A WORD TO READERS:

This Blog is intended to educate as many as possible. Our story is unique as is each story of a special needs child.

Thank you!











Lisa












Saturday, July 17, 2010

Today Dusseldorf-Tomorrow Fargo: Our final thoughts

Well, tomorrow we will be almost to Chicago and back on US soil. We have had quite a week and while it was enjoyable and a memorable time, we are ready to be home.
I have learned so much this week (including a few German words and how to read train maps) but mostly I've learned about trust and faith. Such little things can sometimes be the hardest things to learn.

Ethan continues to do well, no crazy changes yet but I know that they will appear in the next few weeks...nothing ever comes as you'd like or expect so I'm sure the changes will come as they will. Otherwise, outside of a slight headache which was gone by Friday, he is doing fine and is ready to be home (as we all are).

We wrapped up the final bit of the documentary film this morning. We are so grateful for our friend Machu, who took this opportunity to help tell Ethan's story and to bring awareness about to CP as well as to stem cell treatments. We were lucky and so blessed to have you with us. You are an inspiration and a dear friend. THANK YOU FOR EVERYTHING!

So...until we reach Fargo, this is our last update. I will continue to update as we reach new milestones so don't forget to check in from time to time. I love to hear your comments, thoughts and questions too so please feel free to let me know what's on your mind!

Lisa

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