From a church Halloween party, to eating outside, to making new friends, to my first viewing of Teen Witch, all ending with a murder mystery party here’s how we spent the weekend. In iphone pics of course. (Whatever you do, don’t miss the video at the very end. The. Best. Like, ever.) ...
As many of you may know Ann Coulter, a popular Republican pundant, sent a tweet a few weeks ago calling President Obama a ‘retard.’ Republican or Democrat, this is just not cool. People from around the globe have been calling for her to make an apology–including The Special Olympics–yet she has not backed down and...
Hi! My name is Chelsea. I am the mother to two darling, completely opposite little girls, Cali (4) and Ava (2) and a wife to my best friend, Casey. Almost seven years ago, Casey and I started an uncharted adventure we have come to love and treasure each and every day… even the hard, want-to-crawl-up-in-a-ball...
What a darling little girl! I looked at the blog and what great helps Chelsea has for other parents. I don't have any autistic children but will still use some of her ideas. Best of luck to Cali. She has a lot going for her already with such a wonderful family! Chlesea, what part of Utah are you in? I live in Cache Valley!ReplyCancel
I've been reading a ton of Miggy's posts lately (your blog is so wonderful) and none of the posts have pulled on my heartstrings quite like this one. I was diagnosed Autistic years ago, and I understand a lot of what Cali's experiencing. I understand the frustration of not understanding things everybody else seems to know instinctively, the feeling that you're just not the same as everybody else. It's scary sometimes, but having parents who love and support and try to understand is so wonderful and helpful. And through therapy I've grown so much socially to the point that I feel so much more comfortable now than I did even a year ago and I continue to grow. And seeing Cali takes me right back to that little girl I was and makes me proud of her and happy for her. So thank you Chelsea and thank you Miggy.ReplyCancel
A couple months ago I took the girls to get PSP registered at her new school. As I sat in line my mind started wandering… and I thought about PSP’s new teacher. I wondered if we’d get to request a teacher or have one assigned to us. For some reason the thought came into my...
woah. what a raw, honest, vulnerable post.
thank you.
you know, i think you are brave for talking about this, because you're right, it is taboo and not something people readily admit or talk about, but yeah, everyone is prejudice. i hate that it's true- i wish i wasn't. i am sure it stems from ignorace and misinformation. i remember the people/events in my childhood, too. i wish i knew more people who weren't typical so that i could become more open and comfortable. but, i am grateful for your spotlights. and i agree and thank you for repeating that kids shouldn't be shushed when they see someone different, but they should ask politely. we've had so many good experiences doing that.
love this.ReplyCancel
Excellent post. Your spotlights have really opened my eyes to my own misconceptions, and I had never thought it was a good idea to go up and speak to people with disabilities – just assumed it was disrespectful to bring it to everyone's attention. Thanks for your great blog and the Special Needs Spotlight – I look forward to it every weekReplyCancel
Love your post, so honest. I have learned so much from a few blogs I follow about special needs. It took some work for my mind to switch from seeing "disabled", to "differently abled". We all our unique. We ALL have disabilities, we all have wonderful abilities. Thank you for opening up and sharing your stories. ReplyCancel
I love this post.
As a kid I was fortunate to be exposed to many other children with various physical and mental differences. My grandmother was a foster parent for special needs children. She definitely opened my eyes and my understanding of people that are different. She even ended up adopting one of the little boys with down syndrome.
That being said, I still catch myself shying away a bit from people that are obviously different. My gut reaction too is one of being uncomfortable. I don't know why that is. I know better. It's just something I need to work on.
Thank you for saying this so well. Hopefully all of us will admit and move past our predjudices.ReplyCancel
thank you. this post is honest, raw, and thank you for TRYING to open people's eyes. I have an autism spectrum kiddo, and man, he is awesome. yet my heart breaks every day from the things he has to go through and things other people put him through. when he was younger he 'seemed more normal' to others, but now that he is nearing 10, the difference is becoming more obvious. sometimes i want to move on the off-chance he'd somehow find nicer friends, and then i realize what a gamble that is – they could be worse.
anyway, i'm rambling.ReplyCancel
oh, but I meant to write that an unexpected quality i love about my 'neurotypical' kiddos is that they seem much more open about people with special needs. that makes me SUPER happy. they don't even notice things like that because they live with it, and when they do, they are really accepting – it's just not a big deal. ReplyCancel
thinking about this more, i remembered something from last week. i was talking with my husband's grandfather and caught myself thinking about age prejudice.. like how we condescend to listen to their stories sometimes, or feel like we are being so nice by taking the time to visit. really their worth is not diminished as they age. their importance and significance is just the same. they are the same person they were when they were younger, they have just aged. they have the same value.
