02/19/2010
by Michael Wells I got home after 8:00pm last night (website development meeting) and much to my surprise Brady was asleep and is still sleeping. He is doing so well I just hate the idea of having to start all the craziness of “conditioning” chemotherapy and stem cell transplantation process. He is such a happy, smart little boy; each day is another day of learning news words, new skills and he continues to add “signs” to his signing vocabulary. We just have to beat this nasty disease. This weekend my daughter (Jennifer) and my first born son (Stephen) are coming from Maryland and Florida to visit their brother. This truly touches my heart and I am really excited to see them. Also, Sherrie’s brother Wayne will be coming up from Florida to drop in on his nephew. It should be a very interesting and fun week-end. Well, as usual I’ve got to get going; so until next time please continue to pray, think good thoughts and hug someone for Brady, thank you…“8 Years Later—Still No Cure for Pediatric Cancer” is a series of posts revisiting the journal kept by Sherrie and Michael Wells during the cancer diagnosis and treatment of their son, Brady Michael. Hopefully these entires will provide an understanding of the journey families face when dealing with these horrific diseases and of the important work the Hugs for Brady Foundation does.