|
|
|
|
|
|
Chapter Spotlight: South Florida
|
| Letter from the South Florida Chapter President: |
My motive to get involved with It's My Heart was my daughter Paula, my precious two year old, who was born with Hypoplastic Left Heart Syndrome. Seeing her undergo two open heart surgeries by the time she was three months old, changed my life perspective completely. One of the greatest things that this experience left in my heart was a need to pour out myself to others. I realized that I could let others know that they are not alone and that I had been right there in their shoes. It almost feels that God gave me a to-do list.
The South Florida chapter has only been official for three months. In this short period of time, we have been able to see the impact in our community. We have three cardiac hospitals in our area. We are already working with two of them: Joe
Di Maggio and Miami Children's Hospital. This means that we will be providing them with approximately 460 comfort bags this year, reaching out to all these families in our area. We have our monthly support/volunteers meeting the last Thursday of every month. We are also organizing our first walk for February 2011, one huge fundraiser event for the Summer and a couple of other events before the end of the year. We are already building a very strong network, influencing people as we go telling our stories. It is amazing to find so many people that do not know that heart defects are the number one birth defect, but it also feels good to see that because of us they are now aware of this fact. We have so much to do to spread awareness. We know that awareness equals funding, which equals research, support and resources.
Our expectations are high. In such a short time of establishing this chapter, we have seen how our cause touches hearts and opens doors everywhere we go. Both of the hospitals that we are supporting were thrilled to start implementing our programs. We have a large geographical area to cover that goes from Greater Miami, Broward to the Palm Beaches. We need to add more officers and recruit more volunteers in order to reach our plans for this year. We hope to meet more people that are willing to recognize the need to support congenital heart defects.
Heart hugs,
Urquisa Fernandez
President
It's My Heart South Florida Chapter
South Florida Officers' Meeting |
| National CHD Family Conference & Teen Summit 2010 |
|
It's My Heart's 2nd National CHD Family Conference
June 4 - 6, 2010

A Conference for Adults and Children 5 years and up
- A Teen Summit to address the needs of teenagers living with CHD
- Meet Families Friday night at the Meet & Greet
- Learn about important CHD topics on Saturday at the conference while the children enjoy their own conference activities
- Family Fun Day on Sunday at the Houston Children's Museum
To register go to www.itsmyheart.org
Conference Fee: 13 years and up--$35.00
Children ages 5 to 12 attend for free
NO CHILDREN UNDER 5 PLEASE
Sponsors:
Texas Children's Hospital, Whitney Bank, &
BMC Software | |
 |
|
Quote of the Month |
A kind heart is a fountain of gladness, making everything in its vicinity freshen into smiles.
Washington Irving
|
National Officers & Official Volunteers
|
Corrie Stassen Executive Director
Katy Wolff Vice President
Lauren Simpson Secretary
Alexis Durham Treasurer
Anissa Speight Medical Advisory Board Coordinator
Laurie Hutchings Family Matching Director
Ann Martin Literature Distribution
Ashley Auzenne Project Development
Gail Brasser Project Seamstress
Pamela Floyd Conference Chair
Allison Johnston Newsletter Co-Editor
Amy McCathran Newsletter Co-Editor
Heather Vinson Financial Director
Kate Shamszad Child Life Specialist
Jill Vantine Transition Coordinator
Cailey Fitzgerald We Got Heart Chair
Tiffany Galligan Marketing
Ty McCathran Legislative Liaison
Robyn Steinberg Web Administrator
Tim Hutchings Web Admin Assistant & Graphics
Kim Shadek Chapter Liaison
Pamela Camit Chapter Liaison
|
Follow Us on the Web
|

|
Support It's My Heart
|

 | |
|
| Heart Journey |
This is the heart story or Domenic Joseph Deets as told by his mother Raina Lonardo

