Monday, October 10, 2011

Holiday Shopping & FUNdraising

You may DONATE directly for the NYC marathon by clicking on donate.

Only 26 more days until the NYC 26.2 mile marathon! This is your last chance to make a donation in Hayden's honor.  
Every amount no matter how small is precious and will help advocate about the importance of Folic Acid and giving these wonderful children a chance for their right to life and a good quality of life.
Thank you for every dollar you sponsor me or my sister, Melyssa on the run of our lives!  We are SOOOO EXCITED!
If you are not in Austin to attend our Spina Bifida open house, you may also like a little Holiday Shopping Preview with a percent of proceeds going to the SBA:
The Pampered Chef:
Encantada:
Scentsy:
Spina Bifida Jewelry:

Wednesday, September 28, 2011

Milestones

Hayden has never stood for this long by himself.  He has to wear knee immobilizers for support, but he is getting stronger!  Please see the posts below by clicking the banner above.

Sunday, August 14, 2011

Flamingos migrate from Austin, TX to Billings, MT?

To DONATE click here.  To read the whole story, click on the banner picture above.


With some mixed emotions of gratitude, sadness and relief, after 30 days of moving 2 migrating flocks in 100 degree heat, our Austin, Texas flamingo flocking has come to an end.  Due to the heat, our flamingos have flown the coup.  Many of them lost libs or broke wings in sustaining their efforts.  They have moved to a cooler climate, Billings, Montana where my running partner & marathon sister, Melyssa, will debut her fundraising efforts.
We are sincerely thankful for our wonderful neighbors and friends generous donations to the Spina Bifida Association and motivating support that made our fundraising so fun and heart felt.  Our Texas donations were much more than we anticipated. To date, we have raised more than $4,000!  
Over the course of the 26.2 mile race I will be motivated knowing I have over $150 riding on each mile I endure running.  It really helps give me something to think about while I have been training in this terrible Texas heat. 

Why have we done this?  We want you to know that Spina Bifida CAN largely be prevented by taking prenatal vitamins or daily FOLIC ACID PRIOR to getting pregnant. Spina Bifida occurs at ~20 days gestation, just before the 1st missed period.  Although prenatal vitamins were taken in Hayden’s case, not all diagnosis are known why.  
We have been blessed with abundant medical resources and state support while many families throughout the country are not.  Upon learning the diagnosis at the 20 week ultrasound, MOST mothers are pressured into delivering the baby prematurely to terminate the pregnancy.  Spina Bifida is not a death sentence.  EDUCATION = POWER & HOPE
Where Does The Money Go?  100% of your donation goes directly to the national Spina Bifida Association.  
  • $52.40 will provide 10 diagnosed mothers-to-be and six families living with Spina Bifida with tools, resources, information, and guidance from our National Resource Center for one day.
  • $78.60 will provide a full-day of education and supportive services to a family of three living below the poverty line.  This includes treatment information, access to health-care facilities, and psycho-social programming assistance, among others.  A meal is also included.
  • A $131 contribution provides 550 women with information about preventing Spina Bifida with daily folic acid.
  • $183.40 will support at least two children attending the three-day Kids!Camp – the only such camp in the country that promotes self-confidence, esteem and independence all in a fun atmosphere.
  • $262.20 enhances our college scholarship fund to further a young person with Spina Bifida’s education.
  • $1,000 furthers research in Spina Bifida to develop better treatment for, more understanding about, and new ways to prevent this life threatening birth defect.

Monday, July 18, 2011

NYC SBA marathon fundraising fun

Just finished the graphic that includes all the children of the parents who will be running the NYC marathon for SBA.  They represent just a few of the wonderful people with Spina Bifida that I am honored to represent.

Thank you to all of you who continue to contribute and support our fundraising efforts.  The 3 dozen flamingos that are flocking our neighborhood has started off really well, thanks to the full support of our HOA and our generous neighbors.

I am humbled and more grateful than words can express to all our generous donors!

Wednesday, June 15, 2011

New Runners for SBA in NYC

The New York City Marathon recently announced that it was going to allow for double the number of runners invited on behalf of the Spina Bifida Association as a charity partner.  Originally we had been allotted 5 runners and then recently they gave us 5 more for 10 total.  Each additional spot was quickly filled.

The newest member of Team Hayden.....my Montana sister, Melyssa Ostler!!!!  I am honored by her support and love of my little boy Hayden.
Cate, Melyssa & Hayden.  My sister Cate would have been a great running addition had she be 18.  We still love you Cate.

Monday, May 23, 2011

Help Hayden. Give Hope.

26.2 Miles
5 Boroughs
1 Very Special Kid 
Dear Family and Friends,
As you know, my son Hayden was born with Spina Bifida.  You may have read much about him on our blog at www.texastriggs.blogspot.com.
Because of Hayden, it is my honor along with my awesome sister, Melyssa Oster, to be among the 10 invited to run on behalf of the Spina Bifida Association (SBA) as their 2nd Annual New York City Marathon charity partner.  If you don’t know what Spina Bifida is, it is the most frequently occurring permanently disabling birth defect.  Every day about eight babies born in the United States have Spina Bifida or a similar birth defect of the brain and spine.


