As of January 1, 2019, we have closed our forums. This is a decision we did not come to lightly, but it is necessary. The software our forums run on is just too out-of-date and it poses a significant security risk. The server software itself must be updated, and it cannot be without removing the forums.
So it is with a heavy heart that we say goodbye to our long-running forums. They came online in 2000 and brought together so many wonderful Disney fans. We had friendships form, careers launch, couples marry, children born ... all because of this amazing community.
Thank you to each of you who were a part of this community. You made it possible.
And a very special thank you to our Guides (moderators), past and present, who kept our forums a happy place to be. You are the glue that held everything together, and we are forever grateful to you. Thank you aliceinwdw, Caldercup, MrsM, WillCAD, Fortissimo, GingerJ, HiddenMickey, CRCrazy, Eeyoresmom, disneyknut, disneydani, Cam22, chezp, WDWfan, Luvsun, KMB733, rescuesk, OhToodles!, Colexis Mom, lfredsbo, HiddenMickey, DrDolphin, DopeyGirl, duck addict, Disneybine, PixieMichele, Sandra Bostwick, Eeyore Tattoo, DyanKJ130, Suzy Q'Disney, LilMarcieMouse, AllisonG, Belle*, Chrissi, Brant, DawnDenise, Crystalloubear, Disneymom9092, FanOfMickey, Goofy4Goofy, GoofyMom, Home4us123, iamgrumpy, ilovedisney247, Jennifer2003, Jenny Pooh, KrisLuvsDisney, Ladyt, Laughaholic88, LauraBelle Hime, Lilianna, LizardCop, Loobyoxlip, lukeandbrooksmom, marisag, michnash, MickeyMAC, OffKilter_Lynn, PamelaK, Poor_Eeyore, ripkensnana, RobDVC, SHEANA1226, Shell of the South, snoozin, Statelady01, Tara O'Hara, tigger22, Tink and Co., Tinkerbelz, WDWJAMBA, wdwlovers, Wendyismyname, whoSEZ, WildforWD, and WvuGrrrl. You made the magic.
We want to personally thank Sara Varney, who coordinated our community for many years (among so many other things she did for us), and Cheryl Pendry, our Message Board Manager who helped train our Guides, and Ginger Jabour, who helped us with the PassPorter-specific forums and Live! Guides. Thank you for your time, energy, and enthusiasm. You made it all happen.
There are other changes as well.
Why? Well, the world has changed. And change with it, we must. The lyrics to "We Go On" for IllumiNations say it best:
We go on to the joy and through the tears
We go on to discover new frontiers
Moving on with the current of the years.
We go on
Moving forward now as one
Moving on with a spirit born to run
Ever on with each rising sun.
To a new day, we go on.
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.
But eventually, we must move on and move forward. It is the right thing to do.
So we are retiring this newsletter, as we simply cannot keep up with it. Many thanks to Mouse Fan Travel who supported it all these years, to All Ears and MousePlanet who helped us with news, to our many article contributors, and -- most importantly -- to Sara Varney who edited our newsletter so wonderfully for years and years.
And we are no longer charging for the Live Guides. If you have a subscription, it's yours to keep for the lifetime of the Live Guides at no additional cost. The Live Guides will stay online, barring server issues and technical problems, for all of 2019.
That said, PassPorter is not going away. Most of the resources will remain online for as long as we can support them, and after that we will find ways to make whatever we can available. PassPorter means a great deal to us, and to many of you, and we will do our best to keep it alive in whatever way we can. Our server costs are high, and they'll need to come out of our pockets, so in the future you can expect some changes so we can bring those costs down.
Thank you, thank you, thank you for your amazing support over the years. Without you, there's no way us little guys could have made something like this happen and given the "big guys" a run for their money. PassPorter was consistently the #3 guidebook after the Unofficial and Official guides, which was really unheard of for such a small company to do. We ROCKED it thanks to you and your support and love!
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!
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I know we have had some discussion of this in the Special Needs forum, but not everyone looks there, so here goes.....
For my Child and Adolescent Psych class I have to come up with 15 or more suggestions for families to help their child with Speech Language Disorders, such as stuttering, speech delay, etc.
I have found a few websites that give some good suggestions, but I would like to know: If you have a child with some sort of Speech Language Development issue, what do you you suggest to other families to help your child improve their speech?