When I was 16 weeks pregnant, I went in for my second sonogram. That day I received a phone call from my doctor after hours. When I heard it was my doctor on the phone, I froze, as we all know that an after hours phone call from a doctor is not a good one. She informed me that on the sonogram there was an abnormality in my baby's heart. After more tests, we found out that the baby's pulmonary valve was stuck closed. Fortunately, the valve had been opened at one point because if the valve had never been opened, my son's heart would not have had a right ventricle. As it was, the right ventricle was developed, but it was smaller than average. This condition is called pulmonary atresia.
Domenic was born at Brigham and Woman's Hospital so that the doctors could then take him right over to Children's Hospital Boston. When he was born he was 7 pounds 12 ounces. He was and still is a big boy!
When a child is born, there is a ductus in the heart that starts to close. Domenic had to have a medicine called prostaglandin so that ductus would stay open. A side effect of that medicine for Domenic was that it make him stop breathing! So, at a day old, Domenic was taken to the cath lab for a heart cath to dilate his pulmonary valve. After two weeks and several oxygen saturation problems, Domenic had heart surgery. The doctors put in a BT shunt to reroute the blood flow and surgically close the ductus. The shunt is allowing Domenic's right ventricle to rest so hopefully it will grow to its correct size. If the right ventricle does not grow larger, he will require a few more surgeries.
My son is now 13 months old and weighs 24 pounds! The doctors are shocked at how big he is. Some babies with his condition have feeding issues and have to have a feeding tube for a long time. Domenic has had some developmental delays with sitting up, crawling, and walking. He has been few months behind the average baby reaching these milestones. Right now at 13 months he is not walking yet, but Early Intervention works with him twice a month to help him reach these milestones.
Recently, Domenic was hospitalized for another heart cath. The doctors saw that his right ventricle did grow, but not as large as they wanted. The next step is to have anther surgery which will be a double ventricle repair. The surgeon will stretch the right ventricle to its correct size, and also repair the left ventricle which had been overworked. Right now, I test his oxygen levels twice a day. His numbers will tell the doctors when the next surgery is needed.
I was told that Domenic will always have a CHD, but that this next surgery will hopefully be his last one. My son Domenic is the highlight of my life. I have two older children who are heart healthy. We have no idea why Domenic developed this CHD, but I would not trade my son for anything.
|
| Houston Zoo Day |
|
|

