Team Annhilate ALL: Support Matt Dubrey

Team Annhilate ALL: Support Matt Dubrey Welcome to Team Annihilate ALL (Acute Lymphoblastic Leukemia). This pg was created to support The DuBrey family as they battle this horrible disease.

You can get updates, leave Matt and Amy msgs, see & respond to needs in real time and be involved!

Just a bit over a year ago...I don't expect these pics to fully convey how much I love these people, but...they say a pi...
01/29/2025

Just a bit over a year ago...I don't expect these pics to fully convey how much I love these people, but...they say a picture is worth a thousand words. Well 4,000 ways to express how they are part of my family! I put a challenge down yesterday to see if we could band together and raise $8,400 more to cover some of the out of pocket medical costs. Again, BLOWN AWAY by what a difference can be made when people band together! Thank you! We are over an eigth of the way there in only 24 hours!! Thank youuuuu!

As I said in my last post approximately 1 second ago đŸ˜‰ I don't like the interface for sharing Matt's updates so I am cop...
01/28/2025

As I said in my last post approximately 1 second ago đŸ˜‰ I don't like the interface for sharing Matt's updates so I am copying the text here!
Here is the latest update:
Ok, if the impact of Acute Lymphoblastic Leukemia (ALL) wasn't already real...this is where it starts to sink in. Matt got home from the hospital yesterday, after his 6 day inpatient stay to begin this new phase of treatment. Nicknamed Blina, this medication is a powerhouse in the fight against a disease that wants to just keep comin. As I mentioned, Matt had to have a port surgically put in last Monday, and then he spent the week under close watch to make sure he didnt adversely react to the Blina. Thankfully he didnt, so they swapped out his bag and discharged him to go home. He will return 2xs a week to have bloodwork and change the Blina bag. Sounds easy. Until they receive the news that the Blina isn't covered under their prescription plan because of some loophole that the insurance company has because he gets the bags IN the hospital. Still, no big deal...until you hear the cost of each bag to them is $6,500 PER BAG! After they hit their max out of pocket expense which is $8400, then thank the Lord, the insurance will cover it 100%.
Now, as I have said MANY times by this point, all of your support in ALL OF THE WAYS has kept them going to this point! They are ASTONISHED by how much this Go Fund Me has ALREADY raised!! It has ALL been put to SUCH good use! However it has ALL been put to use, and unfortunately even if they were both able to bring in income, life in 2025 with 2 kids is expensive!
If you've already financially given all you can, please no stress! However, if you CAN give, every single dollar helps! Let's see if we can band together and get them that $8,400!! And please, no matter if you can donate currently, please continue with prayer and share! https://gofund.me/629a03c9

I hate the way Go Fund Me shares the updates. You don't see the update front and center, so it may appear that it's what...
01/28/2025

I hate the way Go Fund Me shares the updates. You don't see the update front and center, so it may appear that it's what you've already seen. So, I am going to share the content of the updates HERE in this post. Here's an update from last week: Matt's latest Bone Marrow Biopsy was MRD- which is what we were praying for! That, coupled with other data indicated he does not need a bone marrow transplant at this time.
The current course of treatment is a medication nicknamed Blina. It's job is to kill any cancer cells that come through as his body replenishes his bloid and bone marrow. It's administered through a port that was surgically placed on Monday. He began this treatment yesterday inpatient at Albany Med with a 24/7 drip. This protocol will be 7 days inpatient, then 3 weeks at home, going in weekly to change the bag, then 2 weeks off. That 6 weeks is 1 round. He will do 2 rounds before they check his bone marrow again. The results of that next biopsy will partially determine how many rounds he will undergo, I believe up to 6.
While the Blina is reported to be much gentler than chemo as far as side effects, there will still be limitations to Matt getting back to " life as usual". For a long time. As I have said before, Matt and Amy are completely blown away by the support, love, and prayers that have been extended to them! That support matters just as much now as this fight turns into more of a " grind" of endurance. As we have seen, donations add up! Prayer changes things! Reaching out brings comfort and smiles. So please, continue the prayer and share and give if you are able! https://gofund.me/629a03c9

First I want to apologize for falling behind on the updates. i went on a trip and picked up Pneumonia and that has had m...
11/24/2024

