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I know that none of you are close enough to know this, yet my son will be in need of this soon and everyone should be educated. My son Landen was diagnosed with Cone Dystrophy and will be in need of stem cells to correct his blindness. His blood has been sent to Germany for testing, but we will not have the results for 2-3 months. Please take some time and write your Congress to help with the passing of it here in the States. Damn Bush!! Being a single mother with not alot of cash, I don't have the resources to fly us to Germany for weeks to get it done.
We treat mishaps like sinking ships and I know that I don't want to be out to drift Well I can see it in your eyes like I taste your lips and They both tell me that we're better than this
I read the article before reading this post, but your personal take on it makes me feel that much more anger at the whole argument against embryonic stem-cell research. Karma (when I have some to give) for being a single-mom in a heart-breaking situation and inspiring this person to do more to educate people about the need for embryonic stem-cell research.
Thanks for your comments.... Landen seems to be adjusting well because he had it when he was born. He is not fully blind. The cones in our eyes work with colors and fine detail, along with other things. I have him on an all organic diet, everything from food to lotions to hand soap to dish detergent. Our bills have gone up at least $200 a month for just household stuff. Organic is so expensive. Anyway, he is color blind and has to read VERY large print books and such, but we (his sister and I) preach acceptance about everything. He is who he is and he is perfect just like that! Very happy boy.
Thank you all for stopping in and for commenting. He is not completely blind, but is considered legally blind by the state. All of your prayers are greatly appreciated.
