Tuesday, February 8, 2011

Last night we attended the city meeting at Belle Plaine Minnesota, we recieved a signed proclamation making FEB 7th-14th CHD Awareness week.
We were asked if we would introduce ourselves & Cameron and then to briefly describe what it's like to be a CHD family.

Being A family with a son who was born with a severe congenital heart defect is scary, it's nerve wracking not knowing what tomorrow is gonna bring, it's always busy with Cardiologist appointments, physical therapy pediatrician appointments, Home nurse visits once a month to give Cameron his RSV shot, it's living in a "bubble" because you are always worrying about exposing him to germs and illness that could land him in the hospital. It's getting up in the middle of the night to make sure he's still breathing, it's daily meds to keep his blood pressure at a normal limit, it's daily baby asprin to keep his blood from clotting, It's struggles to get him to eat good enough that he gains a good amount of weight.
Every day has it's challanges but everyday Cameron accomplishes something wonderful.
&
Everyday We count our blessings that Cameron is a part of our lives.
&
that is what it's like to have a son with a congenital heart defect.


We were also asked to talk about The CHD Facts and we did, we watched the council memebrs mouths drop open and we watched their silent reaction as we told them that there is no cure for CHDs,
WE also touched on how many CHDers we knew through facebook & through the U of M Amplatz, we also told the council members about all the CHD Angels that lost their battle with their congenital heart defects.
All in All it was a nice evening at the city meeting & it felt good to help raise CHD Awareness!
(We have another proclamation signing Wednesday evenening in Henderson MN)


Monday, February 7, 2011

DO YOU KNOW YOUR CHD FACTS?

Today Is one of those days, where I find myself not doing much of anything. I am constantly watching Cameron. Tonight we go to the City of Belle Plaines monthly meeting,
 And Tonight the Belle Plaine mayor will be signing a proclamation making this week CHD Awareness week.
I'm pretty sure I will have a tear or two in my eyes as he gives me a copy of the proclamation. My family doesn't understand the importance of a proclamation making Feb 7th-14th CHD Awareness Week. My husband & I try to explain it to them, but honestly if you aren't living a CHD life then you probably won't understand.

To Me CHD Awareness week means just that spreading awareness about the importance of Congenital Heart Defects. If we spread enough awareness just maybe someday there will be enough funds to help with CONgenital Heart Defect Research. Someday we could have some answers as to what causes CHDs or breakthrough technology.
Every year it seems like they come up with some new technique to help our kids and their special hearts. Someday they will be able to grow a heart from stem cells (that's what one of the Cardiologist told us at one of Cameron's appointments) And then maybe a baby or child will be able to have a heart transplant without waiting so long for one and then they will get a transplant before it's to late.
But without CHD Awareness none of this will be possible.

Another reason CHD AWARENESS is important is because, before I had Cameron i never thought about the possibilty of having a baby with a heart defect. I didn't think it would happen to us,but it did.
Cameron is now 1 in 100! And now we are on a new journey in life, we are now a heart family!
 If we didn't know anything about heart defects in newborns, then I am pretty positive that other first time or even other parents who already have healthy kids don't know about congenital heart defects.

So many times I have had people comeup to me and ask if We are hoping for a boy or girl, I would always reply.. "it doesn't matter to us as long as it has 10 fingers & 10 toes" never once did I think or say it doesn't matter as long as the baby has a whole functioning heart, and i'm pretty sure that other people have said the same thing about as long as it has 10 fingers/10 toes.
 So YES we need to get CHD awareness out their to expecting parents! As soon as I hear about one of my friends or family members expecting, I nicely tell them about Congenital Heart Defects and some of the facts.
 Sometimes the expecting parents are happy to listen other times they think I'm trying to scare them, I'm never trying to scare them..I just want them to have their eyes open...don't worry about the little things and have your mind open to the fact that  Anyone can give birth to a baby with a heart defect.
Doesn't matter if your white, black, Purple with dots... IT CAN HAPPEN TO ANYONE!!!

Here are some CONGENITAL HEART DEFECT FACTS:

