Monthly Archives: July 2010

Friday Photo Fun

Back when they were both happy. Half of them were really sick, one of them was sick. Back before we knew about dialysis, depression, trauma. When we could only imagine what would come. And even then, we couldn’t imagine. Trying … Continue reading

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Spoken in the Mutant Family Household

The scene, I am snuggling with Quinn (which we often do) and Julian tells lame joke. We don’t laugh. Quinn: “You laugh when no other people laugh.” Which made us all laugh. ————— Gage said tonight: “You know when I … Continue reading

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A Nightly Fear.

For the last two weeks I’ve been working on a post about a breakthrough that we had with Gage as a result of him realizing, quite shockingly to all of us, that he was able to feel emotion (that wasn’t … Continue reading

Posted in Gage's new kidney adventure, Going Mental, Good behavior doesn't come cheap, Raising special needs kids | Leave a comment

Love That Max's Mom

So a little bit ago, Ellen, mom to Max and Sabrina, wife to Dave and famous blogger of special needs parenting tweeted that she wanted to get a lunch planned during BlogHer which is fast approaching – August 6-8 in … Continue reading

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Friday Photo Fun

The Quinncess will be returning from camp on Saturday. I will be returning to med duty, whining control but all the while I’ll be getting some serious snuggle time. Post Footer automatically generated by Add Post Footer Plugin for wordpress. … Continue reading

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Spoken in the Mutant Family Household, In Honor of Her Absence

The Ofieses in Gorga By: Quinnlin Roberts Made in July there is many ofieses in Gorga. theres Blue ofieses red, Gren, and yellow My Mom and Dad have an ofiese to. It is red The have inpertent stuff to do. … Continue reading

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Friday Photo Fun, What You Might See

Because by this photo you will know… We go through a lot of prescription bottles We often let the kids sit on the counter if the play warrants it We don’t regularly put seed in our bird feeder What Gage’s … Continue reading

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Taken

Nolen, 6/25/10-7/1/10 I’ve recently been supporting a family who had a prenatal diagnosis with ARPKD. The dad contacted me through the PKD Foundation looking for support and information. We talked several months ago and as their pregnancy progressed, I got … Continue reading

Posted in Raising special needs kids, Story telling, What others take for granted | Leave a comment