I really believe that this is going to help families who are going through what we have gone through. I truly believe, as it grows, it will be such a resource. The blog is the same so... whatever... but it's the other stuff. The resources... the soon to come FAQ, the stories of other kids that will be included... THAT is going to be the heart of this site for me and that stuff is what will be a source of great comfort and much needed CLARITY for so many families.The blog hopefully is interesting enough to keep you coming back but I believe this new platform is going to make it easy for other families that have a child who is newly diagnosed with melanoma to find the site. Ultimately, they are the ones for whom I built it.
I am REALLY excited.
Check out the menu at top to see what will be available on the site. There are some areas still "under construction" because I am waiting for content from others but it will continue to grow and expand. I'm hoping one day to even add a message board so people can come and get their questions answered quickly by folks who have been there, done that. Dr. Hughes has agreed to be my "professional lurker" so that we can get accurate, timely information to people who need it.
Please visit and if you look on the right hand side, you will see a "Sign Me Up!" button. All that does is send you an email when there is a new post. Your email goes no where and I have neither the time, nor the inclination to do anything with it. It just allows the posts to hit your inbox.
If you have added this site to your blogroll, THANK YOU! I would ask that you take the time to change it to the new site. I have lots of people who visit everyday who find me through your sites.
So without further ado, you are all invited to move in with me at: (Click on the picture below.)