Today is the first day of surgery prep. Today Tyler started day 1 of his clear liquid diet. Everyone in the house was going to do it with him, but I think it is better if they don't. The other kids are not used to it so, I was a little worried and told them it might make them sick. I still want them to eat other solid foods so they will be okay. He ate almost everything in the house yesterday so I think he might still be full from that. So far he is doing well with it so far. I will keep this updated day by day to show progress.
Have a blessed day!!
Tyler is a 9 year old boy that has Spina Bifida and Hydrocephalus. It is a miracle and a blessing to have him in our life.
Sunday, January 30, 2011
Tennis and Basketball

On Friday we went to Tyler's tennis class at the Salt Lake Swim and Tennis Club. He had a great time. He was able to have a lot of one on one time with Dean and Ryan. They are both excellent with the younger kids. He is a little sad that he will be out for about a month. He is doing better and better every time he goes. This time they got to use the rackets and actually were able to hit the balls. Dean had Tyler doing drills and obstacle courses. It was really fun to watch. Tyler's aunt and uncle showed up also to show a little support.
On Saturday we went to basketball and had a great time there as well. This will be the last one that he will go to for this season. There is only four weeks left and he will be recovering for at least that long. He really started getting into it and his team won. That made him really happy and he talked about it for the rest of the day.Have a blessed day
Friday, January 28, 2011
Family is everything
In our life we go through so much. So in my life I have found that our family is everything. My family has been there for us since day one and even before. Tyler has such a caring soul and he absolutely loves being around family. More times than not it is hard for all of our family to be together. I have two sisters that are in the USMC and so they are gone a lot.
Tyler has such a great love for his aunts. They were both able to come home this year for a short amount of time. It was to bad that it couldn't be at the same time.
In the first picture Tyler is with his Aunt Sam. She was home in early Jan for pre-deployment leave. It will be close to 15 months before they will see each other again.Sam has told me so many times that Tyler is her hero. She is such an amazing aunt to him.
This picture is Tyler with his Aunt Mandy. She was home on leave before she has to go to MCT and start her schooling. It wont be as long between her visits, but it still seems like forever. She also has been an amazing aunt to him.
Have a blessed day!!
Tyler has such a great love for his aunts. They were both able to come home this year for a short amount of time. It was to bad that it couldn't be at the same time.
In the first picture Tyler is with his Aunt Sam. She was home in early Jan for pre-deployment leave. It will be close to 15 months before they will see each other again.Sam has told me so many times that Tyler is her hero. She is such an amazing aunt to him.This picture is Tyler with his Aunt Mandy. She was home on leave before she has to go to MCT and start her schooling. It wont be as long between her visits, but it still seems like forever. She also has been an amazing aunt to him.
Have a blessed day!!
Monday, January 24, 2011
Tennis and Basketball
A little over a month ago Tyler asked me why I asking about wheelchair sports. "If I am not in a chair now, why do you want me to be in one"? It was kinda funny because after all of this time of telling him he can do anything, telling him that he needed to get out and try a little of everything. Now I am telling him that he should sit in a chair and play sports. I think this is a way for him to still be very active, but have a lot less of a chance to get hurt. Well it didn't take long and he was in love with it.
On Friday the 21st, we went to tennis and he had a blast. His coach, Dean who also has Spina Bifida was wonderful. He spent a lot of time one on one with Tyler. Now he can't wait to go back this friday and do it all over again with the other kids. Coach Dean said one of the hardest things for these kids in the hand eye coordination, but that Tyler did very well.

On Saturday, we went to basketball and Tyler was really excited for that. He got in a chair and pretty much rolled right in there. He played the best that he could and did great. He was able to play with a lot of other kids that had Spina Bifida there as well. He met a kid named Ryan who is 16 and is a champion in tennis. He also plays basketball to help the other kids. Tyler told him at the end that if he was on a team he would want Ryan on his team. It was really nice of Ryan to return with and I would want you on my team too. Again he had a great time and can't wait to go back. We will have to take a little time out during this next surgery, but he will go back.
On Friday the 21st, we went to tennis and he had a blast. His coach, Dean who also has Spina Bifida was wonderful. He spent a lot of time one on one with Tyler. Now he can't wait to go back this friday and do it all over again with the other kids. Coach Dean said one of the hardest things for these kids in the hand eye coordination, but that Tyler did very well.
On Saturday, we went to basketball and Tyler was really excited for that. He got in a chair and pretty much rolled right in there. He played the best that he could and did great. He was able to play with a lot of other kids that had Spina Bifida there as well. He met a kid named Ryan who is 16 and is a champion in tennis. He also plays basketball to help the other kids. Tyler told him at the end that if he was on a team he would want Ryan on his team. It was really nice of Ryan to return with and I would want you on my team too. Again he had a great time and can't wait to go back. We will have to take a little time out during this next surgery, but he will go back.
Friday, January 14, 2011
Soccer
On Wednesday, we went to another HopeKids event at The Complex. Chris Wingert from REAL and some of his friends came out to play with the kids. They ran through some drills first and made it fun. Then we all went over to the other room and had pizza and powerade. They also had a table set up for some crafts. While all of that was going on Chris did autographs and took pictures with the kids. At the end they also gave away a few soccer balls and Chris signed those also.
On Thursday Tyler became really sick. He was asking to go to the doctor. That is not something that he usually does. So I called and got him into his pediatrician. She seemed to be worried about him. She wanted to have him go up to Primary's for observation, x-rays, and some blood work. She ended up giving him an antibiotic for an UTI. I told her I would keep in touch and let her know how he was doing. That if he didn't feel better Friday that I would take him up. Well the antibiotic is a good one cause this morning he felt better. That whole situation was weird cause he hasn't shown symptoms before with UTI's. I am just really glad that he is doing better.
