Showing posts with label Harrison. Show all posts
Showing posts with label Harrison. Show all posts

Sunday, March 27, 2011

An Update on Harrison


Recently my nephew, Harrison, turned 12 and was ordained a deacon. A deacon's responsibility (one of several) includes passing the sacrament to the congregation. Because of his cerebral palsy, passing the sacrament is not a standard procedure for Harrison. To help the process, Harrison's father made this special apparatus that connects to his wheelchair and allows him to participate in this special ordinance. The hooks help to hold the trays for him. Today, Harrison's home teacher pushed his wheel chair as he passed the sacrament.

I have to admit I get teary-eyed seeing this.

Scripture of the Day: Proverbs 3:10

Wednesday, December 9, 2009

An Update on Harrison


My brother sent this to me today, so I thought I would bring everyone up to date on Harrison.

Friends and Family,

Since last August, many of you have come to me inquiring about the status of my son Harrison. It means a great deal to me personally that you all are concerned for the health of my child – even now, months after the fact. This year has been a tremendous challenge for us as a family, so having your support has meant a great deal along the way.

Last year, Harrison’s request of Santa was to have the stem cell treatment done. He prayed regularly for a successful outcome, and his prayers were answered. So this Christmas has a bit more meaning to our family.

Attached is an essay Harrison wrote on his computer last month for a school assignment. That in itself is significant – he used both hands to get it written with minimal assistance, something he was not able to do before. Somehow reading his words brings greater focus on the significance of what has happened.

Thank you all,

Jeff (Harrison's Dad)


My Favorite Thing

by: Harrison

What do you know about stem cell therapy? I know a lot about stem cell research because I had a procedure don in Dusseldorf, Germany in July.

The first thing the doctors did was extract my bone marrow out of my hip with a big needle. They harvested the stem cells by putting the bone marrow in a special tube and putting the tube in a special box. It too two days for them to separate the stem cells from the bone marrow. I had one million two hundred thousand stem cells.

After two days I went back to the hospital, the nurse put an IV in my arm and I went to lala land. Next, the doctors put the stem cells in a tube called a syringe with a ginormous needle. They put that needle in my spine and put the stem cells back in me. Ow!!!!! I had a really bad headache for eight days because of that.

Then I woke up, I pulled the IV out right away. Hahahaha. What the heck! I didn't need that thing anyway.

After the procedure some of the things I can do better are sit by myself, move my chair, and move my hands better. I could not do any of these things before yeah me!


Scripture of the Day: Psalms 96: 4, 6, 8

Monday, September 21, 2009

Housekeeping Issues

1. Recently my publisher encouraged all the authors to get on Facebook and Twitter. All this technology seems to take too much time as I am going through the learning curve. I still need to do Twitter, but I did get on Facebook. I even have a fan page. Feel free to become a fan or send a friend request for my personal Facebook page.

2. Tomorrow will be my 500th post! Woo hoo for me! Be sure to check in... there will very likely be a giveaway!

3. I had word from my publisher last week that the cover design of Home Evening Adventures with the Word of God (scheduled for release next month) will be done within a few weeks. I will be sure to post it as soon as I see it.

4. Those of you who indicated you were interested in reviewing a copy of Home Evening Adventures with the Word of God as part of a blog tour, watch your email. I will be getting that set up in the very near future. If anyone else is interested in joing in on this, leave me a comment and I will be happy to add you to the list.

5. Read this article is on the front page of the Denver Post today if you want an update on Harrison.


Monday, August 31, 2009

Harrison's Progress


The physical therapy is really expanding Harrison's newly healed capabilities. In just the past few weeks his legs have really gained strength and he is standing so well. Check out the pictures on his last few blog posts and you can really see the difference!

Thursday, August 20, 2009

Way to Go Jeff!

Congrats to my brother Jeff who was published today in an online e-newsletter! Click here to read his well-written article titled Healthcare and the Profit Motive. It touches on the Germany trip to get Harrison's stem cell treatment and the experience their family had there.

Monday, August 3, 2009

Member Missionary Moment #12


This post is part of a year long series where each week I strive to complete and item from a list of 101 Ways to do Member Missionary Work. Feel free to join me in the work!

