India Doll

This is Delvin. Isn't he cute!? He's the child we sponsor through Mayan Families. Last year, Eli decided to give $25 of his birthday money to Mayan Families and it just so happened that Delvin's family went to the Mayan Families office asking for food at the same time. When we found out that Delvin needed sponsorship to go to school - and that he's in the same grade as Eli and the same age (4 days apart!) we knew we had to sponsor him.
Delvin is 7 and is in the first grade. He lives in Panajachel, Guatemala. He has three brothers and three sisters. A year ago, his dad died and this past May, his grandfather passed away. His grandfather was the main income earner in the family and they've been really struggling since then. Actually, they were struggling A LOT before then, so the situation now is pretty dire.
One thing that's been on my heart for a long time is that Delvin and his older siblings sleep on the floor. And it rains a lot in Guatemala, so basically they're sleeping in the mud. And that breaks my heart.
We'd love to be able to buy two beds, two mattresses, and four sets of blankets for Delvin's family. Yes, they'll have to share beds, but it's culturally acceptable. In order to do this, we need to raise $400.
That's where Delvin's Dolls comes in! You see, my friend Amy is doing a blog roundup of all the things people are selling to raise money for adoptions or orphans or charities. And, honestly, I'm not crafty at all. Need I remind you that I made a "D" in 8th grade home ec? But I love the idea of clothespin doll ornaments and thought I'd give it a try. So I'd like to introduce you to Delvin's Dolls! Each doll is $15, which includes shipping, and all profits (about $10 per doll) goes towards buying Delvin and his family some beds. If we meet our goal and any extra money is raised, it will go towards Delvin's school fees and, hopefully, maybe, we'll be able to send some of Delvin's siblings to school next year! Wouldn't that be awesome??
There are five dolls to choose from - China, Ethiopia, Guatemala, India, and Korea. I'll have pictures of the Indian & Korean dolls posted by Monday. Each doll is about 5 inches tall and is ready to hang on your Christmas tree! Don't want your doll to be an ornament? Just let us know and we'll be sure to send your doll "hook-free". Each doll comes with a little stand and would look adorable sitting on your shelf!
Sim turned an old washing machine box into The Mystery Machine Van and we all went as the Scooby-Doo Gang.
Nandi (aka "Little Diva") insisted on being Daphne because "Mommmmmy! You look just like Velma!"
I refused to spend $24.99 on a red "Daphne" wig... but I think she looks really beautiful with her dark hair.
The green scarf around her neck was fashioned out a pair of old green tights. Reduce. Reuse. Recycle!
Eli met up with a friend from school (aka Darth Vader) and I had to take a pic because "Hooray! Eli has friends!!". That's actually a big deal if you've been following our blog for awhile.
And do you like the soul patch? Kudos to you, Mr. Sharpie Marker.
The wig is one of those cheap Donald Trump wigs from Walmart. We hacked it off with a pair of scissors and turned it sideways and voila! Hello, Shaggy.
The whole gang... Fred, Velma, Daphne, Velma, Scooby, and The Mystery Machine Van.
Hope you all have a great Halloween that's full of wonderful memories, Reese's Peanut Butter Cups and ghost and ghoul free!
First up, which you'll find in the picture above, are stability balls. I love these! They're my favorite. We use them for everything.. not just Noah's therapy. And, let me tell ya, I'm all about buying Noah equipment that I can use too... especially equipment that promises to firm up my flabby tummy by sitting on it.
Mainly, I sit on one of the balls while I work with Noah on his massage table (you'll hear more about that later). And I also like to sit on one and put Noah on another, hold him by his feet, and roll him back and forth. It really works his trunk muscles... and that kid's got some rocking core strength! We also play "bucking bronco" where he sits on a ball and I grab his legs and start jerking him back and forth and side to side. Warning.. your child MUST have good trunk control for this - otherwise - he'll fall backwards and hit his head on your wood floor.
Don't ask me which kid I tried it with to discover that little gem.
Anyway, we see if Noah can stay on the "bucking bronco" for a count of 8 - and he'll grab my arms before then if he's wanting off. I also like to put him on his tummy and roll him back and forth or bounce him up and down. And another favorite is sandwiching the ball in the corner of a room (you have to stand tight against the ball to keep it from moving) and then I hold Noah's hands while he jumps up and down on the ball. We usually sing songs and such while doing this.