anyways, just something else to think about!ReplyCancel
Thank you for doing the spotlight on special needs series. I'm a daily reader though rare commenter. I grew up with disabled family members (deafness, cerebral palsy, etc) but am uncomfortable knowing how to talk to treat differently-abled people in public. Your series has been helpful for making me acknowledge my own discomfort and prejudices and reminded me that we're all just people, no one more perfect than the other.ReplyCancel
Thanks for your comment. Strange how even when we know/live/love people who are different we can still find ourselves in these awkward hang-ups. And I agree…we are all just people and most of us are doing our best. I hope my post didn't come across as accusing but rather, "hey, this happens to all of us–even people in my position–so lets just get it out in the open." Or something…I had a few objectives I guess but it's hard getting everything across just so. ReplyCancel
Self awareness is half of the battle, in my humble opinion. Rather than believing I'm perfectly unprejudiced, I try to be aware of the assumptions that I make. Ideally the self-awareness leads to overcoming them. But let's be real, that isn't going to happen for every bias we have. Self-awareness still lets me correct for my prejudices before I act on them. Like in you story, yea you *thought* "I hope the teacher isn't in a wheelchair" and that's not a great thought to find yourself having, but you caught yourself long before you said that out loud or acted on that thought in any way. We are all works in progress.ReplyCancel
Alexis–absolutely agree. I'm not trying to suggest we can somehow completely eradicate prejudice, but only to get people thinking about the prejudices they do have and then be willing to work on it. My main point in sharing my stories of prejudice was just so that people understand, even someone who is around differences all the time can still make some bone-headed judgements and that's OK. As long as I'm trying to improve and be better. ReplyCancel
Thanks for bringing awareness to special needs and particularly to people to "look" different.
Chalk this up to another wonderful "bonus" to being the mom of a special needs kid – gaining more awareness of our own prejudices. My daughter, like yours, will have very visible physical differences. If I'm completely honest with myself, one of my biggest fears is that because she looks different, people will assume she is mentally disabled as well, and I worry about this limiting her future in subtle, and not so subtle, ways. But this is exactly the problem you are highlighting – we all still have prejudices, and worry about our kids being "labeled" (in my case, though my daughter is special needs, I still don't want her to be classified as mentally disabled – so there is one of my prejudices to overcome!)
ReplyCancel
Carolyn–I get what you're saying. And I don't think you're necessarily being prejudice by not wanting people to make additional assumptions about your daughters capabilities. There is nothing wrong with having mental disabilities, but your daughter doesn't have them–of course you don't want people to think she does and especially not to base that judgement on her appearance.
Sometimes it's sticky walking these lines between not judging others, not wanting others to judge us and wait…who's judging who here? But I get what you're saying. ReplyCancel
What a great post. You say all the things I am too scared to say. I remember the first time some Dr. was talking to me and said "Your son's birth defect….and special needs." I was so angry that they referred to him like that. But you know what-he was born with a birth defect and he does have very special needs. And they aren't bad things. I just had a prejudice of never wanting those words associated with my son. I can now say I have gotten over that but it took a long time. Thanks for all you do!ReplyCancel
Like a previous commenter, I'm in the UK and despite the initial backlash, Cerrie has become one of CBeebies most beloved presenters. It's a channel for pre-schoolers and there are several regular anchors of which she is one – she is truly fantastic and wonderfully engaging with the children. My son is now 3.5 and I don't think he's ever even noticed her difference – and in fact when we've come across children with limb differences he hasn't noticed (whereas he frequently comments on other more obvious difference – hair style, skin colour etc) and I put this down to his day-to-day viewing contact with Cerrie.
The other programme the previous poster mentioned, Something Special, teaches Makaton (a simplified version of Sign Language used to communicate with children with various disabilities that affect their hearing or speech) and it's very popular here to teach babies and preschoolers baby signing or Makaton now which further increases inclusivity. The presenter of Something Special, Justin Fletcher, has been awarded an OBE for his efforts in this area.