The first year that Hayden was born he underwent 7 surgeries (brain shunt, spine closure, hernia repairs and eye surgeries).  He continues to be a champion in the way of working with as many as 6 therapists per week.  We feel blessed that all his surgeries have proven successful and that he has needed no more and we hope to keep it that way.
Approximately 166,000 people in the United States are living with the challenges of Spina Bifida. Find out more information on this challenging and complex birth defect by visiting www.spinabifidaassociation.org.
SBA is the only national voluntary health agency solely dedicated to enhancing the lives of those with Spina Bifida and those who are touched by this challenging birth defect.  
Now I would like you to join the cause. I will be running the New York City Marathon on November 6, 2011 in honor of Hayden and to benefit SBA.  
Please help make this a memorable run and support an organization that will support my family for a lifetime.  
Would you please consider making a donation of $1 per mile ($26), $2 per mile ($52), $5 per mile ($130), $10 per mile ($260), $20 per mile ($520)?  
Thank you so very much.  I do hope you’ll support this very worthwhile organization.  Please make and on-line donation by clicking the link to  donate now.  
You may read below to know where this money will be put into use.
With much gratitude,
Adrienne Trigg
Where Does The Money Go?
  • $52.40 will provide 10 diagnosed mothers-to-be and six families living with Spina Bifida with tools, resources, information, and guidance from our National Resource Center for one day.
  • $78.60 will provide a full-day of education and supportive services to a family of three living below the poverty line.  This includes treatment information, access to health-care facilities, and psycho-social programming assistance, among others.  A meal is also included.
  • A $131 contribution provides 550 women with information about preventing Spina Bifida with daily folic acid.
  • $183.40 will support at least two children attending the three-day Kids!Camp – the only such camp in the country that promotes self-confidence, esteem and independence all in a fun atmosphere.
  • $262.20 enhances our college scholarship fund to further a young person with Spina Bifida’s education.
  • $1,000 furthers research in Spina Bifida to develop better treatment for, more understanding about, and new ways to prevent this life threatening birth defect.

A Mother's Story of the Spina Bifida diagnosis

I have been fortunate to count many experiences as blessings in my life.  The one that I am going to share with you is my sacred blessing of raising my son, Hayden, with Spina Bifida.  My story begins many years ago prayerfully struggling to become a mother.  I tried various fertility treatments and adoption when I miraculously became pregnant with a little girl five long years later.  After giving birth it felt like I was seeing the world in a way I never had before.  She was all I had wanted for so long, I couldn’t wait to immediately start trying to have another.  After a year passed and I was unable to became pregnant, I underwent invetro fertilization (IVF) and was overjoyed when I became pregnant with twins. I felt God’s love for me in this process and knew that I had made the right decision.  It was this prayerful confirmation of my decision that helped me to carry on with some of the hardest trials I have ever had to endure.
Early on in the pregnancy, I miscarried one of the twins known as, Vanishing Twin Syndrome.  I mourned this loss and felt love and comfort from many close family and friends who had also lost pregnancies.  It was reassuring to know that I was not alone in my grief.  Shortly thereafter, at my 20 week ultrasound I had been sent to a Perinatologist for an in-depth ultrasound.  I had been to her for my first pregnancy, so I felt that I had nothing to fear.  What happened in that office that day turned my life upside down.  My husband and I were told that our child had brain and spine abnormalities and was diagnosed with Spina Bifida.  
The doctor said that we could abort the pregnancy, do an experimental inutero surgery study, or wait and see.  When we came home from the doctor that day full of grief, we began to pray.  The Lord testified to me that day that we were not alone and that he was mindful of our hearts.  Minutes later, our friend unexpectedly paid us a visit.  He felt prompted to stop by and see how we were.  We will never forget that moment.
That day, I began researching as much as I could about this condition.  Our church ward held a fast for our family so that we could participate in the experimental study.  We were selected to participate in the study, but after three days of many test, we received yet more news.  Hayden’s brain had what appeared to be another abnormality that excluded us from the inutero surgery.  Again, without a doubt, we knew that it was the Lord’s will.
When we returned home, I continued to pray and rely on the Lord to guide me.  I read in  our gospel literature that when someone has an ailment or an illness and they are healed as the result of a blessing, their faith is being strengthened.  But for those who aren’t healed but continue faithful, their faith is being perfected.  The first is a faith-promoting experience.  The second is faith-perfecting.
As I reflect upon the past 2 years of work with my happy Hayden, my faith is strengthened from the many things that he has been blessed to overcome.  Seven surgeries within the first year of his life and crawling at 22 months.  While we continue to attend sometimes 6+ therapies per week, my hope is that my faith is perfecting.
Details of our families past two years can be read at www.texastriggs.blogspot.com.