The good thing is that the balls are available everywhere (Target, Walmart, Ross) and are pretty cheap... about $10 - $20 depending on the size. We have the largest size (60cm??) and the one just down from that.
The chair above is Noah's favorite. My mom scored this for about 5 bucks at a garage sale last Christmas. I think it's a video game chair?? Not really sure. It's more of a "Oh my gosh, this chair is perfect for Noah!" chair.
He's constantly in, rocking back and forth. It'll tip all the way back and then he has to use his stomach muscles to pull himself up. And sometimes, he'll drag us to it and we'll sit in it and he'll climb in our lap and we'll go back and forth together - singing songs or trying to read a book.
I don't know exactly how therapeutic it is, but I'm pretty sure it works on one of his sensory issues. Vestibular, maybe? (Man, I should know this stuff!)
Without fail, we can always find Noah on his little yellow swing. And he doesn't care that the whole thing only cost us $25 at a garage sale or that everythings broken on it except the three swings in the middle. He loves that thing. One day, I'd love to get him one of those big wooden ones they sale at Costco and cost the equivalent of a month's salary, but, really, he loves this swing. Doesn't bother him a bit.
He still doesn't know how to swing himself, so I spend a lot of time outside pushing him. But now that he's taller, he can push off a little with his feet. It's not proper swinging, but he still gets the swinging motion from it and he likes that.
Our beloved trampoline. We used to practically live on this thing 4 years ago. I believe we got it at Walmart for about $250 + $100 for the net? I can't really remember. It was definitely worth the money.
Noah doesn't initiate going on it as much as he used to, but when I take him on it, he's all smiles and giggles.
This is the piece d' resistance. Our massage table that my parents snagged at a garage sale for about 15 bucks. They're all over Craigslist, though, so it shouldn't be hard to find one if you need one.
You can tell from the pic that it's in the living room. Basically, it's been everywhere. Our room, Noah's room, Noah's closet. But, I'm pretty much 100% an outta sight - outta mind girl. And if it's not right there in front of me then I won't use it. Which means our living room looks like an Occupational Therapist's dream. Everything is right smack dab in the living room. But, hey, I'm a lot more consistent now with doing Noah's therapies each day than before.
The last piece of equipment... which I forgot to take a picture of because the kids were fighting over it and Sim hid it... is a Bosu Ball.
You can get them at Walmart or Target for about $100, but they're a little cheaper on Amazon. Of course, you have to consider shipping. We got our ball for free from a friend. (Thank you! You know who you are!!)
You can use either side of it. Either side, though, works on your balance and balance activities are some of Noah's favorites.
I hope this gives you an idea of the things we think are essential for Noah's in home "program", so to speak. It took several years to get everything... we've had the trampoline for about 5 years now... and I'm a firm believer in giving gifts that can be used for therapy purposes. (The good thing is that my kids are so used to this that they don't know any different!)
There are a few things that I'd still like to get....an Ipad being the most important. Oh my gosh, have you read about all the apps out there for children with autism? There are some AMAZING reports about nonverbal children using Ipads for communication. I tell you, I have become obsessed with Noah getting one. I'm hoping for Christmas, but it will involve me getting off my rear and cleaning out the garage for a massive garage sale and putting some stuff on Ebay. The wheels are definitely spinning in my head. If you have one and use it for a child with autism, please let me know!
Next time, I'll do a post on some of Noah's favorite things... and things we can't live without. I do plan on doing a post about the exercises we do with Noah, but it'll involve my husband taking pictures... hopefully, he'll have this weekend off.
Have a great weekend!
Photo by liveandlearn.net.au



This is Dr. Rosenthal. He's Noah's chiropractor. And he's really good. (And, no, I didn't take that picture. Come on, now! I swiped it off his website.)
I love chiropractors. They do so much more than just back adjustments. And, honestly, this is just my opinion, I think they're really picking up where a lot of medical doctors leave off - especially in the field of autism. They work with allergies, sensory issues, balance issues. I find the whole field just really fascinating.
Anyway, we've been seeing Dr. R for about the last 16 months. Last summer (2009), we really hit it hard and all three kids saw him twice a week for for about 2 months. We saw enormous changes in Eli that summer. He learned to ride a bike. His balance became stellar (he started walking on ropes tied between two trees. Uh huh, he did!). This was soooo big for a kid who'd been diagnosed by an OT with a coordination disorder 9 months earlier.
