Hi Julie - I hope you don't take this as a negitive response......Over the past four years (since my daughter was diagnosed) I have struggled with your same thought "it is important to support other "foundations" that help CFers with some daily struggles". However, I look at all the other national foundations (cancer, MS, MD, etc.) and see what they have done for their patients in terms of medicine, financial help, etc. and maybe I am a little biased (because I can afford the treatments, barely!!!!!!!!!!!), but they are not any where near the "stage" if you will, that CF is in their research. I do agree that it would be nice to have a lot of help with the very costly medincines, etc., but I also look at the fact that there will probably be a cure for CF WAY before cancer, MS, MD, etc. because of the money they put into research. YEs, it is hard for me and my family to pay for the expensive treatments, but there is help out there that doesn't take away from the hard work that the CF foundations does. Sorry if I went off topic here, but this is how I feel.
Also, I have to say that I did get my bracelets after a couple of weeks, but from what I understand, they are about a month behind in getting them out...this only means that people are ordering them and that the CF foundation is raising more money for a cure!!!!!!!!!!!!!<img src="i/expressions/rose.gif" border="0"><img src="i/expressions/face-icon-small-smile.gif" border="0">