I think you've written a very important post – that to reach inside and challenge your own prejudices is vital – especially as a parent, so that you can teach your children how to challenge prejudice within themselves and in others. Hopefully, there is a less prejudiced future ahead for our children.ReplyCancel
very well said. I work at a preschool that is located in a large building that also cares for adults with disabilities, I must say that I have learned A LOT working there. The classroom I work in is integrated, there are 6 children with disabilites (both physical and cognitive) and 6 "typically developing" children. The kids see around their friends disabilities, they hardly even notice the wheelchairs, walkers, oxygen tanks, prosthetics, etc. When I started working there I was comfortable with the kids no matter what their disability was, but I was a little nervous around the adults. Now, I know most ofthem by name and love chatting with those who are able to talk, and waving and saing hello to those who use different forms of communication:) I still get a bit uncomfortable every now and then but I must say that i have learned alot from my little preschoolers about acceptance.ReplyCancel
I'm a long time follower, but haven't commented before. My sister-in-law (R.B.) and family were in your ward in Cincy. Anyway, this post is really making me think. My sister is 30 weeks pregnant with her first and the baby has just been diagnosed with Dandy-Walker Malformation. You can look that up if you want. Dandy-Walker aside, the syndrome often comes with other challenges andas a family, we are realizing that this child will be a very different experience for us. Other than some interactions with differently abled children, I haven't had too many relationships with them. So I'm now asking myself the same questions. I already love our little niece/nephew– that's not the question. But how do I overcome my initial discomfort or shyness with a child whose needs I've never experienced? How do I talk to my girls about my sister's baby and help them overcome any uncertain feelings they have? This post is perfectly timed and very well written. Thank you.ReplyCancel
LOVE, LOVE, LOVE this post!! Ironically enough, I am not a huge blogger, but seemed to be sucked into yours. You have a way with your words! I had the same realization not too long ago, with a similar situation. Why is this? I've even at one point had the thought What if I have another special needs kids, one without autism, and I was scared and again uncomfortable. Sad truth. Guess I am in need of some self-reflection!!ReplyCancel
First I must say I love you blog. SNSL is awesome. I used to think I wasn't prejudice until I had my daughter, Alicen. She is 8 now but the minute I had I her I started seeing things differantly. She goes to a special school in Mattoon Illinois, Franklin School. On her first day I was so scared because I didn't know what to think, say or do with myself. I literally felt lost in a huge sea of "differantly abled" children. Up to the first day of school the only child I was with was Alicen and she doesn't "look" disabled in the way I thought they looked, other than her wheel chair that is the only way someone would know that she was diabled, I don't like that word anymore. Yes I would say that I am still prejudiced, but I think in a differant sence of the word, maybe. I remember leaving the school that first day saying to my husband You know, we really can do this, because we are not alone, not like I thought we were. Again I love your blog and your girls are adorable.
Thanks for your very thoughtful post. My brother has a nephew who is blind. My kids (six and four) met him a couple of months ago and wouldn't speak to him. I guess they were nervous. Secretly, I was sort of delighted because it gave me the chance to talk to them about people who are different on the outside but the same on the inside. We talked about a couple of other people we know, including a neighbor (she is 19) who has a limb difference. We had a wonderfully candid discussion during family home evening, and it was great to be able to tie in how we are all Heavenly Father's children and He loves us. I am working harder at being kinder and friendlier to others who are different from me, too.ReplyCancel
i love what youre doing with your blog…i've actually never commented on a strangers blog before but…just to drive your point home, i think you should know even people in wheelchairs think "prejudiced thoughts" or whatever youd like to call it….
