Updates & Prayers for Kenzi

 We have officially been home in Vernon for two weeks now and it feels amazing! We were originally going to stay in the Fraser Valley until we knew whether or not Kenzi needed radiation, but our nurse told us that even if she did, it wouldn't start right away, so she recommended we go home. We are so thankful we did, because it has lifted everyone's spirits so much. There really is no place like home. God gave us a beautiful, sunny day to travel and we waved to our friends, who we swapped houses with, as we passed them on the highway.  After being home for a week, we got the phone call we were anxiously waiting for; Kenzi does not need radiation!!! I was picking the kids up from school when the doctor called and the tears were flowing as I stood in the parking lot. I went home and told Wes, Kenzi and his parents, who were at our house and we all celebrated together. Kenzi is now done her treatment and we could not be more thankful! We all feel like a huge weight has been lifted

Kenzi is officially done all her chemo! It was the perfect way to end the year, but to be honest it felt like a premature celebration. While she is done chemo, we are waiting to see if she needs radiation and the chemo is still wearing her down. Once we leave the hospital with her central line gone, then we will have a big party. We had a fairly quiet Christmas. It was nice to do gifts with our little family, but it felt pretty lonely having Christmas dinner by ourselves. Arnie and Cathy (Wes's brother and sister in law) came for 2 nights before Christmas with their girls and it was wonderful to visit with people again. We have kept to ourselves so much this year, just trying to keep everyone healthy and we are really missing in person visits. It seems that any time we plan to see people, someone has a cough or sniffle and we decide it's best to not risk it. My parents also came down after Christmas to celebrate Kenzi's last chemo with us, which was wonderful.  We are still

 Kenzi has finished 13 rounds of chemo and only has 1 left! I can't believe we have made it this far. Our lives have been put on hold and focused solely on cancer treatment for the last 8 months and it feels like it will go on this way forever. To be honest, we don't really know what normal life looks like anymore.  Since the last time I posted, we spent a few days at Ronald McDonald House. Wes and the other kids were thankfully able to drive down to Vancouver and meet us there. We were even able to go to a Canucks game with the whole family, thanks to some generous donors. As wonderful as RMH is, we had the chance to swap houses with our friends, Roger and Cheryl, so we moved into their house in Pitt Meadows and they are staying in our house in Vernon, spending time with family and enjoying the snow. We are so grateful for their generosity. Last Monday, Kenzi was admitted for another 5 days of chemo and the kids were actually able to visit and see what goes on in the hospital.

~ Making Gingerbread Houses ~  After 50 days in Toronto, 46 of those in the hospital, 8 trips to the OR, countless hours in the waiting room, over 100 stitches, 1 giant tumour removed and only 3 short days at home, Kenzi and I (Monica) are back in Vancouver. There is no rest for cancer treatment and it's exhausting. After all the delays with surgery, there are only 3 rounds of chemotherapy left. This will take about 6 weeks and then Kenzi will possibly need radiation which could be another 4-6 weeks. We know there is a light at the end of this dark tunnel, but instead of relief, we just feel weary. The trip to Toronto and all the complications with Kenzi's arm, have broken her spirit. We still see glimpses of her usual self, but they are far fewer than they used to be. We hope and pray that she will adjust to being back in Vancouver soon, since it's familiar, but going home makes leaving so much harder.  We are so grateful to my parents, who put everything on hold and moved

 So haven't posted in awhile been a bit of a chaotic emotional few weeks. I(wes) am writing this blog so it wont be as smooth and grammatically correct as your used to hahahah (sry monica) So as many of you already know kenzi had her surgery. The surgery was very long 17hrs start to finish but it was a success and they were able to remove the tumour which we are thankful for(we will not know for certain if it was a clean remove for a month or so until the pathologist are done inspecting all the edges.)  This is what we have been praying for and waiting for since we started on this crazy stupid road. The surgery ended up being very invasive to say the least which we were hoping it would not be and was kind of a punch to the gut after hearing the tumour was out.  Took a few days to process and wrap our heads around this but we kept coming back to the fact the tumour is gone and this always made us happy. There was a complication with kenzi's arm after the surgery and she had to g

We've been in Toronto for 12 days now and we are slowly making progress. While the first week was chaotic and emotional, we are thankful that Kenzi is feeling well and her care is going smoothly.  We arrived last Monday and were given a gift of goodies and a beautiful card from our flight crew at Air Canada. It went downhill after that. Nothing seemed to go smoothly. From frustrating COVID restrictions, to sketchy hotels (which we immediately left), to lost rental car keys. We were all at our breaking point in an already emotional situation. It felt a lot like the first week of Kenzi's diagnosis and there were plenty of tears to go with it. Through the chaos though, we were able to sneak away to Niagara Falls for a night and Wes and I celebrated our 15th wedding anniversary there. It was our only day "off" since we've arrived and we are very thankful for that.  We had to be back at the hospital last Thursday for Kenzi's first surgery. She was feeling anxious a