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It's time to move on and move forward.

PassPorter is a small business, and for many years it supported our family. But the world changed, print books took a backseat to the Internet, and for a long time now it has been unable to make ends meet. We've had to find new ways to support our family, which means new careers and less and less time available to devote to our first baby, PassPorter.

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If you miss us, you can still find some of us online. Sara started a new blog at DisneyParkPrincess.com -- I strongly urge you to visit and get on her mailing list. She IS the Disney park princess and knows Disney backward and forward. And I am blogging as well at JenniferMaker.com, which is a little craft blog I started a couple of years ago to make ends meet. You can see and hear me in my craft show at https://www.youtube.com/c/jennifermaker . Many PassPorter readers and fans are on Facebook, in groups they formed like the PassPorter Trip Reports and PassPorter Crafting Challenge (if you join, just let them know you read about it in the newsletter). And some of our most devoted community members started a forum of their own at Pixie Dust Lane and all are invited over.

So we encourage you to stay in touch with us and your fellow community members wherever works best for you!

Best wishes for a wonderful and magical new year!

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Old 07-07-2011, 10:33 PM   #46
Sandra Bostwick
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Thanks Sandra, I am always looking for more sites that have things.
You are welcome. Taylan is growing up so nicely! I love the photo in your siggy!
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Old 07-08-2011, 10:21 AM   #47
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You are welcome. Taylan is growing up so nicely! I love the photo in your siggy!
I think you mean Jonathon. LOL Yes, he is growing up very quickly but cute as a bug.
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Old 07-09-2011, 12:29 AM   #48
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There are always people out there who will understand and those who wont. Unfortunately, it always seems like in the times we need people to understand (meltdowns and such) the people surrounding us are not the type!

Be strong, Tabitha! Everyone has had great suggestions!
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Old 07-09-2011, 06:35 AM   #49
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I think you mean Jonathon. LOL Yes, he is growing up very quickly but cute as a bug.
Oh, yes. DUH! I mean Jonathan. I was TWS. (Typing while stupid.)
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Old 07-09-2011, 06:44 AM   #50
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Wilderness Lodge Club Level

Has anyone stayed at the Wilderness Lodge Club Level recently? I have booked a trip for there next year and I have been reading mixed reviews of the resort, any recent reviews would be helpful.
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Old 07-13-2011, 12:37 PM   #51
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Agreed - I understand you wanting the shirt, to make people understand and back off. But that's their problem, not yours.
My sentiments EXACTLY. I totally get where you are coming from, my DS (7) is autistic so I have been where you are with the stares. It used to bother me in the beginning but I've come to realize it is what it is and not my issue. I had gotten my son a button that said "I'm not misbehaving, I'm Autistic, please be patient". Once I got it, took a look and realized: here I am trying to do typical things with him that typical kids do and I'm gonna go and label him for all the world to see & make a judgement BEFORE they even "meet" him? Nope, not gonna pigeonhole him. He will always have a battle ahead of him but doesn't need to be publically labeled. Know what I mean? He has made leaps and bounds from where he was and we couldn't be prouder. That doesn't mean he doesn't still have issues in public. His most recent is when he hears babies/kids cry, he will scream "COVER MY EARS". Yeah, that gets the looks but I don't care anymore. I cover his ears and off we go.
I guess my rambling point is: People will react the way they'll react and anything you "say" or do will not change that. It's how YOU react that makes all the difference. My DD(10) has gotten to the point now of telling overly eager starers "My brother has autism, that's why he's doing (blank)..." I asked her why she felt the need to tell them and she said "Mommy, I want them to know WHY Sean is doing what he's doing and maybe they won't stare next time". Out of the mouths of babes.
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Old 07-21-2011, 09:26 PM   #52
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I'm so glad I saw this post because I was about to post something about Zoey and I have been feeling really down about her situation lately. Thanks. I i wsh you all the best.
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Old 07-22-2011, 12:04 AM   #53
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I'm so glad I saw this post because I was about to post something about Zoey and I have been feeling really down about her situation lately. Thanks. I i wsh you all the best.
I'm so sorry to hear that you've been feeling down about the situation. I hope things start looking brighter soon.
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Old 07-28-2011, 07:32 PM   #54
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Please continue to take your children out to restaurants. How else are they going to learn how to behave out in public, regarless of whether or not they have a disability?

My DS's are now young adults and both have special needs. We have taken them everywhere ... movies, restaurants, long car trips, boat rides, jet skis, Disney, airplanes, Las Vegas, etc. Our very first cruise was in February (not Disney) and I was unsure how they would react to the motion of the ship, activities, etc. as well as how the other passengers would react to them. So many passengers talked to me about my DS's and made comments on how well behaved they were, how they thought their special needs grandchild would love a cruise especially after my sons' examples, etc. It made me want to cry I was so happy. Finally it seemed what we had worked so hard on for so many years finally paid off and people noticed! Passengers even talked to me in the elevator when I was alone about them.

So, go for it and don't fear what other people might think negatively. Your children will be much better off in the end if they learn now.
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Old 08-07-2011, 02:44 PM   #55
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b-Calm | ADHD Treatment, Autism treatment, Adaptive Technology

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Old 08-13-2011, 07:07 PM   #56
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Lots of for you and your family! When I was a teenager and in my early 20's I cared for a child who was autistic, developmentally delayed and deaf. She was a handful, but I never let it get to me. She signed a little, but not much. And she was BIG for her age. People would STARE at me when I let her have her fits, but it was part of her "action plan". Let them stare. They stare because it is outside of THEIR NORMAL! I don't care what other people think. I took her EVERYWHERE!
One thing that was popular in my crowd of friends at the time was a slogan : WHY BE NORMAL. I had it on a pin that I LOVED to wear. C's mom loved that I took PRIDE in bringing her around like a 'friend', and not a "special needs kid". Why be normal... normal is as normal does!
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