First I want to apologize for falling behind on the updates. i went on a trip and picked up Pneumonia and that has had me dragging! Instead of writing 1 massive update, I am going to write a few that you can check out at your leisure. Update #1. Matt came home earlier than expected as I mentioned in the previous update. He had a bit of time to settle in to a new norm as far as low energy and what life will look like for the next little while, with him unable to work and not feeling at all like his old self. Then the family faced additional unexpected tragedy when his Mom, Patty, suddenly passed away on November 10. I don't have the right words to explain how that kind of loss hits so very hard, when you are already battling on every level. Please extend prayers and thoughts of comfort to the whole family.
Matt had his bone marrow biopsy this past Wednesday (11/20) and is waiting for the results which should be in sometime this week. Yesterday he was readmitted to begin the "Consolidation" Phase. Consolidation, or intensification, treatment for acute lymphoblastic leukemia (ALL) is given to prevent leukemia cells from coming back. Consolidation treatment usually lasts a few months. Chemotherapy is the primary consolidation treatment for ALL. The chemotherapy is quite intense because the drugs are usually given in higher doses. Since Matt has the Philadelphia variant/chromosome he will also receive targeted therapy, I believe in the form of a pill. He will have a # of these cycles of inpatient treatment lasting 4-7 days each time depending on how his body responds, then home 10 days to 2 weeks for recovery before going back in for another cycle. 4-6 of these cycles are expected. If you are exhausted just reading this, you are beginning to get the picture of what he is currently and in the short term, facing.
The first week of December he will have his appointments in Boston at Dana Farber to discuss his bone marrow transplant. The estimated time for transplant is early February but will be dependent on responsiveness to treatment and other things. THe transplant will have him out here in Boston for about a month as he acquires his new immune system. These are just the facts. If you sit with these facts for a few minutes and think about what this will all mean in their day to day lives, you can quickly see why they need support! As mentioned previously, Matt is out of work for the foreseeable future. That doesn't mean a few weeks or months, it means he likely will not be able to return to any sort of normal work before this summer. During the time that he is here in Boston Amy is going to need to decide between keeping things as normal as possible for the kids and spending time supporting her husband, no easy task when there's a 3.5 hour drive in between the 2. Not to mention her work. She will need as much help as she can get with all of the things from rides for the kids, to groceries, to babysitting, to tasks Matt normally takes care of. It sounds incredibly daunting because IT IS!
However it is also not impossible. I have been absolutely blown away by the support shown to my family, and I know they have too! I have said it before and I won't stop saying it any time soon. EVERYTHING helps. Not just monetary donations. Sharing this post, sending prayers and thoughts, checking in with them, offering to make a meal, or do a chore. EVERYTHING weaves together into a beautiful blanket of support. They will feel your encouragement, and they need it, so very much!
Love Monique

Hi there, my name is Monique Reese and today I want to share a story about… Monique Reese needs your support for Rally for Matt DuBrey: Beat Leukemia Together

He got to go home early!! Woot!! Matt will still have his bone marrow biopsy done on Monday but he is home!! Phase 2 bri...
11/03/2024

He got to go home early!! Woot!! Matt will still have his bone marrow biopsy done on Monday but he is home!! Phase 2 bring it on!!

Matt Treatment Update 11/1/24 - 11/4/24. (Coming Home from hosp, phase 1 over!)Hey all! Hope everyone had a great Hallow...
11/01/2024

Matt Treatment Update 11/1/24 - 11/4/24. (Coming Home from hosp, phase 1 over!)

Hey all! Hope everyone had a great Halloween, here's a short and sweet update - as I won't rehash the long term process like I did last time.

The GOOD NEWS is I am having my bone marrow biopsy MONDAY (The earliest day I could have had it) and will be sent home Monday or Tuesday to enter phase two of my treatment. The Doctors in charge of my case are very pleased with the blood cell numbers and are confident I am ready for the next steps of treatment. What could have been 4-6 weeks in the hosp is about 3.5 instead, so good news there.

I should be home 2 weeks and back in the hosp for a week, repeating a few times.

I can receive visitors at home and all that, so if anyone wants to say hi (or at the hosp this weekend) I have very little going on, so feel free to drop down. Attached are a couple pictures: As expected the hair started to fall out, so we got on top of it. Ella thinks it looks weird, Mason and Amy are rolling with it. ;)

I really shouldn't need to provide another major update going forward until I hit full remission (Unless I need bone marrow transplant) So I'll plan to keep everyone updated as my situation evolves. Thank you again for all the love and positive feelings, it makes a difference in my treatment and recovery. focus. Just know I am thinking of you all as well.

Love you all, -Matt.

Amy helped Matt with his new do! Unfortunately his hair was falling out in clumps. We think he is rockin this new look! ...
10/31/2024

Amy helped Matt with his new do! Unfortunately his hair was falling out in clumps. We think he is rockin this new look! The latest update is Monday will be a big day! Another bone marrow biopsy will be done and the results of that combined with other blood cell numbers will determine when he will go home and mark the start of stage 2. It is looking like he will be home Monday or Tues if all goes well. Praise God for getting this far in relatively good shape! We've come a long way and we've got a long way to go! Please share https://gofund.me/11cb261c

Address

Schenectady, NY

Alerts

Be the first to know and let us send you an email when Team Annhilate ALL: Support Matt Dubrey posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Shortcuts

Share