my older sister has spinia bifida and has always been in a wheelchair. i still remember when she met a friend of a friend from her basketball team who was born with no limbs. remember, my sister is girl who has a group of friends with a variety of limbs missing, limbs not functioning, senses that dont work, etc etc, that call themselves "the crips" (as in cripples, not the gang). she is not some one who hasnt had experience with people that look different. yet as she tells it, when she met him she was thinking " zero limbs! no legs! no arms! we were all going out to dinner and i couldnt stop staring at him. me! the girl in the wheelchair who hates being stared at couldnt stop staring at the guy in the wheelchair. i felt like a horrible person. i was so distracted when everyone ordered food…i could stop thinking about how he was going to eat the hamburger he just ordered! but sure enough the waiter put his plate down and he just bent down and started eating. no big deal." they became close friends after that. the next year at her birthday party, i got made fun of after i offered to go get drinks for a few people. as i started walking over to the table i realized i didnt know what to do with his drink. how would i hand it to him!? i must have looked panicked as i walked over because they all laughed at me when i got closer and said "you have no idea where to put that drink, right?" ReplyCancel
They crips a great group. They all still make fun of me awkwardly walking around holding a rum and coke and pretending I wasn't freaking out. I've definitely seen people get uncomfortable around their humor, like when my sisters fiance takes off his prosthetic leg and says 'Hey hold this for a second'. Not to say that they don't have to deal with frustrating situations…it is by no means always a comedy show with them, but, I have never met people with better attitudes. I think a lot of people would benefit from hanging out with them for a bit. ReplyCancel
Confession: I'm a little nervous responding to this post because I'm afraid something I write will inadvertently offend someone. But I guess running and hiding won't solve anything either…
I have a 3 year old daughter who is very curious and is constantly asking questions. I also have a 10 year old nephew with mild autism, and so far my daughter hasn't questioned why he's different. Other than him, we don't really know anyone else with special needs. I know the time will come soon when Jane sees someone in public and will want to know why they are different. I hope that when put on the spot I will have a good answer for her, but I have to admit it makes me nervous. I feel like I only have one chance to make the right impression with her. I'm also afraid that something will innocently come out of her mouth that would offend someone. I'm really glad you started the Special Needs Spotlight because I am now more likely to instigate a conversation with the person in question.
Now for a prejudice(?) of my own: it is usually my knee-jerk reaction to feel sorry for someone with special needs, as in, I feel guilty that I have certain abilities that they don't. I am sad that their lives are more difficult because of something completely out of their control. I'm pretty sure that no one with special needs would appreciate being pitied, so I'd like my feelings about this to change. Is that something you'd mind discussing?ReplyCancel
Great post! Really makes you think about what prejudices we all carry around with us.
By the way, if you're interested I found this petition:
Here's a link to a petition you can sign that is asking Ann Coulter to apologize and to quit using the word retard:
http://www.change.org/petitions/ann-coulter-public-apology-for-constantly-using-the-r-word?utm_source=action_alert&utm_medium=email&utm_campaign=12502&alert_id=btTkuxgLSi_ufIGhrgdmwReplyCancel
i love love love this post so much. i spend all day everyday working with kids with special needs, and i love them with all of my heart. BUT, this post is so completely real and true. thank you for sharing and helping us see that we are all prejudice in our own way. besides the truth to it all, your writing is amazing. i loved it so much i'm linking it as one of my favorite posts of the month. http://aubreyzaruba.blogspot.com/2012/10/fave-post-of-month.htmlReplyCancel
first of all you must be wondering why u got a response on this old post suddenly…I discovered your blog recently and I am kind of addicted to it now 🙂 You writing is so wonderful, honest, clear and full of love.
This is a wonderful topic and yes I totally agree that everyone is prejudiced..but what makes it better is realizing that one is prejudiced and working towards it. People just take it for granted and think it is ok to be like that…I am sure I have lot too and after moving to this country I seeing people from different backgrounds and countries, I realized that everyone has equal rights in this world and change starts from within to actually see that happen.
I found your post and loved it. Our daughter has cognitive disablities from a brain tumor and treatment she survived. It is so wonderful to run onto people that can write about their thoughts and feelings, not everyone has that ability…and by that I don't mean "the guts" to write it…I mean the ability to take raw emotion and but it down in words. Thank you for the gift. I understand every word you write above. Thanks. It helps me move onto the next level. ReplyCancel
Thanks for adding to my feelings of hopelessness about life.
I've been that teacher with a disability that you didn't want your child to have. It hurts – it hurts forever. Even if it was just a fleeting thought of yours, it stays with others when you articulate it. Most people would just dismiss such a thought, but you'd probably tell her (or him) Leave it to a parent of a PWD.