The assignment is due tomorrow morning, but any suggestions that come in after that would still be a great help.
I am not sure if this helps at all, but my cousin, when she was little (toddler - 1st grade) had a terrible speech disorder - we actually thought she was deaf or partially deaf. Turns out she wasn't, she has never ending ear infections - BAD ones So long story short, she had tubes put in her ears a few times.....after that she had no issues with speech....
So - although it might be tough and\or non applicable, hearing testing is something that I would start with.
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~ Jenn **Disney is REAL LIFE Magic, so much more than optical illusions **
So - although it might be tough and\or non applicable, hearing testing is something that I would start with.
Actually is ti COMPLETELY applicable. It is one of the first suggestions we have on our list. Also almost every website I have found with suggestions has this as one of their main things to do.
My DS had speech delays when he was younger. Turned out he couldn't hear very well & had low muscle tone in his mouth/tongue. His speech therapist suggested using peanut butter or cream cheese or something thick like that, on the roof of his mouth, behind his front teeth. He had to use his tongue to lick it off. This apparantly improves the muscles. Also, have the dentist or pediatrician check the phreneum (sp. ?), that piece of tissue that attaches the tongue to the bottom of the mouth. Sometimes if it's too tight, it has to be clipped to allow the tongue more movement. He's 18 now, so I'll have to see what else I can remember...Good Luck!!
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First trip DW--Nov. 1975; Senior Class Trip DW--Oct. 1979; First trip w/kids--Oct. 1995; Halloween at DW--Oct. 2002; Spring Break at DW--April 2004; Christmas/Pop Warner Nationals-POR--Dec. 2005;Cruisin'--April 2008; Mom/Son trip-POP--March 2010;Taggin' along w/DD on DH's conference-BWI--Oct. 2011; 50th birthday with the Gartner Geeks--Adults only!--BWI--Oct. 2012; The Trip That Almost Wasn't--BWI--Oct. 2013; We climbed The Summit (National Cheer Competition)--ASMovies--May 2014
I am an SLP and all of those suggestions are very good. Try looking at this website: www.asha.org
It's the American Speech and Hearing association's website.
For speech delayed children: think about making language more concrete (using pictures or signs). I also love using music, nursery rhymes, etc. Many kids respond well to this.
For children who stutter you can find a good bit of stuff but usually all implemented by SLPs but the Lidcomb program is good for parent involvement like someone said. Also look at www.stutterhelp.org. This is a very good website.
For speech impaired children (speech sound errors) you will want something that would help with practice and carryover.
I often work with 1-3 year olds who are not talking. Lots of times I can give the families ideas to incorporate more language into the home. I know that sounds so simple but with all of the distractions (technology, etc) in society today lots of our kids live in very quiet homes or homes without good quality interactions.
Hope some of this helps!
Emily
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Check out my Pre-Trip Report for our 9/18-9/23/12 trip here:
Two of my children had speech delays.... One thing I remember them doing is making picture cards so that he could point to what he wanted since he was pretty close to being non-verbal.... He had a picture book also.... I don't know that this improved his speech, but it improved his communication skills....
My youngest ds now recently started speech; his communication skills are good, but he is hard to understand at time- they said that it is because he sucks his two fingers and when he does that and talks it presses down on his tounge weakening those muscles- so I was told to always make him pull his fingers out before speaking (easier said than done) and while they didn't mention it- we should probably be working on some way to re-strengthen those muscles...
With my two older ones; who are no longer in speech- I think the bottom line for them was practice makes perfect.... lots of correcting and reiterating....
Not sure how helpful that was, but that was my 2 cents...
I dont know if this helps but I worked as a social work assistant predominantly with older people however I also worked with one young lady told me that onece she had a stutter and was unable to pronounce words very well - she learned maketon which gave her confidence in her ability and now she has no issues with verbal communication. She went to a selective school for those with impairments though so that made makaton more accessible to her. Also im from the UK and the system is very different over here.
hope you get more help soon !
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Clare Loves Stitch
"sometimes the right path is not the easiest one"
Grandmother Willow - Pocahontas
Proud DVC owner at BWV from March 2011
Thanks for all the great help and advice. I was able to get the assignment done and turned in for a 100. Plus I was honored with having two of my suggestions show up on the next quiz and midterm as True/False questions.