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Friday, May 11, 2012

Treatment for May.......


Found a new Friend on our way to R.T.U. his name is Reggie.


Oliver is still our favorite !!!

Just a little wet.
Making wishes and hoping they will come true.
It has been a long time sense I have been blogging. I need to keep up with this but our life is so busy. Looking at other blogs help me to understand what Hunter really go's through. This helps me be his voice to make things better for him. This trip was R.T.U. now Hunter is growing up and he knows what happens to him and he doesn't want any part of it. Before R.T.U. at the clinic we discovered that Hunter had a blood clot in the casing of his port. Normal would be to panic ( I was scared to death !!!) So down we went to R.T.U. I told them that he had a blood clot in his port so they would not be able to draw back on his port. After R.T.U. they started Hunter on tissue-type piasminogen activator ( T.P.A.) Every fifteen minutes they would come in and try to draw back for blood. An hour has passed now still no blood on the draw back our nurse has to go and talk to Dr. Lemons. Dr. Lemons wants to do a boluses This is one or two doses of T.P.A.in a 10,000 unit of urokinase for two hours. Now if this doesn't work then Hunter would be put under to see exactly where his blood clot is.Finally it all worked out their were able to draw back and get blood (Whoot Whoot).This trip I think I aged about ten years with the scare of a life time. We promised Hunter he would be able to go see the Stingrays at the living aquarium and it was well deserved he was a trooper with everything that happened to him.We would like to thank Cheri and Oliver for coming to see us. Oliver is Hunters favorite.... The fountain was finally running and we went to make wishes. Thank you so much for all of your thoughts and prayers. Love the Laub's

Monday, February 20, 2012

Happy Valentines Day......







We drove up Monday 13Th, that night to Salt Lake on our way up we get a call from Uncle Kevin he told us that on the news they were taking about a shortage of chemo and was wondering if this would effect Hunter? I had not heard about this shortage so I was not sure. Hunter was to have two doses of chemo this trip. I didn't think they would have to put him under for R.T.U. because Hunter got the croup Tuesday a week before. So we had him still fast to see what the Doctor had to say. We are at clinic and I had brought some Valentines for the other kids from Hunter (who doesn't like fun dip,right) While Hunter was making a Valentine we got called back fast, clinic was slow that day. Dr.Lemons came in the room and the first thing he talked about was the shortage. I know I was looking at him like a deer caught in the head lights. It's a feeling that hits you straight in your heart and your heart just sinks. I am overwhelm with fear and very scared. It's true and this is going to effect him how? We will not know how this will effect him until it happens. We have been told that if Hunter just stops his treatments today he would be fine for a while but he would relapse and not be so lucky as to have ALL leukemia. It would could back very aggressive into an other leukemia. He would have to have a bone marrow transplant too. I remember the first time we had went up to Primaries Children's and the nurse we had told us when we found out Hunter had ALL Leukemia he said,"this is the one you would hope for." A flood of memories just came rushing over me. Memories that have forever been burned into my sole. Just the right key of words can open my wall that I have built so strong and tall. Now we are back to picking up the pieces and hoping and praying that none of these kids have to go with out this poison that is keeping them all alive and here with us. Hunter did have chemo in his spine this trip but in three months when he is due for it again they are not for sure if it will be available. So a not so Happy Valentines Day but a unforgetable. But you all can help in our fight by send this letter and make those phone call's. Help all of us in our fights.Thank you all for keeping us in your thoughts and prayers.  Love The Laubs                                                                                                                                   CureSearch for Children's Cancer
YOU CAN HELP IN TWO WAYS
Contact the following pharmaceutical companies who produce methotrexate and ask them to:
  1. Prioritize the production of the preservative-free form of methotrexate.
  2. Consider working with the FDA to import preservative-free methotrexate if sources are available.
APP Customer Service1-888-386-1300
Hospira, Inc. Customer Service1-877-946-7747
Mylan Institutional1-888-258-4199
Sandoz Customer Service1-609-627-8500

Second, contact your Representatives and Senators on Capitol Hill and ask them to immediately send a letter to these same pharmaceutical companies requesting that they:
  1. Prioritize the production of the preservative-free form of methotrexate.
  2. Consider working with the FDA to import preservative-free methotrexate if sources are available.
To send a letter to your representative, click here.
Thank you for your support of this important issue!

Thursday, February 16, 2012

Happy Birthday Triston !!!



CAKE  FIGHT!!!!