Honestly, this post seems sort of self serving – like you're saying – "look at me, How enlightened." Truth is, we all have fleeting a$$ wipeish thoughts about each other – I do it about my perfect looking, young rich neighbor and I do it about the homeless guy. I even do it about myself – but I don't think of them as evidence of prejudice. They're just several of the 1000 nutty thoughts I have everyday. Sometimes, I think unreasonably nice things about the same people too. And I'd bet it's the same for most people. But by making it about disability – like your only crazy thoughts are about disability, you just seem like a closet ableist. I'm sure you think people don't have these very same thoughts about you but because of your hair, your clothes, your accent, your politics, your whatever but somebody out there things about you what you think of people with disabilities. Someone has crazy negative thoughts about you. Only they recognize it means nothing. You on the other hand…
And as for the woman with the limb difference who you never feel quite comfortable with…do you ever think about what she might be thinking bout you???ReplyCancel
Sure, we all do have nutty thoughts–some fleeting, some not–about people around us all the time. And OF COURSE people with disabilities are allowed to have negative thoughts about me–I don't find that shocking or out of the question. I'm sorry hearing this hurts your feelings, but you're wrong in thinking that I would have said something to a person's face. I wouldn't. AND you're also wrong in thinking a fleeting thought can't be more hurtful in the long run. Fleeting thoughts can be the underlying beliefs we don't admit to, which can lead to exclusion, and more. That was basically the point of my article. While I think it would be stupid for everyone to go around and shouting their negative thoughts from the rooftops–or telling them to people's faces–admitting them to yourself is pretty important if you want to actually change. The reason I shared mine was so others would maybe feel a little better about admitting their own prejudice thoughts, and then then ideally change those thought patterns.
I do think this is an important yet touchy subject to address and I'm sure I could have articulated it better.ReplyCancel
Kids are so good at enjoying the sweet and simple things in life. Dirt, rocks, grass, a little purple planter, and the company of a sister. Sometimes I hate the pressure I feel in this digital age to capture every moment–blog about it, instagram, FB, tweet, print it out, scrapbook it and make sure...
I’ve been meaning to do a series of photo editing tutorials from my favorite on-line editing tool Pic Monkey. However, when I hopped on yesterday I got super distracted with their Halloween editing tools. I planned to just play around for a few minutes and ended up creating an array of spooky family photos. If...
CEI is an online based clipping path and image masking service provider that provides high quality photoshop clipping path service at affordable rate.ReplyCancel
Super editing! Just a quick note to tell you that I have a passion for the topic "Photo editing issue" at hand. You know I was seeking for to know and see something new. Thanks!
Photo editing servicesReplyCancel
This photo editing looks great! I just want to learn this ASAP.
Thanks for sharing this information and beautiful picture.They are really stunning… You did a great job of Image Editing ServicesReplyCancel
It was a decent post in fact. I completely delighted in understanding it in my lunch time. Will unquestionably come and visit this blog all the more regularly. A debt of gratitude is in order for sharing. action photoshop
ReplyCancel
Thanks for the author posting such an interesting post. Highly recommend to everyone. Thanks for sharing. best lightroom presets
ReplyCancel
unbelievable post, really i appreciate it. Thanks a lot for your nice sharing.
Clipping Path / Clipping Path service / new movies / civil engineering /
WordPress SpecialistReplyCancel
To finish up, on the off chance that you require the most expert and uncompromising take a gander at your site and an all around outfitted picture portrayal of your items then it is best to go for administrations that are utilized to deal with such undertakings with incredible accuracy. Photo masking
ReplyCancel
Software publisher's graphics are grouped into vector graphics, 3D modelers and bitmap editor. A designer manages, enhances and transforms images with these primary tools. Photo Editing
ReplyCancel
Even an uninteresting photograph can be transformed into an eye-catching one through editing. Jewelry photo retouching
ReplyCancel
On the off chance that you need to include more creatures in your ranch photo, you can likewise do it through the cloning apparatus. pinkmirror
ReplyCancel
Well your Halloween photo editing . I like your creative job and appreciate this post . Image Masking Service | Remove White Background | Product Photo EditingReplyCancel
I must thank you for sharing this useful topic. Really a worth reading post ! it explains it all so easliy ! thank you for sharing this article !!
https://www.photoeditinghq.com/ReplyCancel
Hi. My name is Amanda and I am married to my best friend Neil. We have 2 wonderful little boys. Carter is 4 and Jackson is 17 months old. After having 90% of his small intestine removed on day 1, Jackson is left with a condition called Short Bowel Syndrome… AKA Short Gut. There is...
