September 2008

Vol 3, Issue 9

 
                       CHD Awareness Pamphlet

IMH Heart Connections

Greetings!

Every 12 minutes a child is born with Congenital Heart Disease in the United States. After you are done reading this newsletter, two new families will have been affected by Congenital Heart Disease.  By this time tomorrow, approximately 110 babies will have been diagnosed. These numbers do not include those people who are diagnosed later in life or those children who will contract a virus which will lead to heart disease.
 
This information can be overwhelming but a perfect display as to why It's My Heart must continue the Comfort Bag program. This program has grown to be in over 50 hospitals in the United States including many top cardiac hospitals. It is estimated that we provide Comfort Bags to nearly 8,000 families and there are many more hospitals ready to start the program. The bag and contents inside are valued at $40.00 and with buying in bulk we are able to cut that cost in half to $20.00 per bag. We are spending almost $200,000.00 per year to fund this program and could not do it without donations from our dedicated members. Many donations received are under $25 and provides one third of our funding. Not everyone is able to donate money but we always are needing folders, crayons, notebooks and pens, which are on sale for back to school. If you would like to donate items, please see your nearest chapter or send to our national address:
 
It's My Heart, Inc.
19728 Saums Rd.
PMB #137
Houston, TX 77084
 
With school back in session, it is the perfect time to request a Comfort Bag Drive. Corporations, churches, daycares, public and private schools are always looking for community service projects.  The Comfort Bag drive not only helps to bring support to those inside the hospital but also brings awareness to your surrounding community.  Both are two great purposes.  
 
I hope everyone had a safe and happy summer and the new school year will bring many new friends and experiences to each other and our children.

Heart Hugs,
Corrie Stassen 
Volunteer Meetings
Thursday, September 11, 2008

 

Meeting times and location vary by chapter.

 

"...no matter how big government gets, and no matter how many services it provides, it can never take the place of volunteers."

- Ronald Reagan, 40th U.S. president

 

For more information in your area, go to www.itsmyheart.org, Click on "IMH Chapters" to see specifics about upcoming events.  Make sure you sign up on line to receive e-mails from your chapter by clicking on the link at the bottom of this email.

 

As always, please be considerate about germs and take precautions if you've been around anyone who has been sick. Most of our children have compromised health.

In This Issue
Volunteer Meetings
Dr. Heart to Heart
Heart Journey
CHD Birthdays
In the Media
Donations
IMH Chapters
Donate
Join Our Mailing List!

Quote of the Month


 Happiness resides not in possessions and not in gold, the feeling of happiness dwells in the soul.

 - Democritus, (460?-370? BC)

Visit our Yahoo! Groups

Chapter Pages

 Dr. Heart to Heart 

School has started and I am a nervous wreck that the school will not take my child's heart condition seriously.   

 
Many parents struggle with the worries and stresses of their little ones being in the care of school employees.  With the added concerns for children with heart defects, it is even more important to make sure your voice is heard by the teachers, nurses, and staff at the school. 
 
There are many ways to communicate the necessary information to the school.  Some parents set a meeting with the principal and teacher before school starts, or at the preview/open house night.  You can ask your child's doctor to write a specific note outlining the condition and necessary precautions for your child.  Having something in writing, whether from the doctor or from you, will help the teacher have a better chance of processing the information.  Include with the note a heart shaped candy or candle -  something that will make the conversation or note stand out in their mind and associate your child with a heart condition.  Many schools overload the teachers and the beginning of the year is no exception for any staff member. 
 
Make sure you communicate how important and special the teacher or staff member is to the wellbeing of your child.  Everyone loves to feel appreciated and they will be more likely to give an extra careful eye to the precautions or signs of problems you outlined.
 
Follow up after the conversation and see if the teacher has any other questions.  Keeping the lines of communication open will help in case concerns came up after your initial discussion. 
 
Some children will talk about their medical history, but others may not.  If your child is open, maybe the class would like a show-n-tell about heart surgery.  Be creative and spread awareness. 
 
If you can, be involved in your child's school by volunteering.  The more you are at the school, the more the teachers get to know you and your child.   
 
Being an advocate for your child is a never ending and sometimes tiring job.  Decide each year to take on educating the new teachers with a positive attitude.

