! The biggest update, is that we are being discharged tomorrow afternoon some time! The reason this is so crazy is that the Dr. who was on the floor yesterday, was telling us she wanted to keep us here for the entire first month of Jack's treatment. We had begun to think through how we could do this as a family and all the changes that would entail.... and then our nurse came in this morning and told us she was pretty certain we were going home, as early as today if we wanted!! Let me tell you about the past three days that lead up to this decision of our doctor. Firstly, you should know that when Jack was diagnosed with Leukemia, he had a blast count in his blood of 37. That count is now at ZERO!!!! After the central line was put in on Thursday, they began his chemo treatments Friday. He had been having a fever up until that time. He has responded so well to the chemo, and other medications, that he has been fever free since...

.Day by Day.

"The steadfast love of the Lord never ceases; His mercies never come to an end; they are new every morning; great is your faithfulness. The Lord is my portion says my soul. Therefore I will hope in Him." Lamentations 3:22-24 This has been the cry of my heart these past few days. When thoughts of the future loom ahead and what this is going to look like in a week, month, year are ever present, we are seeking to take things one day at a time. And even as we take it one day at a time, each morning, we are faced with more of the unknown- what the day will bring, how Jack will be feeling, how he will respond to his meds, how he will respond to the staff here, when the nasty side-effects of chemo will begin... the list of unknowns are seemingly endless. Not only is the thought of what the day will bring full of unknowns, but we are also very tired, as we are not sleeping much at night and so we are tempted to view the day through the filter of weariness. So yes, it is a fight each...