Cashy I miss you so much that times like these…Read more »
Well it’s almost been three weeks since you’ve been gone Cashy. We all miss you so much, the pain is indescribable. I catch myself expecting to hear you yell for me down the hall or I double take looking at your spot on the couch where you should be. I miss your sweet voice, your soft touch, your sassy attitude and most of all I miss holding you in my arms at night. Our bed is so lonely at night without you, you’ve slept with us your whole life. Now it’s just a big empty king size bed.
The other night we had both Colten and the baby sleep with us. It made it feel a little better and less spacious. Colty needed it. He misses his brother. He has woke up the last two nights and told me he’s been dreaming of you. He said that in his dream you were here in the house but I couldn’t see you only Colty could see you, he said you ran down the hall and came up to me and gave me a huge kiss and disappeared, but I couldn’t see or feel you only he could. In His dream last night he said you were here on your spot on the couch and yet again only he could see you. He said you were able to talk so clearly and well. This makes me happy that your coming to your brother in his dreams. He needs that, he’s so sad and it breaks my heart even more. (Which is almost impossible because its already broken into pieces).
We made it home from SLC on Tuesday night around 11. It sure was another long week without you. I swear if I watch that slide show of your sweet face one more time you might have to commit me to a looney bin. I do ok most the time but the second I see pictures of you and videos I’m a complete wreck.
Your funeral in SLC was nice. Lots of your family and friends attended. Even our neighbors Nathaniel’s and Liems parents came to it as they were in SLC for the holiday. John and Corinne flew in from Cali and CJ flew in from Texas.
The minute I walked up to your grave site for your burial I got an uneasy feeling and seeing how deep the grave was (it was nearly 12 feet or more deep) gave me chills and a vomit feeling came over my stomach and I felt dizzy. I held it together though. Thinking of you being down there in that cold dark grave forever really made things real. That you’re gone and I can no longer see your delicate face or hold your sweet hand anymore. There is room in your grave for two more coffins and 5 cremations. Ugh, the thought of more people dying and being put down there with you is unsettling. The ceremony at the grave site was beautiful though, which I’m sure you know because I know you were there holding our hands. We released a bunch of yellow, green and red balloons and as they took off in the sky a beautiful hawk soared near. We knew it was you with us that very moment, flying free. Like a free bird. Mike played that song as we sat on the couch the other night and I just broke down into tears. It’s like I literally can’t breath sometimes. God I miss you so much. The reception afterwards was lovely and grandma and everyone made some delicious food!
Sunday night we went up to primary children’s hospital where you lived for over 10 months of your life while we battled what ultimately took your life. We donated 6 reggae and rockin’ runners in your name buddy. It really hit home when we were up on the 4th floor and you weren’t with us. I started crying on our way out thinking, crap I’d give anything to have you up there fighting cancer, even if it was you getting chemo again. I’d live up there again forever if I could have you back. Even though I know it’s not what you wanted, and what kind of life would that be? I know you’re better off where you are, but that selfish part of me wants you here still fighting the fight. I left the oncology floor in tears and my heart in a million pieces. It felt good to leave a part of you up there again. I know you had a giant smile on your face and that you were so happy that your sissy tested and approved each of the runners. It’s her new job now!
Now we’re home, trying to get back in a normal routine. But what is normal without you here?? Nothing, I literally feel like I’m stuck in a torture chamber, looking at all your pictures, your toys, your dresser full of clothes. I folded the last of your dirty clothes that were laundered, no more washing your Jammie’s on quick wash. Now we just have 4 piles of clothes when I do laundry instead of 5. It’s just pure agony. I want so badly for you to be here with us forever.
I put your medicine box on top of the fridge. I can’t bare to throw it out yet and neither can daddy. I even yelled at it the other day. The oil and everything was supposed to make you better, make you well. We thought we were beating this, you seemed to be doing so well compared to how you were in July and August. Maybe we were just in denial. But I truly never felt like I would lose you. I always had that positive attitude and perseverance to keep going and I definitely thought you’d be here for Christmas this year. Our first Christmas home since you were 1 year old. I wanted you to be here and experience it.
I remember last Christmas while in California we took you to see Santa at the Bass Pro shop, we waited in line and you were so patient and also not feeling well as you had received radiation earlier that day. When we got up to take our turn you got up out of the stroller and ran up to Santa and hugged him. It was so cute. Now this year our Santa picture will be missing your beautiful smile and your little sissy will be there. Maybe we will skip the whole Santa thing this year, makes me nauseated to even think about it without you. I love you buddy. I hope your safe.
We were brought the most perfect Christmas tree on Saturday morning by a friend from work, (thanks Jen!) it was so sweet of her and her daughter to do, as picking one out myself would of been a waterfall of tears. So we set the tree up that night with Colty’s buddy Owen who came for a sleep over. (Colty needed that, he misses his buddy Owen). I tried to hide my tears as we put up the ornaments. I found the most perfect ornament for him , it’s a sock monkey with angel wings, seemed so fitting.
Everything just reminds me of Cashy. Everything I see or do. I think of him every second of the day. I seem to be able to hold it together when I’m around people and even when we talk about Cashy I’m always able to keep it cool. But when I’m alone, especially at home or in the car, I cry and I’m constantly telling you that I love you, that I miss you so much, and that I’m sorry that you suffered so much.” I pretty much repeat that over and over. I hope he hears me but I hope he isn’t sad that we are all so sad.
I get tears when I see things that he loved so much. Playdough and cars at Target (I couldn’t even go down the Matchbox cars isle) bug juice at the gas station. I even went as far as I bought him a bug juice on our trip to SLC. Weird and silly I know, but it would of been more painful if I ignored it and didn’t buy it and validated that he’s gone. Ugh. It’s all so new and raw and nothing seems right without him.
We even got rid of the minivan, Mike felt it was just way too hard to be in it. We let Mike’s cousin Jesse take it to help him get on his feet, he’s got a baby boy and he needs to be able to see him as much as he can. I know that’s what Cashy would have wanted, us to keep helping others even though we’ve lost everything.
So I’m really excited and grateful Mike has worked so hard on building Cashy’s Foundation. He’s done a great job. This way everything Cashy went through will not be in vain and we can keep spreading pediatric cancer awareness as well as spreading our knowledge on cannabis as a valid form of treatment. Even though it didn’t work for Cashy doesn’t mean it doesn’t work, we just need valid testing and research done so they can know exactly how much of a dose is needed and how often and ultimately different routes of delivery such as IV.
The time will come and I truly believe because of Cashy it will come sooner than later!
To learn more about or to help out the Cash Hyde Foundation, please visit www.CashHydeFoundation.com or to follow Cashy’s Battle Blog.
UnitedPatientsGroup.com and The Cash Hyde Foundation team up to fight pediatric cancer! Thank you for your support!
UnitedPatientsGroup and The Cash Hyde Foundation:
Our Journey has brought us some amazing stories…
Doobons.com and The Cash Hyde Foundation team up to fight Pediatric Cancer
- United Patients Group Spearheads Cash Hyde Foundation Medical Marijuana Reform Movement