All Blogs Relating To "VCFS"

posted 02/08/2011, comments (10)

Am I Supposed to be Here

Last night I was wondering to myself, what if I wasn't supposed to be here? I'm not saying that I was a mistake, but I was just curious because if I was born 10 years earlier, I would not be living today because they didn't have the technology to keep people alive. If you think about it, it's not natural to keep somebody on life support. ... Read more

posted 01/31/2011, comments (0)

Mission 22q of Nebraska - Our Website

Please visit the Nebraska support group's website to see what we've been up to:   mission22q.webs.com   Thanks,   Anne

posted 01/11/2011, comments (15)

Expert Mom?

Quinn, You asked for experts on a Facebook VCFS page I just joined. What about an expert mom? Seriously, maybe not me but I'm sure there are many moms like myself who have put blood, sweat, and many tears into the lives of thier children with VCFS. I do weekly research, the school knows my face well (lol), Vocational rehab, SSI, Specialists around... Read more

posted 01/08/2011, comments (3)

Logan's story

My little boy Logan Alexander is 5 months old, born 8/2/10, and was diagnosed with VCFS just under a month ago. We're currently testing to find out exactly what we're dealing with medically so far. He had extra amniotic fluid, has a slightly recessed chin, was born with enlarged (properly functioning mind you) kidneys, and had problems... Read more

posted 12/30/2010, comments (0)

Athletes with Disabilities

I just found your site while i was looking up information about athletes with disabilities. I have a learning disability and have been luckly to have great teachers who have helped me to achieve all of my dreams. I am the founder of Future Collegiate Athletes with Disabilities.com. I started this website due to the fact that when i went to college... Read more