This week I accomplished something similar to #8 from the Internet section of the list: "Share photos online of a temple trip, baptism or a baby blessing." I shared the photo of Harrison and his miraculous experience both online on my blog and through e-mail notes to friends, family, and co-workers. I had lots of positive responses from co-workers who are not LDS, so I felt this was a successful missionary moment.

Above: Harrison's family is now in France; he has been nauseous and sick the past few days but is still able to sit on his own.

Scripture of the Day: Matt 6:24

Thursday, July 30, 2009

The First Miracles for Harrison


My parents just had a call from Germany and Harrison has been sitting up on his own for the past 10 minutes or so; this is the first time in his entire life he has been able to sit up alone for more than a few seconds. It has been less than 48 hours since he had the stem cell treatment and they are certain this is directly attributable to the care he received.

Additionally, he is exhibiting greater muscle control in his arms, he is holding his head up much better, and his right hand seems to be improved and relaxed (previously his hands were typically in fists). Even Harrison's overall demeanor seems calmer, his parents reported.

We are waiting for the internet to deliver pics of Harrison sitting up. As soon as I get one I will update this post with one.

As a family we are feeling so blessed and grateful for these miracles. Please join with us and add a word of gratitude in your prayers tonight for Harrison's miracles.

Scripture of the Day: Daniel 2:44-45

Sunday, July 26, 2009

An Update on Harrison

My nephew Harrison and his family made it to Germany for the stem cell treatment, which starts tomorrow. You can read about their first few days there on Harrison's blog (click and scroll to beneath the law mowing pictures). We are so excited for this week to see what happens!

Wednesday, July 1, 2009

Stem-Cell Treatment Offers Hope to Colorado Boys

This article about my nephew Harrison and his friend Dominic appears in today's Denver Post. I thought you might enjoy a little update. They leave on their trip in 3 weeks.

Dominic King didn't have much to say.

Worn out from horseback riding, the 10-year-old sat quietly on a recent summer afternoon, smiling, amused by his best friend, Harrison Spiers.

Harrison, for his part, was hosting a one-man yak-fest, and his topic was one any 10-year-old boy, or former 10-year-old boy, should relate to: baseball.

Neither boy, though, volunteered comment about what will surely be the most memorable event of their activity-packed summer: the trip to Germany they're about to take. Asked about it, the boys shrug it off. No big deal. We've flown in airplanes before.

No big deal, except that this trip isn't about a relaxing summer getaway to the land of bratwurst and the Brandenburg Gate.

This is a trip about hope.

Dominic and Harrison, friends, classmates since preschool, have cerebral palsy.

And after years of watching physical therapy and speech therapy, of watching their sons — who are as smart as anybody else's 10-year-olds — struggle inside their own bodies, the boys' parents have found, maybe, real promise.

That promise is a stem-cell treatment, one that isn't available in the United States. So both boys and their families will head to the XCell Center in Köln, Germany, late in July.

There, technicians will collect stem cells from the boys' bone marrow. According to the clinic, the marrow is then checked for quality and quantity of stem cells. Then, several days later, the cells are re-injected, through the spine.

"It's not invasive, but they will have to be under anesthesia because you don't want them to move around," said Dominic's mom, Christina King.

According to XCell's website, "these re-injected stem cells have the potential to transform into multiple types of cells and are capable of regenerating damaged tissue."

XCell statistics indicate that 70 percent of patients who undergo the treatment for cerebral palsy experience some improvement, including decreased spasticity, better coordination and motor function, improved stability or better speech.

Voicing tentative hope

Cerebral palsy is a group of chronic conditions that affect body movement and muscle coordination. It is caused by damage to the brain, usually during fetal development or during or shortly after birth.

The March of Dimes estimates it occurs in two or three of every 1,000 births.

For many of the 800,000 people in the United States who have it, the disorder causes difficulty controlling movement and speech. Some with the condition experience spasticity.

For Dominic and Harrison, the condition has meant life in wheelchairs. It means that Dominic often communicates via a computer and that Harrison doesn't get to play football and baseball.

