Friday, May 6, 2011 would be Blake’s 2nd birthday. My daughter decide for this year to celebrate we would invite people to wear yellow and to inform people of WH. We made of fliers with this website and some information about Blake asking people in the community to find out about WH and then to wear yellow and tell as many people as they could about the syndrome. We have had a great response and are very excited. I want to ask any of you that would like to wear yellow also to please do so. I didn’tknow it even existed until Blake was born with it and no one around here knew anyting about it. I hope that this little effort will help to educate others. Tahnks so much for this web site. I wish we would have had it when balke was born and am very happy that those of you who has these precious blessings have this support. I pray for each of you and your children daily and pray that Godwill bless each of you.
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I will definitely wear yellow for Blake!!!! I wear a lot of yellow because it’s my favorite….cheery and bright:) But wearing it for Blake will give it so much more meaning. Great job to your sweet daughter educating others too. That’s wonderful. I’ll be thinking of you on Friday.Thanks for your prayers to our families as well.
Thank you for posting and letting us know that you are spreading the word. I too wish something like this was available when Kendall was diagnosed. We can only hope that more and more people will tell their stories so that new families will have hope.
Again, I am so sorry for your loss. It is great that you are spreading the word and educating your community. Thank You. Best of luck to you.