Some news

Well while at work I got a call from my original Dr, Dr Martinez's office, and his nurse said that he wants to see us at least once a week.  I talked to a friend who went to Dr Blanco (the high risk Dr) and she said that she went to her original Dr and Dr Blanco each week as well. So it looks like we will be going to see them and hopefully get more results/news and hopefully know more of what we can do each week. We are going tomorrow to see Dr Martinez, and then we will go back to Dr Blanco's office on Nov 5th to meet with the genetics counselor and see one of his colleague Dr's that work there as well. We should be receiving the results from the past 2 blood tests that they did at the end of last week at this appt too. (The chromosomal test on trisomy 18 and trisomy 21, and infection test.) 

Day's have been getting better, as I said in the entry from earlier it gets difficult to be positive with the unknown, but I know that its not health for Lucas for me to worry about the things that I can't change. We have many friends who have been very kind to check on us, and make sure we are doing alright, which Chris and I are very thankful for. A friend from work also found a website with moms who see to of went through similar things as us, if anyone would like to check it out and maybe be able to get a better understanding for what we are experiencing here it is:
http://parents.berkeley.edu/advice/pregnancy/choroidplexuscyst.html

If anyone else knows someone who's went through this, or similar tests or anything please let us know, we are open to any advice or help that can be offered in figuring out how to make Lucas all better.