Last year, we stopped going as much - mainly because our insurance changed and also because we were trying to save gas by not driving to Dallas so much. But this past summer, at the beginning of June, Noah started having huge meltdowns and started banging and hitting his head over and over again. So we experimented a bit and realized that if we go more than one week without Noah getting adjusted, then he'd start screaming and headbanging.
I don't really understand the science there, but he loves going to see Dr R. He loves getting stretched out and twisted like a pretzel. And it keeps him happy. So we do it.
Anyway, Dr. R adjusts Noah and does certain exercises with him each week and then gives us homework. I love that part! No, really, I do. I love being a part of Noah's therapy and seeing small bits of progress here and there.
Now, honestly, I can't really - in a medical type way - explain exactly what Dr R does. It involves phrases like "firing up neutrons" and "getting both sides of the brain to communicate" and other stuff that just flies straight over my head.
What I can tell you is that it involves cranial sacral therapy (which is on top of my "I really really recommend this therapy" list, body adjustments, stretching, balance games, and exercises.
And while I'll go over the exercises and equipment used in another post... just to give you an idea though, at home, we follow Dr R's exercises for Noah by using a large stability ball, a bosu ball, and a massage table. Most of the stretching is done with Noah on a massage table (that we bought at a garage sale) while I sit on a stability ball. I do a lot of foot stretching and massaging (remember, Noah also has cerebral palsy), midline crossing... cross crawl patterns, body brushing, massaging, etc. Noah stands on the bosu ball and does Captain Morgans against the wall to open up his chest (he leans forward while he walks and this has really helped his posture). We sit him on the stability ball and play "bucking bronco" while holding onto his feet. He looooves this! We'll put the stability ball in a corner and hold Noah's hands while he hops up and down on it. We'll put him in a swivel chair and spin him around and around. Things like that.
It looks really easy.... all these things that Dr R does in his office. And, I admit, there was a time when I thought to myself... "This is really nothing. I can get all of this at OT. I don't understand. How is this helping? Am I wasting my time? Am I wasting my money?" And, truthfully, if our insurance hadn't changed (again!) and allowed us to see him for less than we had been paying before, I might have stopped. It's only because our insurance changed that we can afford to see him once a week.
However, after going for a year and seeing the difference in Noah from going once a month to once a week and then seeing the change from Noah only going once a week without me working at home with him to seeing the improvements from me working at home with him... (wow, is that a long sentence or what?) I can honestly say that it's a therapy we recommend.
The plus side is that he does accept insurance. Yay! Most people who work with children with autism DON'T take insurance. After we pay our deductible, it only costs us $12.80 a session. Yee haw!
Another plus side is that we only go once a week for 30 minutes and then I get exercises to do at home for the rest of the week. I'm not dragging him here and there and everywhere all week long. I get to spend time with him at home while doing his exercises. I do see progress being made.... it's terribly, painfully slow, but it's happening. And he loves it!
The downside is that it is in Dallas.... so we drive 3 hours RT once a week for a 30 minute appointment. He also has a lot of clients and gets booked up fast. The initial consultation is also a little expensive. But if he takes your insurance and your deductible is met, it can be a really cost effective therapy. Don't expect instant results (although we saw near instant results with Eli), but if you want a slower, non-invasive therapy that your child will probably like and that you can maintain at home, then you'll definitely want to check him out.
Also, if you just strictly want Cranial Sacral Therapy, Dr Adele Kestner works in the same building. We saw her for 3 years and she is amazing. She doesn't take insurance and I think (unless her prices have gone up), she charges $50 for 30 minutes. I will say, though, that cranial sacral therapy is one of my favorite therapies. Noah had really bad headaches and sleep patterns at one time... screaming and screeching and crying all the time. Cranial Sacral Therapy helped relieve that head pressure. In the beginning, we went 3x a week, then 2x, then 1x, then once every 2 weeks, then once every month.
Can you see why we ended up in so much debt? And this was the cheapest therapy we were doing at the time! (And let me tell you... if I had to do it over again, I would. In the beginning, it cost a ton, but I cannot begin to tell you how much cranial sacral helped.)
Both Dr Kestner and Dr R are Christians. They are also both very honest. They care about the patient - not the $$$. In fact, Dr Kestner referred us to Dr Rosenthal because he takes insurance. She knew we'd stop seeing her, but it didn't matter. She really cares about Noah.
You can find Dr Rosenthal's info HERE .
You can find Dr Kestner's info HERE.
Next time, I'll talk about Soma and RPM. We saw Soma last Saturday and Noah blew me away with his smarts!