|
Enjoy a day at the Houston Zoo with
It's My Heart!
Saturday, May 8, 2010 Ticket pickup at the front gate at 9:00 a.m. Picnic lunch at the reflections pool at 11:30 a.m.
Tickets are free, but please register online: http://itsmyheart.kintera.org/houstonzoo | | |
| Fort Worth Fun Walk-Run |
 |
Fort Worth Chapter Family Fun Walk-Run May 1, 2010 at Northwood University
It's My Heart Fort Worth is hosting our first annual CHD Awareness Run/Walk on Saturday, May 1, 2010 at Northwood University in Cedar Hill, Texas. All proceeds benefit It's My Heart mission to provide support, spread awareness, educate and advocate those affected by Congenital Heart Defects by creating alliances with fellow families, hospitals, support groups and community. Register Online Now! | |
|
Read all about it! CHDs in the NEWS |
| Key mechanism that guides cells to form heart tissue identified
Washington, DC: A key cellular mechanism that guides embryonic heart tissue formation-a process which, if disrupted, can lead to a number of common congenital heart defects - has been identified by scientists at the Keck School of Medicine of the University of Southern California (USC).
Heart tissue forms in two distinct phases known as the First Heart Field, which includes the left ventricle and portions of both atrial chambers, and the Second Heart Field (SHF), which consists of the right ventricle and outflow tract. In humans, the process occurs within the fourth week of development. Using animal models, Keck School of Medicine researchers found that retinoic acid (RA), a derivative of vitamin A, regulates the SHF tissue formation and the septation, or division, of the outflow tract into the ascending aorta and the pulmonary artery.
"This study provides us with a much deeper understanding of the biology of second heart field development," said principal investigator Henry Sucov, Ph.D., associate professor of Cell and Neurobiology at the Keck School of Medicine and a researcher at the Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC. "We now know that vitamin A is a critical regulator of this process, and too much or too little RA can lead to common congenital defects."
RA is a signaling molecule that causes progenitor cells (cells that have the capacity to differentiate into many different kinds of cells) to take the first step towards differentiating into heart tissue. Using specific molecular markers, researchers were able to observe the process by which the cells moved to the outflow tract and began to form essential heart tissue.
The process of moving cells to form the outflow tract is similar to a conveyer belt, Sucov explained. However, in animal models that were mutated to have an RA receptor deficiency, the entire process was halted, resulting in an outflow tract that was shortened and misaligned.
When development of the SHF is compromised, alignment defects such as double outlet right ventricle (DORV; the aorta and pulmonary trunk both exit from the right ventricle) or overriding aorta (when the aorta straddles the interventricular septum) occur. Problems in SHF development can also compromise the septation process resulting in a single outflow vessel - a condition known as persistent truncus arteriosus. These malformations occur commonly in human infants.
"This exciting research shows how retinoic acid, a vitamin A derivative, acts to guide cells in the embryo to form parts of the heart and the major blood vessels that emerge from it," said Martin Pera, PhD, director of the Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research at USC. "Defects in this developmental pathway can result in serious congenital malformations of the heart in the fetus and newborns, that may be fatal if not corrected surgically."
A link to this article as well as many other articles on CHDs can be found on the It's My Heart Facebook page. Become a fan today! |
| CHD Birthdays |
Hunter Vinson Hailee Victoria Fountain Abigail Rorick March 21, 2004 April 5, 2007 April 9, 2009
April 15, 2007 April 23, 2008 April 27, 2004
Is your child born in May? Please send us your child's birthday and picture so we can all celebrate your child's birth with you!
We also want to celebrate all your angels birthday's too! So, please send us their information so we can include them as well! E-mail to newsletter@itsmyheart.org. |
| Family Matching |
How do I cope with all of the procedures and hospital stays my child endures?
Are there any other children out there with the same diagnosis as my child? How are they doing following their surgery?
Who can I talk to that has had a similar experience?
If you have these questions and more, our Family Matching Program may be able to help you. We can "match" you with another family with the same CHD .We have more adults signing up for family matching each month .If you are an adult with congenital heart disease please consider signing up for Family Matching. You are a true inspiration for families.
|
| Donations |
Recurring monthly donations from:*Beth Jacobson One time donations from:
Karia Colon Laureano in honor of Daelyn Giovanni Cain
Stacey Klostermann, Pete Plum, Tim Smith, Lynn Hatter in
Memory of Colin Kain
Byron Oujesky in support of the cause
Sarah Dioguardi for Tudor Investment Corporation as a
matching
gift donation for Barbara Vasil
Michelle Bellitto in memory of Parker Seuffert from the
Freshman Academy!
Amanda Winter in honor of our niece Fiona Grace Myers
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.
|
| Someone loves IMH! |
|
"I'm excited to find such a group! My son, Joseph, is 19 months old. He was born with an ASD. He had surgery in October and is doing great!
|
|
It's My Heart Chapters |
|
The mission of It's My Heart provides strength and support for those affected by Heart Defects. It's My Heart exists to provide support to and advocating for those affected by Acquired and Congenital Heart Defects. Through awareness, resources and education, It's My Heart creates alliances and networks among families, groups, hospitals, and the community.
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 walk in your area, please contact the It's My Heart National Office at (713) 334.4244 or (888) HEART.07 or e-mail chapters@itsmyheart.org.
Click here to find the IMH Chapter nearest you:
Fresno, California
South Florida
Michigan (Michiana Chapter) Northern New Jersey Cleveland, Ohio Columbus, Ohio Portland, Oregon
Fort Worth, Texas Houston, Texas
Seattle, Washington
| |
|
|
|
|