Neither boy's intellect is impaired. As Harrison's mother, Alicia Spiers, puts it, he understands everything he's missing.

"But he has a really good attitude. He doesn't get down too often," she said.

The boys' mothers can't let themselves voice their hopes for the treatment.

Dominic and Harrison, with their 10-year-old trust, have no such hesitation.

"He's hoping his speech becomes clearer," Christina King said of Dominic.

And improved motor skills would be nice, she said. "He drives his wheelchair and uses his computer with his head. He's hoping he can touch the computer screen."

Harrison wants nothing less than to play football.

"His wish from Santa last Christmas was new stem cells," Alicia Spiers said.

The boys, who just completed fourth grade at Cottonwood Creek Elementary in the Cherry Creek School District, spend most of their days in regular classrooms — aides help them eat, move around school and get their books out of their backpacks.

They go to birthday parties and have buddies they eat with, their moms said.

But the relationship between the boys is special.

"He has lots of friends," Harrison's mom said of her son. "But Dominic gets him."

A community united

The treatment isn't approved in the United States, and it definitely isn't covered by insurance. So the families and their friends and relatives have been pitching in, hoping to raise $12,000 apiece for the treatments.

On June 14, a hair salon offered "Haircuts for Hope," which raised about $1,600. Before that, runners and walkers tromped around the boys' elementary school and raised hundreds.

"And some little girls at swim team made bracelets they sold for $1 each and are giving the money to us," King said.

One of the girls' moms told King she was learning a lot during the fundraising process, about cerebral palsy, about stem-cell treatment.

Both moms said they've learned a lot too — about their neighbors.

"We're not alone," King said. "This community is just wonderful."

Friday, May 22, 2009

A Note from Harrison's Parents

Family,

It gives us great pleasure to inform you that we met our goal for Harrison’s trip yesterday. As it stands, we now have airfare, accommodations, and enough to pay for the procedure. Thank you! The burden of caring for a child with CP is tremendous enough by itself. Your assistance in helping us overcome this financial burden is very much appreciated.

As of now, we have moved the procedure up to the week of July 27th to allow for cheaper airfare and hotel availability.

You should also be aware of the great good that is coming of this. Harrison’s friend from school is also going to have the procedure done. Another friend with CP has begun making preparations for the same. The school and community have rallied around these two boys like you wouldn’t believe (go to http://www.thebighope.com/ to see for yourself). There is a 5K run this Saturday at the elementary school right before our pool opens. Spots are running on the radio, the NBC station interviewed Alicia and H this morning, the Denver Post will run a story, and the Aurora Sentinel is doing a story too. In all of this, we are firm in our testimony and make it clear to all that we recognize the hand of our Heavenly Father in this.

About 10 years ago, when H was diagnosed with his disability, Alicia and I said to each other that we would see a long list of miracles with this child. We count this achievement as yet another in the long list of miracles we have witnessed together as a family already. Please feel free to share our sentiments with all interested family and friends not listed above.

All our love,

Jeff and Alicia

Monday, May 18, 2009

An Update on Harrison


It has been a while since I have updated everyone on my nephew Harrison. You may recall recall I have written about Harrison and his upcoming stem cell treatments in Germany this summer. Harrison and a close friend/school mate will both be going to Germany. For the past several months their families and school have been fund raising to help raise the money needed. Their efforts have been greatly blessed in this area, which you can read about on Harrison's blog. This upcoming weekend there is a fun run--so if you live in the Denver area, be sure to participate!

Tip: Scroll down a ways on his blog to get to some links to some gorgeous temple pictures (like this one) you can download.


Scripture of the Day: Luke 2:19

Tuesday, March 3, 2009

An Update on Harrison

My nephew Harrison has been accepted to receive stem cell treatment from a German facility this upcoming summer. My brother and his family have been tremendously blessed for this upcoming trip. His boss has offered to pay for their lodging. And a client sent them a voucher for their flights (all six of them!). All of this kindness has been more than they or we ever expected and gratitude fills our hearts. We are so hopeful Harrison will see some improvement in his capabilities from the stem cell treatment. I will let you know what happens when it happens.