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I just read this online:

The most highly ranked dog crate, regardless of breed, is the Midwest Life Stages Dog Crate. Dog forums and dog owners alike love this crate because it is safe, functional, grows with the dog and is almost impossible to escape.

Yes! This is the one we have!

Guess who got a paw onto the latch, pushed it over, and squeezed out of her crate in the middle of the night to sleep on our couch?

I am soooooo busted

The best thing is that now she is trying to get back INTO her crate to get her peanut-butter stuffed Kong.

Tonight we will instead wrap her in a straightjacket and hang her from her back paws. I expect she’ll escape in less than three hours.

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note: we will not really be hanging her from her back paws. . .but we’re considering the straightjacket.

Just over a year and a half ago, I wrote about a little girl named Megan with Juvenile Myositis, a rare autoimmune disease that attacks, then can lay in wait for years until ready to attack again.

Sadly, Megan, who is only 11, is again under attack.

Her parents, Kevin from Always Home and Uncool and his wife Rhonda are asking anyone who can spare a little to donate to Cure JM Foundation.

And, even better, if you can donate before June 25, your gift will be matched, up to $3,000.

I can’t think of a better Father’s Day gift for these families than finding a cure.

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want more info? keep reading Kevin’s words to understand why this is so important:

Dear Friend,

We have more urgency than usual to our annual appeal for donations to Cure JM Foundation, the nonprofit search for better treatments and a cure for juvenile myositis diseases.

Our daughter Megan, who was diagnosed a JM disease in 2002, recently experienced a flare, or relapse. She essentially had been symptom free for the past three years and weaning off medications until then. In the past month, she has resumed treatment with IV medication – to date seven infusions of steroids, one of the refined human blood product IVIG.

You can help Megan and children like her by sponsoring our family in the Seattle Rock ‘n’ Roll Marathon on June 25, 2011. Rhonda is running while Kevin and the kids will hand water to runners on race day.

Your donation will help Cure JM continue funding two vital programs that fulfill its mission to one day make sure no child suffers from juvenile myositis diseases ever again:

* medical research centers, which the foundation helped start, at leading hospitals in Chicago and Washington, D.C., that search for the cause and cure for juvenile myositis diseases, and

* online, print and in-person support to educate people about the disease and help families coping with JM’s effects on their children and lives.

Donations of any size help as no one knows which dollar will be the one that finally funds a cure. Since Cure JM is an all-volunteer organization rest assured that about 98 percent of the money we raise goes directly to the cause instead of salaries, overhead or fundraising consultants.

You can help by making a tax-deductible donation in one of two ways:

1) Use a credit card online via FirstGiving. Our fundraising page is:
http://www.firstgiving.com/fundraiser/rhondaandkevinmckeever/2011?fge=ask

2) Print and fill out the form on this Google documents site at
http://tinyurl.com/3avtba8, write a check to “Cure JM Foundation” (put in the memo section that you are sponsoring Kevin and Rhonda McKeever), and then mail it to:

Cure JM Foundation
836 Lynwood Drive
Encinitas, CA 92024

Matching gift forms may also be sent to that address or faxed to (760) 230-2243.

On behalf of all children and their families afflicted with JM, especially ours, thank you for your generous support.

The McKeever Family
(Kevin, Rhonda, Megan, Calvin and Murphy, too)

We adopted Houdini

Happy Father’s Day!

Make this father’s day

Welcome!

Looking for something?

Isn’t that special?

I think he’s pretty great

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