The cdiff has been on and off since late June. We have heard stories of people going years to get rid of it. We can't really sit and wait on this. With Casey always just barely hydrated, each recurrence of cdiff takes more and more fluids that she just can't spare. This last run of cdiff caused her a lot of pain as well. After talking with Casey's pediatrician and palliative doctor we are going to take Casey to see Infectious Disease this week. Hopefully they can help us come up with a way to be rid of cdiff for good this time.
We are going to try to get back onto a normal schedule this week. Casey has school, and dance. She has barley done any school so far this year (I think only 2 days). I guess this is just one of the many reasons we opted for homebound school for her.
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Some friends of ours have done something really special for Casey. Their little girls are some of Casey's friends and are all doing girl scouts this year. They knew that I was not interested in signing Casey up if she was going to get stuck in a group of girls she may/may not know. Instead our friends decided to go through all of the training, background checks, etc in order to start their own group. This way Casey will be with girls that she already knows. This is HUGE!!!! Knowing that the girls are all good around Casey, knowing the environment is one Casey does well in, and it only being a few times a month makes Girl Scouts something Casey CAN do. Our friends doing this so that Casey can participate means so much to us. Casey is very excited! This week will be their first troop meeting. I am not sure if her troop will be selling cookies or not, but if so, she will be hitting you all up soon :)
I will post soon with more details on the ID appointment, how Casey likes Girl Scouts, and more. Until then we hope everyone is doing well.