Thank you for sharing your day with Hunter.

What was left !!!
Happy Birthday Triston !!! Who would have ever thought we would have two BEAUTIFUL boys in our life's today.(So blessed we are) Mom and Dad want you to know how much we love you. With all of our hearts and then some !!!! How proud we are of you !!! You are the very best big brother ever. Hunter thinks the world of you and I know you might not know what is really going on with your brother right now but when you are older you will read this blog you will remember some things that went on this part of your life. Remember that Hunter admires you and wants to be just like you. You help Hunter keep fighting strong everyday Thank you so much for that. You both are not just brothers but best of friends for life. Happy Birthday Triston !!!! We love you with all of our hearts, Dad, Mom and Hunter

Friday, January 27, 2012

Treatment for December and January.........



Hunter LOVES visit from Oliver !!!



Hunter making snow angles.

Our little polar bears.
Hunter was sick for November treatment he was to get two doses. So December 20Th Hunter got his back poke and his Vincristine. We had a visitor on our way out we got to see Oliver !! We gave him a quick squeeze and took some pictures before we left now off to find Daddy and Triston. This December did not bring hardly any snow our boys look forward to the snow when we get to Salt lake. It was snowing while we were walking out from Primaries Children's the boys were so EXCITED !!! We were the only ones playing in it at the Hospital. The next day on our way for home where we stay on the roof still had some snow for the boys to play in. Hunter just about did the camera in this trip.(the proof is in the photo) Now for January treatment.......... this was a long day we drove up and back that same day. It had snowed the day before so the boys could not wait to play in it. After leaving Primaries we headed over to see Uncle Kevin and Aunt Jen and they had a lot of SNOW in their parking lot. The boys had a ball they were rolling around in it because they wanted to look like polar bears. Sorry for not posting sooner our life gets to crazy some times. Happy New Year to all of you and thank you for keeping us in your thoughts and prayers. Love the Laub's

Friday, December 2, 2011

Happy Birthday Hunter !!!



Hunter won the Birthday cake from KONY !!!!

Birthday cards from the Schmitt family,Thank you !!!

What was left.
Hunter turns 4 (HAPPY BIRTHDAY, BIRTHDAY BOY !!!) and winter is finally here because both of our boy's have the crop. We didn't have much of a party for Hunter because he was sick and TWO boy's on STERIODS just was not happy birthday party but..... unforgettable! But as tradition will show you all he enjoyed his birthday. We had a R.T.U. appointment this treatment and it was canceled because of him having the crop. It worries me so because this chemo is measured by age and now it will go up. So are next trip will be right before Christmas. Everything Hunter has to go through and still he has a smile on his adorable little face. We love you Hunter !!! Our life is a lot CRAZY right now. My blogs are not up to date like they should be,"I do have to apologize to you all."  November was a challenge my mother in law who has alzheimer's had a small stroke, Hunter birthday and at the same time both of our boy's having the crop, and our 17Th Anniversary. HAPPY ANNIVERSARY HONEY !!!! I DO LOVE YOU !!! But things could be worse "a lot worse! " So Happy Belated Thanksgiving we hope that Lot's of memories were made. Thank you for keeping us in your thoughts and prays. Love the Laub's

Friday, October 7, 2011

Loosing grandpa Harvey and a treatment for August.......








Loosing grandpa Harvey is a great loss in our family. Our boys still talk about him today and I hope they never forget him. This was a loss that didn't have to happen. He will truly be missed. We were very blessed to have spent his last days with him. It was an honer to be with him. As young as our boys are I hope these memories stay with them for the rest of their lives. Triston and Hunter both have grandpa's crooked little smile and Triston has his hands. Little reminders that will help us to never forget him so very grateful for reminders. I told the boys in there questions about grandpa, why and what was happening to him that grandpa was going to help be their guarding angle. To watch over them both and to keep them safe and we will see him again some day.


I told them that the brightest star in the sky they will see at night will be grandpa watching over them. When we least expect it and running out the door at night or when we are coming home in the evening and the stars are shining so very bright the boys will shout out,"we miss you grandpa Harvey !!!" Rick and I both look at each other and just smile. If we have learned anything in our journey with fighting cancer is life is to short and your life is what you make of it. We will never know how long we all have but I hope that when that time comes, I can be remembered with a smile on my family's face. Harvey was a tell you like it is kind of a man. You might not have like the answer he gave you but it was the truth straight from his mouth. He treated me just like is own. I am very grateful for that. He will be missed but never forgotten. We buried grandpa and a week later we left to go for Hunter's treatment.