Just a quick note tonight with him feeling better we are going to wheelchair tennis. It was cancelled, but we talked to a gentleman who's son plays bb. So we are going to try that too.
Have a BLESSED DAY
On Thursday Tyler became really sick. He was asking to go to the doctor. That is not something that he usually does. So I called and got him into his pediatrician. She seemed to be worried about him. She wanted to have him go up to Primary's for observation, x-rays, and some blood work. She ended up giving him an antibiotic for an UTI. I told her I would keep in touch and let her know how he was doing. That if he didn't feel better Friday that I would take him up. Well the antibiotic is a good one cause this morning he felt better. That whole situation was weird cause he hasn't shown symptoms before with UTI's. I am just really glad that he is doing better.
Just a quick note tonight with him feeling better we are going to wheelchair tennis. It was cancelled, but we talked to a gentleman who's son plays bb. So we are going to try that too.
Have a BLESSED DAY
Tuesday, January 11, 2011
The next big step
Tyler is still having problems with his leaking. This is after he had a stoma put in his belly button. He has also has 3 deflux injections, a botox injection, and an artificial urinary sphincter. Now they are going to do a bladder augmentation. I am not sure how this is going to help him to stop leaking, but I am listening to his urologist on this one. The surgery is pretty major. From what I understand it is 3-6 hours long with a 7-10 day hospital stay. This is our last option so I am really hoping and praying that this will work. I will keep posting and updating as he goes.
Now the fun stuff we went to another fun HopeKids event last night at The Paradise Bakery. There were cookies and soda provided by the bakery. Then at different tables were different games. We played Uno and meet another family there. It was a lot of fun and we really do enjoy doing things with family. Tyler really likes to meet new people.
Thank you for reading Tyler's Luv and have a blessed day.
Now the fun stuff we went to another fun HopeKids event last night at The Paradise Bakery. There were cookies and soda provided by the bakery. Then at different tables were different games. We played Uno and meet another family there. It was a lot of fun and we really do enjoy doing things with family. Tyler really likes to meet new people.
Thank you for reading Tyler's Luv and have a blessed day.
Monday, January 10, 2011
A day out
On Saturday Tyler was able to attend the Hopekids event at the Mega Plex Theatre. We went to Jordan Commons and watched Disney's Tangled. It was Tyler, Savannah, and myself. He had an absolutely wonderful time and talked about the movie for the rest of the day.
Then on Sunday we went over to his grandma and papa's and had our Sunday dinner. It was a great time and he loves seeing his family. He really loves his aunt who is home on leave. We had pork and cactus burritos and then his papa and aunt made dessert. It was really fun and I just love to see him smile.
Then on Sunday we went over to his grandma and papa's and had our Sunday dinner. It was a great time and he loves seeing his family. He really loves his aunt who is home on leave. We had pork and cactus burritos and then his papa and aunt made dessert. It was really fun and I just love to see him smile.
Sunday, January 9, 2011
All New
Hello this is a very new project for me and I hope you will enjoy following Tyler through his trials and tribulations. Tyler was born on July 16, 2001 in Salt Lake. He was diagnosed with Mylomeningecil (Spina Bifida) and Hydrocephalus when he was 4 months in utero. I had the hardest time accepting this because I didn't understand it. I had recently became a single mom with 2 older children. Savannah was 5 and Christian was 1. I was lost and just knew that I could not handle whatever I was just given. I had no idea what was in store for us. I only knew that our entire lives had changed forever.
I was told that my son would not walk or talk and that he would be in a wheelchair as a vegetable his entire life. I was told to get all of his medical equipment ready. I thought to myself this can not be. How am I supposed to take care of my other children and him. I struggeled with that thought for awhile. I was also told that he may not make it. Then after a lot of tears and time to think I realized that if he was meant to be he would be. My grandma told me that God doesn't give us more than we can handle. I didn't understand that and why why me. Well I realized that I was strong enough to handle this and I would do it. I had a lot of support from my mom and dad as well.
Tyler came into this world and he was perfect. Yes his head was a little bigger, he had an open spot on his back, and his feet were severely clubbed, but he was just perfect. I was not able to hold him right away as he had to be kept in a sterile environment. His first trial happened when he was only 17 hours old. He had his back closure surgery. He was able to go home from Primary's when he was a week old. And just a week later he was back in to have his shunt placed. Since that time he has had over 20 surgeries and procedures. Tyler is my hero as he is the strongest little man I know. Now he is 9 and he runs, jumps, plays, and talks. He is in the top percent in his class at school.
Tyler is an amazing person and I hope you enjoy going through his journey with him.
I was told that my son would not walk or talk and that he would be in a wheelchair as a vegetable his entire life. I was told to get all of his medical equipment ready. I thought to myself this can not be. How am I supposed to take care of my other children and him. I struggeled with that thought for awhile. I was also told that he may not make it. Then after a lot of tears and time to think I realized that if he was meant to be he would be. My grandma told me that God doesn't give us more than we can handle. I didn't understand that and why why me. Well I realized that I was strong enough to handle this and I would do it. I had a lot of support from my mom and dad as well.
Tyler came into this world and he was perfect. Yes his head was a little bigger, he had an open spot on his back, and his feet were severely clubbed, but he was just perfect. I was not able to hold him right away as he had to be kept in a sterile environment. His first trial happened when he was only 17 hours old. He had his back closure surgery. He was able to go home from Primary's when he was a week old. And just a week later he was back in to have his shunt placed. Since that time he has had over 20 surgeries and procedures. Tyler is my hero as he is the strongest little man I know. Now he is 9 and he runs, jumps, plays, and talks. He is in the top percent in his class at school.
Tyler is an amazing person and I hope you enjoy going through his journey with him.
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