Dr. Heart to Heart would love to hear your questions, please e-mail newsletter@itsmyheat.org.
 Heart Journey - Graceful Heron
Graceful's story as told by her mother, Kristy Tompkins. 
 Graceful Heron
My husband and I were seated in the waiting room, excited to see our child's, which we affectionately called "Little Lump", image and hear a heartbeat during our comprehensive ultrasound.  We told the technician we did not want to know the sex as she began the ultrasound.  We listened to the beautiful sound of the heartbeat; the sound of a miraculous life inside my body.  It brought tears to our eyes.
 
"I'm not seeing everything I want to see in the heart," the technician states.  (It's okay, I'm staying positive.  'Lump' can tell when I am stressed or anxious.  Yoga breathing...)  After her reassurance that 90% of the time "it's nothing",  we were referred to a specialist.   We said a prayer and tried not to feel the injustice of a not-going-perfectly first pregnancy.  Initially, we felt very blessed.  McKenzie and I were married for three years and within only a month of trying to start a family, we were successful.  We never dreamed the baby might not be healthy.
 
The ultrasound at the specialist's office was horribly quiet.  The air was thick with anticipation, worry, and tension.  For 45 minutes I prayed to the Lord to keep me calm so the baby wouldn't feel any negative vibes.  (Why was it taking so long?  Why was nobody talking?)  Finally, in walked our doctor.  He proceeded to tell us that all of our hopes and dreams were shattered for a healthy baby.  All of our expectations were thrown out the window.  Everything I had been doing and avoiding to give our baby the best chance at life was worthless.  We felt like we had messed up, and big time.  We were losers before the game ever started.  It felt as though I must have done something to cause or deserve this...  Actually, the doctor said our baby had multiple complex heart defects, but all I could hear was an enormous wave push me into my husband's arms and swallow us up.  

Despite the emotional turmoil, I loved being pregnant.  After about 48 hours of contractions, my water broke at midnight on July 5th, 2006 with the sound of fireworks in the background.  It was the most exciting time of my life.  By 2:48 a.m., we were surprised and blessed with a baby girl born by c-section.  We named our daughter, Graceful Heron.  We praised the Lord that we could hold our baby shortly after delivery and that she did not need emergency surgery as expected.

The doctors were no longer able to see coarctation of the aorta.   Her other defects remained, but seemed to be working together to her benefit.  Graceful was born with double-outlet right ventricle, transposition of the great vessels, ASD, VSD, pulmonary stenosis, and an under-developed left ventricle.  Fortunately, we did not see any of those medical problems.  We saw an amazingly beautiful miracle baby and fell instantly hopelessly in love!  

Within a week, we were able to take Graceful home once her eating improved.  We were told to keep track of how much she was eating since her weight gain was of such importance. The doctors wanted her as big as possible before any surgery was performed.  We were offering Graceful milk at the slightest hint she may be hungry.  Sometimes it seemed that was all we did.  A quarter ounce here, half an ounce there; we celebrated when she drank two ounces.  

After the follow-up appointment with her cardiologist, we were told Graceful's oxygen level was too low and she needed surgery that week.  A few days later, in the narrow, empty hallway of the hospital basement, we handed the love of our lives over to a stranger who would be preparing her for surgery.  At 23 days old, Graceful had a thoracotomy. The doctors performed an atrial septostomy and placed a BT shunt; just palliative fixes until she was strong enough for the complete repair.   

Five days later, we took our baby home and tried to organize some kind of routine existence for our family.  Her oxygen level was still just in the high seventies to low eighties, so we were told not to let her cry for more than 5 minutes.  We could handle that.  We were so in love and in awe of our little blessing, we would do anything for her.  

I was searching for a book on congenital heart defects at the library when I came across a novel about an author's experience shadowing an elite pediatric cardiac surgeon.  My husband and I could not put it down.  We were bawling as we read, but it all hit home.  That is when we decided to contact Texas Children's Hospital and get Dr. Charles Fraser to do Graceful's upcoming "big" surgery.  He is one of the best pediatric cardiac surgeons in the country, if not the world.  We wanted our daughter to have the best chance for survival.  We would make it happen, no question.  

