tag:blogger.com,1999:blog-3542279065732178895.post4180321431109214731..comments2008-09-16T19:59:46.041-04:00Andy and Linda Johnsonhttp://www.blogger.com/profile/13903781886135766678noreply@blogger.comBlogger1125tag:blogger.com,1999:blog-3542279065732178895.post-22993493158775445362008-09-16T19:59:00.000-04:002008-09-16T19:59:00.000-04:002008-09-16T19:59:00.000-04:00i have a cousin with this diagnosis, and it is just as heartbreaking, and probably more than these peopole make it out to be, my cousin is my number one ande he is always there for me, i remember the days when we were younger and we used to play baeball, tag, hide and seek together and he would all constantly,he would roll over his ankles and cry, i think his progression is much more rapid than the people i have seen in this video, he is wheelchair bound and has been for a while, he just turned 13, same as myself, we try to play online together on video games as much as possile, but it makes it hard on me for school, sports, and social life when all i do is play video games at homewith him, but i think it's worth it, because the day he passes i know he will always have a special plae in my heart, and i one in his. i think the people who make these efforts are angels, and should continue their work, i hope to go into the medical field when i am an adult, and believe there may be hope in genetics research, but in all honesty i hope to god these guys beat me to it, for my cousins and everyones elses's loved ones sake whose time is running out.spencernoreply@blogger.com