♥ Congenital Heart Defects are the #1 birth defect (Source: March of Dimes)
♥ Congenital Heart Defects are the #1 cause of birth defect related deaths (Source: March of Dimes)
♥ About 1 out of every 100 babies are born each year with some type of CHD (approx 40,000/year) (Source: Children's heart Foundation)
♥ Nearly twice as many chilren die from Congenital Heart Defects in the USA each year as from all forms of childhood cancers combined, yet funding for pediatric cancer research is 5 times higher then funding for CHD. (Source: Children's Heart Foundation)
♥ This year approx 4,000 babies will not live to see their first birthday because of Congenital Heart Defects (source: Children's Heart Foundation)
♥ The cost of  inpatient surgery to repair CHDs exceeds over $2.2 billion a year (Source: Children's Heart Foundation)
♥ Of every dollar the government spends on medical funding ONLY a fraction of a penny is directed towards  Congenital Heart Defect research (Source: Children's Heart Foundation)
♥Though research is ongoing, at least 35 Heart defects have now been identified.
♥ 4-8% born with CHD have Hypoplastic Left Heart Syndrome
♥ 4-10% born withCHD Have Atrioventriclar Septal Defects
♥ 8-11% born with CHD have Coarctation of the Aorta
♥ 9-14% born with CHD have Tetralogy of Fallot
♥10-11% born with CHD have Transposition of the great Arteries
♥14-16% born with CHD have Ventricu;ar Septal Defects
♥ Although some babies will be diagnosed during gestation or at birth, sometimes the diagnosos is not made until days, weeks, monthd or even years after. In some cases, CHD is not detected until adolescence or adulthood. (Source: March of Dimes)
♥ It is a proven fact that the earlier CHD is detected and treated, it is more likely the affected child will survive and have less long term health complications (Source: March of Dimes)

Cameron is the reason I feel the need to help raise awareness to such a ugly CHD...
♥ Cameron after his 1st OHS Hybrid ♥

♥ Cameron's shirt says it all, CHD WARRIOR ♥
 EVERYTHING I DO I DO FOR CAMERON, he is my inspiration during this.
                         ♥♥♥I LOVE YOU CAMERON CHASE! ♥♥♥

Wednesday, February 2, 2011

CHD AWARENESS MONTH

For the last couple weeks i have been thinking non stop about what I want to say at the proclamation signings that I was invited to from the city of Henderson & the City of Belle Plaine.
 Both Mayors contacted me and said they would be honored to sign the proclamatin making Feb 7th-14th 2011 Congenital Heart Defect Awareness Week. They both asked me to go in front of the city officials and the public that will be at the meetings and introduce my family & most importantly tell them why "heart day" is important to me and then to give some CHD/HLHS facts.
  I am beyond nervous, i have never been great with speaking to a room full of people, i have never been great with looking at people in the eye. What if I sound dumb, what if  they ask me a question and I don't have the best answer?
 My mom who knows how nervous I am, says "Shawna, you just gotta speak from your heart, don't be nervous, you're doing it for Cameron & all families affected by Congenital Heart Defects"
And as always my mom is right, I just gotta get over my fear of speaking in public and shout out the importance of CHD Awareness week!

Here are some CHD questions & answers (provided by March of Dimes)

Congenital heart defects

About 35,000 infants (1 out of every 125) are born with heart defects each year in the United States (1). The defect may be so slight that the baby appears healthy for many years after birth, or so severe that his life is in immediate danger.


Heart defects are among the most common birth defects and are the leading cause of birth defect-related deaths (2). However, advances in diagnosis and surgical treatment have led to dramatic increases in survival for children with serious heart defects. In the United States, about 1.4 million children and adults live with congenital heart defects today (3). Almost all are able to lead active, productive lives (1).


What is a congenital heart defect? A congenital heart defect is an abnormality in any part of the heart that is present at birth. Heart defects originate in the early weeks of pregnancy when the heart is forming.


How does the heart work? The heart is a muscle that pumps blood to the body. It is divided into four hollow parts called chambers. Two chambers are located on the right side of the heart, and two are on the left. Within the heart are four valves (one-way openings) that let the blood go forward and keep it from going back. Blood goes from the heart to the lungs where it picks up oxygen. From the lungs, the blood carrying oxygen, which appears bright red, goes back to the heart. The heart then pumps the oxygen-rich blood through the body by way of arteries. As the oxygen is used up by the body's tissues and organs, the blood becomes dark and returns by way of veins to the heart, where the process starts over again.


How do heart defects affect a child? Some babies and children with heart defects experience no symptoms. The heart defect may be diagnosed if the health care provider hears an abnormal sound, called a murmur. Children with normal hearts also can have heart murmurs, called innocent or functional murmurs. A provider may suggest tests to rule out a heart defect.


Certain heart defects can cause congestive heart failure.
In this condition, the heart can’t pump adequate blood to the lungs or other parts of the body. It can lead to fluid build-up in the heart, lungs and other parts of the body. An affected child may experience a rapid heartbeat and breathing difficulties, especially during exercise. Infants may experience these difficulties during feeding, sometimes resulting in poor weight gain. Affected infants and children also may have swelling of the legs or abdomen or around the eyes.


