Tuesday, February 23, 2010

Walk, Lindsay Bear Baskets, Update On Aunt Jeanne

Jon, Tanner, Case and I as well as 20 other family and friends are once again walking in memory of Lindsay on June 13, 2010 for NSTAR'S walk for Children's Hosptial Boston. As most of you know we were hoping to do this last year but Case decided to come into the world the day before. The rest of the team went and walked but Jon and I stayed behind and got to know Case. So this year we will be there and we are so excited about it. In order for us to do this we need to raise some money. If you are interested in sponsoring one of us here is the links to our pages. Tanner gets to raise money this year and he is very excited about it.

We are once again starting to collect things for the Lindsay Bear Baskets. My mom, mother in law, my sister, and I got some awesome deals on Valentine's bears for the baskets this past week. We have enough for this round and a start for the next round. If you are interested in helping again please email me at jonnlaura@hotmail.com. We will be putting them together sometime in May with my MOPS group.
My Aunt Jeanne is doing great. She was in the hospital with some blood clots in her leg and arms. They got them under control and she is back home and back to work. The biggest new this week is that her blood test results from the chemo are down to 47 from 937 :). They want them to be at 21 so she can have her surgery. We are all praising the Lord that the numbers are dropping. Please continue to pray for her. I know she appreciates all the prayers she can get.
Thanks again for your continued prayers for our family. Lindsay still lives in all of us and we love and miss her all the time. Case is starting to look like her more and more each day.

We love you all!!!

Thursday, February 11, 2010

CHD Awareness Week

This week marks CHD week. CHD stands for Congenital Heart Defect. I thought some of you would be interested in some information about this and can some how raise more awareness for it.

~ CHDs are the #1 birth defect and the #1 cause of infant death related to birth defects. 1 in every 100 babies born will have a CHD (1 in every 800-1000 babies born has Down Syndrome).

~ 1 in 10 of those born with a CHD will have a fatal defect.

~ In the US there are nearly twice as many deaths due to CHDs than that of all forms of childhood cancers combined. Yet there is 5 times more research for pediatric cancer than for CHDs.

~ The cost of inpatient surgery alone for CHDs exceeds 2.2 billion dollars per year.

~ There are approximately 35 known Congenital Heart Defects.

~ Causes for CHDs are still being studied. While there is no known definitive cause, it is said that both genetics and environmental factors can play a role. Scientists have actually identified over 100 mutations that are directly linked to the heart.

~There is no known cure for CHDs. However, the mortality rate after surgery has significantly decreased in the past 20-30 years. On average it is about 5% compared to the 30% it was. At the same time, the rate of incidence of CHDs has remained unchanged.

~ With advances in medicine, many of those born with a CHD will have their first and sometimes only corrective surgery before age 2.

~ Many of those living with a CHD go on to lead normal to near normal lives. Those with complex CHDs will also go on to lead longer and more active lives than before. Most will have some physical limitations, but almost all learn to move pass them.

~ Only about 30% of the children who need a heart transplant receive one in time.

~ About 40,000 units of blood are used every day yet only about 5% of the adults, the only ones who are eligible to donate blood, do so. Someone needs blood every three seconds in the United States; that someone is often one of our heart children.

~ Education is the first step in helping these children live happier, healthier lives!

In honor of this week my very good friend Jessica Twigg who also lost her little boy Ethin is having a basketball game on February 16, 2010 in Newaygo, MI to raise awareness as well as funds to help with CHD research. She asked me to send her a picture of Lindsay as well as a paragraph about her and what her CHD's were. I have to tell you that was hard to do. Because it brought back so many memories and well as just the reality that this has happened and that she is no longer here with us. But I am glad I did it and that she will be remembered during that game. Each team member is playing either in honor of or in memory of a child with a CHD. I am so excited to see how this goes for Jessica and to see pictures. She had special shirts made up and the player will wear a shirt with Lindsay's name. We will then get the shirt sent to us. So look for another update on how it goes and pictures. I thank God for sending Jessica my way. I have been able to chat with her on face book as well as on the phone. I have seen her go through the highs and lows of grief. I hope that in some small way I have helped her during this difficult time in her and our lives. You can check on Ethin's blog here on the right hand side under heart family. Please continue to pray for her.
Thanks Jessica for allowing us to have Lindsay remembered in this game. I know that Ethin and Lindsay are playing and having a great time together in heaven!