So we went to have Hunter accessed here in town and I saw that it wasn't the right bandage for him. I asked the nurse and she said,"I looked in his charted and this is the one." I asked again and told her that it is brown. And Child life was in there and she agreed with me. She said,"she is right it is brown." This nurse insisted that it was the right band aid and I believed her. I should have listen to my gut. "I know better then this." So we leave for Primaries and this time it is RTU. We go up stairs to do more blood work and as they put in the saline and Hunter started to cry and grabbed his chest. My heart just sank, I was sick, Hunter de-accessed him self. This means that Hunter can not be numbed again because the spray burns him worse then the band aids. So now that he is re accesses we are heading down stairs to RTU. We had to wait for an hour and a half. Mom is still kicking my self for this. Now it is our turn and we get into RTU and the anesthesiology just pushes in the meds into his port. He always grabs me so tightly before he falls asleep but not this time Hunter stared to cry, yes Hunter has de-accessed him self again. Now Hunter is very swollen and they have to re access him and it is not working so they have to pick the needle up and down at least five or six times to try to get it in. They can not get Hunter accessed. By this time Hunter is hysterical. The anesthesiology had to order him some liquid Versed to clam him down. They had to shoot this up in his nose with a nurse on each side of him. It took six adults to hold him down through all of this. Now they had to call a nurse from up stairs to RTU to access Hunter. This worked (yeah) now they can give him his chemo. As I walked outside to wait for Hunter I lost it. I felt so guilty I should have listen to my gut. I think the hardest part is knowing what all Hunter has to go through and I could have prevented this. Waiting for Hunter The Doctor came out to tell me that she had missed in his spine so he will have two pokes in his back. They think he will be a little while waking up from all the meds and how sorry she was (which made me cry more) so they will see me up stair when he wakes up. Two minutes later Hunter woke up screaming to get away from him. So I went back he wanted out of there,he wanted his dad and he wanted to go home. I told him we had to go up stairs he stared to cry this broke my heart even more. We get up stairs and we run into Sherry and Oliver this always makes Hunter's day (not today!) had to apologize to her for Hunter. Hunter is so done this trip,he has had enough this time. He didn't even want to make his wish outside this time. The next day I had to call Primaries because Hunter was not eating anything and he is on a high dose of dexamethasone, six tablets twice a day and I had to ask them about a rash he was starting to get on his face. I was told that if it get worse then bring him in. We got ready to head home arrived just in St.George just before 9:30pm to go to Red Rock pediatrics to have Hunter checked out because now his rash is all over his face and he is itchy. Hunter had an allergic reaction to the versed they shot up his noise. We never got home until after 11:00pm. We unpacked and went to bed. I got up early to get things done before I had to be to work and Hunter started throwing up every where. Hunter was screaming and saying," my head is hurting!" I thought he was having an aneurysm but come to find out when they missed on his spinal it caused him to leak spinal fluid so Hunter was having migraine head aches. Hunter had to be put back on Oxycontin and Zofran to help with his head ache and to stop him from throwing up. This lasted for a week and a half. Our blog is late we made it through another treatment. Thank you for keeping us in your thoughts and prayers. Love,The Laub's

Tuesday, June 14, 2011

Needing some prayers our way !!!

First I do have to apologies for not posting sooner !!! I promise to show and tell every detail on Hunter's Make-a-wish trip soon !! While we were in Florida Hunter's grandpa was admitted in the rest home for cellulitis infection. Grandma was watching our boy's while Daddy and Mommy works and brought home the Rhino flu from visiting grandpa. Hunter got it the next day because of his immune system. Then Daddy,Triston and yes,even grandma got it too. Daddy and Triston had to be checked out and two day's later Triston came home with the croup. While we were up to Primaries for treatment last Tuesday they did not do Hunter's RTU because he has been sick. We were Quentin to our room on this trip. Now last night back again to the hospital for fever now throwing up. Got home about 4:00am and this morning and another fever at 8:00am we will be going back later today for more antibiotic through his port. So Hunter has the Rhino flu with croup that keeps hanging on and now throwing up with fever. This has been a ROUGH FOUR WEEKS. This mommy is asking please,for some prayers to be sent his way !!! Thank you for keeping us in your thoughts and prayers !! Love,The Laub's