-
Recent Posts
Recent Comments
Archives
Categories
- A gripe
- Friday Photo Fun
- Gage's liver
- Gage's new kidney adventure
- General Family
- Going Mental
- Good behavior doesn't come cheap
- Homespun Therapy
- Kidneys in general
- Nothing to do with kidneys
- Plugging SfSN site!
- Quinn's new kidney adventure
- Quinnlin's liver
- Raising special needs kids
- Spoken in the Mutant Family
- Story telling
- Tips for parents, families and friends
- Uncategorized
- What others take for granted
- Working through it.
Monthly Archives: February 2008
Friday Photo Fun
Muddy fun, compliments of rain and a few kids who love to dig up the foundation of a house on a hill! Post Footer automatically generated by Add Post Footer Plugin for wordpress. Bookmark on Delicious Digg this post Recommend … Continue reading
Posted in Friday Photo Fun
Leave a comment
Clinic Highlights and Remembering
Bullets are all my brain can take right now. 1. One doctor for the entire lot of us for Thursday clinic. I have no idea how many that is but I saw about 13 kids during the time we were … Continue reading
Posted in Gage's new kidney adventure
Leave a comment
Try this! And that!
I’ve been searching my brain to find a solution to Gage’s bad-mouthing of school. When we say anything like “it’s time to get up for school!” or “let’s do your homework” we hear nothing but disdain spewing from that cute … Continue reading
Eleven.
Jody, Can you believe we are pushing a year since you gave a kidney to Gage? I can and I can’t believe it in this very moment. It seems so very far away but also like it was yesterday. How … Continue reading
Posted in Gage's new kidney adventure
Leave a comment
Where do crappy kidneys go?
On an earlier post, Bree asked why were we able to donate Gage’s old kidney… Here’s some information from the nurse that helped us facilitate getting Gage’s kidney in the hands of researchers* and how doing so is helpful. Teresa … Continue reading
Posted in Gage's new kidney adventure
Leave a comment
This might sum it up for you.
In the car, about an hour into our drive home from our appointment with Dr. Wonderful: Me: “So. That wasn’t so bad. Right?” Julian: “Well, hearing about our kids’ kidney failure doesn’t shock us anymore.” Me: “Yeah, your right…the words … Continue reading
Posted in Quinn's new kidney adventure
Leave a comment
Housekeeping.
If you are by way of the PKD Foundation’s newsletter released today (or Dawn’s post)…head on over to our about page to the right. That will bring you up to speed. And welcome. Pull up a chair and stay a … Continue reading
Posted in General Family
Leave a comment
A Study in Weighing Factors
We’re headed when the kids are out of school to the NIH (National Institute of Health) for a study on cystic diseases. For 5 days we’ll be staying at the Children’s Inn while the kids have tests each day. It’s … Continue reading
Anticipation.
We’re headed soon to see Dr. Wonderful on our day trip with the kids. As always, I look forward to these trips because I always learn something – even if it’s not great news – about the care of the … Continue reading
Posted in Kidneys in general
Leave a comment
Seeing a new baby through this momma's eyes.
Our very good friends Linda and Don had Baby Tessa last September. I was lucky enough to be there when she was born – not actually in the room since Linda had a c-section – but I was one of … Continue reading
Posted in Raising special needs kids
Leave a comment




