We never finished reading Fortunately, the Milk by Neil Gaiman. Cassie fell asleep the night I finished it, so I read the rest to Walt. Cassie never heard the end of the story. Cassie never got to see Frozen, or Welcome to Nightvale live in New Orleans. C...
'She will never grow old, nor age weary her' ... or words to that effect. (I have nothing better. sorry.)
Have a care, breathy deeply, feel the sads, get through another day.
You're a true hero!
It's very hard to wrap my head around the idea that it's almost Thanksgiving. I remember last year so clearly; listening to Welcome to Nightvale with Cassie on the way to Christina's house for dinner, Cassie thinking there was too much nutmeg in the pumpkin...
It's been quite a while since I posted. I feel like I don't have the words for what I'm feeling most of them time, so I just don't. I have a job now, Walt has made the decision to transition genders and lives as Tyra now, and is back in public school. The j...
- Marvel Puzzle Quest Dark Reign
José González Teams With Zero 7 on "Last Light" | News | Pitchfork
From Zero 7's new EP
Help River get to Ohio! | Medical Expenses - YouCaring.com
River is 17 months old and has Hirschsprung's, which requires a major bowel surgery. There are no specialists for this in Louisiana, so we n
Louisiana girl with rare condition to be honored in anime movie
Cassie England died on Jan. 10 after a lifelong battle with a rare skin disease. Her goal was to be an artist and she loved the Japanese ani
Anime cartoon based on local girl who died from rare disease
Cassie England died last month at age 16 from a rare and extremely painful skin disease called E.B.
The Paragon of Audience Outreach? Robbie Bryan Talks Black Hat - Filmmak...
Any panel, roundtable or seminar that concerns technological advancements in film is bound to hit upon the issue of audience engagement. How
Dancing helps East Texas boy overcome rare skin disorder | KETK | East T...
Tyler, Longview and Jacksonville News from KETKnbc.com. Your source for local news, weather and sports for Tyler, Longview, Jacksonville, Lu
Obamacare Offers Hope for People With Rare Diseases
Megan Barron, 22, has epidermolysis bullosa, a rare skin condition, but the Affordable Care Act could be a huge help for her. (Credit: Court
Study Suggests a Special Needs Child is the Most Important Friend Your K...
Like many children, my son is friendly with the kids in his classroom. Unlike many children, those are his only friends.
Let’s Talk, In All the Wrong Ways « Confetti Skin, Beauty Within
We are excited to have SooAnn Roberts Pisano join us today! SooAnn is the mother of two boys with two different forms of epidermolysis bullo
Revolution Season 2 Casting News – New Recurring Character Cast
Revolution Season 2 Casting News - New Recurring Character Cast NBC Revolution is widening its cast of characters. Steven Culp (Grey's Anato