I know that my children have a website at another location, but I will be using that for all kinds of other fun things. This site is for the nitty gritty details about what’s going on medically and such with Braden. Of course, we’ll throw some fun in here too! It’s our goal to make this the go to site for the most up to date information on what’s going on. I will put up what happened at therapy, what doctor we see next, the whens, whys, and hows as we learn them. We hope to teach others about this disease, reach out to those who have gone before us, and those that are sure to follow.
So, next up we have physical and speech therapy on Monday. I called the therapists on Thursday so that we wouldn’t have to go into a deep discussion about it in front of Braden. The more normal I can make his life the better. Not to mention, I just don’t want to cry in a public place if I don’t have to. I’m getting better at saying it out loud, and that’s progress. I know that this new diagnosis will change his course of therapy, and I’m interested to see how. I will let you know.