Merry Christmas and Happy New Year (in advance)!
I’m happy to tell you guys that I’ll be able to go spend a day at home with Kat and my family for Christmas! I’m escaping Alcatraz again (my favorite joke ).
Boy have I come a long way since my ICU days and re-learning how to walk about 4 weeks ago! You guys would be proud of me! My body is definitely recuperating, but unfortunately there’s still a lot of cancer present ☹ . I’m almost off oxygen, walking really good (although I’m constricted to 100 square feet) and now able to get up from the toilet bowl … yup lol! My kidneys are getting better and my moral is still as good and positive as always! I’m so ready for this and can’t wait to get to this new step… but one day at a time and one dollar at a time!
FINALLY on our way home (by home, I mean our home hospital… 😑 ) after four long months of being away!
We’re really excited to come home for the holidays, even with the crazy snow today! I’ll continue to recover at the hospital and maybe do a bridge treatment to keep my cancer under control until I’m stable and we raise enough money to get to Seattle! Hopefully I’ll be able to get a pass to be home for Christmas!
Make sure to enjoy every second with your family and friends. Hold them a little tighter, because you are lucky enough to all be together! ❤️️
We really need a BIG $ BOOST to Help Save my Life!
Do you think we could get over 10,000 Likes & Shares for this post?! Let’s try to make it happen and reach as many people as possible, all around the world, because the whole world has so much LOVE to give!
Remember, this treatment which is not available in Canada has an 85-95% remission success rate in Acute Lymphoblastic Leukemia and is my ONLY chance at surviving this horrendous cancer! But I need the funds and your support to receive the treatment in Seattle!!!
Hello bighearted angels around the world!
I feel like I’ve been asleep for the past days, weeks, but am now awakening to an outpouring of love I need to respond to ASAP! The ICU has been difficult, but I feel like right from left, up from down, everything is re-distinguishing itself and now I can properly give true thanks to the events that have been occurring during my “mental absence”.
The shares, the likes, the comments, the humanity. I’ve been so grateful, with tears of joy washing down my cheeks every day, reading as many comments as I can, responding to as many as I can, feeling supported and loved by so many: family, friends and complete strangers (who I feel like I know personally too by the way!).
I just wanted to give you all a quick update on Matt.
He is currently in the ICU, as a preventative measure, because they started stronger chemotherapy today Continue reading
Dearest family, friends, and loving strangers,
We have lots of news and I’m not exactly sure how to go about this update, so when in doubt, just dive right in I guess…
**Update since I wrote this last night: Matt started a raging continuous fever! Go T-cells go!
Here’s a long awaited update! I’ve been wanting to update everyone for so long but I just didn’t have any clear answers on what was going on! As we know, Matt is quite unique…
It’s happening right now! The CAR-T22 cells are going in! Let’s do this! 💪🏼
As always, the roller coaster continues. Soon, we’ll hopefully be off of this ride and never get back on it again! Lol
On Wednesday morning, the fever reappeared, after only a mere 24 hours of stopping the steroids. Matt was admitted into the hospital once again. The plan was to admit him next Tuesday, which is when the treatment was set to begin. Good news, Bad news. Unfortunately, or as Matt would say, fortunately, there was a change of plans!!