Sorry i forgot to mention that part. The main artery that should have supplied blood flow to the intestines was weak. The surgeon said his small bowel looked like a big chain of sausage links. Since there was little to no blood supply to the bowel they were basically dead and had to be removed. ReplyCancel
Wow. Very inspiring story. I have never heard of that condition before too. It sounds hard, but seeing Ms. Amanda's positive attitude now, I can see everything will be alright. Just by looking at Jackson, you can already tell that he's a wonder child. You're right Amanda, we can't fix everything. But we can accept them, right? I salute you!ReplyCancel
My nephew has Eosinophilic Enteritis with less than 10 foods he's allowed to eat at this point in time (hopefully more as they discover what his body can take) so he also does not have the typical social experiences associated with food. It feels good to know that there are others who understand and other little boys who learn to celebrate birthdays differently, but happily 🙂 I admire your daily hard work and positive attitude- thanks for uplifting me and teaching us about short bowel syndrome.ReplyCancel
What an adorable little boy he is! And his big brother is a cutie, too. My brother recently had a feeding tube inserted and can't take anything by mouth, possibly never. We never realized how much life can revolve around food until now. I'll sure be praying for sweet Jackson's steady progress!ReplyCancel
I really do love and appreciate this series. Last week I was at a coffee shop and a little girl came in and sat down next to my son. I invited the mom to sit by me as there wasn't much space. Her daughter had devices hooked up to the back of her head and was using hearing devices as well. Because of this series, I knew it would be okay to ask this mother about her daughter, what her circumstances were. It was an amazing experience and I could tell the mother was grateful for the chance to talk about her beautiful daughter and explain what their lives were like. I would never have had the courage to have asked before and my son might have missed out on an opportunity to play with this sweet girl. Thank you, thank you, thank you!ReplyCancel
Jackson is adorable. It is so nice to read about another mom with a situation similar to mine. My 16-month-old daughter (our fifth child) lost most of her terminal ilium on the day she was born due to a duplication cyst on her small intestine. After three months on TPN in the NICU, and four surgeries later, she was able to come home. We have never been on the charts for weight (sigh), and see a GI specialist regularly, but we are grateful for the progress she has made. She is active, happy, and smart, and I have to remind myself that amidst all the diarrhea and food struggles, we are in a good place. Were you at Primary's? Maybe we overlapped. 🙂 Best wishes to you and your cute family!ReplyCancel
Hey, I'm Amy!
I'm an author, artist, and disability advocate. I live with my handsome husband and three beautiful daughters in Cincinnati, Ohio.
categories
purchase when charley met emma
Let's be friends!
© 2025 This Little Miggy|ProPhoto Blog Template|Designed by Hirschi Creative
Oh my gosh, oh my gosh, oh my gosh…I wish I could come over to your house and play right now. I simply can't take Lampy…she KILLS me! And seriously, PSP, you are your mother's daughter. Fhgwagads. And Bracken, ow ow! Nice moves.
That was so completely hilarious! I love the way PSP & Lamp interact. Such firecrackers, the two of them! And I've always suspected such talent had a stage-dad behind it. 🙂
I love Lamp's background vocals..but then she takes the lead "BACK TOGETHER" at one point, belting it out. I hope taylor swift (or ellen) sees this! 2 stars on your hands!
Holy smokes that video was awesome! I see it going viral 😉
Miss these girls! Truely talented … 😉 I LOVED your vintage bride and groom costumes and am glad you got in on a halloween mystery party.
OMGosh… the video is precious!
Love the video! My almost 4yo. has been singing this all the time. I'm due to deliver my second daughter in two days and – the thought of TWO little girls singing? – just The Best. Thanks for sharing!
ha ha ha ha ha ha ha! That is the best ever 😀
Someone needs to send this to Taylor Swift. Miss PSP and Lamp need to meet her….maybe Ellen can arrange that??? hehehe
Love, Love this! All my little ones (and their teenage siblings) sing this. The song is so addictive. Gets stuck in your head. And how do they know all the words? Can't wait for my kiddos to watch this. They will love it : ) Jan
Holy. O. M. Gsh!! So amazing! And B… for reals?? His dance moves are amazing:) haha! I'm dying here! And they remind me so much of my girls I wish we lived closer!! Love. it.
Bravo! That video is incredible.
bahahaha! So funny! Isn't it amazing how kids pick up on songs? And your hubs! Mine would kill me if I'd posted that, but he would have def been dancing like that too 🙂
Ohhh wow! That's hilarious and so cute! I love it!! Thanks for sharing!
That video is amazing! Marry me, W family!!
Sorry I am late to this party…'Cause that was AWESOME.
Your husband is hilarious. He almost made me think of a stage mom singing in the wings.
PSP has some great facial expressions. She knows how to emote. The part where she acted out the line about the Indy record was incredible…and that Lamp? So awesome.