Some heart defects result in a pale grayish or bluish coloring of the skin called cyanosis. This usually appears soon after birth or during infancy and should be evaluated immediately by a health care provider. On occasion, cyanosis may be delayed until later in childhood. Cyanosis is a sign of defects that prevent the blood from getting enough oxygen. Children with cyanosis may tire easily. Symptoms, such as shortness of breath and fainting, often worsen when the child exerts himself. Some youngsters may squat frequently to ease their shortness of breath.


What tests are used to diagnose heart defects? Babies and children who are suspected of having a heart defect are usually referred to a pediatric cardiologist (children’s heart disease specialist). This doctor can do a physical examination and often recommends one or more of the following tests:
  • Chest X-ray
  • Electrocardiogram, a test that records heart rate patterns
  • Echocardiogram, a special form of ultrasound that uses sound waves to take pictures of the heart
All of these tests are painless and noninvasive (nothing enters the child’s body). Some children with heart disease also may need to undergo a procedure called cardiac catheterization. In this procedure, a thin, flexible tube is inserted into the heart after the child is given medications to make him sleepy. This test provides detailed information about the heart and how it is working.


What causes congenital heart defects?
In most cases, scientists do not know what makes a baby's heart develop abnormally. Genetic and environmental factors appear to play roles.


Scientists are making progress in understanding the genetics of heart defects. Since the 1990s, they have identified about 10 gene mutations (changes) that can cause isolated (not accompanied by other birth defects) heart defects (3). For example, a March of Dimes grantee identified a gene that can cause a heart defect called an atrial septal defect (a hole between the upper chambers of the heart), and one that may contribute to hypoplastic left heart syndrome (underdevelopment of the heart’s main pumping chamber) (4, 5).


Environmental factors can contribute to congenital heart defects. Women who contract rubella (German measles) during the first three months of pregnancy have a high risk of having a baby with a heart defect. Other viral infections, such as the flu, also may contribute, as may exposure to certain industrial chemicals (solvents) (2). Some studies suggest that drinking alcohol or using cocaine in pregnancy may increase the risk of heart defects (2).


Certain medications increase the risk. These include (2):
  • The acne medication isotretinoin (Accutane and other brand names)
  • Thalidomide (approved only for a rare, severe skin disorder, but sometimes used for other conditions)
  • Certain anti-seizure medications
Some studies suggest that first-trimester use of trimethoprim-sulfonamide (a combination of antibiotics sometimes used to treat urinary-tract infections) may increase the risk of heart defects (2).


Certain chronic illnesses in the mother, such as diabetes, may contribute to heart defects (2). However, women with diabetes can reduce their risk by making sure their blood sugar levels are well controlled before becoming pregnant.


Heart defects can be part of a wider pattern of birth defects. For example, at least 30 percent of children with chromosomal abnormalities, such as Down syndrome (mental retardation and physical birth defects) and Turner syndrome (short stature and lack of sexual development), have heart defects (3). Children with Down syndrome, Turner syndrome and certain other chromosomal abnormalities should be routinely evaluated for heart defects.


Heart defects also are common in children with a variety of inherited disorders, including Noonan syndrome (short stature, learning disabilities), velocardiofacial syndrome (craniofacial defects and immune deficiencies), Holt-Oram syndrome (limb defects) and Alagille syndrome (liver, skeletal and eye defects) (3).


What are some of the most common heart defects, and how are they treated?
  • Patent ductus arteriosus (PDA): Before birth, a large artery (ductus arteriosus) lets the blood bypass the lungs because the fetus gets its oxygen through the placenta. The ductus normally closes soon after birth so that blood can travel to the lungs and pick up oxygen. If it doesn’t close, the baby may develop heart failure. This problem occurs most frequently in premature babies. Treatment with medicine during the early days of life often can close the ductus. If that doesn't work, surgery is needed.
  • Septal defect: This is a hole in the wall (septum) that divides the right and left sides of the heart. A hole in the wall between the heart’s two upper chambers is called an atrial septal defect, while a hole between the lower chambers is called a ventricular septal defect. These defects can cause the blood to circulate improperly, so the heart has to work harder. Some atrial septal defects can be repaired without surgery by inserting a thin, flexible tube into the heart and then releasing a device that plugs the hole. A surgeon also can close an atrial or ventricular septal defect by sewing or patching the hole. Small holes may heal by themselves or not need repair at all.
  • Coarctation of the aorta: Part of the aorta, the large artery that sends blood from the heart to the rest of the body, may be too narrow for the blood to flow evenly. A surgeon can cut away the narrow part and sew the open ends together, replace the constricted section with man-made material, or patch it with part of a blood vessel taken from elsewhere in the body. Sometimes, this narrowed area can be widened by inflating a balloon on the tip of a catheter (tube) inserted through an artery.
  • Heart valve abnormalities: Some babies are born with heart valves that do not close normally or are narrowed or blocked, so blood can’t flow smoothly. Surgeons usually can repair the valves or replace them with man-made ones. Balloons on catheters also are frequently used to fix faulty valves.
  • Tetralogy of Fallot: This combination of four heart defects keeps some blood from getting to the lungs. As a result, the blood that is pumped to the body may not have enough oxygen. Affected babies have episodes of cyanosis and may grow poorly. This defect is usually surgically repaired in the early months of life.
  • Transposition of the great arteries: Transposition occurs when the positions of the two major arteries leaving the heart are reversed, so that each arises from the wrong pumping chamber. Affected newborns suffer from severe cyanosis due to a lack of oxygen in the blood. Recent surgical advances make it possible to correct this serious defect in the newborn period.
  • Hypoplastic left heart syndrome: This combination of defects results in a left ventricle (the heart’s main pumping chamber) that is too small to support life. Without treatment, this defect is usually fatal in the first few weeks of life. However, over the last 25 years, survival rates have dramatically improved with new surgical procedures and, less frequently, heart transplants (6).
At what age do children have surgery to repair heart defects? Many children who require surgical repair of heart defects now undergo surgery in the first months of life. Until recently, it was often necessary to make temporary repairs and postpone corrective surgery until later in childhood. Now, early corrective surgery often prevents development of additional complications and allows the child to live a normal life.


