Please help spread awareness.
Monday, February 11, 2013
Win this necklace
Sorry I didnt post yesterday. But I am here today and I am glad to show you this week's prize.
This is the 18kt Gold-Plated Silver Genuine Heart Pendant With a Diamond at the top of the heart. and you have a chance to win it. :) All you have to do is leave ask a question in the comments section or help spread awareness either through your blog, Google+, or facebook and send me the link so that I can see it. Sorry I dont have twitter.
Please help spread awareness.
Please help spread awareness.
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5 comments:
Hi! What a beautiful necklace! I have a little boy Joshua who was born with Pulmonary Atresia with VSD and MAPCAs and an absent pulmonary artery. He had his 3rd open heart surgery yesterday and was in the operating room for 17.5hrs! There were complications, but he's doing okay now. He has a FB page called Joshua's Journey which I've been using to spread CHD awareness.
I also joined the City Of Hearts 2013 event on Facebook and spread it to the UK. I made over 200 clay hearts, each with a name of a heart warrior, their condition and date of birth/passing. I made fact sheets and displayed some in my doctor's office and some in the town centre. So hopefully the word about CHD is getting out there!
I wish from the bottom of my heart that we didn't have to spread awareness, that there was no CHD to start with...
Here's a link to my boy's page!
www.facebook.com/joshuasjourneychd
My son is a CHD warrior who has Atrioventricular Canal Defect. He will be having surgery this year. I have a facebook page for him,and this week I have been featuring a CHD child every day. I would give information on the child, and their CHD that affects/affected them. I also share various facts and videos as often as I can on his page. I try and spread awareness to the people on his page. I also share facts on my own personal page, and tell all of my friends about Vincent and his defect. My sons page can be found following the link below. I have featured seven different children, and several different CHD's. I even have a list in my notes section there that talks about several different CHD's.
http://www.facebook.com/PrayersForVincent
Hello, Thank You again for the Beautiful necklace i won last year. I wear it all the time.
This Necklace is also Very Beautiful. It wouldn't be fair if i won again. Just wanted to chime in about all the great CHD posts. I am sure i am getting on my Facebook friends nerves with all my CHD posts. I just love it though when someone shares them. But it is usually one of the CHD friends who does the sharing, and not all the classmates/friends. I don't post much on my Google+ because there isn't much activity there. I will have to go post something.
https://www.facebook.com/diane.kowalik.7
https://plus.google.com/104942721612867619441/posts
I think it is great that you are spreading the word. I will post on my Facebook. :)
Hello, I am a mom to a heart angel. Our son Will was born in 2006 with HLHS and TAPVR. He passed away at 4 days old. I try to spread CHD awareness on facebook and have been planning on doing some sort of project in his memory, but it has not happened yet. My oldest son is doing Jump Rope for Heart and is jumping in Will's memory. This is the link to his page: http://jumpgsa.kintera.org/faf/donorReg/donorPledge.asp?msource=Gigya&ievent=1036375&supId=376482865 Thanks for all you are doing to spread awareness for CHD.
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