The amazing Dr. Mainwaring, PA Dinice and me (in the middle) I love these two people!
I now know Child/Adult CPR. My husband, Carl, who is a PICU RN, purchased a home/mannequin CPR kit and I learned the technique in 30 minutes. It was pretty amazing that I never had learned it since I have a child/adult with a congenital heart defect. I couldn't believe how easy it was! As a celebration of learning a new skill........
........I was doing some research for "giveaway" items at our Parent Evening CHD Symposium and ran across a baseball hat that I personally cannot live without.So, I ordered one for myself (see right picture) and decided to order another as a giveaway on this blog. I will be giving it away on August 11th. How you can receive this amazing hat, you might ask......post in the comment area of this Blog by midnight August 10th, your most creative reason you absolutely cannot live without a hat displaying a CHD logo (I love reading interesting writing) and I will let everyone know who won on Saturday, August 12th morning.
Can't wait to read all of the entries (at least I hope there are a bunch).
Thursday, July 26, 2007
What I learned yesterday.........
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11 comments:
Some hospitals have parents take CPR before taking your child home but we didn't have to because Evan came home with a pacemaker.
Five reasons I cannot live without a baseball cap with the CHD logo:
5. This is the first time I've visited your blog, and maybe I'd find out what CHD stands for.
4. It would help make a connection to the family in Sacramento I rarely see but often think of.
3. I so admire Alexia's strength and courage, and it would be a reminder of her.
4. A blog giveaway would be a great reason to send mail to Minnesota.
...and...
5. A CHD baseball cap would be a wonderful addition to my beautiful husband's beautiful bald head.
The reason I cannot live without a CHD baseball cap is because I would love to give it to my almost 3-yr-old son, Isaiah, who was born with a complex CHD (HLHS, DORV) and allow him to show everyone that he is a CHD survivor!
I can't live with out the hat because I need something to display so that other people will ask me more about CHD.
Let's see...I can't live without that awesome CHD hat because Drew (3 1/2) loves to wear his American Heart Association hat and it would be great if I could have a coordinating CHD hat so we could be matchers! Plus I really like the symbol of the heart mended with the bandaid.
I cannot live wthout the baseball hat because I am the mom of two VERY ACTIVE little boys, and I need something to hide the greys. Even though my toddler has a CHD, it doesn't stop him from jumping, flipping, screaming, swinging, hanging, and destroying every part of the house. And I love every second of it! ;0)
I can't live without the hat because I think it would be an interesting conversation starter. In the small town where we live, many even think cancer and pregnancy are contagious. No, sadly, I'm not kidding. I would love someone to see my hat, wonder what it means, and ask about it. Then I could start explaining. I know there has to be others in this area who have been to you know where and back with their child just as we all have, but you never hear of it in this area. Maybe I could get more people to open up and speak out and raise awareness.
I cannot live without the CHD baseball cap because I will do ANYTHING to bring awareness to CHD's! Someone in my family would wear it all the time so that we can all enlighten someone about CHD everywhere we go. Besides, I don't have a hat, and this one would be PERFECT!
I am not sure, I may be too late...but the reason I must have that CHD hat is because everyone in my family, and I mean EVERYONE, has a hat but me! I cannot even believe it myself, but I do not own a single hat for my head. But more seriously, it would be so nice to be able to spread more awareness about CHD because NO ONE knows what it means and it might help get more attention and more money to go in the direction of heart research.
It is a commonly expressed reason, that I cannot live without the hat, so that I too can raise awareness for CHD. Prior to the birth of my son a knew very little about CHD. I had no idea how it would impact our lives. It is very true that we are one of the "lucky" families. In Jacob's first hours, his CHD, Transposition, threatened his life. In the following days, he had surgery at 6 days old. In the following months, he's done beautifully, and we live a near normal existence. I'm grateful for all I've learned, and I hope to continue to learn more. I seek out others who know about CHD, and I seek to communicate what I know about CHD to other raise awareness.
I think I'll first give the hat to my husband to wear, so he can figure out what CHD means, ;-) - he actually just asked what I was doing, I told him and he said, what is CHD... looks like I have my work cut out for me!
they asked us to take cpr and izzy has a pacemaker. we did not take it at the hospital because we had taken before she was born, before we knew what CHD meant.
we can live with out the hat,we have our little girl:) she smiles at strangers and they ask why she looks a little differently and I tell them about CHD and PHACES. I also have a great mended hearts sweatshirt. The hat is wonderful and is a wonderful way to spread the word about chds!! this is a wonderful idea! I have met many CHD parents while wearing the sweatshirt. spreading the word can help save lives, izzy went undx for 6 weeks and was ins ever heart failure when we found out about her CHD
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