Thursday, February 2, 2012
20 Weeks & Counting....
The Day A Mother Never Forgets!
Another trip to Huntsman....
Sunday, January 8, 2012
Update on Jared...
Wednesday, October 12, 2011
Halle's Broken Arm....
By the next day it was pretty swollen! Dr. Bean wanted to take her picture...
putting on the partial cast - she was very nervous!
her moral support with Brooklyn, Grace, and Randa and blankie!
All better!
Our sweet little Halle broke her arm! I was with the girls and Miranda at parent teacher confrences. Halle and Randa stayed and played outside while Brooklyn and I went to visit with her teacher. A little while later Halle came running in crying and Randa told us how she had fallen off the Monkey Bars...how many millions of times a day does that happen! I made her sit on my lap and tried to calm her down while I finished (I know...bad mom!) but it didnt look broken? By the time we were finished, I knew something was wrong. Halle is my tough little girl (she takes after me) and she was still sad and wimpering. So whenever my kids get hurt I always call my next door neighbor Alisa, she can deal with all the blood and stuff much better than me! She convinced me that something was wrong, so I took her in. The doctor who saw her that first night didnt see anything on the xray, but by the next morning they were calling me back to tell me it was broken just below her elbow. So we took her to Dr. Bean at Layton Tanner Clinic, who is not only a great orthopedic doctor, but just a great, great guy! He came walking out into the waiting room and said, "Wheres my little Halle with the hurt arm?" He was sooo cute with her and made her feel right at ease. He took us all back into his office where his desk was. He gave all the girls bone suckers and told us he went around to different schools and talked to kids about being safe on the playground. He asked Halle if he could take a picture of her because she was just about the prettiest thing he could ever show the kids. Her arm was too swollen to cast so she will have to wear a partial cast for a week before they can put a real cast on it. Which is a good thing, because she will need a week to decide what color cast she will choose!
Sunday, August 28, 2011
Fletcher Family Pics!
Mom & Dad with all the grandkids
Mom & Dad with all us kids
Brooklyn, Jared & Halle
Mitch & Mom
Kylie & SteveFor those of you that know, I come from a big family with 8 siblings. My mom has wanted to do another (or final) family picture for awhile now. Weve got 2 nephews on their missions and another, Deven leaving in just 2 weeks, and Kylie & Steve just getting back from a summer internship in New York City, so our time was growing short, but we mamaged to pull it off the day of Devens farewell. We all went out to Thanksgiving Point. It was very fun and soo beautiful, exactly what my mom wanted. Soo to spite my dads discontent (and most of the other guys)..here are a few pics of my sweet family!
Tuesday, July 12, 2011
Update on the Family....
Monday, June 27, 2011
St George trip with the Fletcher Family!
Wednesday, June 22, 2011
Jared's Tumor Update...
Our last appointment at the Huntsman was yesterday, June 21st. We went each month, but he only had an MRI every other month. At this last appointment we found that his tumor hadnt really changed much, which was a disappointment. Each time we go Jared will always say, wouldnt it be great if they looked at the MRI and the tumor was completly gone! Yes would be a miracle..but not reality unfortunatly :(. So he was a little bummed.
As we talked with the doctors, they said he could be on Chemo anywhere from 6 months up to 2 years, as long as the patient can tolerate it. But the down side is that with this Chemo, they dont have any studies that prove that it is still effective after the first 6 months. Also another down side, is that if he stays on the Chemo for too long, he can contract another form of Cancer from taking the Chemo, like Leukemia. Wow who would have thought you could get cancer, from taking Chemo?
Soo we left last time, a little bummed. But I keep telling Jared, the Lord is in complete control!! And you will be on this earth, as long as he needs you! Im soo greatful we know what we do. Its gives us alot of peace.
We will now go to Huntsman, every other month. And he will have bloodwork done here at Davis hospital after the chemo treatment the months he dosent go to Huntsman. But so far his bloodwork has looked great! They say that his levels look just like a health man. So thats great!
Saturday, June 11, 2011
Jared turns 40!!




Tuesday, March 22, 2011
Update on my sweet Jared.....
But even worse he has been sooooo tired. Tired like when you havent sleep all night and cant think straight. But for Jared he was sleeping all the time! The worst days were probably the end of last week. thursday, friday and saturday I think he was asleep longer than he was awake. It was killing him. And I worried about him driving to work and stuff. It made me really stop and think about how you always hear people say....if the cancer dosent kill them, the chemotherapy will. It literally zapped the life right out of him. It was soo hard to see him go from doing soo well, happy & motivated, to soo tired that he was a zombie, not functioning and when he was awake, he was down about how tired he felt all the time.
Then on saturday night, he started feeling itchy all over. His head, his back, his arms, everything itched. He started putting anti-itch cream on, but that only locked in the heat and made it worse. By sunday morning we were calling the pharmacy, he said its probably a reaction to the Temodar, so they had him take Zyrtec and it helped.
So fast-forward to today, tuesday...I think I finally have my husband back YEA! Although he says his food still tastes weird, he is eating again. And even better, he only slept for about an hour today!
We will go back to Huntsman next tuesday, March 29th, have more blood drawn, and get a prescription for another month of Chemotherapy. Yuck! Dr. Coleman wants to up his dose again, this time to 400mg per day, but I say no way!! Hopefully he will let him take a lower dose for more days or something. At least until his body can adjust to the posion he's putting in it! Another option is to reduce the anti-sezure medicine he's on. That slows your brain down too and can make you tired. Its a double edged sword! Hopefully we can get some answers next week when we go!
Tuesday, February 15, 2011
Great News....Its Shrinking!
This is the Radiation department gals...they LOVED Jared! After his 33 treatments they gave him a blanket and a certificate and LOTS of hugs! He wanted to bring them in some donuts to say thanks! Jared was able to touch a lot of peoples lives, also having radiation. He was an inspiration!
I decided to take you on a journey of what we do and see each time we go to the Huntsman Center. Outside we drive up to the front and guys are waiting to valet park our car. They are college boys, and they are not allowed to take tips of any kind. Above there's a shot of the main entrance. The Radiation department is straight ahead. The Neuro-oncology department is up the stairs on the second floor. Once were upstairs we got to Clinic E. We check in and then go to Clinic Lab (blood drawn) first, just down the hall.We know that we are soo blessed to be at the Huntsman Center and associated with these amazing people who have blessed our lives. They truly are wonderful!
Jared will have a little bit of a break, and start Chemo again on Monday March 7th. And then we will go back to see Dr. Coleman at the end of the month on March 29th. So until then Jared can have a normal life for awhile!
Monday, February 7, 2011
All Done!
We go next monday..Valentines day, for his MRI. Then on tuesday we meet with Dr. Coleman for the results from his MRI. We are very Hopeful, that it will be good news! We will keep you posted!
Thanks again for all the Love & Prayers!