Dr. Fraser accepted Graceful's case and the adventure began.  We scoured the internet and asked everyone we knew for ideas on how to get to Houston without completely going into financial ruin.  It took much perseverance and motivation on our part, but the Lord paved our path. With donated plane tickets, Ronald McDonald House for housing, and a church at home backing us up with prayers and financial assistance for bills, we were on our way.  

November 5th, Graceful turned 16 months old, met Dr. Fraser for the first time, and took her first unassisted steps back and forth through our room at the Ronald McDonald House.  Three days later she endured her open-heart surgery, a modified REV procedure.  Dr. Fraser used a bovine conduit to connect her right ventricle to her pulmonary artery and patched Graceful's large VSD with her own pericardial tissue.  

McKenzie and I meditated on Isaiah 42:16 during the 12 hour surgery.  Our heads spun around each time anyone entered the waiting area, hoping it would be the nurse with an update for us.  When we finally got to sit down with Dr. Fraser, I don't think either of us was breathing.  "Surgery went well.. Graceful in on her way to the ICU... It was a difficult surgery due to the placement of..."  Dr. Fraser went on to explain the procedure to us.  I felt immense gratitude, respect, admiration, and awe for this amazing man of God who held my daughter's future in his earthly hands and gave her a chance for a near-normal life. 

Graceful successfully battled a high fever after surgery and overcame acute renal failure.  She had a few appointments after discharge from Texas Children's Hospital to monitor fluid build-up around her heart.  Our family felt very blessed with a relatively uneventful recovery.  We saw and heard of families that were not as fortunate.  

We were able to fly home to Oregon exactly one month after arriving in Texas.  The changes we saw in our daughter were dramatic.  She left Portland still a baby and came home a little girl.  We are amazed by Graceful daily.  To describe her energy level now, we often use the term 'crazy monkey'.  Her appetite is that of a heart-healthy toddler.  Graceful will need more surgery as her body grows, but for now we are celebrating life as a family.  She loves the outdoors, swinging, reading and hiking.  Graceful told us she wanted to climb mountains like her daddy who climbed Mt. Hood for her.  As we try to teach her about the world, Graceful shows us how to feel and truly exist in it.  

Do you have a heart journey to share?  E-mail newsletter@itsmyheart.org for more details.
CHD Birthdays
 Ajay Greenwood 
 Alexandra Mosby
 September 26, 2001
  
 

Please send us your child's birthday and picture so we can all celebrate your child's birth!

 

We also want to celebrate all our angels birthday's too! So, please send us their information so we can include them as well! E-mail to

newsletter@itsmyheart.org.
In the Media
 
An ACHA (Adult Congenital Heart Association) Member will be on Lifetime Television on the show "How to Look Good Naked".  During the second season finale, Heather Magee will be featured.  Heather was born with a congenital heart defect that has had surgeries from the age of 7 months until recently, at age 38.  She had been told for most of her life to expect death, but she has now, since her last surgery, been given hope of a lengthy future.
 
September 9, 2008 at 10:00 p.m. EST (check your local listing to verify time and channel)
Donations

In Honor of Melena Abeita. This donation is a birthday present to Melena's mom, Rosie Abeita, from Jesse & Cindy Ramirez.

Donations "In Honor Of", "Memory Of", in recognition of a birthday, anniversary or "Just Because" can be made to It's My Heart. Not only will your donation go towards helping those affected by CHD, but also let someone special know you are thinking of them in a very special way.  All donations are tax deductible.  Your donation will further the work of spreading awareness of CHDs, fund programs such as the Comfort Bags and Care Packages to the hospitals, etc.

It's My Heart Chapters

It's My Heart is dedicated to our mission which is to provide support, spread awareness, educate and advocate for those affected by Congenital Heart Defects by creating alliances with fellow families, hospitals, support groups, and the community. Creating chapters of IMH throughout the country is imperative to our ability in achieving our mission.

 

The objective of chapter development advances our opportunity to increase awareness, support and thereby advocate for those affected by CHD.

 
If you are interested in organizing a chapter or becoming a Regional Coordinator in your area, please contact the It's My Heart National Office at (281) 578.7343 or (888) HEART.07 or e-mail
chapters@itsmyheart.org.
It's My Heart, Inc.