My Photo
Erick Wills
Rexburg, Idaho, United States
Grew up in California. Married an Idaho girl. Raising my kids in America's Family Community. I coach football, baseball, girl's basketball, and fastpitch softball. I love to work with kids.
View my complete profile

Thursday, June 18, 2009

Kicking Cancer's Butt


Please visit http://www.ikickedcancersbutt.org/ and follow Aubri's cousin ride a bike from Reno, NV to Salt Lake City, UT for cancer research. Mike Nelson and his son Taylor are part of a group of great guys who ride to raise money for the Huntsman Cancer Institute. More than the money however, is the fact that they would sacrifice themselves on behalf of others. Thanks guys!

Friday, April 24, 2009

A Father's Reflections


I found this column and found that it matched my own feelings and experiences perfectly...

I suppose that the general Dad experience is one of anger and helplessness. Dads are supposed to be the protectors of their families. Burglars, thieves, cutthroats, and murderers lurk outside the gate, and will be dealt with summarily if they chance to invade our kingdoms. There is a powerful fantasy of defending the castle against all comers, even laying down our lives to keep our children safe.

A diagnosis of a grave illness is sneaky, however. A spy, an assassin that has entered our lives through the sewer grate. Suddenly we realize that the princess is held captive in her own room, with a knife at her throat, and we are standing helplessly, stupidly, in the courtyard with useless weapons in our hands.

At the moment of our daughter's diagnosis, my wife and I set out on different journeys to rescue our child. More like two different takes on the same mission, two complementary approaches. For Mom, it was about comfort. Make our baby comfortable, make our family comfortable, share feelings and insights with visitors, things she was willing to do 24 hours a day at the expense of her own health. For me, it was about facts. What, exactly, is the diagnosis? What are the odds of complete recovery? What will be the results of the surgery? Where will we stay? What about the insurance people? Who will feed the dog?

Interestingly, the doctors told me not to read books. Current therapy and practice are advancing so rapidly, that a book is far out of date the day it’s published. So I went to the medical library at the hospital and read current periodicals and extracts. Good news. I asked tough questions at the doctor's conferences. Good numbers. I wrote regular newsletters so that we wouldn't have to tell the same stories over and over. Good work.

Meanwhile, my wife sat by our daughter's bedside and watched her sleep. She sat out in the hallway and talked to visitors, nurses, doctors, strangers, patients, janitors, technicians, maintenance men, pizza delivery guys until she was exhausted, and I knew we had to have a plan.

1. Analyze your strengths. Nancy was the caregiver, I was the utility player. She stayed at the hospital during the week, supervised our daughter's daily fight, and I stayed home and played Mom.

2. Allow your friends to help. When someone asks you what you need, tell them. Our friends did our laundry, mowed our lawn, cleaned our house, cared for our other children (took them Trick or Treating, swimming, to games, to sleepovers)

3. Try to keep the good and ignore the bad. While Mom was gone to the hospital all week, the other kids slept with me, had dinner with me, watched TV with me, and generally treated me with care. It was our job to be as normal and happy as possible.

4. Try to get some rest. Once we had established our plan, it had to produce good results for the patient. I told my wife that she was allowed to cry when she was not in the patient's presence, but she needed to be healthy and cheerful whenever she went in the room. Personal care is necessary for the patient's benefit. Take time off to sleep, shower, eat, and return with a good attitude. I came for the weekends; that was my time to relieve my wife, and take my turn on watch.

5. Accept the reality of your new life. One of the strangest results of our new routine was an incredible sense of peace for me. On the scale of values, weeds and bills sank to an all time low, and time at the hospital rose right to the top. At my most helpless, I found the strongest sense of God's presence. In my weakness, my only weapon was my time, my patience, and my support. As a man, it was humbling, as a father, it was transforming.

I don't mean to take away from the pain and difficulty of this experience; it was both painful and difficult. But I do believe that while this illness can destroy a family, it also has the potential to build one too. I think the bottom line rests with Dad. Dad's job as the warrior is to lay down his wants and desires, to fight with himself, and make the noblest sacrifice of his time so that his family might survive. In the end, it may be the best thing that you have ever done.

Joe, father of a childhood cancer survivor

Thursday, April 16, 2009

Sarcoma Awareness Foundation

We are in the process of creating a Sarcoma awareness Foundation to help Aubri help others. She feels so greatly blessed by all the kindness, generousity, and prayers on her behalf that she wants to share with those in her same situation. We plan on having a yearly dance/dinner each summer, as well as other events to help raise money for the Huntsman Cancer Institute (specifically for Sarcoma research) and for others that have needs to help with their individual treatment. If any of you have ideas or would like to help, please let us know at erickwills@yahoo.com



Here is her foundation logo.

Wednesday, March 11, 2009

Aubri in the news

Here is a recent story about Aubri.

http://www.localnews8.com/Global/story.asp?s=9809219

Friday, February 6, 2009

Pride


Another lesson learned...

This week as my wife and I were watching the local high school basketball game broadcast over the internet (http://www.eisnlive.com/), we were caught off guard by a halftime guest. The broadcaster was interviewing my father-in-law on a subject they called "serious and sensitive." It was regarding our daughter Aubri and the cost of the treatment she has undergone and will continue to endure over the next year. He mentioned that a fund had been setup in her name at Zion'z Bank and that they would be holding other fundraisers on her behalf.

A flood of emotions hit me during the broadcast. Embarassment - I thought, "man I should be able to take care of myself and my family" (a recurring theme in my selfish, prideful mind.) Anger - why had noone told me they were doing this? Sadness - I thought again for the billionth time about what my daughter would have to endure in her young life. Happiness - to know that we had friends and family who cared enough to want to help.

My wife and I have been told many times that people want to help, but don't know how. My mother-in-law and sister-in-law have scolded us (nicely) that we need to let them, for their sakes as well as ours. We are trying to listen.

So, thank you. We love you all, we love the help, we love the thoughts, we love the prayers. We are touched by your compassion and love. I only hope that someday we can repay the kindness. God bless you all.

Thursday, January 15, 2009

Aubri Update

Aubri went through surgery this morning. It was set to take 2 and half hours and went a little over 3. The doctor said there was a lot of scaring from the firt surgery, but they took out what they could including the skin that had been exposed. He said the chest scan was clear as well. Other than a little radiation and a MRI/CT Scan every 3 months, she is free and clear. There is always a chance that it could reoccur, but this was best case scenario. Thank you for all your prayers, thoughts, cards, care packages, meals, and financial help. We have been overwhelmed with emotion at all the friendships that have been strengthened and developed. We love you all.

Wednesday, December 17, 2008

Daughter With Cancer

Cancer. Never thought I would hear this word spoken in relationship to one of my children. My daughter Aubri found a large lump under her arm near the middle of the bicep. After antibotics for what the doctors thought was infection, anti-inflamatory medication for the swelling, an ultrasound, and several doctors visits they decided to take it out. After it was removed and sent away for pathology work the results came back inconclusive. They said is was an "Atypical Spindle Cell Neoplasm". That's doctor speak for an unusual growth made of spindle cells. After further stain testing they determined it was fast growing and nondiferentiate (what ever that means), but still could not determine where it came from, what is was made from, or whether is was benign or malignant. It has now been sent to the Mayo Clinic and to the Huntsman Cancer Institute for genetic testing to determine it's origin. We also visited a specialist at Primary Children's Hospital in Salt Lake City and they performed some tests and took an MRI of the arm.

I know the statistics both good and bad, but not knowing what this is and what we can do about it drives me nuts. So now we sit and wait for a couple of weeks.