Following surgery, children should have periodic heart checkups with a cardiologist. Children and adults with certain heart defects, even after surgical repair, remain at increased risk of infection involving the heart and its valves. Parents of children with heart defects and adults with repaired heart defects should discuss with their provider whether they need to take antibiotics before dental visits and other procedures to prevent these infections. Antibiotic treatment is recommended only for those considered at highest risk for infection, including those with man-made heart valves (7).


Is there a prenatal test for congenital heart defects? Echocardiography can be used before birth to accurately identify many heart defects. If this test shows that a fetus’s heart is beating too fast or too slowly (called an arrhythmia), the mother can be treated with medications that may restore a normal heart rhythm in the fetus. This treatment often prevents fetal heart failure. In other cases, where the heart defect can't be treated before birth, parents and providers can plan the delivery so that the baby can receive necessary evaluation and treatment soon after birth.


Can congenital heart defects be prevented? Most congenital heart defects cannot be prevented. However, there are some steps a woman can take before and during pregnancy that may help reduce the risk of having a baby with a heart defect:
  • Take a multivitamin containing 400 micrograms of folic acid daily, starting before pregnancy. This helps to prevent serious birth defects of the brain and spinal cord and may also help prevent heart defects.
  • Go for a preconception visit with her health care provider. At this visit, a woman should be tested for immunity to rubella and be vaccinated if she is not immune. Women with chronic health conditions, such as diabetes and phenylketonuria (PKU), should discuss adjusting their medications and/or eating habits to keep these conditions under control before and during pregnancy.
  • Discuss all medications with their provider, even over-the-counter or herbal medicines.
  • Avoid people who have the flu or other illnesses with fever.
  • Avoid exposure to organic solvents, used in products such as paints, varnishes and degreasing/cleaning agents.
Are heart defects likely to recur in another pregnancy?
Parents who have already had a child with a heart defect do have an increased risk of having other affected children, often with the same heart defect. In many cases, the risk is low. Some heart defects have about a 2 to 3 percent chance of happening again (8). However, the risk may differ, depending on the specific heart defect. If a child’s heart defect is part of a syndrome of other birth defects, the recurrence risk in another pregnancy may be much higher.


Parents who have had a child with a heart defect should consult their pediatric cardiologist and can consult a genetic counselor to find out the risks to any future children. Parents who themselves have a heart defect also are at increased risk of having an affected child and should consider consulting a genetic counselor.


Is pregnancy safe for women with heart defects? Many women with congenital heart defects can safely become pregnant and have healthy babies. However, women with congenital heart defects always should check with their cardiologist before they become pregnant. Pregnancy can be risky for women with certain types of heart disease (including those with poorly functioning ventricles or high blood pressure in the lungs) (9).


In some cases, the mother’s heart disease or the medications she takes to treat it can affect the fetus, causing poor growth, premature delivery or other problems (9). Some women with heart disease may need careful monitoring by a high-risk obstetrician, as well as their cardiologist, throughout pregnancy.


Does the March of Dimes support research on congenital heart defects? A number of scientists funded by the March of Dimes are studying genes that may underlie specific heart defects or seeking to identify new genes that may cause heart defects. The goal of this research is to better understand the causes of congenital heart defects, in order to develop ways to prevent them. Grantees also are looking at how environmental factors (such as a form of vitamin A called retinoic acid) may contribute to congenital heart defects. One grantee is seeking to understand why some babies with serious heart defects develop brain injuries, in order to learn how to prevent and treat them.