We went to a superbowl party at a friend’s house today. It was great to get out and socialize again, and Ethan and Abby had such a good time with the other kids. They had a betting pool for the game with 100 squares. After everyone chose their squares, there were only 7 left […]
[Continue reading...]Make-A-Wish, we are eternally grateful!

Anyone who knows us knows that our Make-A-Wish to Disney World last April was the best time of our family’s life with Hannah. I’m disappointed that I never had the chance to really blog about it, but I am so glad that we have over 800 pictures from the trip. It was Disney World. […]
[Continue reading...]It all fits into a box

It is done. All of the clothes of Hannah’s I want to keep fit snuggly in a Christmas storage tub. For now, anyway. Eventually, I will get a hope chest for her clothes, but this will do for now. I didn’t intend to do it, especially after the tailspin it threw me into […]
[Continue reading...]Hannah’s fight against childhood rare disease

Today is the World Rare Disease Day blog-hop, 30 days before World Rare Disease Day on February 29th. Dozen of rare disease bloggers across the world are coming together to share our personal stories of how childhood rare disease has affected our lives. (Please check out their stories below) If you take a look […]
[Continue reading...]It’s just friggin’ fabric!!
It has been a really rough couple of days. Well, it hasn’t been like an all day thing, but I have had my moments of major breakdowns. I mean, be pissy at everyone, crawl into bed, and just bawl breakdowns. It started Thursday when I made the decision that I was finally strong enough […]
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