This is a blog that all School Students will want to comment on, as well as parents. It is that lovely time of year again. YES! School is out for the summer. woo hoo. Lets talk about some of the fun things we can suggest for those who don’t have a clue of what to do for the little ones who have all this time to spend at home. And for those of us who have nieces and nephews that want something fun to do, post it here. Something that will keep them busy and the uncle happy because they are happy having so much fun. See then everyone is happy all summer long.
[flv:/wp-content/uploads/2009/05/reggieInMI.flv 480 320]
Sorry for the inconvenience but the blog wasn’t allowing any new comments on posts 14 days old or older. That is fixed and now anyone can comment on any post at any time. Don’t you just love technology.
Thank you for your interest in helping raise awareness for NF. With your help, I hope to spread the word about neurofibromatosis through web, viral, web-related resources, and personal appearances at events throughout the country
Unfortunately due to my not being rich, i.e. poor, I don’t have the financial resources to underwrite all the funding we need to meet my objectives. Thanks to Lou, I have been able to attend all of the functions you see in these photos courtesy of Lou.
I want to raise awareness of neurofibromatosis so that people affected as severely as myself can be accepted into society and lead a “normal” life. That’s why Lou and I and Matt and Geo and William and Shana go out together. When people see other people acting normal around something they don’t understand, they feel ok about it and figure there’s nothing wierd happening and they’re fine. Continue reading Tax Deductible Donations Now Being Accepted by the Just Ask Foundation